322 NP_001070868 A604T not found in SNVbox database
371 NP_001070868 K508N not found in SNVbox database
865 NP_001070868 D521N not found in SNVbox database
1185 NP_001070868 W116R not found in SNVbox database
1433 NP_001070868 D567H not found in SNVbox database
1638 NP_001070868 T422A not found in SNVbox database
2145 NP_001070868 V70M not found in SNVbox database
2339 NP_001070868 R423H not found in SNVbox database
2791 NP_001070868 G14R not found in SNVbox database
2826 NP_001070868 N694Y not found in SNVbox database
3419 NP_001070868 F617L not found in SNVbox database
3984 NP_001070868 A594T not found in SNVbox database
4995 NP_001070868 Q348E not found in SNVbox database
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:16257093 C>T maps to NM_015001.2 S1453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:16257093 C>T maps to NM_015001.2 S1453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:17958925 C>T maps to NM_018125.3 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:17958925 C>T maps to NM_018125.3 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:158576524 C>T maps to NM_001004478.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:158576524 C>T maps to NM_001004478.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr2:177034057 C>T maps to NM_006898.4 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr2:177034057 C>T maps to NM_006898.4 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr2:210993850 A>C maps to NM_152519.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr2:210993850 A>C maps to NM_152519.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:21755849 G>A maps to NM_004061.3 Q579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:21755849 G>A maps to NM_004061.3 Q579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:54635835 A>G did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:54635835 A>G did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:138643656 A>C maps to ENST00000394800 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:138643656 A>C maps to ENST00000394800 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:148408100 A>G maps to NM_024577.3 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:148408100 A>G maps to NM_024577.3 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:26407899 A>T maps to NM_007048.5 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:26407899 A>T maps to NM_007048.5 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:42975222 C>T maps to NM_006245.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:42975222 C>T maps to NM_006245.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:117663707 C>A did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:117663707 C>A did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr7:84694821 A>G maps to NM_152754.2 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr7:84694821 A>G maps to NM_152754.2 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr8:27605730 G>C maps to NM_018246.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr8:27605730 G>C maps to NM_018246.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr9:101748354 C>T maps to NM_001855.3 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr9:101748354 C>T maps to NM_001855.3 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:56043917 C>T maps to NM_001004745.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:56043917 C>T maps to NM_001004745.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:61034969 C>T maps to NM_152718.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:61034969 C>T maps to NM_152718.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:65123662 A>G maps to NM_145719.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:65123662 A>G maps to NM_145719.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:66259192 C>T maps to NM_005700.3 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:66259192 C>T maps to NM_005700.3 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:71293805 A>T maps to ENST00000376535 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:71293805 A>T maps to ENST00000376535 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:103090669 T>G maps to NM_001080463.1 L2953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:103090669 T>G maps to NM_001080463.1 L2953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr12:57962798 C>T maps to NM_004984.2 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr12:57962798 C>T maps to NM_004984.2 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr13:19755936 G>A did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr13:19755936 G>A did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:33990172 C>T maps to NM_001036.3 N2075N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:33990172 C>T maps to NM_001036.3 N2075N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:62978868 G>T maps to NM_015059.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:62978868 G>T maps to NM_015059.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:79051879 C>T maps to ENST00000258883 T1651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:79051879 C>T maps to ENST00000258883 T1651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:79051885 G>A maps to ENST00000258883 C1649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:79051885 G>A maps to ENST00000258883 C1649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr16:3640680 G>A maps to NM_032444.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr16:3640680 G>A maps to NM_032444.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr16:20370790 C>T maps to NM_174924.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr16:20370790 C>T maps to NM_174924.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr17:54969321 G>A maps to NM_005082.4 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr17:54969321 G>A maps to NM_005082.4 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:5965621 G>A maps to NM_032485.4 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:5965621 G>A maps to NM_032485.4 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:47845306 C>T maps to NM_017895.7 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:47845306 C>T maps to NM_017895.7 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:56099192 C>T maps to ENST00000423479 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:56099192 C>T maps to ENST00000423479 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:62597693 T>G maps to NM_020713.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:62597693 T>G maps to NM_020713.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr1:203316789 C>T maps to NM_002023.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr1:203316789 C>T maps to NM_002023.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr1:203819751 G>A maps to NM_014827.4 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr1:203819751 G>A maps to NM_014827.4 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr2:198570299 G>T maps to NM_138395.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr2:198570299 G>T maps to NM_138395.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr8:1616639 G>A maps to ENST00000357934 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr8:1616639 G>A maps to ENST00000357934 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr11:1093367 G>A maps to ENST00000441003 T1729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr11:1093367 G>A maps to ENST00000441003 T1729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr11:1093409 C>A maps to ENST00000441003 T1743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr11:1093409 C>A maps to ENST00000441003 T1743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr11:1093451 G>A maps to ENST00000441003 P1757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr11:1093451 G>A maps to ENST00000441003 P1757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr12:123875310 C>T maps to NM_020382.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr12:123875310 C>T maps to NM_020382.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr14:20764584 A>C maps to NM_138376.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr14:20764584 A>C maps to NM_138376.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr17:18137335 C>T maps to NM_004140.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr17:18137335 C>T maps to NM_004140.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr17:79668551 C>T maps to NM_004712.4 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr17:79668551 C>T maps to NM_004712.4 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr19:51219978 G>A maps to ENST00000391814 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr19:51219978 G>A maps to ENST00000391814 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr19:53270591 A>C maps to NM_198457.2 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr19:53270591 A>C maps to NM_198457.2 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr20:5965621 G>A maps to NM_032485.4 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr20:5965621 G>A maps to NM_032485.4 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr21:16338591 G>T maps to NM_003489.3 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr21:16338591 G>T maps to NM_003489.3 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr22:30688747 G>A maps to ENST00000403477 C388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr22:30688747 G>A maps to ENST00000403477 C388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr22:33260925 T>C maps to NM_003490.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr22:33260925 T>C maps to NM_003490.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chrX:70472906 C>A maps to ENST00000373988 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chrX:70472906 C>A maps to ENST00000373988 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chrX:84561265 G>T maps to ENST00000373145 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chrX:84561265 G>T maps to ENST00000373145 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chrX:151869831 C>T maps to NM_005363.2 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chrX:151869831 C>T maps to NM_005363.2 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:23650123 T>C maps to ENST00000414299 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:23650123 T>C maps to ENST00000414299 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:52823498 C>A maps to NM_032449.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:52823498 C>A maps to NM_032449.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:68906684 T>C did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:68906684 T>C did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:9595848 C>G maps to NM_016207.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:9595848 C>G maps to NM_016207.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:68882251 G>T maps to NM_138964.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:68882251 G>T maps to NM_138964.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:128408803 G>A maps to NM_005291.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:128408803 G>A maps to NM_005291.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:201846108 G>A maps to NM_173822.3 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:201846108 G>A maps to NM_173822.3 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:53905309 C>A maps to NM_022899.4 G506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:53905309 C>A maps to NM_022899.4 G506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:3990603 G>A maps to NM_152744.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:3990603 G>A maps to NM_152744.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:141635652 T>C maps to NM_013252.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:141635652 T>C maps to NM_013252.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr9:111617061 G>T maps to NM_006686.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr9:111617061 G>T maps to NM_006686.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:62038407 G>C maps to NM_002411.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:62038407 G>C maps to NM_002411.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:89531567 T>C maps to NM_020358.2 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:89531567 T>C maps to NM_020358.2 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr13:45523878 T>C maps to NM_012345.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr13:45523878 T>C maps to NM_012345.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr13:47269053 G>T maps to NM_001164211.1 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr13:47269053 G>T maps to NM_001164211.1 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr15:65685845 G>A maps to NM_020962.1 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr15:65685845 G>A maps to NM_020962.1 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:40474447 A>G maps to NM_139276.2 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:40474447 A>G maps to NM_139276.2 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:45234385 G>T maps to NM_001114091.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:45234385 G>T maps to NM_001114091.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr1:236760201 C>G maps to NM_018072.5 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr1:236760201 C>G maps to NM_018072.5 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr6:52285246 G>A maps to NM_018100.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr6:52285246 G>A maps to NM_018100.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr6:76604977 G>A did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr6:76604977 G>A did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr6:159191837 G>T maps to NM_001111077.1 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr6:159191837 G>T maps to NM_001111077.1 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr8:103664290 T>A did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr8:103664290 T>A did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr12:125398089 C>T maps to NM_021009.5 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr12:125398089 C>T maps to NM_021009.5 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr13:25376710 T>A did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr13:25376710 T>A did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr15:101938638 A>C maps to NM_002570.3 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr15:101938638 A>C maps to NM_002570.3 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr17:26680001 G>A maps to NM_015584.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr17:26680001 G>A maps to NM_015584.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr19:7174735 C>A maps to NM_000208.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr19:7174735 C>A maps to NM_000208.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr19:7670196 G>T maps to NM_001080429.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr19:7670196 G>T maps to NM_001080429.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr19:55324634 T>C maps to ENST00000396289 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr19:55324634 T>C maps to ENST00000396289 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr20:30584458 C>T maps to NM_001011718.1 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr20:30584458 C>T maps to NM_001011718.1 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr20:30904101 C>T maps to NM_004798.3 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr20:30904101 C>T maps to NM_004798.3 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr1:24676594 C>G maps to NM_021180.3 Y564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr1:24676594 C>G maps to NM_021180.3 Y564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr4:20751287 G>A maps to ENST00000382152 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr4:20751287 G>A maps to ENST00000382152 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:54791831 A>T maps to NM_170587.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:54791831 A>T maps to NM_170587.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:124705462 G>A maps to NM_001003954.1 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:124705462 G>A maps to NM_001003954.1 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:145150821 G>A maps to NM_001916.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:145150821 G>A maps to NM_001916.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr10:118441314 G>T maps to NM_025015.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr10:118441314 G>T maps to NM_025015.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:5905956 C>T maps to NM_001005165.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:5905956 C>T maps to NM_001005165.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:88781127 G>A did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:88781127 G>A did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:101946633 G>T maps to NM_032930.2 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:101946633 G>T maps to NM_032930.2 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr14:102474612 C>A maps to NM_001376.4 S1972S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr14:102474612 C>A maps to NM_001376.4 S1972S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr15:79051879 C>T maps to ENST00000258883 T1651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr15:79051879 C>T maps to ENST00000258883 T1651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr16:15122750 C>T maps to NM_015027.2 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr16:15122750 C>T maps to NM_015027.2 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr17:900588 C>A maps to NM_013337.2 C69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr17:900588 C>A maps to NM_013337.2 C69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr17:72949180 C>A maps to NM_030630.2 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr17:72949180 C>A maps to NM_030630.2 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr18:14757888 C>G maps to NM_001145029.1 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr18:14757888 C>G maps to NM_001145029.1 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr18:31326360 T>C maps to NM_030632.1 N2183N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr18:31326360 T>C maps to NM_030632.1 N2183N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr19:3600347 C>T maps to NM_201636.2 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr19:3600347 C>T maps to NM_201636.2 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr19:54760065 G>T maps to NM_001081442.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr19:54760065 G>T maps to NM_001081442.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr20:31825549 C>T maps to NM_130852.2 Y11Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr20:31825549 C>T maps to NM_130852.2 Y11Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chrX:9912814 C>T maps to NM_001649.2 P1482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chrX:9912814 C>T maps to NM_001649.2 P1482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chrX:70471026 C>A did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chrX:70471026 C>A did not map to a codon.
Sequencing variant TCGA-CH-5743-01A-21D-1576-08 chr17:21203906 T>C maps to NM_145109.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5743-01A-21D-1576-08 chr17:21203906 T>C maps to NM_145109.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5743-01A-21D-1576-08 chr21:34635096 G>A did not map to a codon.
Sequencing variant TCGA-CH-5743-01A-21D-1576-08 chr21:34635096 G>A did not map to a codon.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr1:12726316 C>T maps to NM_001013630.1 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr1:12726316 C>T maps to NM_001013630.1 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr1:181725166 C>T maps to ENST00000357570 Y1355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr1:181725166 C>T maps to ENST00000357570 Y1355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr1:197313414 A>G maps to NM_201253.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr1:197313414 A>G maps to NM_201253.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr2:55561489 C>A maps to ENST00000436346 E823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr2:55561489 C>A maps to ENST00000436346 E823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr3:51101985 G>A maps to NM_004947.4 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr3:51101985 G>A maps to NM_004947.4 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr3:51102012 G>A maps to NM_004947.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr3:51102012 G>A maps to NM_004947.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr3:112993396 T>C maps to ENST00000273395 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr3:112993396 T>C maps to ENST00000273395 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr6:29797405 G>A maps to ENST00000376828 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr6:29797405 G>A maps to ENST00000376828 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr6:29797435 T>C maps to ENST00000376828 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr6:29797435 T>C maps to ENST00000376828 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:118343970 T>C maps to NM_001197104.1 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:118343970 T>C maps to NM_001197104.1 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:123893784 C>T maps to NM_001001953.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:123893784 C>T maps to NM_001001953.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:123909642 G>A maps to NM_001004463.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:123909642 G>A maps to NM_001004463.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr12:50474349 C>A maps to NM_020039.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr12:50474349 C>A maps to NM_020039.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr12:101876610 A>G maps to ENST00000299272 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr12:101876610 A>G maps to ENST00000299272 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr16:3440103 T>A maps to ENST00000396852 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr16:3440103 T>A maps to ENST00000396852 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:17950418 T>A maps to NM_000215.3 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:17950418 T>A maps to NM_000215.3 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:50248601 C>T maps to NM_021733.1 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:50248601 C>T maps to NM_021733.1 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:53117460 C>T maps to NM_018300.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:53117460 C>T maps to NM_018300.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:58565059 C>A maps to NM_182572.3 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:58565059 C>A maps to NM_182572.3 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chrX:70280883 C>A maps to NM_013346.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chrX:70280883 C>A maps to NM_013346.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr3:197497067 G>A maps to NM_032288.6 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr3:197497067 G>A maps to NM_032288.6 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr6:3850734 C>T maps to NM_012135.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr6:3850734 C>T maps to NM_012135.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr8:144995012 G>T maps to NM_201380.2 I3129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr8:144995012 G>T maps to NM_201380.2 I3129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr10:115527187 C>T maps to NM_182601.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr10:115527187 C>T maps to NM_182601.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr12:125397357 T>C maps to NM_021009.5 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr12:125397357 T>C maps to NM_021009.5 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr16:11785488 G>A maps to ENST00000356957 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr16:11785488 G>A maps to ENST00000356957 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr16:27782956 G>A maps to NM_015202.2 P1394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr16:27782956 G>A maps to NM_015202.2 P1394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr17:10430103 G>A maps to NM_017534.5 N1333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr17:10430103 G>A maps to NM_017534.5 N1333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr17:37830250 G>A maps to NM_033419.3 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr17:37830250 G>A maps to NM_033419.3 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr20:61444844 G>A maps to NM_007346.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr20:61444844 G>A maps to NM_007346.2 P626P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CH-5745-01A-11D-1576-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CH-5745-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chrX:70344180 T>C maps to ENST00000333646 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chrX:70344180 T>C maps to ENST00000333646 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chrX:153200993 G>T maps to NM_002910.5 Y371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chrX:153200993 G>T maps to NM_002910.5 Y371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr1:26691328 C>A maps to ENST00000436292 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr1:26691328 C>A maps to ENST00000436292 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr2:202591576 G>T maps to NM_020919.3 R998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr2:202591576 G>T maps to NM_020919.3 R998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr3:148786107 C>T maps to NM_003071.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr3:148786107 C>T maps to NM_003071.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr5:133914475 G>A maps to ENST00000448712 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr5:133914475 G>A maps to ENST00000448712 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr6:35930383 A>C maps to NM_052961.3 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr6:35930383 A>C maps to NM_052961.3 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr6:43183064 G>T did not map to a codon.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr6:43183064 G>T did not map to a codon.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr8:22974414 G>A maps to ENST00000356864 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr8:22974414 G>A maps to ENST00000356864 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr8:87563329 T>G did not map to a codon.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr8:87563329 T>G did not map to a codon.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr8:144945348 G>T maps to NM_031308.1 Y691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr8:144945348 G>T maps to NM_031308.1 Y691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr9:111718090 G>T maps to NM_003798.2 Y536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr9:111718090 G>T maps to NM_003798.2 Y536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr10:115422473 A>G maps to ENST00000369358 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr10:115422473 A>G maps to ENST00000369358 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr11:10622487 G>T maps to NM_001098579.1 S656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr11:10622487 G>T maps to NM_001098579.1 S656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr12:120899911 G>T maps to NM_003769.2 Y192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr12:120899911 G>T maps to NM_003769.2 Y192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr16:30731616 A>C maps to NM_006662.2 P984P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr16:30731616 A>C maps to NM_006662.2 P984P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr17:38938610 G>A maps to NM_181537.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr17:38938610 G>A maps to NM_181537.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr17:45219281 G>A maps to NM_001114091.1 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr17:45219281 G>A maps to NM_001114091.1 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr18:3075745 G>A maps to NM_003803.3 A1554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr18:3075745 G>A maps to NM_003803.3 A1554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr19:11558390 G>A maps to ENST00000436195 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr19:11558390 G>A maps to ENST00000436195 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr19:22363642 C>T maps to NM_001001411.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr19:22363642 C>T maps to NM_001001411.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr22:24622216 C>A maps to NM_001099781.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr22:24622216 C>A maps to NM_001099781.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr1:55457538 C>T maps to NM_182532.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr1:55457538 C>T maps to NM_182532.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:38818745 G>C maps to NM_138394.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:38818745 G>C maps to NM_138394.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:109381815 G>A maps to NM_006267.4 E1607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:109381815 G>A maps to NM_006267.4 E1607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:193056698 T>C maps to NM_016192.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:193056698 T>C maps to NM_016192.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:232577518 C>T maps to ENST00000409321 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:232577518 C>T maps to ENST00000409321 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr3:141497116 G>A did not map to a codon.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr3:141497116 G>A did not map to a codon.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr3:154042070 A>C maps to NM_020865.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr3:154042070 A>C maps to NM_020865.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr4:8235131 G>A maps to NM_018986.3 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr4:8235131 G>A maps to NM_018986.3 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr4:48994015 T>C maps to NM_025087.2 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr4:48994015 T>C maps to NM_025087.2 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr5:140559492 C>T maps to NM_019120.2 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr5:140559492 C>T maps to NM_019120.2 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr6:87725480 C>A maps to NM_000865.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr6:87725480 C>A maps to NM_000865.2 I143I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5748-01A-11D-1576-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CH-5748-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr9:94495689 C>T maps to NM_004560.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr9:94495689 C>T maps to NM_004560.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr9:138378218 C>T maps to NM_014811.3 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr9:138378218 C>T maps to NM_014811.3 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:721930 C>T maps to NM_022772.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:721930 C>T maps to NM_022772.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:1093511 C>A maps to ENST00000441003 T1777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:1093511 C>A maps to ENST00000441003 T1777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:59282921 C>T maps to NM_001004711.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:59282921 C>T maps to NM_001004711.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:108032026 A>G maps to NM_002519.2 S1262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:108032026 A>G maps to NM_002519.2 S1262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr12:7177942 C>T maps to NM_001734.3 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr12:7177942 C>T maps to NM_001734.3 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr12:117768454 C>T maps to ENST00000338101 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr12:117768454 C>T maps to ENST00000338101 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr13:39262557 T>C maps to NM_207361.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr13:39262557 T>C maps to NM_207361.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr16:3786755 A>G maps to NM_004380.2 H1485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr16:3786755 A>G maps to NM_004380.2 H1485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr16:51173558 G>A maps to ENST00000251020 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr16:51173558 G>A maps to ENST00000251020 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr17:33462275 C>T maps to NM_018096.3 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr17:33462275 C>T maps to NM_018096.3 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr17:39742893 G>A maps to NM_000526.4 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr17:39742893 G>A maps to NM_000526.4 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr17:39742897 G>A maps to NM_000526.4 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr17:39742897 G>A maps to NM_000526.4 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr19:10798202 G>C maps to NM_017620.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr19:10798202 G>C maps to NM_017620.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr19:22940553 A>G maps to ENST00000397104 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr19:22940553 A>G maps to ENST00000397104 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr20:4770304 G>A maps to NM_014737.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr20:4770304 G>A maps to NM_014737.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr20:18142563 A>G maps to NM_020536.4 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr20:18142563 A>G maps to NM_020536.4 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr22:44892838 G>A maps to NM_032287.2 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr22:44892838 G>A maps to NM_032287.2 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr1:108247661 A>G maps to NM_006113.4 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr1:108247661 A>G maps to NM_006113.4 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr1:110950281 G>A maps to NM_006402.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr1:110950281 G>A maps to NM_006402.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr2:79349166 C>T maps to NM_002909.4 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr2:79349166 C>T maps to NM_002909.4 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:41382447 G>A maps to NM_001005473.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:41382447 G>A maps to NM_001005473.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:131531125 C>A maps to NM_001142599.1 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:131531125 C>A maps to NM_001142599.1 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:149755318 C>T maps to ENST00000451292 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:149755318 C>T maps to ENST00000451292 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr6:28227391 C>T maps to NM_001007531.1 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr6:28227391 C>T maps to NM_001007531.1 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr6:160237000 T>C maps to NM_173516.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr6:160237000 T>C maps to NM_173516.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr7:27565970 G>A maps to NM_152740.3 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr7:27565970 G>A maps to NM_152740.3 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr8:113657356 A>T maps to NM_198123.1 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr8:113657356 A>T maps to NM_198123.1 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:88650292 A>G maps to ENST00000376023 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:88650292 A>G maps to ENST00000376023 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:97080947 A>G maps to NM_017561.1 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:97080947 A>G maps to NM_017561.1 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:100971251 G>A maps to NM_018421.3 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:100971251 G>A maps to NM_018421.3 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:116858373 C>A maps to ENST00000259410 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:116858373 C>A maps to ENST00000259410 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr10:51584845 G>A maps to NM_001145260.1 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr10:51584845 G>A maps to NM_001145260.1 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr12:32764088 T>C maps to NM_139241.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr12:32764088 T>C maps to NM_139241.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr12:123875310 C>T maps to NM_020382.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr12:123875310 C>T maps to NM_020382.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr13:21557699 G>A maps to NM_014572.2 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr13:21557699 G>A maps to NM_014572.2 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr13:45523878 T>C maps to NM_012345.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr13:45523878 T>C maps to NM_012345.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:7657341 T>G did not map to a codon.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:7657341 T>G did not map to a codon.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:19041571 T>C maps to NM_024847.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:19041571 T>C maps to NM_024847.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:31499067 G>A maps to ENST00000431354 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:31499067 G>A maps to ENST00000431354 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr17:1840947 G>A maps to NM_178568.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr17:1840947 G>A maps to NM_178568.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr17:6673969 T>C maps to NM_017523.2 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr17:6673969 T>C maps to NM_017523.2 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr19:10335296 A>T maps to NM_004230.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr19:10335296 A>T maps to NM_004230.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr19:20026166 C>T maps to NM_031218.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr19:20026166 C>T maps to NM_031218.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr19:46020978 C>A maps to NM_003370.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr19:46020978 C>A maps to NM_003370.