6712 NP_001070868 A406S not found in SNVbox database
7647 NP_705833 S703L not found in SNVbox database
7686 NP_705833 H662D not found in SNVbox database
2297 NP_705833 M520T not found in SNVbox database
2804 NP_001070868 D309V not found in SNVbox database
4670 NP_001070868 K474N not found in SNVbox database
4760 NP_001070868 F280L not found in SNVbox database
4896 NP_705833 D143H not found in SNVbox database
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:58864485 G>A maps to NM_130786.3 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:58863921 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr19:58863847 C>T maps to NM_130786.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr19:58864317 T>A maps to NM_130786.3 K106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:52573751 G>T maps to NM_138932.2 Y404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:52575976 A>T maps to NM_138932.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr10:52576012 G>A maps to NM_138932.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:52575946 G>A maps to NM_138932.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:52573625 G>A maps to NM_138932.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:52573679 C>T maps to NM_138932.2 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr10:52595897 G>A maps to NM_138932.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr16:7629789 C>T maps to NM_145891.2 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:7568150 T>C maps to NM_145891.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr16:7568363 C>T maps to NM_145891.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr16:7629798 G>C maps to NM_145891.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr16:7645621 G>T maps to NM_145891.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr16:7383040 C>T maps to NM_145891.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:9262517 C>T maps to NM_000014.4 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:9227269 G>C maps to NM_000014.4 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr12:9256906 G>A maps to NM_000014.4 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr12:9251235 G>A maps to NM_000014.4 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr12:9265042 C>T maps to NM_000014.4 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr12:9229399 T>A maps to NM_000014.4 K1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr12:8994101 C>T maps to NM_144670.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr22:43089135 G>A maps to NM_017436.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr3:137843342 G>T maps to NM_016161.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:137843366 G>A maps to NM_016161.2 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:137843690 G>T maps to NM_016161.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:53709521 G>C maps to NM_015665.5 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr12:53715144 G>A maps to NM_015665.5 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr12:125587271 T>C maps to NM_023928.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr3:151545494 C>G maps to NM_001086.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr3:151545710 G>C maps to NM_001086.2 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:12785335 C>A maps to NM_001103170.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr1:12785420 C>T maps to NM_001103170.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:12726744 G>A maps to NM_001013630.1 *408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:170989839 T>G did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr4:170999664 G>A maps to ENST00000509167 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:170983103 G>C maps to ENST00000509167 S396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr2:69870147 G>A maps to NM_014911.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr6:44272034 C>T maps to NM_020745.2 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:44273501 G>C maps to NM_020745.2 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:44275103 G>A maps to NM_020745.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr4:57244555 G>A maps to NM_181806.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:57221513 G>A maps to NM_181806.2 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr4:57204792 C>A maps to NM_181806.2 P1024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:105950302 C>G maps to NM_015423.2 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr7:121738532 G>A maps to NM_005763.3 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr7:121738886 C>T maps to NM_005763.3 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:121756933 T>A maps to NM_005763.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr17:35306511 G>A maps to NM_012138.3 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:79094651 C>T maps to NM_001080395.2 P1028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr17:79108260 G>A maps to NM_001080395.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr16:8862754 G>A maps to NM_001127448.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr16:8829601 C>T maps to NM_001127448.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:8875250 C>A maps to NM_001127448.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:8862733 C>T maps to NM_001127448.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr9:107558477 C>G maps to NM_005502.3 G1746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr9:107568575 G>A maps to NM_005502.3 I1470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr9:107547892 T>C maps to NM_005502.3 V2143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:107560848 G>A maps to NM_005502.3 S1658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:107594012 A>G maps to NM_005502.3 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr9:107562200 G>A maps to NM_005502.3 L1614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:67150090 G>A maps to NM_080282.3 F1282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:67186543 C>A maps to NM_080282.3 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr17:67218722 A>G maps to NM_080282.3 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr17:67149443 A>T did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr17:67178386 A>G maps to NM_080282.3 C892C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr2:215880299 G>A maps to NM_173076.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr2:216002860 A>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:215976317 A>T did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr2:215880314 T>A maps to NM_173076.2 K619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr2:215914476 G>C maps to NM_173076.2 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:215840690 G>C maps to NM_173076.2 L1733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr2:215809783 G>C maps to NM_173076.2 L2428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr2:215852509 G>A maps to NM_173076.2 Y1279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr2:215840594 G>T maps to NM_173076.2 G1765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:48285512 C>A maps to NM_152701.