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr20:61525226 G>A maps to NM_033081.2 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr20:61525226 G>A maps to NM_033081.2 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chrX:118604366 C>T maps to NM_001152.4 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chrX:118604366 C>T maps to NM_001152.4 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chrX:140985037 C>T maps to NM_138702.1 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chrX:140985037 C>T maps to NM_138702.1 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr1:115005787 G>A maps to NM_015906.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr1:115005787 G>A maps to NM_015906.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr5:140865885 C>T maps to NM_018928.2 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr5:140865885 C>T maps to NM_018928.2 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr6:25472739 G>T maps to NM_017640.5 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr6:25472739 G>T maps to NM_017640.5 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr6:33377449 C>T maps to NM_002263.3 Q669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr6:33377449 C>T maps to NM_002263.3 Q669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr7:86848786 G>A maps to NM_024315.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr7:86848786 G>A maps to NM_024315.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr8:21768189 C>T maps to NM_003974.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr8:21768189 C>T maps to NM_003974.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr10:52595981 G>T maps to NM_138932.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr10:52595981 G>T maps to NM_138932.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr11:28058050 A>G maps to NM_031217.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr11:28058050 A>G maps to NM_031217.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr11:65793238 G>A maps to NM_053054.3 H204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr11:65793238 G>A maps to NM_053054.3 H204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr12:22035726 G>A maps to NM_005691.2 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr12:22035726 G>A maps to NM_005691.2 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr12:52680992 C>T maps to NM_002281.3 Q380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr12:52680992 C>T maps to NM_002281.3 Q380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr14:66208992 G>C maps to NM_178155.1 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr14:66208992 G>C maps to NM_178155.1 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr16:84402274 G>C maps to ENST00000416219 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr16:84402274 G>C maps to ENST00000416219 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr19:3661951 G>T maps to NM_012398.2 Y89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr19:3661951 G>T maps to NM_012398.2 Y89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr22:42524923 A>G maps to NM_000106.4 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr22:42524923 A>G maps to NM_000106.4 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:27755319 G>A maps to NM_006990.2 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:27755319 G>A maps to NM_006990.2 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:89587610 G>C maps to NM_004120.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:89587610 G>C maps to NM_004120.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:158612200 C>T maps to NM_003126.2 K1579K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:158612200 C>T maps to NM_003126.2 K1579K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr2:131096731 G>C maps to NM_032357.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr2:131096731 G>C maps to NM_032357.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr2:171862700 A>G maps to ENST00000360843 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr2:171862700 A>G maps to ENST00000360843 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr3:45761022 A>G maps to NM_014016.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr3:45761022 A>G maps to NM_014016.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr3:176755960 C>G did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr3:176755960 C>G did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:9629678 G>A maps to NM_019599.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:9629678 G>A maps to NM_019599.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:140564008 C>T maps to NM_020957.1 R625R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:140564008 C>T maps to NM_020957.1 R625R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:140568868 G>T maps to NM_019119.3 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:140568868 G>T maps to NM_019119.3 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:177022270 C>T maps to NM_017510.4 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:177022270 C>T maps to NM_017510.4 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr6:52400645 T>A did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr6:52400645 T>A did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr6:129601259 C>T maps to NM_000426.3 C835C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr6:129601259 C>T maps to NM_000426.3 C835C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr7:87082327 A>G maps to NM_018849.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr7:87082327 A>G maps to NM_018849.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr8:53045684 G>A maps to NM_014682.2 C792C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr8:53045684 G>A maps to NM_014682.2 C792C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr8:142161763 C>A maps to NM_014957.2 S221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr8:142161763 C>A maps to NM_014957.2 S221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr9:43627186 C>T maps to NM_001145196.1 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr9:43627186 C>T maps to NM_001145196.1 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr10:17032434 C>T maps to NM_001081.3 E1416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr10:17032434 C>T maps to NM_001081.3 E1416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr11:56756564 G>A maps to NM_001005323.1 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr11:56756564 G>A maps to NM_001005323.1 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr11:61111397 G>A maps to NM_015533.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr11:61111397 G>A maps to NM_015533.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr12:82792602 C>A maps to NM_032230.2 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr12:82792602 C>A maps to NM_032230.2 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr13:27649443 T>A maps to NM_182488.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr13:27649443 T>A maps to NM_182488.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr14:102891313 A>T did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr14:102891313 A>T did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr14:105419144 G>C maps to NM_138420.2 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr14:105419144 G>C maps to NM_138420.2 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr15:89074915 G>A maps to NM_017996.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr15:89074915 G>A maps to NM_017996.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr16:84906611 C>T maps to NM_031476.3 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr16:84906611 C>T maps to NM_031476.3 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr19:58863781 C>T maps to NM_130786.3 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr19:58863781 C>T maps to NM_130786.3 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:34389528 T>G did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:34389528 T>G did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:43926837 C>T maps to ENST00000372754 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:43926837 C>T maps to ENST00000372754 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:62178594 G>A maps to NM_080823.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:62178594 G>A maps to NM_080823.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr22:39421245 C>T maps to NM_152426.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr22:39421245 C>T maps to NM_152426.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr1:159163313 C>A maps to NM_021189.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr1:159163313 C>A maps to NM_021189.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr3:43618736 G>T maps to NM_018075.3 Y203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr3:43618736 G>T maps to NM_018075.3 Y203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr3:50879109 G>A maps to NM_004947.4 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr3:50879109 G>A maps to NM_004947.4 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr4:91760119 C>T maps to NM_183049.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr4:91760119 C>T maps to NM_183049.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr7:98460808 G>A maps to NM_001134450.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr7:98460808 G>A maps to NM_001134450.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr7:157903564 G>A maps to NM_002847.3 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr7:157903564 G>A maps to NM_002847.3 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr8:11667247 G>A maps to NM_004462.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr8:11667247 G>A maps to NM_004462.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr8:113277664 C>T maps to NM_198123.1 W3221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr8:113277664 C>T maps to NM_198123.1 W3221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr9:139651557 C>T maps to ENST00000371689 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr9:139651557 C>T maps to ENST00000371689 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr11:66188670 C>A maps to NM_178864.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr11:66188670 C>A maps to NM_178864.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr13:19751195 G>A maps to NM_006001.1 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr13:19751195 G>A maps to NM_006001.1 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr15:33835895 C>T maps to NM_001036.3 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr15:33835895 C>T maps to NM_001036.3 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr15:43896962 G>A maps to NM_153700.2 R1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr15:43896962 G>A maps to NM_153700.2 R1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr16:2827128 C>T did not map to a codon.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr16:2827128 C>T did not map to a codon.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr16:3190969 G>A maps to NM_001134655.1 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr16:3190969 G>A maps to NM_001134655.1 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr16:67199715 C>A maps to NM_001040667.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr16:67199715 C>A maps to NM_001040667.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr17:60654068 G>A did not map to a codon.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr17:60654068 G>A did not map to a codon.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr20:44515341 G>A maps to NM_080608.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr20:44515341 G>A maps to NM_080608.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr22:22988910 G>A maps to ENST00000215938 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr22:22988910 G>A maps to ENST00000215938 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:2419085 C>A maps to NM_014638.2 Y388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:2419085 C>A maps to NM_014638.2 Y388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:10231329 G>A maps to NM_001105562.2 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:10231329 G>A maps to NM_001105562.2 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:92262993 A>T maps to NM_003243.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:92262993 A>T maps to NM_003243.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:179638342 T>C maps to ENST00000444136 N888N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:179638342 T>C maps to ENST00000444136 N888N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr2:112551672 G>A maps to NM_022662.2 S1500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr2:112551672 G>A maps to NM_022662.2 S1500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr2:220348802 C>T maps to NM_005876.4 P2206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr2:220348802 C>T maps to NM_005876.4 P2206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:36524553 C>T maps to NM_003149.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:36524553 C>T maps to NM_003149.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:38618224 G>A maps to NM_001099404.1 N1146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:38618224 G>A maps to NM_001099404.1 N1146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:194126842 C>T maps to NM_024524.3 E1162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:194126842 C>T maps to NM_024524.3 E1162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr4:162577599 A>G maps to NM_020116.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr4:162577599 A>G maps to NM_020116.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr5:10256076 T>G maps to NM_012073.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr5:10256076 T>G maps to NM_012073.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr5:140515666 T>G maps to NM_015669.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr5:140515666 T>G maps to NM_015669.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr6:56341000 T>C maps to ENST00000361203 K7059K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr6:56341000 T>C maps to ENST00000361203 K7059K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr6:151671235 T>C maps to NM_005100.3 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr6:151671235 T>C maps to NM_005100.3 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:99474213 G>T maps to NM_001005276.1 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:99474213 G>T maps to NM_001005276.1 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:100775169 T>C maps to NM_000602.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:100775169 T>C maps to NM_000602.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:100775171 G>A maps to NM_000602.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:100775171 G>A maps to NM_000602.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:135106937 A>C maps to NM_001190850.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:135106937 A>C maps to NM_001190850.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:143043270 C>A maps to NM_000083.2 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:143043270 C>A maps to NM_000083.2 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr8:121554094 T>A maps to NM_021021.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr8:121554094 T>A maps to NM_021021.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr8:141567319 C>T maps to NM_012154.3 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr8:141567319 C>T maps to NM_012154.3 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr9:129595972 C>T maps to NM_014007.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr9:129595972 C>T maps to NM_014007.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:5948525 G>A maps to NM_032807.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:5948525 G>A maps to NM_032807.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:48390796 C>A maps to NM_002900.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:48390796 C>A maps to NM_002900.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:99655148 G>A maps to NM_018058.4 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:99655148 G>A maps to NM_018058.4 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:67173157 G>A maps to NM_198517.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:67173157 G>A maps to NM_198517.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:71277007 T>G maps to ENST00000422553 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:71277007 T>G maps to ENST00000422553 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:74421956 G>T maps to NM_015424.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:74421956 G>T maps to NM_015424.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:92570899 C>T maps to ENST00000298047 V3432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:92570899 C>T maps to ENST00000298047 V3432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:117335685 G>A maps to NM_020693.2 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:117335685 G>A maps to NM_020693.2 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr12:11546798 G>A maps to NM_006248.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr12:11546798 G>A maps to NM_006248.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr13:114514744 C>T maps to NM_182614.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr13:114514744 C>T maps to NM_182614.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr14:45639924 T>G maps to NM_020937.2 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr14:45639924 T>G maps to NM_020937.2 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr14:71514562 G>A maps to NM_014982.2 L1400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr14:71514562 G>A maps to NM_014982.2 L1400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr15:35185965 G>C maps to NM_014691.2 G823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr15:35185965 G>C maps to NM_014691.2 G823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr16:31498983 C>G maps to ENST00000431354 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr16:31498983 C>G maps to ENST00000431354 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:26851603 C>T maps to NM_003593.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:26851603 C>T maps to NM_003593.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:38172079 A>G maps to NM_000759.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:38172079 A>G maps to NM_000759.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:9071590 G>T maps to NM_024690.2 P5285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:9071590 G>T maps to NM_024690.2 P5285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:30935326 C>T maps to NM_014717.1 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:30935326 C>T maps to NM_014717.1 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:50979131 G>A maps to ENST00000391816 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:50979131 G>A maps to ENST00000391816 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr22:46658214 G>T maps to NM_006071.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr22:46658214 G>T maps to NM_006071.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chrX:47039693 C>G maps to NM_005676.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chrX:47039693 C>G maps to NM_005676.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:212251656 C>A maps to NM_005235.2 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:212251656 C>A maps to NM_005235.2 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:227729678 G>A maps to NM_001167608.1 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:227729678 G>A maps to NM_001167608.1 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:2613234 C>A maps to NM_175607.1 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:2613234 C>A maps to NM_175607.1 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:9482198 G>A maps to ENST00000407969 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:9482198 G>A maps to ENST00000407969 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:36874131 C>T maps to NM_014831.2 L2270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:36874131 C>T maps to NM_014831.2 L2270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:50147120 G>A maps to NM_005778.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:50147120 G>A maps to NM_005778.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr4:57272693 G>A maps to NM_002703.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr4:57272693 G>A maps to NM_002703.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:100350274 A>G maps to ENST00000349350 K849K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:100350274 A>G maps to ENST00000349350 K849K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:120381667 C>A maps to NM_012281.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:120381667 C>A maps to NM_012281.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:141754595 C>T maps to ENST00000475668 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:141754595 C>T maps to ENST00000475668 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr9:123805396 C>T maps to NM_001735.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr9:123805396 C>T maps to NM_001735.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:64065642 C>T maps to ENST00000422670 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:64065642 C>T maps to ENST00000422670 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86662612 G>A maps to NM_012193.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86662612 G>A maps to NM_012193.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86662879 G>A maps to NM_012193.2 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86662879 G>A maps to NM_012193.2 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86663023 G>A maps to NM_012193.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86663023 G>A maps to NM_012193.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr12:6153555 C>A maps to NM_000552.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr12:6153555 C>A maps to NM_000552.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr15:35189160 C>A maps to NM_014691.2 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr15:35189160 C>A maps to NM_014691.2 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr15:45695157 G>A maps to NM_024063.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr15:45695157 G>A maps to NM_024063.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr15:91549290 T>A did not map to a codon.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr15:91549290 T>A did not map to a codon.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr16:3304572 G>T maps to NM_000243.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr16:3304572 G>T maps to NM_000243.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr16:46943651 C>T maps to NM_133443.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr16:46943651 C>T maps to NM_133443.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr17:46622153 C>G maps to NM_002145.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr17:46622153 C>G maps to NM_002145.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr21:11097589 G>A maps to NM_182482.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr21:11097589 G>A maps to NM_182482.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chrX:51075900 G>A maps to NM_153183.2 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chrX:51075900 G>A maps to NM_153183.2 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:10292481 C>T maps to ENST00000377086 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:10292481 C>T maps to ENST00000377086 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:26138261 T>C maps to NM_020451.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:26138261 T>C maps to NM_020451.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:110217412 C>G maps to ENST00000369830 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:110217412 C>G maps to ENST00000369830 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:145209365 A>G did not map to a codon.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:145209365 A>G did not map to a codon.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:128399722 C>A maps to NM_017980.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:128399722 C>A maps to NM_017980.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr6:57499034 T>C maps to NM_000947.2 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr6:57499034 T>C maps to NM_000947.2 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr7:43659291 C>T maps to NM_004760.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr7:43659291 C>T maps to NM_004760.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr8:87563329 T>G did not map to a codon.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr8:87563329 T>G did not map to a codon.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr8:101589257 G>A maps to NM_152628.3 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr8:101589257 G>A maps to NM_152628.3 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr9:95784667 A>C maps to NM_033086.2 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr9:95784667 A>C maps to NM_033086.2 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr10:74034534 G>A maps to NM_019058.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr10:74034534 G>A maps to NM_019058.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr11:66192367 C>T maps to NM_178864.3 D669D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr11:66192367 C>T maps to NM_178864.3 D669D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr11:77911273 C>T maps to NM_020798.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr11:77911273 C>T maps to NM_020798.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:11214314 T>A maps to ENST00000422992 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:11214314 T>A maps to ENST00000422992 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:116457670 C>T maps to NM_015335.4 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:116457670 C>T maps to NM_015335.4 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:133428222 C>T maps to NM_001161344.1 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:133428222 C>T maps to NM_001161344.1 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr15:65502036 C>A maps to NM_003613.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr15:65502036 C>A maps to NM_003613.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr16:30731616 A>C maps to NM_006662.2 P984P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr16:30731616 A>C maps to NM_006662.2 P984P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr16:30731625 C>A maps to NM_006662.2 P987P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr16:30731625 C>A maps to NM_006662.2 P987P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chrX:5821236 G>C maps to ENST00000381093 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chrX:5821236 G>C maps to ENST00000381093 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chrX:153940642 G>C maps to NM_001081573.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chrX:153940642 G>C maps to NM_001081573.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr1:19439346 C>T maps to ENST00000375267 S3824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr1:19439346 C>T maps to ENST00000375267 S3824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr1:240977012 C>A maps to ENST00000407727 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr1:240977012 C>A maps to ENST00000407727 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr2:183846058 A>G maps to NM_205842.1 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr2:183846058 A>G maps to NM_205842.1 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr2:218683367 C>T maps to NM_022648.4 P1125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr2:218683367 C>T maps to NM_022648.4 P1125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr2:236708165 C>T maps to NM_001037131.1 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr2:236708165 C>T maps to NM_001037131.1 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr4:122075726 A>G maps to ENST00000509841 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr4:122075726 A>G maps to ENST00000509841 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr9:131503067 C>T maps to NM_006336.2 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr9:131503067 C>T maps to NM_006336.2 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr12:116446660 C>A maps to NM_015335.4 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr12:116446660 C>A maps to NM_015335.4 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr12:133197606 T>C maps to NM_170683.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr12:133197606 T>C maps to NM_170683.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr13:20006718 C>G did not map to a codon.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr13:20006718 C>G did not map to a codon.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr20:62193018 C>T maps to NM_001037335.2 P2257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr20:62193018 C>T maps to NM_001037335.2 P2257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:16257157 C>T maps to NM_015001.2 R1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:16257157 C>T maps to NM_015001.2 R1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:51826840 A>G did not map to a codon.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:51826840 A>G did not map to a codon.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:207737311 T>C maps to NM_000651.4 Y1230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:207737311 T>C maps to NM_000651.4 Y1230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:227152756 G>A maps to NM_020247.4 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:227152756 G>A maps to NM_020247.4 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr2:209190766 C>T maps to NM_015040.3 R1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr2:209190766 C>T maps to NM_015040.3 R1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr3:10108897 A>G maps to NM_033084.3 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr3:10108897 A>G maps to NM_033084.3 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr5:5303542 G>A maps to NM_139056.2 Q984Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr5:5303542 G>A maps to NM_139056.2 Q984Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr5:137485405 G>A maps to NM_139199.1 G1067G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr5:137485405 G>A maps to NM_139199.1 G1067G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr7:91631336 A>G maps to NM_005751.4 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr7:91631336 A>G maps to NM_005751.4 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr9:33797991 C>T maps to NM_007343.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr9:33797991 C>T maps to NM_007343.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr10:100013410 G>T maps to NM_032211.6 Y578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr10:100013410 G>T maps to NM_032211.6 Y578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr12:32135027 C>A maps to NM_018169.3 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr12:32135027 C>A maps to NM_018169.3 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr12:64173823 C>T maps to NM_014254.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr12:64173823 C>T maps to NM_014254.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr17:39633888 G>A maps to NM_002280.4 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr17:39633888 G>A maps to NM_002280.4 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr22:38120299 T>C maps to NM_001039141.2 C579C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr22:38120299 T>C maps to NM_001039141.2 C579C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:36563466 G>T maps to NM_005202.2 Y605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:36563466 G>T maps to NM_005202.2 Y605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:157504476 T>C maps to NM_031281.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:157504476 T>C maps to NM_031281.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:206566194 C>T maps to ENST00000414359 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:206566194 C>T maps to ENST00000414359 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:216052410 G>A maps to ENST00000366943 N2751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:216052410 G>A maps to ENST00000366943 N2751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:247695756 G>A maps to NM_198074.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:247695756 G>A maps to NM_198074.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr2:191922751 G>A maps to NM_003151.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr2:191922751 G>A maps to NM_003151.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr4:122063931 C>A did not map to a codon.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr4:122063931 C>A did not map to a codon.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr6:34495227 C>A maps to NM_020804.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr6:34495227 C>A maps to NM_020804.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr6:35930383 A>C maps to NM_052961.3 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr6:35930383 A>C maps to NM_052961.3 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr8:131792812 G>A maps to NM_001115.2 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr8:131792812 G>A maps to NM_001115.2 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr9:111718090 G>T maps to NM_003798.2 Y536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr9:111718090 G>T maps to NM_003798.2 Y536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr9:140330680 G>T maps to NM_001033113.1 Y278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr9:140330680 G>T maps to NM_001033113.1 Y278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr10:104679670 C>A maps to NM_017649.3 Y478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr10:104679670 C>A maps to NM_017649.3 Y478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr11:59608633 A>G maps to NM_005142.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr11:59608633 A>G maps to NM_005142.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr12:122825727 C>A maps to ENST00000302528 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr12:122825727 C>A maps to ENST00000302528 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr13:29599665 C>T maps to NM_001033602.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr13:29599665 C>T maps to NM_001033602.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr13:115090480 G>A maps to NM_032436.2 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr13:115090480 G>A maps to NM_032436.2 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr14:23828654 C>T maps to NM_005864.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr14:23828654 C>T maps to NM_005864.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr14:26917260 T>C maps to ENST00000449198 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr14:26917260 T>C maps to ENST00000449198 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr14:105615534 G>C maps to NM_002226.3 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr14:105615534 G>C maps to NM_002226.3 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr16:2506606 C>T maps to NM_001761.2 C649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr16:2506606 C>T maps to NM_001761.2 C649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr16:30731616 A>C maps to NM_006662.2 P984P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr16:30731616 A>C maps to NM_006662.2 P984P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:40485823 A>C maps to NM_006503.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:40485823 A>C maps to NM_006503.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:44564708 G>A maps to NM_013361.4 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:44564708 G>A maps to NM_013361.4 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:55324634 T>C maps to ENST00000396289 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:55324634 T>C maps to ENST00000396289 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:56539872 A>G maps to NM_153447.4 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:56539872 A>G maps to NM_153447.4 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr20:861912 A>C maps to NM_015985.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr20:861912 A>C maps to NM_015985.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr20:18123555 A>C maps to NM_020536.4 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr20:18123555 A>C maps to NM_020536.4 I84I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5765-01A-11D-1576-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CH-5765-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chrX:142718072 G>T maps to NM_001184749.1 Y284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chrX:142718072 G>T maps to NM_001184749.1 Y284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr1:223971996 G>T maps to NM_001031685.2 G1061G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr1:223971996 G>T maps to NM_001031685.2 G1061G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr1:245849236 C>A maps to NM_018012.3 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr1:245849236 C>A maps to NM_018012.3 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:13542246 C>T maps to NM_024827.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:13542246 C>T maps to NM_024827.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:38135138 T>C maps to NM_007335.2 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:38135138 T>C maps to NM_007335.2 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr5:139744178 C>T maps to ENST00000507527 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr5:139744178 C>T maps to ENST00000507527 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr7:100348485 C>A maps to ENST00000349350 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr7:100348485 C>A maps to ENST00000349350 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr9:138651632 G>A maps to ENST00000298480 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr9:138651632 G>A maps to ENST00000298480 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr11:1904666 C>T maps to ENST00000381758 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr11:1904666 C>T maps to ENST00000381758 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr12:3390976 C>T maps to ENST00000407263 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr12:3390976 C>T maps to ENST00000407263 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr14:64580249 C>T maps to NM_182914.2 D4267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr14:64580249 C>T maps to NM_182914.2 D4267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr14:77236394 G>T did not map to a codon.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr14:77236394 G>T did not map to a codon.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr19:41062019 G>A maps to NM_020971.2 V1705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr19:41062019 G>A maps to NM_020971.2 V1705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr21:47421897 G>A maps to NM_001848.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr21:47421897 G>A maps to NM_001848.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr1:120539833 A>T maps to NM_024408.2 C179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr1:120539833 A>T maps to NM_024408.2 C179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr2:179585678 G>A maps to NM_133378.4 D6445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr2:179585678 G>A maps to NM_133378.4 D6445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr3:126160694 G>T maps to NM_025112.4 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr3:126160694 G>T maps to NM_025112.4 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr4:9783991 C>T maps to NM_000798.4 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr4:9783991 C>T maps to NM_000798.4 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr5:112876725 T>C maps to NM_022828.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr5:112876725 T>C maps to NM_022828.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr6:29910621 C>T maps to ENST00000376806 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr6:29910621 C>T maps to ENST00000376806 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr6:38548003 G>A maps to NM_052893.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr6:38548003 G>A maps to NM_052893.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr7:73604628 C>T maps to NM_022170.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr7:73604628 C>T maps to NM_022170.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr9:117359984 C>A maps to NM_004888.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr9:117359984 C>A maps to NM_004888.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr11:44626915 C>T maps to NM_002231.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr11:44626915 C>T maps to NM_002231.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr12:11546066 A>G maps to NM_006248.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr12:11546066 A>G maps to NM_006248.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr16:70508757 C>T maps to NM_145059.2 R741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr16:70508757 C>T maps to NM_145059.2 R741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr17:45664676 C>T maps to NM_006310.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr17:45664676 C>T maps to NM_006310.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr17:77808783 A>C maps to NM_003655.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr17:77808783 A>C maps to NM_003655.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr17:79873381 G>A maps to NM_016538.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr17:79873381 G>A maps to NM_016538.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr19:39334539 A>G maps to ENST00000221419 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr19:39334539 A>G maps to ENST00000221419 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr19:52130799 G>A maps to ENST00000222107 H399H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr19:52130799 G>A maps to ENST00000222107 H399H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr1:108307708 G>A maps to NM_006113.4 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr1:108307708 G>A maps to NM_006113.4 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr1:158368836 C>T maps to NM_001004475.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr1:158368836 C>T maps to NM_001004475.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr1:179452331 C>T maps to NM_144696.4 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr1:179452331 C>T maps to NM_144696.4 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:29295480 G>A maps to NM_001029883.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:29295480 G>A maps to NM_001029883.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:170677647 G>A maps to NM_014168.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:170677647 G>A maps to NM_014168.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:189874961 T>C maps to NM_000090.3 C1294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:189874961 T>C maps to NM_000090.3 C1294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr5:171299982 C>A maps to NM_012300.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr5:171299982 C>A maps to NM_012300.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr7:137082143 A>T maps to NM_004717.2 L987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr7:137082143 A>T maps to NM_004717.2 L987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr8:14095116 G>A maps to NM_139167.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr8:14095116 G>A maps to NM_139167.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr8:142226016 G>A maps to NM_001080431.1 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr8:142226016 G>A maps to NM_001080431.1 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr10:26581401 C>T maps to NM_001134366.1 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr10:26581401 C>T maps to NM_001134366.1 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr10:127737878 G>A maps to NM_003474.4 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr10:127737878 G>A maps to NM_003474.4 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr12:133249851 C>T maps to ENST00000455752 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr12:133249851 C>T maps to ENST00000455752 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr14:21796692 C>A maps to NM_020366.3 Y1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr14:21796692 C>A maps to NM_020366.3 Y1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr16:2903246 G>A maps to NM_022119.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr16:2903246 G>A maps to NM_022119.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr16:7645570 C>T maps to NM_145891.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr16:7645570 C>T maps to NM_145891.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr17:15976857 A>C maps to ENST00000395857 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr17:15976857 A>C maps to ENST00000395857 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr18:30517983 G>A maps to NM_001105528.1 N865N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr18:30517983 G>A maps to NM_001105528.1 N865N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr19:17571712 G>A did not map to a codon.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr19:17571712 G>A did not map to a codon.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr19:31769516 C>T maps to NM_020856.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr19:31769516 C>T maps to NM_020856.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chrX:117700565 G>T maps to ENST00000276204 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chrX:117700565 G>T maps to ENST00000276204 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chrX:128599697 G>T maps to NM_003069.3 Y943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chrX:128599697 G>T maps to NM_003069.3 Y943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:7723411 G>T did not map to a codon.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:7723411 G>T did not map to a codon.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:62393500 C>T maps to NM_176877.2 Q1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:62393500 C>T maps to NM_176877.2 Q1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:89480251 G>A maps to NM_018284.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:89480251 G>A maps to NM_018284.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:149885320 C>T maps to NM_014849.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:149885320 C>T maps to NM_014849.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:156221225 C>T maps to NM_015327.2 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:156221225 C>T maps to NM_015327.2 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:156316721 A>G maps to NM_144627.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:156316721 A>G maps to NM_144627.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:185269160 A>G maps to NM_006469.4 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:185269160 A>G maps to NM_006469.4 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:228456387 C>T maps to NM_001098623.1 R1673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:228456387 C>T maps to NM_001098623.1 R1673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:9630611 C>A maps to NM_003183.4 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:9630611 C>A maps to NM_003183.4 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:99861763 G>A maps to NM_175735.3 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:99861763 G>A maps to NM_175735.3 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:101656774 G>A maps to NM_001102426.1 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:101656774 G>A maps to NM_001102426.1 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:170938347 C>T maps to ENST00000442603 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:170938347 C>T maps to ENST00000442603 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr3:33194350 A>C maps to NM_015551.1 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr3:33194350 A>C maps to NM_015551.1 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr3:196388400 C>T maps to NM_198565.1 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr3:196388400 C>T maps to NM_198565.1 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr4:141074097 G>T maps to ENST00000509479 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr4:141074097 G>T maps to ENST00000509479 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr5:1814478 G>A maps to ENST00000469176 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr5:1814478 G>A maps to ENST00000469176 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr5:140188640 C>T maps to NM_018907.2 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr5:140188640 C>T maps to NM_018907.2 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr6:10882020 C>T maps to NM_004752.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr6:10882020 C>T maps to NM_004752.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr6:56999544 C>T maps to NM_001031623.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr6:56999544 C>T maps to NM_001031623.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:4823970 C>T maps to ENST00000450194 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:4823970 C>T maps to ENST00000450194 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:100275275 C>T maps to NM_005273.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:100275275 C>T maps to NM_005273.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:102087009 G>A maps to NM_032831.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:102087009 G>A maps to NM_032831.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:143771566 G>A maps to NM_001004488.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:143771566 G>A maps to NM_001004488.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr8:22051964 C>T maps to NM_006129.4 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr8:22051964 C>T maps to NM_006129.4 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr8:27779151 G>A maps to NM_173833.5 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr8:27779151 G>A maps to NM_173833.5 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr9:101980872 G>A maps to NM_033087.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr9:101980872 G>A maps to NM_033087.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr11:61018743 T>C maps to ENST00000422676 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr11:61018743 T>C maps to ENST00000422676 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr11:69063453 G>A maps to NM_138768.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr11:69063453 G>A maps to NM_138768.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr11:74979963 G>A maps to NM_004041.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr11:74979963 G>A maps to NM_004041.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr12:52911442 C>T maps to NM_000424.3 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr12:52911442 C>T maps to NM_000424.3 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:108861450 C>T maps to NM_001098268.1 K722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:108861450 C>T maps to NM_001098268.1 K722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:111156529 G>T maps to NM_001846.2 G1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:111156529 G>T maps to NM_001846.2 G1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:111298322 C>T maps to NM_024537.2 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:111298322 C>T maps to NM_024537.2 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:63175049 G>A maps to NM_139318.3 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:63175049 G>A maps to NM_139318.3 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:90650707 C>T maps to NM_022054.2 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:90650707 C>T maps to NM_022054.2 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:91647608 T>C maps to NM_001102368.1 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:91647608 T>C maps to NM_001102368.1 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:94756666 T>C maps to NM_001100607.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:94756666 T>C maps to NM_001100607.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr15:66618501 C>T maps to NM_001143688.1 H667H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr15:66618501 C>T maps to NM_001143688.1 H667H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr15:80884041 C>T maps to NM_014862.3 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr15:80884041 C>T maps to NM_014862.3 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr16:2239047 G>A maps to NM_020764.3 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr16:2239047 G>A maps to NM_020764.3 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr16:89212410 C>T maps to NM_174917.2 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr16:89212410 C>T maps to NM_174917.2 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:5033902 C>T maps to NM_004505.2 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:5033902 C>T maps to NM_004505.2 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:6381354 C>T maps to NM_031220.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:6381354 C>T maps to NM_031220.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:40557265 G>A maps to NM_012232.5 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:40557265 G>A maps to NM_012232.5 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:42636102 G>A maps to NM_001466.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:42636102 G>A maps to NM_001466.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:55339543 G>A maps to NM_138962.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:55339543 G>A maps to NM_138962.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:65026807 G>A maps to NM_014405.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:65026807 G>A maps to NM_014405.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr18:77896568 T>C maps to NM_014913.3 F1091F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr18:77896568 T>C maps to NM_014913.3 F1091F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:1068741 C>T maps to NM_012292.2 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:1068741 C>T maps to NM_012292.2 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:3595922 G>A maps to NM_201636.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:3595922 G>A maps to NM_201636.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:8319478 G>A maps to NM_024552.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:8319478 G>A maps to NM_024552.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:18313412 C>T maps to NM_002866.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:18313412 C>T maps to NM_002866.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr21:43412179 G>A maps to NM_020727.4 C675C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr21:43412179 G>A maps to NM_020727.4 C675C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chrX:153587626 G>A maps to NM_001110556.1 G1430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chrX:153587626 G>A maps to NM_001110556.1 G1430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr1:8398052 G>T did not map to a codon.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr1:8398052 G>T did not map to a codon.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr1:36935382 G>T maps to NM_156039.3 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr1:36935382 G>T maps to NM_156039.3 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr1:174987688 G>T maps to NM_022100.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr1:174987688 G>T maps to NM_022100.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr4:1388997 G>A maps to NM_175918.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr4:1388997 G>A maps to NM_175918.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr5:75427790 C>T maps to NM_014979.1 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr5:75427790 C>T maps to NM_014979.1 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr5:140052311 T>G maps to NM_194249.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr5:140052311 T>G maps to NM_194249.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr5:140052330 G>T maps to NM_194249.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr5:140052330 G>T maps to NM_194249.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr5:162886897 C>A maps to NM_145266.4 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr5:162886897 C>A maps to NM_145266.4 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr7:149518960 T>C maps to NM_198455.2 A4259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr7:149518960 T>C maps to NM_198455.2 A4259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr8:55540710 T>A maps to NM_006269.1 C1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr8:55540710 T>A maps to NM_006269.1 C1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr11:117988096 C>T maps to NM_019894.3 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr11:117988096 C>T maps to NM_019894.3 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr12:75601571 C>A maps to NM_139137.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr12:75601571 C>A maps to NM_139137.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr12:123834910 A>G maps to NM_001167856.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr12:123834910 A>G maps to NM_001167856.1 I26I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5771-01A-21D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr14:23397823 C>A maps to NM_006109.3 G37G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5771-01A-21D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr14:23397823 C>A maps to NM_006109.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr14:96800091 G>A maps to NM_018036.5 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr14:96800091 G>A maps to NM_018036.5 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr16:418563 C>T maps to NM_006428.4 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr16:418563 C>T maps to NM_006428.4 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr17:7366920 T>G maps to NM_020899.3 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr17:7366920 T>G maps to NM_020899.3 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr20:57290252 C>T maps to NM_024663.3 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr20:57290252 C>T maps to NM_024663.3 A481A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5771-01A-21D-1576-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CH-5771-01A-21D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:25617206 G>A maps to ENST00000357542 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:25617206 G>A maps to ENST00000357542 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:153391727 C>T maps to NM_176823.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:153391727 C>T maps to NM_176823.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:155028576 C>T maps to NM_207197.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:155028576 C>T maps to NM_207197.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:158592859 G>A maps to NM_003126.2 A2011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:158592859 G>A maps to NM_003126.2 A2011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:212274087 T>C maps to NM_016448.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:212274087 T>C maps to NM_016448.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:248551358 C>T maps to NM_001005471.1 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:248551358 C>T maps to NM_001005471.1 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr2:80530233 C>A maps to NM_178839.4 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr2:80530233 C>A maps to NM_178839.4 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr2:109381815 G>A maps to NM_006267.4 E1607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr2:109381815 G>A maps to NM_006267.4 E1607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr2:215890473 G>A maps to NM_173076.2 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr2:215890473 G>A maps to NM_173076.2 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr2:242758175 C>A maps to NM_001167599.1 Y432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr2:242758175 C>A maps to NM_001167599.1 Y432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr4:48422299 C>T maps to NM_020846.1 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr4:48422299 C>T maps to NM_020846.1 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr4:69693266 G>A did not map to a codon.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr4:69693266 G>A did not map to a codon.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140237081 G>A maps to NM_018901.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140237081 G>A maps to NM_018901.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140559492 C>T maps to NM_019120.2 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140559492 C>T maps to NM_019120.2 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140574044 C>G maps to NM_018930.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140574044 C>G maps to NM_018930.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140720421 G>A maps to NM_018915.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140720421 G>A maps to NM_018915.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140794394 G>A maps to NM_018913.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140794394 G>A maps to NM_018913.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr6:1390757 G>A maps to NM_001452.1 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr6:1390757 G>A maps to NM_001452.1 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr7:43484981 C>T maps to NM_015052.3 D737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr7:43484981 C>T maps to NM_015052.3 D737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr8:97605799 C>T maps to NM_002998.3 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr8:97605799 C>T maps to NM_002998.3 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr9:15744746 A>G maps to NM_173550.2 G842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr9:15744746 A>G maps to NM_173550.2 G842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr9:100684718 A>C maps to NM_016481.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr9:100684718 A>C maps to NM_016481.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr9:130630298 G>A maps to ENST00000223836 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr9:130630298 G>A maps to ENST00000223836 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr10:105798242 G>A maps to NM_000494.3 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr10:105798242 G>A maps to NM_000494.3 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:1093511 C>A maps to ENST00000441003 T1777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:1093511 C>A maps to ENST00000441003 T1777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:1642975 A>C maps to ENST00000359229 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:1642975 A>C maps to ENST00000359229 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:66469125 G>A maps to NM_006946.2 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:66469125 G>A maps to NM_006946.2 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:92088334 C>A maps to ENST00000298047 V1019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:92088334 C>A maps to ENST00000298047 V1019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:128844093 C>A maps to NM_001142685.1 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:128844093 C>A maps to NM_001142685.1 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:133712383 G>A maps to NM_174927.1 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:133712383 G>A maps to NM_174927.1 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:11244165 G>C maps to NM_176884.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:11244165 G>C maps to NM_176884.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:11546798 G>A maps to NM_006248.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:11546798 G>A maps to NM_006248.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:13717456 G>T maps to NM_000834.3 A905A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:13717456 G>T maps to NM_000834.3 A905A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:63543827 A>G maps to NM_000706.3 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:63543827 A>G maps to NM_000706.3 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr13:45008836 A>G maps to NM_183422.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr13:45008836 A>G maps to NM_183422.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr14:88459433 G>T maps to NM_000153.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr14:88459433 G>T maps to NM_000153.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr15:89871739 G>A maps to NM_002693.2 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr15:89871739 G>A maps to NM_002693.2 D399D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CH-5772-01A-11D-1576-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CH-5772-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr16:83704516 G>C maps to ENST00000268613 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr16:83704516 G>C maps to ENST00000268613 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr17:8792522 C>T maps to NM_001142633.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr17:8792522 C>T maps to NM_001142633.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr17:39280113 T>C maps to NM_031854.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr17:39280113 T>C maps to NM_031854.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr17:48557075 T>C maps to NM_018346.1 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr17:48557075 T>C maps to NM_018346.1 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr19:45656260 C>A maps to NM_198478.3 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr19:45656260 C>A maps to NM_198478.3 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr19:57175471 G>A maps to NM_001005850.1 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr19:57175471 G>A maps to NM_001005850.1 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr20:44751804 C>T maps to NM_001250.4 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr20:44751804 C>T maps to NM_001250.4 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr20:44869812 G>A maps to NM_021248.1 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr20:44869812 G>A maps to NM_021248.1 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr22:26701984 C>T maps to NM_021115.4 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr22:26701984 C>T maps to NM_021115.4 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chrX:24516990 C>T maps to NM_001142386.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chrX:24516990 C>T maps to NM_001142386.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chrX:99662412 G>A maps to NM_001184880.1 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chrX:99662412 G>A maps to NM_001184880.1 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chrX:138713595 G>T maps to ENST00000370578 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chrX:138713595 G>T maps to ENST00000370578 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr1:202245637 C>T maps to NM_001017403.1 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr1:202245637 C>T maps to NM_001017403.1 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr2:74072295 A>G maps to NM_213622.1 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr2:74072295 A>G maps to NM_213622.1 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr2:109382169 A>G maps to NM_006267.4 E1725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr2:109382169 A>G maps to NM_006267.4 E1725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr4:15569017 G>A maps to NM_001080522.2 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr4:15569017 G>A maps to NM_001080522.2 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:98192173 C>T maps to NM_001270.2 Q1681Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:98192173 C>T maps to NM_001270.2 Q1681Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:140553129 C>T maps to NM_018940.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:140553129 C>T maps to NM_018940.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:162868106 T>A maps to NM_199246.1 C96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:162868106 T>A maps to NM_199246.1 C96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr7:96339203 A>T did not map to a codon.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr7:96339203 A>T did not map to a codon.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:23290498 C>T maps to NM_004901.3 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:23290498 C>T maps to NM_004901.3 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:72963063 G>A maps to NM_007332.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:72963063 G>A maps to NM_007332.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:128428779 A>C maps to NM_001159542.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:128428779 A>C maps to NM_001159542.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr11:33373267 T>C maps to NM_005734.3 H974H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr11:33373267 T>C maps to NM_005734.3 H974H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr15:55964736 C>T maps to NM_173814.4 Q649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr15:55964736 C>T maps to NM_173814.4 Q649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:3778252 C>T maps to NM_004380.2 A2265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:3778252 C>T maps to NM_004380.2 A2265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:67234422 G>A maps to NM_024712.3 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:67234422 G>A maps to NM_024712.3 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:67305046 C>T maps to NM_004594.2 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:67305046 C>T maps to NM_004594.2 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr19:15756623 C>A maps to NM_000896.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr19:15756623 C>A maps to NM_000896.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr19:57065113 G>A maps to NM_020828.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr19:57065113 G>A maps to NM_020828.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr22:36960763 G>A maps to NM_006078.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr22:36960763 G>A maps to NM_006078.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr1:237801683 C>T maps to NM_001035.2 L2274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr1:237801683 C>T maps to NM_001035.2 L2274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr2:33172886 T>C did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr2:33172886 T>C did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr2:88478452 G>A maps to NM_018271.3 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr2:88478452 G>A maps to NM_018271.3 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr2:112551672 G>A maps to NM_022662.2 S1500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr2:112551672 G>A maps to NM_022662.2 S1500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr6:33287899 C>T maps to NM_001350.4 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr6:33287899 C>T maps to NM_001350.4 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr7:45744118 C>A maps to NM_021116.2 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr7:45744118 C>A maps to NM_021116.2 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr7:92147135 G>A maps to NM_000466.2 N231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr7:92147135 G>A maps to NM_000466.2 N231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr8:23114022 C>T maps to NM_152272.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr8:23114022 C>T maps to NM_152272.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr9:90535289 T>C maps to NM_001145124.1 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr9:90535289 T>C maps to NM_001145124.1 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr9:104152774 G>A maps to NM_019051.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr9:104152774 G>A maps to NM_019051.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr10:56287577 G>T maps to NM_001142763.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr10:56287577 G>T maps to NM_001142763.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr11:18524117 G>T maps to NM_006292.2 Y185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr11:18524117 G>T maps to NM_006292.2 Y185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr11:117864124 G>A maps to NM_001558.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr11:117864124 G>A maps to NM_001558.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr14:92608696 T>C did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr14:92608696 T>C did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr16:84402274 G>C maps to ENST00000416219 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr16:84402274 G>C maps to ENST00000416219 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr19:9075832 C>T maps to NM_024690.2 E3871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr19:9075832 C>T maps to NM_024690.2 E3871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr20:1433674 C>T did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr20:1433674 C>T did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chrX:26212304 T>G maps to NM_173523.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chrX:26212304 T>G maps to NM_173523.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr1:152284211 C>T maps to NM_002016.1 P1050P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr1:152284211 C>T maps to NM_002016.1 P1050P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr2:27258871 G>A maps to NM_017727.4 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr2:27258871 G>A maps to NM_017727.4 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:10251300 G>A maps to NM_001570.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:10251300 G>A maps to NM_001570.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:48624752 C>T maps to NM_000094.3 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:48624752 C>T maps to NM_000094.3 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:51746688 C>T maps to NM_000839.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:51746688 C>T maps to NM_000839.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr6:146480671 C>T maps to NM_000838.3 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr6:146480671 C>T maps to NM_000838.3 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr8:139278044 G>A maps to NM_015912.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr8:139278044 G>A maps to NM_015912.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr10:32337437 T>C maps to NM_004521.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr10:32337437 T>C maps to NM_004521.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr11:1093367 G>A maps to ENST00000441003 T1729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr11:1093367 G>A maps to ENST00000441003 T1729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr16:85936701 T>C maps to NM_002163.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr16:85936701 T>C maps to NM_002163.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr18:8113636 C>A maps to NM_001105244.1 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr18:8113636 C>A maps to NM_001105244.1 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr19:33584365 C>T maps to NM_018025.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr19:33584365 C>T maps to NM_018025.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr20:31427558 C>G maps to NM_012325.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr20:31427558 C>G maps to NM_012325.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chrX:142718072 G>T maps to NM_001184749.1 Y284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chrX:142718072 G>T maps to NM_001184749.1 Y284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr1:12939673 C>G maps to ENST00000376192 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr1:12939673 C>G maps to ENST00000376192 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr1:196971636 G>A maps to ENST00000367414 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr1:196971636 G>A maps to ENST00000367414 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr1:230338964 C>T maps to NM_004481.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr1:230338964 C>T maps to NM_004481.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr2:228155517 C>A maps to NM_000091.4 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr2:228155517 C>A maps to NM_000091.4 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr2:229890758 T>A maps to NM_017933.4 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr2:229890758 T>A maps to NM_017933.4 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr3:47376265 C>A maps to NM_025010.4 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr3:47376265 C>A maps to NM_025010.4 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr3:53886920 C>T maps to NM_018725.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr3:53886920 C>T maps to NM_018725.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr7:21939031 C>A maps to NM_003777.3 L4383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr7:21939031 C>A maps to NM_003777.3 L4383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr8:77764256 C>T maps to NM_024721.4 H1700H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr8:77764256 C>T maps to NM_024721.4 H1700H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr8:133196584 G>A maps to NM_004519.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr8:133196584 G>A maps to NM_004519.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr9:137707833 G>A maps to NM_000093.3 T1374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr9:137707833 G>A maps to NM_000093.3 T1374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr10:89690801 G>A did not map to a codon.