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr7:48411939 C>G maps to NM_152701.3 S3660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr7:48682990 T>G did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr7:48284271 G>A maps to NM_152701.3 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr7:48390324 C>T maps to NM_152701.3 C3430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:48443310 C>T maps to NM_152701.3 Q3969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:48314866 T>C maps to NM_152701.3 G1868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr7:48318539 A>G maps to NM_152701.3 T2583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr7:48319202 T>C maps to NM_152701.3 S2804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr7:48391977 C>T maps to NM_152701.3 Q3528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr7:48545977 G>A maps to NM_152701.3 K4446K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr7:48312991 T>G maps to NM_152701.3 V1243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr7:48559722 C>A maps to NM_152701.3 C4628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr9:139912244 G>C maps to ENST00000355090 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr9:139906445 G>A maps to ENST00000355090 I1825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr9:139905641 C>T maps to ENST00000355090 K2003K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr9:139904518 G>A maps to ENST00000355090 D2167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr9:139903014 C>T maps to ENST00000355090 P2406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr9:139904518 G>A maps to ENST00000355090 D2167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr16:2376443 C>T maps to NM_001089.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr16:2339464 C>T maps to NM_001089.2 E890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr16:2333283 G>C maps to NM_001089.2 S1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr16:2369815 G>A maps to NM_001089.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:2329014 C>T maps to NM_001089.2 G1492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr16:2347778 G>A maps to NM_001089.2 I680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr16:2376269 C>T maps to NM_001089.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:2369820 G>A maps to NM_001089.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr16:2376013 G>A maps to NM_001089.2 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:2347420 G>A maps to NM_001089.2 D724D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:94526179 G>A maps to NM_000350.2 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr1:94463632 G>T maps to NM_000350.2 I2171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:94577115 C>G maps to NM_000350.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:94505665 C>T maps to NM_000350.2 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:94496610 G>A maps to NM_000350.2 G1398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr1:94506779 T>C maps to NM_000350.2 Q1169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:94496003 G>T maps to NM_000350.2 C1444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr1:94496667 G>C maps to NM_000350.2 L1379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:67287393 C>T maps to ENST00000392677 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:67094138 C>T maps to NM_080284.2 P1014P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:67094144 C>T maps to NM_080284.2 G1012G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:67111519 C>A maps to NM_080284.2 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr17:67102346 C>A maps to NM_080284.2 E799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr17:67081771 A>T maps to NM_080284.2 A1341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:67080593 T>C maps to NM_080284.2 L1413L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-TN-A7HI-01A-11D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr17:67129852 G>A maps to NM_080284.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:1055345 C>T maps to NM_019112.3 Q1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:1062257 G>A maps to NM_019112.3 E1886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:1043250 G>A did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:1042122 G>T maps to NM_019112.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr19:1043351 G>C maps to NM_019112.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:1056929 C>T maps to NM_019112.3 L1537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr19:1049415 G>T maps to NM_019112.3 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:1045191 C>T maps to NM_019112.3 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:1043402 G>A maps to NM_019112.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:66871462 T>A maps to NM_007168.2 A1483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:66871843 C>G maps to NM_007168.2 T1427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr17:66978738 G>A maps to NM_080283.3 R1562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr17:67031932 C>T maps to NM_080283.3 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr17:67020424 G>T maps to NM_080283.3 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:66972083 C>T maps to NM_080283.3 W1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:87179525 G>C maps to NM_000927.3 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:87179591 C>G maps to NM_000927.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr7:87195484 G>A maps to NM_000927.3 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr7:87170746 G>A maps to NM_000927.3 R749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:169791839 G>T maps to NM_003742.2 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:169783743 G>A maps to NM_003742.2 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:169780146 T>C maps to NM_003742.2 G1317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr2:169791936 T>C did not map to a codon.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr2:169826656 G>A maps to NM_003742.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:87072721 C>T maps to NM_018849.2 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr7:87072739 C>T maps to NM_018849.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr7:87051438 G>A maps to NM_018849.2 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr7:87056097 G>A maps to NM_018849.2 Q678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr7:87037430 C>A maps to NM_018849.2 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr7:87072992 G>A maps to NM_018849.2 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr7:87035603 G>A maps to NM_018849.2 H1169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr7:87079402 G>A maps to NM_018849.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr7:20706379 A>T did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr7:20682806 G>A maps to NM_001163941.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:20762763 C>T maps to NM_001163941.1 A849A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr7:20689664 C>G maps to NM_001163941.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:20739703 G>T maps to NM_001163941.1 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr7:20725390 C>T maps to NM_001163941.1 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr7:20744405 C>A maps to NM_001163941.1 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:20685401 G>A maps to NM_001163941.1 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:20683155 G>C maps to NM_001163941.