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr10:89690801 G>A did not map to a codon.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr10:101455822 C>T maps to NM_020354.3 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr10:101455822 C>T maps to NM_020354.3 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr11:124857793 C>T maps to NM_025004.2 Q558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr11:124857793 C>T maps to NM_025004.2 Q558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr11:124947148 G>A maps to NM_198277.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr11:124947148 G>A maps to NM_198277.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:48737262 C>A maps to NM_152320.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:48737262 C>A maps to NM_152320.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:109290786 C>T maps to NM_001917.4 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:109290786 C>T maps to NM_001917.4 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:120615276 G>A maps to NM_006836.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:120615276 G>A maps to NM_006836.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr16:9892212 G>T maps to NM_000833.3 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr16:9892212 G>T maps to NM_000833.3 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr16:58750603 G>A maps to NM_002080.2 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr16:58750603 G>A maps to NM_002080.2 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr17:3992019 C>T maps to NM_015113.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr17:3992019 C>T maps to NM_015113.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr19:22271811 G>A maps to NM_033468.2 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr19:22271811 G>A maps to NM_033468.2 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr21:18924179 G>A maps to NM_001338.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr21:18924179 G>A maps to NM_001338.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr21:47570138 G>T maps to ENST00000397748 S267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr21:47570138 G>T maps to ENST00000397748 S267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chrX:131212511 A>G maps to NM_194277.2 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chrX:131212511 A>G maps to NM_194277.2 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:55166841 C>T maps to ENST00000454855 P1073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:55166841 C>T maps to ENST00000454855 P1073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:158576872 C>T maps to NM_001004478.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:158576872 C>T maps to NM_001004478.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:182550488 G>A maps to NM_021133.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:182550488 G>A maps to NM_021133.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:248308778 C>T maps to NM_001004690.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:248308778 C>T maps to NM_001004690.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr2:48915654 A>T maps to NM_000233.3 Y427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr2:48915654 A>T maps to NM_000233.3 Y427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr3:49928942 C>T maps to NM_002447.2 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr3:49928942 C>T maps to NM_002447.2 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr5:53751987 T>C maps to NM_006308.2 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr5:53751987 T>C maps to NM_006308.2 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr5:79029069 A>G maps to NM_153610.3 K1494K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr5:79029069 A>G maps to NM_153610.3 K1494K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr5:140564008 C>T maps to NM_020957.1 R625R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr5:140564008 C>T maps to NM_020957.1 R625R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr6:29910621 C>T maps to ENST00000376806 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr6:29910621 C>T maps to ENST00000376806 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr7:100807836 G>A maps to NM_003378.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr7:100807836 G>A maps to NM_003378.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr7:141796214 T>C maps to ENST00000475668 R2565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr7:141796214 T>C maps to ENST00000475668 R2565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr8:3889496 G>A maps to NM_033225.5 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr8:3889496 G>A maps to NM_033225.5 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr9:94172249 G>C maps to NM_005384.2 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr9:94172249 G>C maps to NM_005384.2 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:34147367 C>T maps to NM_139215.1 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:34147367 C>T maps to NM_139215.1 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:74473093 G>T maps to NM_024599.5 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:74473093 G>T maps to NM_024599.5 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:74732289 T>A maps to NM_003016.4 K207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:74732289 T>A maps to NM_003016.4 K207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:74732290 C>A maps to NM_003016.4 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:74732290 C>A maps to NM_003016.4 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr19:10089566 C>T maps to NM_015719.3 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr19:10089566 C>T maps to NM_015719.3 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr19:40224985 A>G maps to NM_001828.4 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr19:40224985 A>G maps to NM_001828.4 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr19:50726569 G>A maps to NM_001145809.1 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr19:50726569 G>A maps to NM_001145809.1 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr20:31424468 A>G maps to NM_012325.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr20:31424468 A>G maps to NM_012325.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr22:40054947 T>C maps to NM_021096.3 I719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr22:40054947 T>C maps to NM_021096.3 I719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr1:5926506 T>C maps to NM_015102.2 E1190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr1:5926506 T>C maps to NM_015102.2 E1190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr1:16361924 G>A did not map to a codon.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr1:16361924 G>A did not map to a codon.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr1:16385177 G>A maps to NM_182623.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr1:16385177 G>A maps to NM_182623.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr1:158585064 G>A maps to NM_003126.2 D2243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr1:158585064 G>A maps to NM_003126.2 D2243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr2:182376433 T>C maps to NM_000885.4 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr2:182376433 T>C maps to NM_000885.4 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr3:49755884 G>A maps to NM_198722.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr3:49755884 G>A maps to NM_198722.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr3:112005629 T>C maps to NM_183061.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr3:112005629 T>C maps to NM_183061.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:34826504 C>G maps to NM_001145521.1 S907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:34826504 C>G maps to NM_001145521.1 S907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:45262493 C>T maps to NM_021072.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:45262493 C>T maps to NM_021072.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:101813485 G>A maps to NM_173488.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:101813485 G>A maps to NM_173488.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr6:1624709 G>A maps to NM_001500.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr6:1624709 G>A maps to NM_001500.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr7:99686976 C>G maps to NM_006833.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr7:99686976 C>G maps to NM_006833.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr9:104192138 G>A maps to NM_000035.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr9:104192138 G>A maps to NM_000035.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr9:133799130 C>A maps to NM_001145106.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr9:133799130 C>A maps to NM_001145106.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr10:93554 C>T maps to NM_177987.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr10:93554 C>T maps to NM_177987.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr12:110765383 T>A maps to NM_170665.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr12:110765383 T>A maps to NM_170665.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr18:12955466 T>C maps to NM_001013437.1 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr18:12955466 T>C maps to NM_001013437.1 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr19:39965234 G>T maps to NM_003169.3 T967T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr19:39965234 G>T maps to NM_003169.3 T967T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr22:32794015 A>G maps to NM_014306.4 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr22:32794015 A>G maps to NM_014306.4 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr4:41621298 G>A maps to NM_014988.2 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr4:41621298 G>A maps to NM_014988.2 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr4:52861921 G>A maps to NM_001024611.1 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr4:52861921 G>A maps to NM_001024611.1 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr5:140188928 C>T maps to NM_018907.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr5:140188928 C>T maps to NM_018907.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr5:140554609 C>T maps to NM_018940.2 R732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr5:140554609 C>T maps to NM_018940.2 R732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr8:86249176 G>A maps to NM_001738.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr8:86249176 G>A maps to NM_001738.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr11:55606580 G>A maps to NM_001005496.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr11:55606580 G>A maps to NM_001005496.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr12:111652017 C>T maps to NM_015267.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr12:111652017 C>T maps to NM_015267.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr12:130935763 G>A maps to NM_015347.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr12:130935763 G>A maps to NM_015347.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr14:38060571 A>C maps to NM_004496.2 *473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr14:38060571 A>C maps to NM_004496.2 *473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr18:21426326 C>T maps to ENST00000416669 G1264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr18:21426326 C>T maps to ENST00000416669 G1264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chrX:102337711 G>A maps to NM_022052.1 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chrX:102337711 G>A maps to NM_022052.1 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:5964827 C>T maps to NM_015102.2 K664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:5964827 C>T maps to NM_015102.2 K664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:16559012 G>T maps to NM_030907.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:16559012 G>T maps to NM_030907.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:16918793 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:16918793 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:21103088 C>G did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:21103088 C>G did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:186276290 A>G maps to NM_005807.3 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:186276290 A>G maps to NM_005807.3 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr2:105706376 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr2:105706376 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr3:121563354 T>C maps to NM_018456.4 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr3:121563354 T>C maps to NM_018456.4 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr4:13601500 G>A maps to NM_148894.2 S2341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr4:13601500 G>A maps to NM_148894.2 S2341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr4:119161794 G>A maps to NM_004784.2 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr4:119161794 G>A maps to NM_004784.2 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr4:175897498 G>T maps to NM_014269.4 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr4:175897498 G>T maps to NM_014269.4 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:32023934 G>T maps to ENST00000375244 T2720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:32023934 G>T maps to ENST00000375244 T2720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:54735286 T>C maps to NM_001010872.1 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:54735286 T>C maps to NM_001010872.1 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:96651186 C>T maps to NM_006581.3 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:96651186 C>T maps to NM_006581.3 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:155451341 C>T maps to ENST00000456144 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:155451341 C>T maps to ENST00000456144 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:160864676 G>A maps to ENST00000392145 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:160864676 G>A maps to ENST00000392145 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr7:3681626 A>T maps to NM_152744.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr7:3681626 A>T maps to NM_152744.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr8:99440308 G>T maps to NM_020697.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr8:99440308 G>T maps to NM_020697.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr9:32541531 A>G maps to NM_005802.4 D997D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr9:32541531 A>G maps to NM_005802.4 D997D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr10:48389851 C>T maps to NM_002900.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr10:48389851 C>T maps to NM_002900.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr11:57182086 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr11:57182086 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:49443871 C>A maps to NM_003482.3 E1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:49443871 C>A maps to NM_003482.3 E1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:62946845 G>A maps to ENST00000393630 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:62946845 G>A maps to ENST00000393630 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:66725337 A>G maps to NM_033647.2 V1025V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:66725337 A>G maps to NM_033647.2 V1025V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr16:20043983 G>T maps to NM_001002911.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr16:20043983 G>T maps to NM_001002911.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr16:27802747 G>C maps to NM_001109763.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr16:27802747 G>C maps to NM_001109763.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:7673933 G>A maps to NM_020877.2 K1386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:7673933 G>A maps to NM_020877.2 K1386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:18528455 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:18528455 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:18528456 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:18528456 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:60140572 G>A maps to NM_005121.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:60140572 G>A maps to NM_005121.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr18:48327814 G>A maps to NM_001127176.1 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr18:48327814 G>A maps to NM_001127176.1 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:3643242 G>A maps to NM_012398.2 Y549Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:3643242 G>A maps to NM_012398.2 Y549Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:8212298 G>A maps to NM_032447.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:8212298 G>A maps to NM_032447.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:45316806 C>T maps to NM_005581.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:45316806 C>T maps to NM_005581.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:54725994 G>A maps to NM_001081450.1 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:54725994 G>A maps to NM_001081450.1 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr20:32379197 G>T maps to ENST00000375200 E814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr20:32379197 G>T maps to ENST00000375200 E814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr21:27840879 G>T maps to ENST00000435845 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr21:27840879 G>T maps to ENST00000435845 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr22:35742924 T>G maps to ENST00000451197 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr22:35742924 T>G maps to ENST00000451197 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:27106760 A>G maps to NM_006015.4 K2124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:27106760 A>G maps to NM_006015.4 K2124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:29314299 A>G maps to NM_001166005.1 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:29314299 A>G maps to NM_001166005.1 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:119576826 G>A maps to NM_015836.3 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:119576826 G>A maps to NM_015836.3 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:240371216 A>T maps to ENST00000406993 P1178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:240371216 A>T maps to ENST00000406993 P1178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr2:141751590 C>A maps to NM_018557.2 G873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr2:141751590 C>A maps to NM_018557.2 G873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr3:31710252 C>T maps to NM_017784.4 W659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr3:31710252 C>T maps to NM_017784.4 W659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:70721016 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:70721016 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:123192754 G>A maps to NM_015312.3 V2692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:123192754 G>A maps to NM_015312.3 V2692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:170913386 C>T maps to NM_021647.6 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:170913386 C>T maps to NM_021647.6 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:53813829 A>C maps to NM_052870.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:53813829 A>C maps to NM_052870.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:74091852 A>G did not map to a codon.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:74091852 A>G did not map to a codon.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:130766662 G>A maps to ENST00000514667 Q1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:130766662 G>A maps to ENST00000514667 Q1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:149247705 G>A maps to NM_000440.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:149247705 G>A maps to NM_000440.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr6:119510997 G>A maps to NM_005907.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr6:119510997 G>A maps to NM_005907.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr10:73472476 C>A maps to ENST00000398860 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr10:73472476 C>A maps to ENST00000398860 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr10:99410789 T>C maps to ENST00000416867 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr10:99410789 T>C maps to ENST00000416867 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr15:78403581 G>A maps to NM_006383.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr15:78403581 G>A maps to NM_006383.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr16:81944187 C>T maps to NM_002661.2 Y599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr16:81944187 C>T maps to NM_002661.2 Y599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr17:42293126 G>A maps to NM_014233.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr17:42293126 G>A maps to NM_014233.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr17:66267451 T>C maps to NM_004694.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr17:66267451 T>C maps to NM_004694.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr19:22574556 C>A maps to NM_001098626.1 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr19:22574556 C>A maps to NM_001098626.1 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr19:42312920 G>A maps to NM_001815.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr19:42312920 G>A maps to NM_001815.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr19:53644133 A>T maps to NM_001172674.1 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr19:53644133 A>T maps to NM_001172674.1 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr20:31023727 G>A maps to ENST00000375687 A1071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr20:31023727 G>A maps to ENST00000375687 A1071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr21:45959772 C>T maps to NM_198691.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr21:45959772 C>T maps to NM_198691.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr1:24998070 G>A maps to NM_005839.3 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr1:24998070 G>A maps to NM_005839.3 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr1:240371468 C>T maps to ENST00000406993 P1262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr1:240371468 C>T maps to ENST00000406993 P1262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr2:211454903 G>A maps to NM_001122633.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr2:211454903 G>A maps to NM_001122633.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr3:112005629 T>C maps to NM_183061.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr3:112005629 T>C maps to NM_183061.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr4:2831382 T>G maps to NM_001145856.1 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr4:2831382 T>G maps to NM_001145856.1 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr5:139201585 G>A maps to NM_032289.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr5:139201585 G>A maps to NM_032289.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr5:140176552 G>A maps to NM_018905.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr5:140176552 G>A maps to NM_018905.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr6:31595604 C>A maps to NM_080686.2 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr6:31595604 C>A maps to NM_080686.2 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr8:145534872 C>T maps to NM_005526.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr8:145534872 C>T maps to NM_005526.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr9:40702846 C>A maps to NM_001083124.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr9:40702846 C>A maps to NM_001083124.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr11:134054636 C>T maps to NM_015261.2 K782K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr11:134054636 C>T maps to NM_015261.2 K782K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr15:79067062 A>G maps to ENST00000258883 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr15:79067062 A>G maps to ENST00000258883 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr17:7366920 T>G maps to NM_020899.3 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr17:7366920 T>G maps to NM_020899.3 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr19:14829746 C>T maps to NM_032433.2 C536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr19:14829746 C>T maps to NM_032433.2 C536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr19:35232874 C>G maps to ENST00000392232 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr19:35232874 C>G maps to ENST00000392232 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr20:31021260 C>T maps to ENST00000375687 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr20:31021260 C>T maps to ENST00000375687 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr20:34458922 A>G maps to NM_016436.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr20:34458922 A>G maps to NM_016436.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr1:145367738 A>G maps to NM_001039703.4 K3445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr1:145367738 A>G maps to NM_001039703.4 K3445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr1:197104364 G>C maps to NM_018136.4 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr1:197104364 G>C maps to NM_018136.4 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr2:48059589 C>T maps to NM_001190274.1 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr2:48059589 C>T maps to NM_001190274.1 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr2:61415487 C>A maps to NM_014709.3 E3464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr2:61415487 C>A maps to NM_014709.3 E3464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr2:143790836 C>T maps to NM_003937.2 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr2:143790836 C>T maps to NM_003937.2 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr3:108112994 G>A maps to NM_014981.1 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr3:108112994 G>A maps to NM_014981.1 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr3:188327127 T>C maps to NM_005578.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr3:188327127 T>C maps to NM_005578.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr6:30884892 G>T maps to NM_001167734.1 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr6:30884892 G>T maps to NM_001167734.1 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr7:48327659 G>A maps to NM_152701.3 A2980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr7:48327659 G>A maps to NM_152701.3 A2980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr7:121943287 G>A maps to NM_001024613.2 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr7:121943287 G>A maps to NM_001024613.2 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr9:117791637 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr9:117791637 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr9:139847393 G>A maps to NM_178536.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr9:139847393 G>A maps to NM_178536.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr10:106974253 C>T maps to NM_014978.1 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr10:106974253 C>T maps to NM_014978.1 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr12:53189691 G>A maps to ENST00000309505 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr12:53189691 G>A maps to ENST00000309505 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr12:55820711 C>T maps to NM_001005183.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr12:55820711 C>T maps to NM_001005183.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr14:105354292 A>G maps to ENST00000453495 S1240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr14:105354292 A>G maps to ENST00000453495 S1240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr15:33954938 C>T maps to NM_001036.3 G1736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr15:33954938 C>T maps to NM_001036.3 G1736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr17:58288801 A>G maps to NM_032582.3 C751C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr17:58288801 A>G maps to NM_032582.3 C751C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr19:43579779 C>T maps to NM_031246.3 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr19:43579779 C>T maps to NM_031246.3 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr19:44352237 C>G maps to NM_181845.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr19:44352237 C>G maps to NM_181845.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr20:35668589 C>T maps to NM_002895.2 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr20:35668589 C>T maps to NM_002895.2 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr21:41684281 C>T maps to NM_001389.3 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr21:41684281 C>T maps to NM_001389.3 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr1:152732099 G>A maps to NM_001025231.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr1:152732099 G>A maps to NM_001025231.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr2:97883086 A>G maps to NM_001164315.1 T1277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr2:97883086 A>G maps to NM_001164315.1 T1277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr2:166165900 G>A maps to NM_001040142.1 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr2:166165900 G>A maps to NM_001040142.1 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr4:155254245 G>A maps to NM_017639.3 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr4:155254245 G>A maps to NM_017639.3 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr5:140563549 C>T maps to NM_020957.1 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr5:140563549 C>T maps to NM_020957.1 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr5:140573540 C>T maps to NM_018930.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr5:140573540 C>T maps to NM_018930.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr6:131490306 A>G maps to ENST00000431975 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr6:131490306 A>G maps to ENST00000431975 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr14:65239588 G>T maps to ENST00000389723 I1758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr14:65239588 G>T maps to ENST00000389723 I1758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr14:100728719 A>G maps to NM_003403.3 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr14:100728719 A>G maps to NM_003403.3 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr15:65917479 A>G maps to NM_004727.2 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr15:65917479 A>G maps to NM_004727.2 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:22001954 T>G maps to NM_003423.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:22001954 T>G maps to NM_003423.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:42301581 G>A maps to NM_001815.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:42301581 G>A maps to NM_001815.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:55106787 G>A maps to NM_006863.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:55106787 G>A maps to NM_006863.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr1:145367738 A>G maps to NM_001039703.4 K3445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr1:145367738 A>G maps to NM_001039703.4 K3445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:25467185 C>T maps to NM_175629.1 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:25467185 C>T maps to NM_175629.1 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:121746684 C>T maps to NM_005270.4 D1065D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:121746684 C>T maps to NM_005270.4 D1065D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:129026418 G>A maps to NM_004807.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:129026418 G>A maps to NM_004807.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:132237010 G>C maps to NM_080386.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:132237010 G>C maps to NM_080386.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr5:205600 G>A maps to NM_145265.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr5:205600 G>A maps to NM_145265.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr5:2749499 G>A maps to NM_033267.4 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr5:2749499 G>A maps to NM_033267.4 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr5:80409728 T>C maps to NM_006909.1 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr5:80409728 T>C maps to NM_006909.1 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr10:12200104 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr10:12200104 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr11:133790979 G>A maps to NM_014987.1 A880A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr11:133790979 G>A maps to NM_014987.1 A880A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr17:79207798 C>T maps to NM_144679.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr17:79207798 C>T maps to NM_144679.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr20:47692014 C>T maps to NM_001316.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr20:47692014 C>T maps to NM_001316.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr2:141259354 G>A maps to NM_018557.2 G2917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr2:141259354 G>A maps to NM_018557.2 G2917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr5:140605444 C>T maps to NM_018934.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr5:140605444 C>T maps to NM_018934.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr6:57393111 T>C maps to NM_000947.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr6:57393111 T>C maps to NM_000947.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr8:28385110 A>T maps to NM_017412.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr8:28385110 A>T maps to NM_017412.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr1:152328410 A>G maps to NM_001014342.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr1:152328410 A>G maps to NM_001014342.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr1:174987688 G>T maps to NM_022100.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr1:174987688 G>T maps to NM_022100.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr3:112546283 G>A maps to NM_001008784.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr3:112546283 G>A maps to NM_001008784.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr5:36225708 C>A maps to NM_001085411.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr5:36225708 C>A maps to NM_001085411.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr5:82849207 G>A maps to NM_004385.4 W3173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr5:82849207 G>A maps to NM_004385.4 W3173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr6:43400461 C>T maps to NM_033450.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr6:43400461 C>T maps to NM_033450.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr9:428368 C>A maps to NM_203447.3 S1449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr9:428368 C>A maps to NM_203447.3 S1449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr10:24880836 A>G maps to NM_020824.3 I1327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr10:24880836 A>G maps to NM_020824.3 I1327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr10:118394421 T>A maps to NM_005396.4 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr10:118394421 T>A maps to NM_005396.4 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr11:2182080 G>A maps to NM_001042376.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr11:2182080 G>A maps to NM_001042376.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr12:40631790 T>C maps to NM_198578.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr12:40631790 T>C maps to NM_198578.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr14:100728719 A>G maps to NM_003403.3 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr14:100728719 A>G maps to NM_003403.3 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr16:52478214 C>T maps to ENST00000407228 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr16:52478214 C>T maps to ENST00000407228 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr16:72139183 C>A maps to NM_014003.3 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr16:72139183 C>A maps to NM_014003.3 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr17:33769198 G>A maps to NM_144682.5 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr17:33769198 G>A maps to NM_144682.5 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr17:48263704 G>A maps to NM_000088.3 F1326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr17:48263704 G>A maps to NM_000088.3 F1326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr20:50071157 G>A maps to NM_012340.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr20:50071157 G>A maps to NM_012340.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr22:25016295 G>A maps to NM_005265.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr22:25016295 G>A maps to NM_005265.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chrX:54224912 C>A maps to NM_020922.4 G1749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chrX:54224912 C>A maps to NM_020922.4 G1749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chrX:70823594 G>A maps to NM_052957.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chrX:70823594 G>A maps to NM_052957.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr1:55521762 C>T maps to NM_174936.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr1:55521762 C>T maps to NM_174936.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr1:163122354 C>T maps to NM_003617.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr1:163122354 C>T maps to NM_003617.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr2:175618297 G>A maps to NM_001039523.2 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr2:175618297 G>A maps to NM_001039523.2 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr2:219353101 G>T maps to NM_020935.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr2:219353101 G>T maps to NM_020935.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr3:108347995 A>G maps to NM_014648.3 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr3:108347995 A>G maps to NM_014648.3 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr4:1980395 C>T maps to NM_133335.3 D1286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr4:1980395 C>T maps to NM_133335.3 D1286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr5:173067 C>T maps to NM_052909.3 C1013C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr5:173067 C>T maps to NM_052909.3 C1013C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr6:28294581 G>T maps to NM_030899.4 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr6:28294581 G>T maps to NM_030899.4 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr6:132203594 C>T maps to NM_006208.2 Y737Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr6:132203594 C>T maps to NM_006208.2 Y737Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr7:121652282 G>A maps to NM_002851.2 E1061E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr7:121652282 G>A maps to NM_002851.2 E1061E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr9:129642272 C>T maps to ENST00000319119 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr9:129642272 C>T maps to ENST00000319119 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr10:64159481 C>T maps to NM_014951.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr10:64159481 C>T maps to NM_014951.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr10:127525311 C>A maps to NM_018180.2 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr10:127525311 C>A maps to NM_018180.2 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr11:1643251 A>G maps to ENST00000359229 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr11:1643251 A>G maps to ENST00000359229 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr11:119002675 C>G maps to NM_198971.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr11:119002675 C>G maps to NM_198971.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr12:56030938 G>A maps to NM_206899.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr12:56030938 G>A maps to NM_206899.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr12:131498746 C>T maps to NM_198827.3 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr12:131498746 C>T maps to NM_198827.3 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr13:52661538 T>G maps to NM_199289.1 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr13:52661538 T>G maps to NM_199289.1 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr14:24613438 G>A maps to ENST00000429021 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr14:24613438 G>A maps to ENST00000429021 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr15:30938315 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr15:30938315 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr15:65491057 G>T maps to NM_003613.3 Y522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr15:65491057 G>T maps to NM_003613.3 Y522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr17:16285382 T>C maps to NM_018955.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr17:16285382 T>C maps to NM_018955.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr19:22940553 A>G maps to ENST00000397104 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr19:22940553 A>G maps to ENST00000397104 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr20:8755242 T>C maps to NM_015192.2 A996A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr20:8755242 T>C maps to NM_015192.2 A996A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chrX:14748514 C>T maps to NM_002063.3 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chrX:14748514 C>T maps to NM_002063.3 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr1:155451979 A>T maps to ENST00000368346 C227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr1:155451979 A>T maps to ENST00000368346 C227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr2:209358095 G>T maps to NM_005048.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr2:209358095 G>T maps to NM_005048.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr3:169486065 A>G maps to NM_032487.4 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr3:169486065 A>G maps to NM_032487.4 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr4:155256173 C>G maps to NM_017639.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr4:155256173 C>G maps to NM_017639.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr5:115298377 C>T maps to NM_173800.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr5:115298377 C>T maps to NM_173800.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr6:31797487 C>G maps to NM_005346.4 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr6:31797487 C>G maps to NM_005346.4 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr11:122848488 G>A maps to NM_001098169.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr11:122848488 G>A maps to NM_001098169.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr13:45523878 T>C maps to NM_012345.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr13:45523878 T>C maps to NM_012345.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr15:59064094 T>G maps to NM_001040450.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr15:59064094 T>G maps to NM_001040450.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chrX:51075840 A>G maps to NM_153183.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chrX:51075840 A>G maps to NM_153183.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chrX:153224169 A>C maps to ENST00000369984 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chrX:153224169 A>C maps to ENST00000369984 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr2:203157537 A>G maps to NM_015934.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr2:203157537 A>G maps to NM_015934.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr2:235951818 A>G maps to NM_014521.2 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr2:235951818 A>G maps to NM_014521.2 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr2:242794938 G>T maps to NM_005018.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr2:242794938 G>T maps to NM_005018.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr3:196509543 T>C maps to NM_002577.4 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr3:196509543 T>C maps to NM_002577.4 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr8:8749968 C>A maps to NM_004225.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr8:8749968 C>A maps to NM_004225.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr8:135621024 G>T maps to NM_020863.3 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr8:135621024 G>T maps to NM_020863.3 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr9:35042437 C>T maps to NM_203299.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr9:35042437 C>T maps to NM_203299.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr10:429976 G>A maps to NM_014974.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr10:429976 G>A maps to NM_014974.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr11:43513625 C>T maps to NM_018259.5 D1069D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr11:43513625 C>T maps to NM_018259.5 D1069D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr12:104487294 T>G maps to NM_013320.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr12:104487294 T>G maps to NM_013320.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr15:74368263 C>T maps to NM_001038640.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr15:74368263 C>T maps to NM_001038640.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr16:72130067 C>T maps to NM_014003.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr16:72130067 C>T maps to NM_014003.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr17:40476776 G>A maps to NM_139276.2 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr17:40476776 G>A maps to NM_139276.2 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr21:30439984 A>G maps to NM_006585.2 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr21:30439984 A>G maps to NM_006585.2 H91H. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EJ-5506-01A-01D-1576-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-EJ-5506-01A-01D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr1:55521820 C>A maps to NM_174936.3 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr1:55521820 C>A maps to NM_174936.3 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr1:149884959 G>A maps to NM_014849.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr1:149884959 G>A maps to NM_014849.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr2:238259790 G>T maps to NM_004369.3 T2266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr2:238259790 G>T maps to NM_004369.3 T2266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:47036898 A>G maps to NM_015175.1 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:47036898 A>G maps to NM_015175.1 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:51347718 C>T maps to NM_004947.4 F993F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:51347718 C>T maps to NM_004947.4 F993F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:129247551 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:129247551 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:195510155 G>A maps to NM_018406.5 H2765H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:195510155 G>A maps to NM_018406.5 H2765H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr6:51524057 G>A maps to NM_138694.3 C3622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr6:51524057 G>A maps to NM_138694.3 C3622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr6:108985091 C>G maps to NM_001455.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr6:108985091 C>G maps to NM_001455.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr6:111726772 C>T maps to NM_002912.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr6:111726772 C>T maps to NM_002912.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr7:106509964 C>T maps to NM_002649.2 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr7:106509964 C>T maps to NM_002649.2 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr9:77448964 T>C maps to NM_017662.4 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr9:77448964 T>C maps to NM_017662.4 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr9:138586194 C>T maps to NM_001012415.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr9:138586194 C>T maps to NM_001012415.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr13:45594564 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr13:45594564 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr19:19625912 G>T maps to NM_032037.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr19:19625912 G>T maps to NM_032037.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr20:20493221 G>A maps to NM_020343.3 P1597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr20:20493221 G>A maps to NM_020343.3 P1597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr20:39990960 G>A maps to NM_052846.1 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr20:39990960 G>A maps to NM_052846.1 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr22:26688422 C>A maps to NM_021115.4 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr22:26688422 C>A maps to NM_021115.4 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr22:31059966 G>A maps to NM_152511.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr22:31059966 G>A maps to NM_152511.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr1:186915808 A>G maps to NM_024420.2 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr1:186915808 A>G maps to NM_024420.2 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr4:126370708 C>T maps to NM_024582.4 S2846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr4:126370708 C>T maps to NM_024582.4 S2846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr5:148206405 C>T maps to NM_000024.5 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr5:148206405 C>T maps to NM_000024.5 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr6:41029414 G>A maps to NM_006789.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr6:41029414 G>A maps to NM_006789.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr6:87969898 A>G maps to NM_015021.1 Q2184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr6:87969898 A>G maps to NM_015021.1 Q2184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr7:6865861 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr7:6865861 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr7:87104730 C>T maps to NM_018849.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr7:87104730 C>T maps to NM_018849.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr11:71850177 G>T maps to ENST00000442948 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr11:71850177 G>T maps to ENST00000442948 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr14:36039875 T>G maps to NM_194301.2 T1975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr14:36039875 T>G maps to NM_194301.2 T1975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr17:39742897 G>A maps to NM_000526.4 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr17:39742897 G>A maps to NM_000526.4 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr18:19154389 T>A maps to NM_052911.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr18:19154389 T>A maps to NM_052911.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr19:53855283 G>A maps to NM_138374.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr19:53855283 G>A maps to NM_138374.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr21:30255332 A>G maps to NM_013240.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr21:30255332 A>G maps to NM_013240.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr1:12921384 C>T maps to NM_023014.1 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr1:12921384 C>T maps to NM_023014.1 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr1:16255571 C>A maps to NM_015001.2 S946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr1:16255571 C>A maps to NM_015001.2 S946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr1:152975738 T>C maps to NM_005416.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr1:152975738 T>C maps to NM_005416.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr2:189875580 A>T maps to NM_000090.3 K1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr2:189875580 A>T maps to NM_000090.3 K1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr3:33400491 C>T maps to NM_012157.3 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr3:33400491 C>T maps to NM_012157.3 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr4:74005374 T>G maps to NM_032217.3 G986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr4:74005374 T>G maps to NM_032217.3 G986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr4:153881742 C>T maps to NM_033393.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr4:153881742 C>T maps to NM_033393.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr6:27861557 G>A maps to NM_003527.4 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr6:27861557 G>A maps to NM_003527.4 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr7:100693834 T>C maps to NM_001040105.1 L4265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr7:100693834 T>C maps to NM_001040105.1 L4265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr8:37623075 G>A maps to NM_007198.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr8:37623075 G>A maps to NM_007198.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr10:82185668 C>T maps to NM_032333.4 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr10:82185668 C>T maps to NM_032333.4 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr11:119045199 C>T maps to NM_024618.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr11:119045199 C>T maps to NM_024618.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr12:6787621 C>T maps to NM_001135734.1 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr12:6787621 C>T maps to NM_001135734.1 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr12:88568464 T>C maps to NM_181783.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr12:88568464 T>C maps to NM_181783.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr15:89195525 A>G maps to NM_002201.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr15:89195525 A>G maps to NM_002201.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr17:30533969 A>G maps to NM_001033568.1 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr17:30533969 A>G maps to NM_001033568.1 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr17:39383040 C>T maps to NM_031961.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr17:39383040 C>T maps to NM_031961.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr17:39406007 A>C maps to ENST00000431129 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr17:39406007 A>C maps to ENST00000431129 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr17:45664676 C>T maps to NM_006310.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr17:45664676 C>T maps to NM_006310.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr17:71384168 C>T maps to NM_001144952.1 P1400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr17:71384168 C>T maps to NM_001144952.1 P1400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr20:57769547 G>A maps to NM_178457.1 T1158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr20:57769547 G>A maps to NM_178457.1 T1158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr1:198233328 A>G maps to NM_133494.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr1:198233328 A>G maps to NM_133494.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr3:63898513 G>A maps to NM_001177387.1 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr3:63898513 G>A maps to NM_001177387.1 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr3:64554180 G>A maps to NM_182920.1 Q1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr3:64554180 G>A maps to NM_182920.1 Q1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr6:27879449 T>G maps to NM_033057.2 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr6:27879449 T>G maps to NM_033057.2 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr10:17204220 A>C maps to NM_004412.5 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr10:17204220 A>C maps to NM_004412.5 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr11:43345104 A>C maps to NM_001142930.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr11:43345104 A>C maps to NM_001142930.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:43777765 A>G maps to ENST00000389420 C1489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:43777765 A>G maps to ENST00000389420 C1489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:120150459 G>T maps to ENST00000392521 P1540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:120150459 G>T maps to ENST00000392521 P1540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:120635151 C>T maps to NM_053275.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:120635151 C>T maps to NM_053275.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr13:109779875 G>A maps to NM_015011.1 A1321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr13:109779875 G>A maps to NM_015011.1 A1321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chrX:37027784 C>T maps to NM_001013736.2 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chrX:37027784 C>T maps to NM_001013736.2 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr1:145015937 C>T maps to NM_001198832.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr1:145015937 C>T maps to NM_001198832.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr1:240371111 G>T maps to ENST00000406993 P1143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr1:240371111 G>T maps to ENST00000406993 P1143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr3:184647412 T>C maps to ENST00000437079 D920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr3:184647412 T>C maps to ENST00000437079 D920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr4:983808 C>T maps to NM_213613.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr4:983808 C>T maps to NM_213613.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr4:91229662 T>C maps to NM_001145065.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr4:91229662 T>C maps to NM_001145065.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr5:156184678 C>T maps to NM_000337.5 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr5:156184678 C>T maps to NM_000337.5 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr6:152832184 T>A maps to NM_182961.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr6:152832184 T>A maps to NM_182961.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr9:112185101 C>T maps to NM_002829.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr9:112185101 C>T maps to NM_002829.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr9:134497350 C>T maps to NM_198679.1 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr9:134497350 C>T maps to NM_198679.1 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr11:133790583 G>T maps to NM_014987.1 I1012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr11:133790583 G>T maps to NM_014987.1 I1012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr15:85326136 G>A maps to NM_014630.2 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr15:85326136 G>A maps to NM_014630.2 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:30986137 G>A maps to NM_015194.1 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:30986137 G>A maps to NM_015194.1 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:41611324 G>A maps to NM_001079675.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:41611324 G>A maps to NM_001079675.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42635478 C>T maps to NM_001466.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42635478 C>T maps to NM_001466.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636060 C>G maps to NM_001466.3 Y335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636060 C>G maps to NM_001466.3 Y335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636210 C>T maps to NM_001466.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636210 C>T maps to NM_001466.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636498 C>T maps to NM_001466.3 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636498 C>T maps to NM_001466.3 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr19:41595958 G>A maps to NM_000766.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr19:41595958 G>A maps to NM_000766.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr1:158669836 G>T maps to NM_001005279.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr1:158669836 G>T maps to NM_001005279.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr3:149040065 C>A maps to NM_138786.3 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr3:149040065 C>A maps to NM_138786.3 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr6:106764040 G>A maps to NM_004849.2 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr6:106764040 G>A maps to NM_004849.2 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr7:141315345 G>T maps to NM_018238.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr7:141315345 G>T maps to NM_018238.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr10:93600427 A>G maps to NM_025235.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr10:93600427 A>G maps to NM_025235.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr11:93754496 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr11:93754496 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr12:14628822 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr12:14628822 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr15:33261342 T>G maps to NM_001103184.2 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr15:33261342 T>G maps to NM_001103184.2 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr15:42676688 C>T maps to NM_000070.2 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr15:42676688 C>T maps to NM_000070.2 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr15:45965848 G>T maps to NM_021199.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr15:45965848 G>T maps to NM_021199.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr16:87678350 C>T maps to NM_020655.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr16:87678350 C>T maps to NM_020655.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr17:62007650 G>A maps to NM_001039933.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr17:62007650 G>A maps to NM_001039933.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr20:1559074 G>A maps to NM_006065.3 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr20:1559074 G>A maps to NM_006065.3 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr1:55280636 C>T maps to NM_001110533.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr1:55280636 C>T maps to NM_001110533.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr1:113636958 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr1:113636958 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:15468433 C>T maps to NM_015909.2 G1450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:15468433 C>T maps to NM_015909.2 G1450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:29148006 T>G maps to NM_015131.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:29148006 T>G maps to NM_015131.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:109382169 A>G maps to NM_006267.4 E1725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:109382169 A>G maps to NM_006267.4 E1725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:209292994 G>T maps to NM_005048.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:209292994 G>T maps to NM_005048.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:213886795 C>G maps to ENST00000342002 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:213886795 C>G maps to ENST00000342002 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr4:9828094 T>G maps to NM_020041.2 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr4:9828094 T>G maps to NM_020041.2 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr4:79747249 C>A maps to NM_198892.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr4:79747249 C>A maps to NM_198892.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr5:79026180 C>T maps to NM_153610.3 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr5:79026180 C>T maps to NM_153610.3 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr5:82808054 C>T maps to NM_004385.4 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr5:82808054 C>T maps to NM_004385.4 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr7:95750980 A>G maps to NM_001160210.1 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr7:95750980 A>G maps to NM_001160210.1 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr10:118357364 C>T maps to NM_006229.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr10:118357364 C>T maps to NM_006229.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr11:8969884 C>T maps to NM_020644.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr11:8969884 C>T maps to NM_020644.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr12:102158762 T>C maps to NM_024312.4 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr12:102158762 T>C maps to NM_024312.4 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr12:125396376 A>G maps to NM_021009.5 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr12:125396376 A>G maps to NM_021009.5 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr14:21871247 A>G maps to NM_001170629.1 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr14:21871247 A>G maps to NM_001170629.1 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr15:42602621 G>A maps to NM_198141.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr15:42602621 G>A maps to NM_198141.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr16:24373177 C>T maps to NM_006539.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr16:24373177 C>T maps to NM_006539.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr16:25251247 G>T maps to NM_001012981.4 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr16:25251247 G>T maps to NM_001012981.4 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr17:7495580 T>C maps to NM_004860.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr17:7495580 T>C maps to NM_004860.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr17:39135204 A>G maps to NM_182497.3 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr17:39135204 A>G maps to NM_182497.3 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr17:73887231 C>T maps to NM_173547.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr17:73887231 C>T maps to NM_173547.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr19:5598869 G>A maps to NM_014649.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr19:5598869 G>A maps to NM_014649.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr19:9237434 A>G maps to NM_001001958.1 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr19:9237434 A>G maps to NM_001001958.1 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chrX:2407935 G>A maps to NM_004729.3 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chrX:2407935 G>A maps to NM_004729.3 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chrX:107159357 A>G maps to NM_012216.3 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chrX:107159357 A>G maps to NM_012216.3 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chrX:144337273 G>T maps to NM_001009614.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chrX:144337273 G>T maps to NM_001009614.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr1:46073596 A>G maps to NM_002482.3 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr1:46073596 A>G maps to NM_002482.3 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr2:160737620 C>T maps to NM_001198759.1 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr2:160737620 C>T maps to NM_001198759.1 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr11:66082755 C>T maps to NM_020404.2 Q581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr11:66082755 C>T maps to NM_020404.2 Q581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr12:132547086 G>A maps to ENST00000333577 Q2761Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr12:132547086 G>A maps to ENST00000333577 Q2761Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr16:52484401 C>T maps to ENST00000407228 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr16:52484401 C>T maps to ENST00000407228 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr17:33690214 G>T maps to NM_152270.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr17:33690214 G>T maps to NM_152270.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr18:8609871 C>A maps to NM_001025300.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr18:8609871 C>A maps to NM_001025300.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr18:42532844 C>A maps to NM_015559.2 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr18:42532844 C>A maps to NM_015559.2 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr19:12940771 G>A maps to NM_031429.1 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr19:12940771 G>A maps to NM_031429.1 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr19:48622426 A>G maps to NM_000234.1 D802D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr19:48622426 A>G maps to NM_000234.1 D802D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chrX:30254529 A>G maps to NM_002365.4 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chrX:30254529 A>G maps to NM_002365.4 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr1:12336132 C>T maps to NM_015378.2 R830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr1:12336132 C>T maps to NM_015378.2 R830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr1:91843737 T>A maps to NM_001017975.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr1:91843737 T>A maps to NM_001017975.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr2:160688256 C>T maps to NM_001198759.1 E1294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr2:160688256 C>T maps to NM_001198759.1 E1294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr2:160710868 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr2:160710868 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr3:113152409 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr3:113152409 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr4:9828062 G>A maps to NM_020041.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr4:9828062 G>A maps to NM_020041.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr4:158257611 C>T maps to NM_000826.3 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr4:158257611 C>T maps to NM_000826.3 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr6:30954962 G>A maps to NM_001010909.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr6:30954962 G>A maps to NM_001010909.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr6:57393159 G>A maps to NM_000947.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr6:57393159 G>A maps to NM_000947.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr6:158505087 A>G maps to NM_003898.3 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr6:158505087 A>G maps to NM_003898.3 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr6:161032667 A>G maps to NM_005577.2 T843T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr6:161032667 A>G maps to NM_005577.2 T843T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr7:138437473 G>A maps to NM_130840.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr7:138437473 G>A maps to NM_130840.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr10:5435917 G>A maps to NM_024803.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr10:5435917 G>A maps to NM_024803.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr11:13424826 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr11:13424826 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr11:18579844 G>C maps to NM_001040697.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr11:18579844 G>C maps to NM_001040697.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr13:25376710 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr13:25376710 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr15:30938315 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr15:30938315 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr15:43827081 G>A maps to NM_001130858.2 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr15:43827081 G>A maps to NM_001130858.2 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr15:101464914 T>C maps to NM_024652.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr15:101464914 T>C maps to NM_024652.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr19:5456786 C>T maps to NM_181710.3 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr19:5456786 C>T maps to NM_181710.3 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr19:12492035 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr19:12492035 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr19:12492038 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr19:12492038 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr20:32212689 C>T maps to NM_005093.3 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr20:32212689 C>T maps to NM_005093.3 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr20:37547206 G>A maps to NM_015568.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr20:37547206 G>A maps to NM_015568.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr20:61471945 C>T maps to NM_001853.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr20:61471945 C>T maps to NM_001853.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr22:51008808 G>A maps to NM_152245.2 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr22:51008808 G>A maps to NM_152245.2 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr1:12855751 G>A maps to NM_023013.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr1:12855751 G>A maps to NM_023013.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr2:118771565 C>A maps to NM_019044.4 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr2:118771565 C>A maps to NM_019044.4 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr2:198283304 T>C maps to NM_012433.2 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr2:198283304 T>C maps to NM_012433.2 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr4:155242137 C>T maps to NM_017639.3 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr4:155242137 C>T maps to NM_017639.3 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr5:137277735 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr5:137277735 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr5:140558061 T>A maps to NM_019120.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr5:140558061 T>A maps to NM_019120.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr6:39828786 G>A maps to ENST00000398904 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr6:39828786 G>A maps to ENST00000398904 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr7:154667654 C>T maps to NM_130797.2 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr7:154667654 C>T maps to NM_130797.2 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr9:88903618 T>C maps to NM_024617.3 S1487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr9:88903618 T>C maps to NM_024617.3 S1487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr11:117789385 A>C maps to ENST00000413475 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr11:117789385 A>C maps to ENST00000413475 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr12:113733847 A>T maps to NM_001143819.1 P878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr12:113733847 A>T maps to NM_001143819.1 P878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr16:55601018 C>T maps to NM_032330.1 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr16:55601018 C>T maps to NM_032330.1 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr17:725621 C>A maps to NM_022463.3 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr17:725621 C>A maps to NM_022463.3 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr19:9063352 G>A maps to NM_024690.2 S8031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr19:9063352 G>A maps to NM_024690.2 S8031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr19:36430857 C>A maps to NM_024509.1 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr19:36430857 C>A maps to NM_024509.1 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr19:52937266 G>A maps to NM_001143939.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr19:52937266 G>A maps to NM_001143939.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr22:45128195 G>C maps to ENST00000352766 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr22:45128195 G>C maps to ENST00000352766 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chrX:41000650 G>A maps to NM_001039590.2 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chrX:41000650 G>A maps to NM_001039590.2 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr1:15546031 C>T maps to NM_018022.2 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr1:15546031 C>T maps to NM_018022.2 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr1:70502286 T>C maps to NM_020794.2 H718H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr1:70502286 T>C maps to NM_020794.2 H718H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:25469137 C>T maps to NM_175629.1 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:25469137 C>T maps to NM_175629.1 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:28117447 C>T maps to NM_004899.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:28117447 C>T maps to NM_004899.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:241831175 C>T maps to NM_001085437.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:241831175 C>T maps to NM_001085437.