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:20721229 G>T maps to NM_001163941.1 G604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr7:20782526 C>T maps to NM_001163941.1 R1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr7:20682902 G>A maps to NM_001163941.1 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:220079137 T>A maps to NM_005689.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr2:220081143 C>T maps to NM_005689.2 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr2:220078890 G>A maps to NM_005689.2 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr2:220078865 G>A maps to NM_005689.2 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr2:220082998 G>T maps to NM_005689.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:74289142 T>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:74288933 C>T did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr23:74334621 T>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:74282245 C>T did not map to a codon.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr23:74288842 T>C did not map to a codon.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr23:74376043 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr7:150730890 G>T maps to ENST00000297504 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr12:123444338 C>T maps to NM_203444.2 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr16:16205395 G>A maps to ENST00000399408 T1022T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr16:16101761 C>T maps to ENST00000399408 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:16103673 C>G maps to ENST00000399408 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr16:16232271 G>A maps to ENST00000399408 T1458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr16:16146636 C>A maps to ENST00000399408 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr16:16184308 C>T maps to ENST00000399408 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr16:16205305 C>T maps to ENST00000399408 F992F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:16218717 C>T maps to ENST00000399408 S1231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:16177362 C>T maps to ENST00000399408 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr16:16142159 G>A maps to ENST00000399408 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr16:16216016 C>T maps to ENST00000399408 S1202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr6:43403843 A>G maps to NM_033450.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr6:43406407 C>T maps to NM_033450.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr16:48211015 G>A maps to NM_032583.3 V1119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr16:48256715 T>C maps to NM_032583.3 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr16:48250114 C>T maps to NM_032583.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr16:48261721 G>A maps to NM_032583.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr16:48249114 G>A maps to NM_032583.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr16:48138102 A>G maps to NM_033226.2 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr16:48174624 C>T maps to NM_033226.2 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:101591438 G>A maps to NM_000392.3 A985A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr10:101559037 G>A maps to NM_000392.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:101591888 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:48735815 C>T maps to NM_003786.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr17:48745370 G>A did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr17:48753912 C>A maps to NM_003786.3 V1114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:95858998 G>A maps to NM_005845.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:95815403 A>G maps to NM_005845.3 D760D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr3:183699569 G>T maps to NM_005688.2 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr3:183681280 G>A maps to NM_005688.2 D709D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr3:183679423 C>A maps to NM_005688.2 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr3:183681352 C>T maps to NM_005688.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr3:183679418 C>T maps to NM_005688.2 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:16255390 C>T maps to NM_001171.5 G1179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:16286776 G>A maps to NM_001171.5 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:17426126 G>A maps to ENST00000302539 F1164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr11:17432095 G>A maps to ENST00000302539 T888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr11:17428293 C>T maps to ENST00000302539 T1069T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:17428227 C>T maps to ENST00000302539 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:22013988 C>T maps to NM_005691.2 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:22063216 G>T maps to NM_005691.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr12:21991021 G>T maps to NM_005691.2 R1186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:22069955 G>C maps to NM_005691.2 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:21970132 C>A maps to NM_005691.2 E1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:22068688 A>G maps to NM_005691.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:21998611 G>A maps to NM_005691.2 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr23:153001568 C>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr23:153009061 C>A did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:153006072 G>A did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr23:153006170 G>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:153001627 A>G did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr23:152991458 C>T did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:39947880 C>A maps to NM_005164.3 E686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:40012817 A>G maps to NM_005164.3 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:94964202 G>T maps to ENST00000454898 G502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:74761851 T>A maps to NM_005050.3 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:74759944 C>A maps to NM_005050.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr14:74757039 C>T maps to NM_005050.3 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr14:74766970 C>T maps to NM_005050.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr14:74759534 C>G maps to NM_005050.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr6:30547712 A>G maps to NM_001025091.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr6:30545864 C>T maps to NM_001025091.1 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:150916224 C>T maps to NM_005692.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr21:43714734 G>T maps to NM_004915.3 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr4:89039300 G>A maps to NM_004827.2 H267H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr4:89013472 C>T maps to NM_004827.2 W627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr11:119029005 C>G maps to NM_001142505.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr11:119031273 C>T maps to NM_001142505.1 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr11:119020844 C>G maps to NM_001142505.1 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr11:119020797 G>A maps to NM_001142505.1 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr2:44065003 G>A maps to NM_022436.