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:36778887 G>A maps to NM_033403.1 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:36778887 G>A maps to NM_033403.1 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:51456278 G>A maps to ENST00000273612 F1096F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:51456278 G>A maps to ENST00000273612 F1096F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:121413150 T>C maps to ENST00000393667 E2073E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:121413150 T>C maps to ENST00000393667 E2073E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EJ-5518-01A-01D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:187451334 G>A maps to ENST00000449623 R51R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EJ-5518-01A-01D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:187451334 G>A maps to ENST00000449623 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr6:46623670 C>A maps to NM_004277.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr6:46623670 C>A maps to NM_004277.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr7:48315046 C>T maps to NM_152701.3 V1928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr7:48315046 C>T maps to NM_152701.3 V1928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr10:70940277 C>T maps to NM_003171.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr10:70940277 C>T maps to NM_003171.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr10:103789493 G>A maps to NM_024541.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr10:103789493 G>A maps to NM_024541.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr11:113704217 G>C maps to NM_020886.2 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr11:113704217 G>C maps to NM_020886.2 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr12:78515854 G>T maps to NM_014903.4 T1295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr12:78515854 G>T maps to NM_014903.4 T1295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr15:51750825 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr15:51750825 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr16:23999907 C>T maps to NM_002738.6 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr16:23999907 C>T maps to NM_002738.6 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr16:83065741 C>T maps to ENST00000268613 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr16:83065741 C>T maps to ENST00000268613 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr17:75205503 C>G maps to NM_001039573.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr17:75205503 C>G maps to NM_001039573.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr19:40383985 G>A maps to NM_003890.2 C3208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr19:40383985 G>A maps to NM_003890.2 C3208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr21:47773102 C>A maps to NM_006031.5 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr21:47773102 C>A maps to NM_006031.5 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chrX:13337264 C>T maps to NM_001135995.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chrX:13337264 C>T maps to NM_001135995.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:85510884 G>A maps to NM_018298.9 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:85510884 G>A maps to NM_018298.9 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:152275292 A>G maps to NM_002016.1 D4023D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:152275292 A>G maps to NM_002016.1 D4023D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:186055462 T>G maps to NM_031935.2 G2990G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:186055462 T>G maps to NM_031935.2 G2990G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:33745724 C>T maps to NM_170672.2 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:33745724 C>T maps to NM_170672.2 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:44040308 A>T maps to NM_022436.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:44040308 A>T maps to NM_022436.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:215645850 G>A maps to NM_000465.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:215645850 G>A maps to NM_000465.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:226447104 G>A maps to NM_020864.1 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:226447104 G>A maps to NM_020864.1 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr3:44399286 G>C maps to NM_173826.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr3:44399286 G>C maps to NM_173826.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr3:45942585 C>T maps to NM_031200.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr3:45942585 C>T maps to NM_031200.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr4:76813114 G>A maps to NM_006239.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr4:76813114 G>A maps to NM_006239.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr5:115238634 T>C maps to NM_001284.2 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr5:115238634 T>C maps to NM_001284.2 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr5:129520760 A>G maps to NM_175856.4 E642E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr5:129520760 A>G maps to NM_175856.4 E642E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:32156279 G>T maps to NM_002586.4 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:32156279 G>T maps to NM_002586.4 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:34100898 C>T maps to NM_000841.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:34100898 C>T maps to NM_000841.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:87969736 C>T maps to NM_015021.1 N2130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:87969736 C>T maps to NM_015021.1 N2130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:108985268 C>T maps to NM_001455.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:108985268 C>T maps to NM_001455.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:110752469 C>T maps to NM_033125.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:110752469 C>T maps to NM_033125.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr7:48318293 T>C maps to NM_152701.3 T2501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr7:48318293 T>C maps to NM_152701.3 T2501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr7:151932987 T>A maps to ENST00000355193 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr7:151932987 T>A maps to ENST00000355193 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:17169088 C>T maps to NM_004686.4 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:17169088 C>T maps to NM_004686.4 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:25745378 C>A maps to NM_022659.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:25745378 C>A maps to NM_022659.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:53071574 G>A maps to NM_014682.2 Y563Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:53071574 G>A maps to NM_014682.2 Y563Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:82371573 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:82371573 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:95158180 G>A maps to NM_001144663.1 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:95158180 G>A maps to NM_001144663.1 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:95676989 C>G maps to NM_017697.3 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:95676989 C>G maps to NM_017697.3 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:131249204 C>G maps to NM_018482.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:131249204 C>G maps to NM_018482.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr11:119228894 G>A maps to NM_004205.4 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr11:119228894 G>A maps to NM_004205.4 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:32135814 C>T maps to NM_018169.3 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:32135814 C>T maps to NM_018169.3 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:46757762 C>G maps to NM_018976.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:46757762 C>G maps to NM_018976.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:69094532 C>A maps to NM_020401.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:69094532 C>A maps to NM_020401.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:97098575 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:97098575 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:123875310 C>T maps to NM_020382.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:123875310 C>T maps to NM_020382.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr13:50123714 G>A maps to NM_018191.3 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr13:50123714 G>A maps to NM_018191.3 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr16:69056742 C>G maps to NM_024562.1 S952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr16:69056742 C>G maps to NM_024562.1 S952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:5264855 A>G maps to NM_004703.4 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:5264855 A>G maps to NM_004703.4 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:7827735 G>T maps to NM_004732.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:7827735 G>T maps to NM_004732.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:17412830 C>T maps to NM_148172.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:17412830 C>T maps to NM_148172.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:56598641 G>A maps to NM_004574.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:56598641 G>A maps to NM_004574.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr18:12706676 G>T maps to NM_020232.4 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr18:12706676 G>T maps to NM_020232.4 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:2878236 C>T maps to NM_024967.1 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:2878236 C>T maps to NM_024967.1 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:14910837 G>C maps to NM_198944.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:14910837 G>C maps to NM_198944.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:14938094 C>A maps to NM_017506.1 *320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:14938094 C>A maps to NM_017506.1 *320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr20:16360551 C>A maps to NM_024704.4 E699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr20:16360551 C>A maps to NM_024704.4 E699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr21:45959619 C>T maps to NM_198691.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr21:45959619 C>T maps to NM_198691.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr22:30736750 T>C maps to NM_005877.4 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr22:30736750 T>C maps to NM_005877.4 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr1:111147493 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr1:111147493 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr1:158064570 C>T maps to ENST00000368173 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr1:158064570 C>T maps to ENST00000368173 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr1:247614411 G>T maps to NM_001004492.1 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr1:247614411 G>T maps to NM_001004492.1 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:15378657 C>T maps to NM_015909.2 E1959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:15378657 C>T maps to NM_015909.2 E1959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:25505421 G>A maps to NM_175629.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:25505421 G>A maps to NM_175629.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:101607289 C>T maps to NM_002518.3 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:101607289 C>T maps to NM_002518.3 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr3:148760004 A>T maps to NM_003071.3 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr3:148760004 A>T maps to NM_003071.3 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr3:151545614 C>T maps to NM_001086.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr3:151545614 C>T maps to NM_001086.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:126371607 T>A maps to NM_024582.4 L3146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:126371607 T>A maps to NM_024582.4 L3146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:126371767 T>C maps to NM_024582.4 Y3199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:126371767 T>C maps to NM_024582.4 Y3199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:159790452 C>T maps to ENST00000379346 R912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:159790452 C>T maps to ENST00000379346 R912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:163204 G>C maps to NM_052909.3 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:163204 G>C maps to NM_052909.3 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:72370578 G>T maps to NM_138782.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:72370578 G>T maps to NM_138782.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:156899409 C>T maps to NM_001099287.1 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:156899409 C>T maps to NM_001099287.1 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:180582178 G>A maps to NM_206880.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:180582178 G>A maps to NM_206880.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr9:71628978 G>A maps to NM_002732.3 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr9:71628978 G>A maps to NM_002732.3 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr9:130653031 G>A maps to NM_013443.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr9:130653031 G>A maps to NM_013443.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr11:4791051 A>T maps to ENST00000380383 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr11:4791051 A>T maps to ENST00000380383 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr12:7061280 C>T maps to ENST00000416215 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr12:7061280 C>T maps to ENST00000416215 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr12:55420975 C>A maps to NM_021191.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr12:55420975 C>A maps to NM_021191.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr13:102047575 C>T maps to NM_052867.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr13:102047575 C>T maps to NM_052867.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr15:65790301 G>A maps to NM_197960.2 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr15:65790301 G>A maps to NM_197960.2 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr16:70506906 T>C maps to NM_145059.2 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr16:70506906 T>C maps to NM_145059.2 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr17:58288801 A>G maps to NM_032582.3 C751C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr17:58288801 A>G maps to NM_032582.3 C751C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:5784047 T>C maps to NM_001134316.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:5784047 T>C maps to NM_001134316.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:10394817 G>A maps to NM_000201.2 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:10394817 G>A maps to NM_000201.2 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:10625417 G>A maps to NM_001166215.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:10625417 G>A maps to NM_001166215.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr20:17622554 T>A maps to ENST00000377813 K691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr20:17622554 T>A maps to ENST00000377813 K691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr20:42161555 T>C maps to NM_032107.4 Y454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr20:42161555 T>C maps to NM_032107.4 Y454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr22:17663640 A>C maps to NM_017424.2 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr22:17663640 A>C maps to NM_017424.2 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr22:25016295 G>A maps to NM_005265.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr22:25016295 G>A maps to NM_005265.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr1:1333665 G>A maps to NM_030937.4 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr1:1333665 G>A maps to NM_030937.4 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr1:8420608 T>G maps to NM_012102.3 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr1:8420608 T>G maps to NM_012102.3 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr1:154988947 C>A maps to ENST00000417934 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr1:154988947 C>A maps to ENST00000417934 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr2:241404316 C>T maps to NM_002081.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr2:241404316 C>T maps to NM_002081.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr2:242138765 C>T maps to NM_001001891.3 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr2:242138765 C>T maps to NM_001001891.3 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr3:44672663 G>A maps to NM_006991.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr3:44672663 G>A maps to NM_006991.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr4:48851970 T>C maps to NM_001168254.1 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr4:48851970 T>C maps to NM_001168254.1 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:74646120 G>A maps to NM_000859.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:74646120 G>A maps to NM_000859.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:140725402 C>T maps to NM_018916.3 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:140725402 C>T maps to NM_018916.3 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:140735372 C>T maps to NM_018917.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:140735372 C>T maps to NM_018917.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:1497833 G>A maps to ENST00000357934 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:1497833 G>A maps to ENST00000357934 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:2910128 T>A maps to NM_033225.5 S2505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:2910128 T>A maps to NM_033225.5 S2505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:41572580 G>A maps to ENST00000415018 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:41572580 G>A maps to ENST00000415018 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr9:139751940 C>T maps to ENST00000392881 F826F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr9:139751940 C>T maps to ENST00000392881 F826F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr10:85904773 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr10:85904773 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr11:64109489 C>A maps to NM_032251.5 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr11:64109489 C>A maps to NM_032251.5 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr11:64981471 G>C maps to ENST00000438990 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr11:64981471 G>C maps to ENST00000438990 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr12:68050893 C>A maps to NM_006482.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr12:68050893 C>A maps to NM_006482.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr12:101764853 C>T maps to NM_014503.2 L2236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr12:101764853 C>T maps to NM_014503.2 L2236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr14:105415556 G>A maps to NM_138420.2 P2077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr14:105415556 G>A maps to NM_138420.2 P2077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr17:46053333 A>G maps to NM_176096.1 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr17:46053333 A>G maps to NM_176096.1 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr17:56345180 C>T maps to NM_006151.2 N655N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr17:56345180 C>T maps to NM_006151.2 N655N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr19:13211895 T>G maps to NM_005583.4 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr19:13211895 T>G maps to NM_005583.4 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr21:37716974 C>A maps to ENST00000290384 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr21:37716974 C>A maps to ENST00000290384 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chrX:50054015 A>G maps to NM_033031.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chrX:50054015 A>G maps to NM_033031.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr1:981930 A>G maps to NM_198576.2 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr1:981930 A>G maps to NM_198576.2 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr1:3807510 G>A maps to NM_207356.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr1:3807510 G>A maps to NM_207356.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr1:86916414 C>T maps to NM_006536.5 N718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr1:86916414 C>T maps to NM_006536.5 N718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr2:160706544 C>T maps to NM_001198759.1 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr2:160706544 C>T maps to NM_001198759.1 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr2:211421555 A>G maps to NM_001122633.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr2:211421555 A>G maps to NM_001122633.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr3:8787219 T>C maps to NM_001234.3 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr3:8787219 T>C maps to NM_001234.3 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr6:38781865 C>G maps to ENST00000327475 S1086S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr6:38781865 C>G maps to ENST00000327475 S1086S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr8:134488006 G>A maps to NM_173344.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr8:134488006 G>A maps to NM_173344.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr9:35662634 C>T maps to NM_032818.2 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr9:35662634 C>T maps to NM_032818.2 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr10:63520697 T>C maps to NM_173554.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr10:63520697 T>C maps to NM_173554.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr10:129900971 G>C maps to NM_002417.4 P3044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr10:129900971 G>C maps to NM_002417.4 P3044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr11:134158744 A>G maps to NM_001080407.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr11:134158744 A>G maps to NM_001080407.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr12:25148934 C>T maps to NM_001101339.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr12:25148934 C>T maps to NM_001101339.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr12:124395092 G>A maps to NM_207437.3 K3218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr12:124395092 G>A maps to NM_207437.3 K3218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr13:76409435 A>G maps to ENST00000357063 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr13:76409435 A>G maps to ENST00000357063 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr13:96506663 A>G maps to NM_020121.3 T1358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr13:96506663 A>G maps to NM_020121.3 T1358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr15:41483681 A>G maps to NM_152596.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr15:41483681 A>G maps to NM_152596.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr15:78825561 C>T maps to NM_001013619.2 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr15:78825561 C>T maps to NM_001013619.2 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr17:8416900 C>T maps to ENST00000360416 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr17:8416900 C>T maps to ENST00000360416 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr17:42085836 C>T maps to NM_153006.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr17:42085836 C>T maps to NM_153006.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr17:73627744 G>A maps to NM_004259.5 C411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr17:73627744 G>A maps to NM_004259.5 C411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr18:54591237 G>A maps to NM_015285.2 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr18:54591237 G>A maps to NM_015285.2 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr18:55221647 T>C maps to NM_001012515.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr18:55221647 T>C maps to NM_001012515.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr18:72347481 T>C maps to NM_017757.2 L1503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr18:72347481 T>C maps to NM_017757.2 L1503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:68947727 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:68947727 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:92185485 C>T maps to NM_003243.4 E459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:92185485 C>T maps to NM_003243.4 E459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:120342380 C>T maps to NM_032044.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:120342380 C>T maps to NM_032044.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:161512866 G>A maps to NM_000569.6 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:161512866 G>A maps to NM_000569.6 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:227153069 C>T maps to NM_020247.4 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:227153069 C>T maps to NM_020247.4 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr2:237489878 C>T maps to NM_020311.2 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr2:237489878 C>T maps to NM_020311.2 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr4:141074097 G>T maps to ENST00000509479 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr4:141074097 G>T maps to ENST00000509479 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr6:106969053 T>A maps to NM_001624.2 L916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr6:106969053 T>A maps to NM_001624.2 L916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr6:132195476 A>G maps to NM_006208.2 Q545Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr6:132195476 A>G maps to NM_006208.2 Q545Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr9:132400167 C>T maps to NM_017873.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr9:132400167 C>T maps to NM_017873.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr10:99623790 C>T maps to NM_001010917.1 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr10:99623790 C>T maps to NM_001010917.1 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr10:134942934 T>C maps to ENST00000368577 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr10:134942934 T>C maps to ENST00000368577 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr11:1093511 C>A maps to ENST00000441003 T1777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr11:1093511 C>A maps to ENST00000441003 T1777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr11:18362865 A>G maps to NM_005316.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr11:18362865 A>G maps to NM_005316.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr12:94763728 T>C maps to NM_001042399.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr12:94763728 T>C maps to NM_001042399.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr12:130839527 C>T maps to NM_004764.4 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr12:130839527 C>T maps to NM_004764.4 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr13:26788079 G>A maps to NM_005977.3 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr13:26788079 G>A maps to NM_005977.3 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr14:94004550 G>T maps to ENST00000393153 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr14:94004550 G>T maps to ENST00000393153 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr15:31294405 G>A maps to NM_002420.4 I1477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr15:31294405 G>A maps to NM_002420.4 I1477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr17:30349139 A>C maps to ENST00000327564 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr17:30349139 A>C maps to ENST00000327564 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr17:38905555 G>C maps to NM_181534.3 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr17:38905555 G>C maps to NM_181534.3 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr18:8088780 T>A maps to NM_001105244.1 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr18:8088780 T>A maps to NM_001105244.1 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:1058147 C>T maps to NM_019112.3 L1677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:1058147 C>T maps to NM_019112.3 L1677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:9090530 T>C maps to NM_024690.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:9090530 T>C maps to NM_024690.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:44099376 G>A maps to NM_001007561.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:44099376 G>A maps to NM_001007561.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:58101496 C>T maps to NM_001010879.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:58101496 C>T maps to NM_001010879.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr21:45503101 T>C maps to NM_003274.4 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr21:45503101 T>C maps to NM_003274.4 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr22:50987419 G>C maps to NM_138433.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr22:50987419 G>C maps to NM_138433.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr1:214171236 C>T maps to NM_002763.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr1:214171236 C>T maps to NM_002763.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr2:76975913 G>A maps to NM_001134745.1 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr2:76975913 G>A maps to NM_001134745.1 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr6:17292223 C>A maps to NM_001143942.1 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr6:17292223 C>A maps to NM_001143942.1 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr7:63981562 A>G maps to NM_178558.4 C523C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr7:63981562 A>G maps to NM_178558.4 C523C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr15:65041629 G>A maps to NM_194272.1 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr15:65041629 G>A maps to NM_194272.1 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr15:75131660 A>G maps to NM_001099436.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr15:75131660 A>G maps to NM_001099436.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:83999179 C>T maps to NM_013370.3 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:83999179 C>T maps to NM_013370.3 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:88061087 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:88061087 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:88967910 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:88967910 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr19:18898324 C>G maps to NM_000095.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr19:18898324 C>G maps to NM_000095.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr20:42788454 G>A maps to NM_020433.4 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr20:42788454 G>A maps to NM_020433.4 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chrX:34961793 T>C maps to NM_152631.2 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chrX:34961793 T>C maps to NM_152631.2 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:48865160 T>C maps to NM_019073.2 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:48865160 T>C maps to NM_019073.2 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:114510460 T>C maps to ENST00000426820 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:114510460 T>C maps to ENST00000426820 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:157558992 C>G did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:157558992 C>G did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr2:168099281 T>G maps to NM_152381.5 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr2:168099281 T>G maps to NM_152381.5 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:25833003 T>C maps to NM_017897.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:25833003 T>C maps to NM_017897.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:37125218 A>G maps to NM_006309.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:37125218 A>G maps to NM_006309.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:108724126 G>A maps to NM_014429.3 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:108724126 G>A maps to NM_014429.3 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:186331025 C>T maps to ENST00000273784 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:186331025 C>T maps to ENST00000273784 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr4:36130283 T>G maps to NM_015230.2 R1171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr4:36130283 T>G maps to NM_015230.2 R1171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr4:55956220 G>A maps to NM_002253.2 R1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr4:55956220 G>A maps to NM_002253.2 R1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:148207350 T>G maps to NM_000024.5 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:148207350 T>G maps to NM_000024.5 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:171821587 T>G maps to NM_001017995.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:171821587 T>G maps to NM_001017995.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr7:86468359 C>T maps to NM_000840.2 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr7:86468359 C>T maps to NM_000840.2 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr7:117188738 T>C maps to NM_000492.3 N418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr7:117188738 T>C maps to NM_000492.3 N418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr12:4874639 G>A maps to NM_017417.1 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr12:4874639 G>A maps to NM_017417.1 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr12:63976242 T>C maps to NM_173812.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr12:63976242 T>C maps to NM_173812.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr14:51446110 G>A maps to ENST00000338969 N769N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr14:51446110 G>A maps to ENST00000338969 N769N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr16:74566027 G>A maps to NM_012201.5 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr16:74566027 G>A maps to NM_012201.5 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr17:19559758 G>A maps to NM_001031806.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr17:19559758 G>A maps to NM_001031806.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr19:1881394 T>C maps to NM_031213.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr19:1881394 T>C maps to NM_031213.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr19:42819343 C>A maps to ENST00000406159 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr19:42819343 C>A maps to ENST00000406159 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr19:46181195 C>A maps to NM_000164.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr19:46181195 C>A maps to NM_000164.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr22:42610894 A>G maps to NM_005650.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr22:42610894 A>G maps to NM_005650.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chrX:39914705 A>G maps to NM_001123385.1 Y1552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chrX:39914705 A>G maps to NM_001123385.1 Y1552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:9171451 G>A maps to NM_024980.4 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:9171451 G>A maps to NM_024980.4 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:22214039 G>A maps to NM_005529.5 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:22214039 G>A maps to NM_005529.5 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:111216033 G>A maps to NM_002232.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:111216033 G>A maps to NM_002232.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:181727099 C>T maps to ENST00000357570 F1449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:181727099 C>T maps to ENST00000357570 F1449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr2:125521375 C>T maps to NM_130773.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr2:125521375 C>T maps to NM_130773.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr2:204039931 C>G maps to NM_001114132.1 S2100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr2:204039931 C>G maps to NM_001114132.1 S2100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr3:105238965 C>T maps to NM_001627.2 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr3:105238965 C>T maps to NM_001627.2 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr3:192517392 G>T maps to NM_178496.3 Y86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr3:192517392 G>T maps to NM_178496.3 Y86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:53752033 T>C maps to NM_006308.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:53752033 T>C maps to NM_006308.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:55472068 C>T maps to NM_024669.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:55472068 C>T maps to NM_024669.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:140250898 G>A maps to NM_018902.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:140250898 G>A maps to NM_018902.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:171639163 C>T maps to NM_152277.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:171639163 C>T maps to NM_152277.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr6:25600967 G>A maps to NM_017640.5 A1182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr6:25600967 G>A maps to NM_017640.5 A1182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr6:32021195 G>A maps to ENST00000375244 R2920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr6:32021195 G>A maps to ENST00000375244 R2920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr6:57393159 G>A maps to NM_000947.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr6:57393159 G>A maps to NM_000947.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr8:28633368 G>A maps to NM_018250.3 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr8:28633368 G>A maps to NM_018250.3 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr8:117878923 G>A maps to NM_006265.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr8:117878923 G>A maps to NM_006265.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr11:45672089 G>A maps to NM_003654.4 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr11:45672089 G>A maps to NM_003654.4 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr11:47345220 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr11:47345220 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr15:34649646 C>T maps to ENST00000438749 D1136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr15:34649646 C>T maps to ENST00000438749 D1136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr15:85410591 C>T maps to NM_020778.4 R1792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr15:85410591 C>T maps to NM_020778.4 R1792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr16:71419499 C>T maps to NM_001740.4 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr16:71419499 C>T maps to NM_001740.4 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr17:73663473 C>T maps to NM_013260.6 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr17:73663473 C>T maps to NM_013260.6 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr19:15132480 G>A maps to NM_173482.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr19:15132480 G>A maps to NM_173482.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr19:36430884 C>A maps to NM_024509.1 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr19:36430884 C>A maps to NM_024509.1 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr20:18505661 C>T maps to NM_001172745.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr20:18505661 C>T maps to NM_001172745.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chrX:83411184 A>T maps to NM_014496.4 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chrX:83411184 A>T maps to NM_014496.4 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr1:86590962 G>T maps to NM_152890.5 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr1:86590962 G>T maps to NM_152890.5 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr1:212118152 C>T maps to NM_015434.3 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr1:212118152 C>T maps to NM_015434.3 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr2:128381807 C>T maps to ENST00000389524 H1294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr2:128381807 C>T maps to ENST00000389524 H1294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr3:49149417 G>T maps to ENST00000434032 Y941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr3:49149417 G>T maps to ENST00000434032 Y941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:54011575 T>C maps to NM_152540.3 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:54011575 T>C maps to NM_152540.3 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:56309991 A>G maps to NM_004898.2 N588N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:56309991 A>G maps to NM_004898.2 N588N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:57190355 G>A maps to NM_020722.1 R1155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:57190355 G>A maps to NM_020722.1 R1155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:57237682 G>A maps to NM_181806.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:57237682 G>A maps to NM_181806.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:57273839 C>G maps to NM_002703.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:57273839 C>G maps to NM_002703.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:57889676 C>T maps to NM_000938.1 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:57889676 C>T maps to NM_000938.1 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:62598688 C>T maps to ENST00000506720 H272H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:62598688 C>T maps to ENST00000506720 H272H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:69870720 A>G maps to ENST00000381096 H481H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:69870720 A>G maps to ENST00000381096 H481H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:69964336 A>T maps to NM_001074.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:69964336 A>T maps to NM_001074.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:70898906 C>T maps to NM_000200.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:70898906 C>T maps to NM_000200.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:71115151 T>C maps to NM_005212.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:71115151 T>C maps to NM_005212.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:71396988 C>T maps to NM_212557.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:71396988 C>T maps to NM_212557.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:79300898 T>C maps to NM_025074.6 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:79300898 T>C maps to NM_025074.6 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:79372929 C>T maps to NM_025074.6 H2156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:79372929 C>T maps to NM_025074.6 H2156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:79387441 C>T maps to NM_025074.6 H2370H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:79387441 C>T maps to NM_025074.6 H2370H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:79437154 C>T maps to NM_025074.6 T3459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:79437154 C>T maps to NM_025074.6 T3459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:81283915 C>T maps to ENST00000508675 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:81283915 C>T maps to ENST00000508675 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:83763392 G>A maps to ENST00000505472 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:83763392 G>A maps to ENST00000505472 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:88902691 T>C maps to NM_001040058.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:88902691 T>C maps to NM_001040058.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:88903852 C>T maps to NM_001040058.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:88903852 C>T maps to NM_001040058.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:94316762 T>G maps to NM_001510.2 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:94316762 T>G maps to NM_001510.2 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:95186054 A>G maps to NM_001128429.1 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:95186054 A>G maps to NM_001128429.1 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:95197519 C>T maps to NM_001128429.1 D613D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:95197519 C>T maps to NM_001128429.1 D613D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:95506841 G>A maps to NM_006457.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:95506841 G>A maps to NM_006457.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:98893436 A>G maps to NM_174952.2 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:98893436 A>G maps to NM_174952.2 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:98893475 C>T maps to NM_174952.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:98893475 C>T maps to NM_174952.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:99808253 G>A maps to NM_001130679.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:99808253 G>A maps to NM_001130679.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:100047811 G>A maps to ENST00000505590 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:100047811 G>A maps to ENST00000505590 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:103189035 G>A maps to NM_001135146.1 H347H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:103189035 G>A maps to NM_001135146.1 H347H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:103555991 A>G maps to NM_005908.3 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:103555991 A>G maps to NM_005908.3 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:110737388 T>C maps to NM_018983.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:110737388 T>C maps to NM_018983.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:119736795 A>C maps to ENST00000379735 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:119736795 A>C maps to ENST00000379735 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:121958090 T>G maps to NM_024574.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:121958090 T>G maps to NM_024574.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:121958186 A>G maps to NM_024574.3 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:121958186 A>G maps to NM_024574.3 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:123145750 T>A maps to NM_015312.3 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:123145750 T>A maps to NM_015312.3 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:123192382 T>C maps to NM_015312.3 D2568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:123192382 T>C maps to NM_015312.3 D2568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:123229131 C>T maps to NM_015312.3 A3290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:123229131 C>T maps to NM_015312.3 A3290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:123664444 C>T maps to NM_152618.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:123664444 C>T maps to NM_152618.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:123868605 C>T maps to NM_145207.2 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:123868605 C>T maps to NM_145207.2 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:126329788 T>C maps to NM_024582.4 D1920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:126329788 T>C maps to NM_024582.4 D1920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:129924976 C>A maps to NM_144643.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:129924976 C>A maps to NM_144643.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:146824229 G>A maps to ENST00000508784 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:146824229 G>A maps to ENST00000508784 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:152609825 A>C maps to NM_004564.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:152609825 A>C maps to NM_004564.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:154216709 G>A maps to NM_015271.3 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:154216709 G>A maps to NM_015271.3 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:154479429 T>C maps to NM_001131007.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:154479429 T>C maps to NM_001131007.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:154525457 C>T maps to NM_001131007.1 A1098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:154525457 C>T maps to NM_001131007.1 A1098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:155256176 A>G maps to NM_017639.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:155256176 A>G maps to NM_017639.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:156721197 C>T maps to ENST00000502959 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:156721197 C>T maps to ENST00000502959 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:156787339 G>A maps to NM_017419.2 N13N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:156787339 G>A maps to NM_017419.2 N13N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:157684247 T>C maps to NM_016205.2 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:157684247 T>C maps to NM_016205.2 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:158238829 T>C maps to NM_000826.3 H229H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:158238829 T>C maps to NM_000826.3 H229H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:164466823 C>T maps to ENST00000514618 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:164466823 C>T maps to ENST00000514618 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:166929101 G>A maps to ENST00000507499 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:166929101 G>A maps to ENST00000507499 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:175184198 T>C maps to NM_012180.2 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:175184198 T>C maps to NM_012180.2 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:175443155 C>T maps to NM_000860.4 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:175443155 C>T maps to NM_000860.4 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:177142610 G>A maps to NM_080874.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:177142610 G>A maps to NM_080874.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:183674696 C>T maps to NM_001080477.1 G1319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:183674696 C>T maps to NM_001080477.1 G1319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:186299259 A>G maps to ENST00000362004 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:186299259 A>G maps to ENST00000362004 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:187629895 G>A maps to ENST00000260147 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:187629895 G>A maps to ENST00000260147 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:189012679 G>A maps to ENST00000326754 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:189012679 G>A maps to ENST00000326754 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr11:1081736 C>T maps to ENST00000441003 N555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr11:1081736 C>T maps to ENST00000441003 N555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr12:49430958 G>A maps to NM_003482.3 Q3394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr12:49430958 G>A maps to NM_003482.3 Q3394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr16:9858033 C>A maps to NM_000833.3 E1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr16:9858033 C>A maps to NM_000833.3 E1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr17:39742897 G>A maps to NM_000526.4 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr17:39742897 G>A maps to NM_000526.4 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr17:62852004 G>T maps to NM_199340.2 I1604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr17:62852004 G>T maps to NM_199340.2 I1604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr1:240371525 G>A maps to ENST00000406993 A1281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr1:240371525 G>A maps to ENST00000406993 A1281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr1:240371600 C>T maps to ENST00000406993 P1306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr1:240371600 C>T maps to ENST00000406993 P1306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr5:149360520 T>A maps to NM_000112.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr5:149360520 T>A maps to NM_000112.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr6:28227526 G>A maps to NM_001007531.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr6:28227526 G>A maps to NM_001007531.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr10:123954656 C>T maps to NM_206862.2 P1979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr10:123954656 C>T maps to NM_206862.2 P1979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr11:76868350 G>A maps to NM_000260.3 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr11:76868350 G>A maps to NM_000260.3 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr12:6172164 C>T maps to NM_000552.3 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr12:6172164 C>T maps to NM_000552.3 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr12:112516058 A>G maps to NM_024953.3 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr12:112516058 A>G maps to NM_024953.3 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr13:29600583 G>A maps to NM_001033602.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr13:29600583 G>A maps to NM_001033602.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr15:51855613 C>T maps to NM_001174116.1 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr15:51855613 C>T maps to NM_001174116.1 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr16:12136838 C>T maps to NM_032167.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr16:12136838 C>T maps to NM_032167.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr17:20910261 G>A maps to ENST00000455117 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr17:20910261 G>A maps to ENST00000455117 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr22:42524923 A>G maps to NM_000106.4 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr22:42524923 A>G maps to NM_000106.4 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr4:155532985 T>C maps to ENST00000407946 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr4:155532985 T>C maps to ENST00000407946 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr5:140183010 C>T maps to NM_018906.2 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr5:140183010 C>T maps to NM_018906.2 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr7:152513618 G>A maps to NM_020445.4 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr7:152513618 G>A maps to NM_020445.4 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr10:50666943 G>A maps to NM_000124.2 R1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr10:50666943 G>A maps to NM_000124.2 R1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr11:74053511 C>T maps to NM_173582.3 K542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr11:74053511 C>T maps to NM_173582.3 K542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr11:117066582 C>T maps to NM_001040455.1 H796H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr11:117066582 C>T maps to NM_001040455.1 H796H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr14:71543124 C>A maps to NM_014982.2 R1776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr14:71543124 C>A maps to NM_014982.2 R1776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr16:3613170 G>A maps to ENST00000448023 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr16:3613170 G>A maps to ENST00000448023 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr17:2076131 C>T maps to NM_017575.4 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr17:2076131 C>T maps to NM_017575.4 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr17:38062139 C>T maps to NM_001165958.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr17:38062139 C>T maps to NM_001165958.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr17:58288801 A>G maps to NM_032582.3 C751C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr17:58288801 A>G maps to NM_032582.3 C751C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:6216423 C>T maps to NM_005934.3 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:6216423 C>T maps to NM_005934.3 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:38810913 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:38810913 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:42569513 C>T maps to NM_002088.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:42569513 C>T maps to NM_002088.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr20:62839352 A>G maps to NM_004535.2 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr20:62839352 A>G maps to NM_004535.2 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:75055354 C>A maps to NM_001002912.4 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:75055354 C>A maps to NM_001002912.4 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:111737240 G>A maps to NM_024901.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:111737240 G>A maps to NM_024901.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:145302713 A>G maps to NM_001039703.4 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:145302713 A>G maps to NM_001039703.4 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:168698283 C>T maps to NM_001937.4 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:168698283 C>T maps to NM_001937.4 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:207787752 C>T maps to NM_000651.4 R2194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:207787752 C>T maps to NM_000651.4 R2194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr2:130872870 C>T maps to NM_001099771.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr2:130872870 C>T maps to NM_001099771.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr2:155115551 T>G maps to NM_052917.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr2:155115551 T>G maps to NM_052917.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr2:169020262 G>A maps to NM_013233.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr2:169020262 G>A maps to NM_013233.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr5:140050925 G>A maps to NM_194249.2 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr5:140050925 G>A maps to NM_194249.2 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr6:1611153 C>T maps to NM_001453.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr6:1611153 C>T maps to NM_001453.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr6:10756711 C>T maps to NM_030969.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr6:10756711 C>T maps to NM_030969.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr9:33395102 G>A maps to NM_001170.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr9:33395102 G>A maps to NM_001170.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr9:35089136 A>C maps to NM_032634.2 G1074G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr9:35089136 A>C maps to NM_032634.2 G1074G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr10:13375854 T>C maps to NM_012247.4 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr10:13375854 T>C maps to NM_012247.4 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr11:5878380 A>G maps to NM_001005168.1 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr11:5878380 A>G maps to NM_001005168.1 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr11:17409275 G>A maps to NM_000525.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr11:17409275 G>A maps to NM_000525.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr11:67052767 G>A maps to NM_001619.3 E639E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr11:67052767 G>A maps to NM_001619.3 E639E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr11:77614591 C>T maps to NM_033547.3 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr11:77614591 C>T maps to NM_033547.3 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr12:11214869 A>T maps to NM_176887.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr12:11214869 A>T maps to NM_176887.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr12:52843580 A>G maps to NM_005555.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr12:52843580 A>G maps to NM_005555.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr15:86838595 G>A maps to NM_152336.2 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr15:86838595 G>A maps to NM_152336.2 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr16:27353478 C>T maps to NM_000418.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr16:27353478 C>T maps to NM_000418.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr17:45234385 G>T maps to NM_001114091.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr17:45234385 G>T maps to NM_001114091.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr17:45234712 T>C maps to NM_001114091.1 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr17:45234712 T>C maps to NM_001114091.1 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr17:45234724 T>C maps to NM_001114091.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr17:45234724 T>C maps to NM_001114091.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr18:76753062 C>T maps to NM_171999.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr18:76753062 C>T maps to NM_171999.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr19:33484927 C>T maps to NM_033103.4 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr19:33484927 C>T maps to NM_033103.4 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr20:33345743 C>T maps to NM_014071.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr20:33345743 C>T maps to NM_014071.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr22:25016295 G>A maps to NM_005265.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr22:25016295 G>A maps to NM_005265.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr22:42910768 G>A maps to NM_015703.4 Y159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr22:42910768 G>A maps to NM_015703.4 Y159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr2:109382169 A>G maps to NM_006267.4 E1725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr2:109382169 A>G maps to NM_006267.4 E1725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr5:83360582 G>A maps to NM_005711.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr5:83360582 G>A maps to NM_005711.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr5:145890176 C>A maps to NM_006706.3 S1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr5:145890176 C>A maps to NM_006706.3 S1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr7:131172447 T>G maps to NM_013255.4 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr7:131172447 T>G maps to NM_013255.4 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr8:52320733 G>T maps to NM_144651.4 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr8:52320733 G>T maps to NM_144651.4 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr10:91162496 A>G maps to NM_001548.3 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr10:91162496 A>G maps to NM_001548.3 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr11:110450381 C>T maps to NM_020809.2 R1096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr11:110450381 C>T maps to NM_020809.2 R1096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr12:57485456 T>C maps to NM_005967.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr12:57485456 T>C maps to NM_005967.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr12:132547137 A>G maps to ENST00000333577 Q2778Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr12:132547137 A>G maps to ENST00000333577 Q2778Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr13:114780694 C>T maps to ENST00000389544 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr13:114780694 C>T maps to ENST00000389544 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr16:74336162 G>A maps to NM_002811.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr16:74336162 G>A maps to NM_002811.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr17:48270009 G>A maps to NM_000088.3 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr17:48270009 G>A maps to NM_000088.3 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:12058936 T>A did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:12058936 T>A did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:149885275 G>A maps to NM_014849.3 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:149885275 G>A maps to NM_014849.3 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:153907305 T>C maps to NM_014856.2 Q901Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:153907305 T>C maps to NM_014856.2 Q901Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:161022537 T>C maps to NM_001025598.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:161022537 T>C maps to NM_001025598.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:175086261 G>A maps to NM_022093.1 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:175086261 G>A maps to NM_022093.1 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:43015710 G>T maps to NM_012205.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:43015710 G>T maps to NM_012205.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:51255225 G>A maps to ENST00000404971 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:51255225 G>A maps to ENST00000404971 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:167142944 C>T maps to ENST00000303354 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:167142944 C>T maps to ENST00000303354 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:167262809 A>T maps to NM_002976.2 I1443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:167262809 A>T maps to NM_002976.2 I1443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr4:175897857 C>T maps to NM_014269.4 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr4:175897857 C>T maps to NM_014269.4 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr5:140574044 C>G maps to NM_018930.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr5:140574044 C>G maps to NM_018930.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr6:130762196 C>A maps to NM_052913.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr6:130762196 C>A maps to NM_052913.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr6:168297652 G>T did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr6:168297652 G>T did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr7:151932960 G>A maps to ENST00000355193 R904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr7:151932960 G>A maps to ENST00000355193 R904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr9:139701516 C>A maps to NM_001039374.4 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr9:139701516 C>A maps to NM_001039374.4 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr10:26575383 C>T maps to NM_001134366.1 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr10:26575383 C>T maps to NM_001134366.1 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr11:65315006 G>A maps to NM_001130144.2 C670C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr11:65315006 G>A maps to NM_001130144.2 C670C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr15:28386774 G>A maps to NM_004667.4 R3940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr15:28386774 G>A maps to NM_004667.4 R3940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr15:30938315 G>A did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr15:30938315 G>A did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr15:63632618 G>A maps to NM_001218.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr15:63632618 G>A maps to NM_001218.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr16:54966501 A>G maps to NM_005853.5 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr16:54966501 A>G maps to NM_005853.5 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:10355524 G>A maps to NM_017533.2 A1157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:10355524 G>A maps to NM_017533.2 A1157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:42333172 G>A maps to NM_000342.3 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:42333172 G>A maps to NM_000342.3 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:61949662 G>A maps to NM_020991.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:61949662 G>A maps to NM_020991.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr19:22940805 G>A maps to ENST00000397104 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr19:22940805 G>A maps to ENST00000397104 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr21:11058247 G>A maps to NM_182482.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr21:11058247 G>A maps to NM_182482.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr22:43267419 G>A maps to NM_001184970.1 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr22:43267419 G>A maps to NM_001184970.1 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr1:227842074 C>T maps to NM_178549.3 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr1:227842074 C>T maps to NM_178549.3 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr2:70130360 C>T maps to NM_006857.1 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr2:70130360 C>T maps to NM_006857.1 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr2:136511816 A>G maps to NM_014607.3 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr2:136511816 A>G maps to NM_014607.3 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr2:207008762 C>A maps to ENST00000455934 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr2:207008762 C>A maps to ENST00000455934 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr2:222290828 C>T maps to NM_004438.3 T960T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr2:222290828 C>T maps to NM_004438.3 T960T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr3:195505862 G>T maps to NM_018406.5 T4196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr3:195505862 G>T maps to NM_018406.5 T4196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr5:648007 G>A maps to NM_018140.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr5:648007 G>A maps to NM_018140.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr5:180374533 G>A maps to NM_001040462.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr5:180374533 G>A maps to NM_001040462.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr6:36931161 A>G maps to NM_153370.2 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr6:36931161 A>G maps to NM_153370.2 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr6:118790442 T>G maps to NM_001042475.2 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr6:118790442 T>G maps to NM_001042475.2 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr8:24199260 C>T maps to NM_014265.4 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr8:24199260 C>T maps to NM_014265.4 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr11:132081913 A>C did not map to a codon.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr11:132081913 A>C did not map to a codon.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr12:6686949 C>T did not map to a codon.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr12:6686949 C>T did not map to a codon.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr12:72036213 A>C did not map to a codon.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr12:72036213 A>C did not map to a codon.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr14:21866025 T>C maps to NM_001170629.1 A1669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr14:21866025 T>C maps to NM_001170629.1 A1669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr14:24808387 A>G maps to NM_006871.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr14:24808387 A>G maps to NM_006871.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr14:64612844 C>T maps to NM_182914.2 I5181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr14:64612844 C>T maps to NM_182914.2 I5181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr15:42446633 C>T maps to ENST00000397272 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr15:42446633 C>T maps to ENST00000397272 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr16:68293319 T>C maps to NM_012320.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr16:68293319 T>C maps to NM_012320.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr17:44111612 A>G maps to NM_015443.3 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr17:44111612 A>G maps to NM_015443.3 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr17:78444657 T>G maps to NM_002522.3 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr17:78444657 T>G maps to NM_002522.3 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr19:15648714 G>A maps to NM_173483.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr19:15648714 G>A maps to NM_173483.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr19:39433298 A>G maps to NM_148169.1 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr19:39433298 A>G maps to NM_148169.1 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr20:4854681 A>G maps to NM_203327.1 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr20:4854681 A>G maps to NM_203327.1 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr20:6064730 C>T maps to NM_017671.4 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr20:6064730 C>T maps to NM_017671.4 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr21:34903823 C>A maps to NM_001136006.1 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr21:34903823 C>A maps to NM_001136006.1 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr22:23438190 C>T maps to NM_002073.2 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr22:23438190 C>T maps to NM_002073.2 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr22:29456732 T>C maps to NM_015370.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr22:29456732 T>C maps to NM_015370.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr22:42341933 A>G maps to NM_024053.3 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr22:42341933 A>G maps to NM_024053.3 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chrX:30261001 A>G maps to NM_002367.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chrX:30261001 A>G maps to NM_002367.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:1271545 G>A maps to ENST00000378888 C688C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:1271545 G>A maps to ENST00000378888 C688C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:17264938 T>C maps to NM_014675.3 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:17264938 T>C maps to NM_014675.3 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:35579020 A>G maps to NM_024772.3 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:35579020 A>G maps to NM_024772.3 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:115454197 C>T maps to NM_003176.2 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:115454197 C>T maps to NM_003176.2 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:145439909 T>C maps to NM_006472.3 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:145439909 T>C maps to NM_006472.3 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:158390383 G>T maps to NM_001004476.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:158390383 G>T maps to NM_001004476.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr2:179412021 G>A maps to NM_133378.4 S28842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr2:179412021 G>A maps to NM_133378.4 S28842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr3:49028270 G>A maps to NM_177938.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr3:49028270 G>A maps to NM_177938.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr3:107096616 C>T maps to NM_032600.2 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr3:107096616 C>T maps to NM_032600.2 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr4:2648483 C>T maps to ENST00000324666 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr4:2648483 C>T maps to ENST00000324666 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:16465317 T>A maps to NM_033414.2 K153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:16465317 T>A maps to NM_033414.2 K153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:78415118 A>T maps to NM_001713.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:78415118 A>T maps to NM_001713.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:81354374 C>G maps to NM_031482.4 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:81354374 C>G maps to NM_031482.4 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:140711177 C>T maps to NM_018912.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:140711177 C>T maps to NM_018912.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:26033604 C>T maps to NM_003513.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:26033604 C>T maps to NM_003513.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:34804090 G>T maps to NM_017754.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:34804090 G>T maps to NM_017754.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:35810382 T>A did not map to a codon.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:35810382 T>A did not map to a codon.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:51915070 C>T maps to NM_138694.3 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:51915070 C>T maps to NM_138694.3 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:69646519 C>A maps to NM_001704.2 C326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:69646519 C>A maps to NM_001704.2 C326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr7:151932960 G>A maps to ENST00000355193 R904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr7:151932960 G>A maps to ENST00000355193 R904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr8:19690801 G>A maps to NM_018142.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr8:19690801 G>A maps to NM_018142.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr9:123171435 C>A maps to NM_018249.4 E1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr9:123171435 C>A maps to NM_018249.4 E1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr9:130854175 A>G maps to ENST00000373066 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr9:130854175 A>G maps to ENST00000373066 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr9:133780630 G>A maps to NM_001145106.1 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr9:133780630 G>A maps to NM_001145106.1 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr11:55999740 C>T maps to NM_001004746.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr11:55999740 C>T maps to NM_001004746.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr11:77612470 G>A maps to NM_033547.3 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr11:77612470 G>A maps to NM_033547.3 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr12:32134716 A>G maps to NM_018169.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr12:32134716 A>G maps to NM_018169.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr12:113748107 G>T maps to NM_024959.2 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr12:113748107 G>T maps to NM_024959.2 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr12:124229428 T>C maps to NM_012463.3 N505N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr12:124229428 T>C maps to NM_012463.3 N505N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr13:100635172 A>G maps to NM_007129.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr13:100635172 A>G maps to NM_007129.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr14:33290882 G>T maps to NM_004274.4 V1288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr14:33290882 G>T maps to NM_004274.4 V1288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr14:74426129 T>C maps to NM_182476.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr14:74426129 T>C maps to NM_182476.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr17:77768835 C>T maps to NM_020649.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr17:77768835 C>T maps to NM_020649.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr19:44103049 T>C maps to NM_024327.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr19:44103049 T>C maps to NM_024327.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr22:29091840 G>A maps to NM_001005735.1 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr22:29091840 G>A maps to NM_001005735.1 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chrX:3227795 G>A maps to NM_015419.3 L2816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chrX:3227795 G>A maps to NM_015419.3 L2816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:46493408 A>T maps to NM_015112.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:46493408 A>T maps to NM_015112.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:65300334 A>C maps to NM_002227.2 Y1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:65300334 A>C maps to NM_002227.2 Y1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:156639635 G>A maps to NM_006617.1 A1448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:156639635 G>A maps to NM_006617.1 A1448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:247014375 G>C maps to ENST00000428671 A1682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:247014375 G>C maps to ENST00000428671 A1682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr2:179537131 A>G did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr2:179537131 A>G did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr2:179543216 C>T maps to NM_133378.4 E10034E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr2:179543216 C>T maps to NM_133378.4 E10034E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr4:109084811 G>T maps to NM_016269.4 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr4:109084811 G>T maps to NM_016269.4 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr5:145641191 G>A maps to NM_018989.1 W671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr5:145641191 G>A maps to NM_018989.1 W671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr6:69758170 C>T maps to NM_001704.2 N734N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr6:69758170 C>T maps to NM_001704.2 N734N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr6:118228996 C>A maps to NM_001029858.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr6:118228996 C>A maps to NM_001029858.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr6:149826609 T>C maps to NM_139126.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr6:149826609 T>C maps to NM_139126.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr10:96970503 G>T maps to NM_207321.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr10:96970503 G>T maps to NM_207321.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr10:118397883 A>G maps to NM_005396.4 *357W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr10:118397883 A>G maps to NM_005396.4 *357W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr11:85459456 A>T maps to NM_001162953.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr11:85459456 A>T maps to NM_001162953.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr12:248154 C>T maps to NM_001170738.1 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr12:248154 C>T maps to NM_001170738.1 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr13:43872564 C>A maps to NM_001127615.1 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr13:43872564 C>A maps to NM_001127615.1 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr15:42109222 T>C maps to NM_001128608.1 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr15:42109222 T>C maps to NM_001128608.1 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr15:83332551 C>A did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr15:83332551 C>A did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr16:50368806 C>A did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr16:50368806 C>A did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:7680785 C>G maps to NM_020877.2 S1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:7680785 C>G maps to NM_020877.2 S1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:67252296 C>T did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:67252296 C>T did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:67513025 C>T maps to NM_002758.3 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:67513025 C>T maps to NM_002758.3 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr2:54753665 G>A maps to NM_003128.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr2:54753665 G>A maps to NM_003128.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr2:129075938 T>A maps to NM_004807.2 K67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr2:129075938 T>A maps to NM_004807.2 K67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr2:179436668 A>C maps to NM_133378.4 G22162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr2:179436668 A>C maps to NM_133378.4 G22162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr4:25678364 C>T maps to NM_006424.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr4:25678364 C>T maps to NM_006424.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr5:169535491 G>A maps to NM_012188.4 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr5:169535491 G>A maps to NM_012188.4 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr6:31238930 G>A maps to ENST00000383329 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr6:31238930 G>A maps to ENST00000383329 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr9:82320808 C>T maps to ENST00000376537 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr9:82320808 C>T maps to ENST00000376537 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr11:71259903 C>T maps to ENST00000422553 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr11:71259903 C>T maps to ENST00000422553 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr12:53343004 G>A maps to NM_000224.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr12:53343004 G>A maps to NM_000224.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr13:21436892 G>T maps to NM_022459.4 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr13:21436892 G>T maps to NM_022459.4 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr13:30107117 A>C maps to NM_003045.4 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr13:30107117 A>C maps to NM_003045.4 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr16:75269476 A>C maps to NM_001170714.1 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr16:75269476 A>C maps to NM_001170714.1 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr17:39274156 G>A maps to NM_033059.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr17:39274156 G>A maps to NM_033059.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr17:39274204 T>C maps to NM_033059.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr17:39274204 T>C maps to NM_033059.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr20:18446021 C>A did not map to a codon.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr20:18446021 C>A did not map to a codon.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr20:47989843 A>C maps to NM_004975.2 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr20:47989843 A>C maps to NM_004975.2 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr22:29091840 G>A maps to NM_001005735.1 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr22:29091840 G>A maps to NM_001005735.1 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chrY:16952766 C>T maps to ENST00000382868 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chrY:16952766 C>T maps to ENST00000382868 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr1:53728130 G>A maps to NM_004631.3 N587N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr1:53728130 G>A maps to NM_004631.3 N587N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr1:152185881 G>A maps to NM_001009931.1 G2741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr1:152185881 G>A maps to NM_001009931.1 G2741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr1:167095420 C>T maps to NM_001080426.1 Y351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr1:167095420 C>T maps to NM_001080426.1 Y351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr5:74056730 T>C maps to NM_032380.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr5:74056730 T>C maps to NM_032380.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr5:158204424 A>G maps to NM_024007.3 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr5:158204424 A>G maps to NM_024007.3 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr7:44185093 A>G did not map to a codon.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr7:44185093 A>G did not map to a codon.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr9:117052372 A>G maps to NM_032888.2 P1414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr9:117052372 A>G maps to NM_032888.2 P1414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr12:110815281 C>A maps to NM_016238.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr12:110815281 C>A maps to NM_016238.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr13:20006619 C>T maps to NM_199254.2 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr13:20006619 C>T maps to NM_199254.2 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr16:70818708 G>A maps to NM_018052.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr16:70818708 G>A maps to NM_018052.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr17:1679917 C>T maps to NM_002615.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr17:1679917 C>T maps to NM_002615.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr17:45234349 C>T maps to NM_001114091.1 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr17:45234349 C>T maps to NM_001114091.1 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr17:45234385 G>T maps to NM_001114091.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr17:45234385 G>T maps to NM_001114091.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr19:43519266 C>A did not map to a codon.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr19:43519266 C>A did not map to a codon.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr20:57415469 C>T maps to NM_016592.2 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr20:57415469 C>T maps to NM_016592.2 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr1:7890009 A>G maps to ENST00000377532 T1001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr1:7890009 A>G maps to ENST00000377532 T1001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr1:153907305 T>C maps to NM_014856.2 Q901Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr1:153907305 T>C maps to NM_014856.2 Q901Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:44153049 T>C maps to NM_133259.3 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:44153049 T>C maps to NM_133259.3 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:169681150 C>T maps to NM_001171631.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:169681150 C>T maps to NM_001171631.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:203149109 G>T maps to NM_015934.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:203149109 G>T maps to NM_015934.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:220162726 C>A maps to NM_002846.3 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:220162726 C>A maps to NM_002846.3 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr3:196743129 T>C maps to NM_005929.5 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr3:196743129 T>C maps to NM_005929.5 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr7:43540886 A>C maps to NM_015052.3 R1199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr7:43540886 A>C maps to NM_015052.3 R1199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr12:1989017 T>C maps to NM_172364.4 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr12:1989017 T>C maps to NM_172364.4 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr14:35782252 A>G maps to NM_002791.1 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr14:35782252 A>G maps to NM_002791.1 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr17:74057618 C>A maps to NM_014230.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr17:74057618 C>A maps to NM_014230.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr19:23927343 T>C maps to NM_138286.2 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr19:23927343 T>C maps to NM_138286.2 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr20:2840772 C>T maps to NM_022575.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr20:2840772 C>T maps to NM_022575.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr20:30527064 T>C maps to NM_001008409.2 H413H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr20:30527064 T>C maps to NM_001008409.2 H413H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr1:16778445 T>C maps to NM_018090.4 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr1:16778445 T>C maps to NM_018090.4 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr3:190345112 A>G maps to NM_002182.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr3:190345112 A>G maps to NM_002182.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr7:124387091 C>G maps to NM_005302.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr7:124387091 C>G maps to NM_005302.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr7:150738256 C>A maps to ENST00000297504 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr7:150738256 C>A maps to ENST00000297504 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr9:125860017 A>G did not map to a codon.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr9:125860017 A>G did not map to a codon.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr17:7386271 C>T maps to NM_001102614.1 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr17:7386271 C>T maps to NM_001102614.1 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr17:39240793 C>A maps to ENST00000377731 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr17:39240793 C>A maps to ENST00000377731 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr1:229666036 C>T maps to NM_012089.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr1:229666036 C>T maps to NM_012089.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr1:237870321 C>T maps to NM_001035.2 I3218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr1:237870321 C>T maps to NM_001035.2 I3218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr2:128377978 C>A maps to ENST00000389524 R1129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr2:128377978 C>A maps to ENST00000389524 R1129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr2:153468106 C>T maps to NM_052905.3 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr2:153468106 C>T maps to NM_052905.3 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr3:107885799 A>G maps to ENST00000457963 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr3:107885799 A>G maps to ENST00000457963 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr4:99030363 T>C maps to NM_174952.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr4:99030363 T>C maps to NM_174952.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr7:139268746 G>A maps to NM_022740.4 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr7:139268746 G>A maps to NM_022740.4 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr7:141752696 C>T maps to ENST00000475668 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr7:141752696 C>T maps to ENST00000475668 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr10:95326920 G>T maps to NM_181745.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr10:95326920 G>T maps to NM_181745.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr11:118498441 C>A maps to NM_015157.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr11:118498441 C>A maps to NM_015157.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr11:119243941 G>A maps to NM_004205.4 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr11:119243941 G>A maps to NM_004205.4 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr11:123900523 G>C maps to NM_001004464.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr11:123900523 G>C maps to NM_001004464.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr12:11546798 G>A maps to NM_006248.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr12:11546798 G>A maps to NM_006248.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr12:133351741 G>A maps to NM_005895.3 R1376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr12:133351741 G>A maps to NM_005895.3 R1376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr18:33767625 G>T maps to NM_017947.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr18:33767625 G>T maps to NM_017947.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr19:43585252 C>T maps to ENST00000449000 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr19:43585252 C>T maps to ENST00000449000 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr19:50103127 C>A maps to NM_020719.1 P1426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr19:50103127 C>A maps to NM_020719.1 P1426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr20:61444844 G>A maps to NM_007346.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr20:61444844 G>A maps to NM_007346.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr2:36691751 C>T maps to NM_016441.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr2:36691751 C>T maps to NM_016441.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr3:155206587 G>A maps to ENST00000340059 N788N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr3:155206587 G>A maps to ENST00000340059 N788N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr3:155314033 A>G maps to ENST00000340059 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr3:155314033 A>G maps to ENST00000340059 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr4:175416698 C>A maps to NM_000860.4 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr4:175416698 C>A maps to NM_000860.4 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr5:95236414 G>A maps to NM_012081.5 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr5:95236414 G>A maps to NM_012081.5 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr6:161139479 C>T maps to NM_000301.3 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr6:161139479 C>T maps to NM_000301.3 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr9:72131721 G>A maps to NM_001163.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr9:72131721 G>A maps to NM_001163.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr9:135374897 T>C maps to NM_207417.1 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr9:135374897 T>C maps to NM_207417.1 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr11:67759286 C>A maps to NM_030930.2 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr11:67759286 C>A maps to NM_030930.2 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr12:133434117 G>A maps to NM_001161344.1 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr12:133434117 G>A maps to NM_001161344.1 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr15:22383188 G>A maps to NM_001005241.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr15:22383188 G>A maps to NM_001005241.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr15:89421404 G>A maps to NM_178232.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr15:89421404 G>A maps to NM_178232.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr16:31336718 G>A maps to NM_001145808.1 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr16:31336718 G>A maps to NM_001145808.1 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr17:6607200 C>A maps to NM_177550.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr17:6607200 C>A maps to NM_177550.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr17:8792170 T>C maps to NM_001142633.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr17:8792170 T>C maps to NM_001142633.1 L311L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G9-6373-01A-11D-1786-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-G9-6373-01A-11D-1786-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr19:41350671 G>A maps to NM_000762.5 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr19:41350671 G>A maps to NM_000762.5 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr22:24384212 G>A maps to NM_000853.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr22:24384212 G>A maps to NM_000853.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr22:50987890 G>A maps to NM_138433.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr22:50987890 G>A maps to NM_138433.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chrX:40506696 A>G maps to NM_144970.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chrX:40506696 A>G maps to NM_144970.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr1:94506836 G>A maps to NM_000350.2 C1150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr1:94506836 G>A maps to NM_000350.2 C1150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr2:32368484 G>T did not map to a codon.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr2:32368484 G>T did not map to a codon.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr5:90106487 C>T maps to NM_032119.3 F5137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr5:90106487 C>T maps to NM_032119.3 F5137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr5:141017908 C>G maps to NM_173828.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr5:141017908 C>G maps to NM_173828.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr6:31940214 C>T maps to NM_032454.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr6:31940214 C>T maps to NM_032454.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr6:32122415 G>A maps to NM_138717.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr6:32122415 G>A maps to NM_138717.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr7:48443342 C>A maps to NM_152701.3 G3979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr7:48443342 C>A maps to NM_152701.3 G3979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr8:8238939 G>C maps to NM_001080826.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr8:8238939 G>C maps to NM_001080826.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr11:66026226 G>T maps to NM_022822.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr11:66026226 G>T maps to NM_022822.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr14:68220895 C>A maps to NM_015346.3 V2340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr14:68220895 C>A maps to NM_015346.3 V2340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:42839683 C>A maps to NM_153260.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:42839683 C>A maps to NM_153260.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:51676021 G>A maps to NM_181789.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:51676021 G>A maps to NM_181789.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:51795001 C>T did not map to a codon.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:51795001 C>T did not map to a codon.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr16:30794664 G>T maps to NM_001080417.1 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr16:30794664 G>T maps to NM_001080417.1 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr17:45234748 A>C maps to NM_001114091.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr17:45234748 A>C maps to NM_001114091.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chrX:151900632 G>A maps to NM_005367.5 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chrX:151900632 G>A maps to NM_005367.5 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr1:158299692 G>A maps to NM_001764.2 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr1:158299692 G>A maps to NM_001764.2 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr2:12863618 C>T maps to NM_021643.3 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr2:12863618 C>T maps to NM_021643.3 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr3:129288692 G>T maps to NM_015103.2 S1286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr3:129288692 G>T maps to NM_015103.2 S1286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr5:99871329 C>T maps to NM_198507.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr5:99871329 C>T maps to NM_198507.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr5:160033838 C>A maps to NM_025153.2 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr5:160033838 C>A maps to NM_025153.2 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr8:144643540 C>T maps to NM_024736.6 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr8:144643540 C>T maps to NM_024736.6 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr11:117152313 A>T did not map to a codon.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr11:117152313 A>T did not map to a codon.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr12:56082024 G>C maps to ENST00000347027 S1050S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr12:56082024 G>C maps to ENST00000347027 S1050S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr14:105361168 A>C maps to ENST00000453495 S1549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr14:105361168 A>C maps to ENST00000453495 S1549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr16:27585274 G>T maps to NM_015202.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr16:27585274 G>T maps to NM_015202.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr16:30620888 A>C maps to NM_138447.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr16:30620888 A>C maps to NM_138447.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr17:39150166 G>A maps to NM_033185.2 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr17:39150166 G>A maps to NM_033185.2 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr18:42532844 C>A maps to NM_015559.2 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr18:42532844 C>A maps to NM_015559.2 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr19:375679 C>T maps to NM_016585.3 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr19:375679 C>T maps to NM_016585.3 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr21:16340288 C>T maps to NM_003489.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr21:16340288 C>T maps to NM_003489.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr22:28194935 C>T maps to NM_002430.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr22:28194935 C>T maps to NM_002430.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr1:228481210 C>T maps to NM_001098623.1 D3675D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr1:228481210 C>T maps to NM_001098623.1 D3675D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr3:64084857 G>A maps to NM_198859.3 R802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr3:64084857 G>A maps to NM_198859.3 R802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr4:71472191 C>A maps to NM_016519.4 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr4:71472191 C>A maps to NM_016519.4 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr6:32163813 C>T maps to NM_004557.3 A1804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr6:32163813 C>T maps to NM_004557.3 A1804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr9:33056917 C>T maps to NM_018225.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr9:33056917 C>T maps to NM_018225.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr14:58896078 A>G did not map to a codon.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr14:58896078 A>G did not map to a codon.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr19:4102448 G>A maps to NM_030662.3 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr19:4102448 G>A maps to NM_030662.3 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr19:52793388 G>A maps to NM_001010851.2 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr19:52793388 G>A maps to NM_001010851.2 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chrX:51076023 G>A maps to NM_153183.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chrX:51076023 G>A maps to NM_153183.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr1:19477276 C>A maps to ENST00000375267 S2408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr1:19477276 C>A maps to ENST00000375267 S2408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr1:91781958 C>A maps to NM_001017975.3 E963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr1:91781958 C>A maps to NM_001017975.3 E963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr1:145367738 A>G maps to NM_001039703.4 K3445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr1:145367738 A>G maps to NM_001039703.4 K3445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr2:45233548 C>T maps to NM_016932.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr2:45233548 C>T maps to NM_016932.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr2:220331956 C>T maps to NM_005876.4 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr2:220331956 C>T maps to NM_005876.4 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr3:98519474 A>C maps to ENST00000326857 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr3:98519474 A>C maps to ENST00000326857 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr6:111498552 C>T maps to NM_018593.4 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr6:111498552 C>T maps to NM_018593.4 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr7:38305253 G>A maps to ENST00000443402 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr7:38305253 G>A maps to ENST00000443402 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr10:44104059 A>T did not map to a codon.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr10:44104059 A>T did not map to a codon.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr10:51749116 G>A maps to NM_001077665.2 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr10:51749116 G>A maps to NM_001077665.2 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr12:113822715 C>G maps to NM_173542.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr12:113822715 C>G maps to NM_173542.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr14:105349540 G>A maps to ENST00000453495 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr14:105349540 G>A maps to ENST00000453495 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr17:38555126 G>T maps to ENST00000357601 S1153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr17:38555126 G>T maps to ENST00000357601 S1153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr19:12501648 T>A maps to NM_001080821.2 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr19:12501648 T>A maps to NM_001080821.2 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr19:44891125 T>A maps to NM_152354.3 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr19:44891125 T>A maps to NM_152354.3 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr20:30363691 G>T maps to ENST00000340513 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr20:30363691 G>T maps to ENST00000340513 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr20:36974955 C>T maps to NM_004139.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr20:36974955 C>T maps to NM_004139.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr20:46295035 G>A maps to NM_001161841.1 Y591Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr20:46295035 G>A maps to NM_001161841.1 Y591Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr1:99422182 G>A maps to NM_001037317.1 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr1:99422182 G>A maps to NM_001037317.1 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr1:145209365 A>G did not map to a codon.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr1:145209365 A>G did not map to a codon.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr2:130832761 T>C maps to NM_001099771.2 K761K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr2:130832761 T>C maps to NM_001099771.2 K761K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr2:166020179 C>T maps to NM_006922.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr2:166020179 C>T maps to NM_006922.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr2:211541793 C>T maps to NM_001122633.1 V1452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr2:211541793 C>T maps to NM_001122633.1 V1452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr3:132075553 T>C maps to NM_001134194.1 Y331Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr3:132075553 T>C maps to NM_001134194.1 Y331Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr3:164764718 C>A maps to NM_001041.3 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr3:164764718 C>A maps to NM_001041.3 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr5:476352 C>T maps to NM_004174.2 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr5:476352 C>T maps to NM_004174.2 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr5:1466918 G>A maps to NM_024830.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr5:1466918 G>A maps to NM_024830.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr5:36142647 A>G maps to NM_001007527.1 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr5:36142647 A>G maps to NM_001007527.1 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr5:126771181 G>C did not map to a codon.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr5:126771181 G>C did not map to a codon.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr6:30075863 A>G maps to NM_007028.3 H283H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr6:30075863 A>G maps to NM_007028.3 H283H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr6:108985052 T>C maps to NM_001455.3 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr6:108985052 T>C maps to NM_001455.3 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr7:76029804 G>A maps to NM_080744.1 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr7:76029804 G>A maps to NM_080744.1 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr7:101845117 C>T maps to ENST00000360264 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr7:101845117 C>T maps to ENST00000360264 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr7:141952405 A>C maps to NM_001001317.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr7:141952405 A>C maps to NM_001001317.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr9:131107631 C>G maps to NM_005094.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr9:131107631 C>G maps to NM_005094.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr10:70446225 G>A maps to NM_030625.2 K1722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr10:70446225 G>A maps to NM_030625.2 K1722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr12:52886489 A>G maps to NM_005554.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr12:52886489 A>G maps to NM_005554.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr12:57108202 A>G maps to NM_001113203.1 I1922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr12:57108202 A>G maps to NM_001113203.1 I1922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr14:101200644 T>C maps to NM_003836.5 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr14:101200644 T>C maps to NM_003836.5 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr17:4542893 A>G maps to NM_001140.3 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr17:4542893 A>G maps to NM_001140.3 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr19:19654188 G>A maps to NM_153221.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr19:19654188 G>A maps to NM_153221.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr20:1600529 G>A maps to NM_006065.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr20:1600529 G>A maps to NM_006065.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr20:46301110 C>A maps to NM_001161841.1 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr20:46301110 C>A maps to NM_001161841.1 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr3:57488128 C>T maps to NM_178504.4 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr3:57488128 C>T maps to NM_178504.4 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chrX:151896700 G>T did not map to a codon.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chrX:151896700 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr17:263704 C>T maps to NM_001013672.4 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr17:263704 C>T maps to NM_001013672.4 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr19:56090150 C>T maps to NM_152600.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr19:56090150 C>T maps to NM_152600.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr16:69364029 G>A maps to NM_022341.1 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr16:69364029 G>A maps to NM_022341.1 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr21:11015011 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr21:11015011 G>A did not map to a codon.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr7:74298856 T>C did not map to a codon.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr7:74298856 T>C did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr7:74298938 G>C did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr7:74298938 G>C did not map to a codon.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr7:74298938 G>C did not map to a codon.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr7:74298938 G>C did not map to a codon.