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:44079963 C>T maps to NM_022437.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:44099197 C>T maps to NM_022437.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:44104828 T>A did not map to a codon.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr2:44104781 T>A maps to NM_022437.2 Y613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr2:44078906 C>T maps to NM_022437.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr2:27352651 C>T maps to NM_032604.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr2:27352633 G>C maps to NM_032604.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr7:73152998 G>A maps to NM_148912.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr20:25284223 C>A maps to NM_015600.3 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:27889908 G>A maps to NM_198147.2 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:89738456 G>C did not map to a codon.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr15:89698751 C>T maps to NM_152924.4 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr18:19244104 G>A maps to NM_138340.4 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr18:19237109 G>A maps to NM_138340.4 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr19:17412026 G>A maps to NM_024527.4 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:17403622 G>A maps to NM_024527.4 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:47299451 G>A did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:100469362 C>T maps to ENST00000471714 G1770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr3:100489650 G>A maps to ENST00000471714 T1550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:100489716 C>T maps to ENST00000471714 E1528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr9:133760622 C>A maps to NM_007313.2 P1001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr9:133738188 G>T maps to NM_007313.2 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:133738361 G>A maps to NM_007313.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr9:133750434 C>A maps to NM_007313.2 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:133760373 G>A maps to NM_007313.2 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:179095630 G>A maps to NM_007314.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr1:179077239 C>T maps to NM_007314.3 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:116213164 G>A maps to ENST00000277895 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr4:8037889 G>A maps to NM_001130083.1 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr5:148590345 G>A maps to NM_014945.2 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:148619422 C>T maps to NM_014945.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr9:136132862 C>T maps to NM_020469.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IF-01A-11D-A31L-08 chr9:136131235 G>A maps to NM_020469.2 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr7:150556007 C>T maps to ENST00000416793 Y576Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:150554745 C>T maps to ENST00000416793 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:961285 C>T did not map to a codon.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr17:1028580 G>A maps to NM_021962.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:915170 C>T maps to NM_021962.2 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr17:1028565 G>A maps to NM_021962.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:107782022 C>T maps to NM_139166.4 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr8:107773699 C>T maps to NM_139166.4 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:107782214 G>A maps to NM_139166.4 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr8:107782151 A>G maps to NM_139166.4 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr6:26597434 C>G maps to NM_013375.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr6:26597371 G>T maps to NM_013375.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr3:127398901 C>T maps to NM_172027.2 C368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr3:127396077 C>T maps to NM_172027.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr3:127395885 C>T maps to NM_172027.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:34219029 C>T maps to NM_145804.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr11:34182506 G>A maps to NM_145804.2 N780N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr11:34175832 C>T maps to NM_145804.2 V953V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:35468547 T>G maps to NM_198834.1 V2161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:35581999 T>C maps to NM_198834.1 S1129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr17:35470192 G>A maps to NM_198834.1 Y2094Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr17:35614746 G>A maps to NM_198834.1 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:109629725 C>T maps to NM_001093.3 C790C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr12:109673452 G>C did not map to a codon.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr12:109634898 G>A maps to NM_001093.3 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:109678917 C>T maps to NM_001093.3 Y1618Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:109684048 C>A maps to NM_001093.3 I1789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:109650675 G>C maps to NM_001093.3 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr12:109696114 G>T maps to NM_001093.3 R2102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:109690902 C>T maps to NM_001093.3 T1995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:109678959 C>G maps to NM_001093.3 V1632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:109685463 G>A maps to NM_001093.3 L1875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr12:112150387 G>A maps to NM_001136538.1 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:112182645 C>T maps to NM_001136538.1 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr12:112130609 C>A maps to NM_001136538.1 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:112194270 C>T maps to NM_001136538.1 R1089R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr12:112150396 G>A maps to NM_001136538.1 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr3:132378463 C>T maps to NM_032169.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr11:134128474 C>T maps to NM_014384.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:211085507 C>T maps to NM_001608.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:121164931 G>A maps to NM_000017.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:124800175 C>G maps to NM_001609.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr10:124800143 G>T maps to NM_001609.3 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:7128358 C>T maps to ENST00000356839 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr17:7127130 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr17:7125376 C>G maps to ENST00000356839 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr15:89400810 A>G maps to NM_013227.3 T1665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr15:89398653 C>T maps to NM_013227.3 G946G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:89402511 G>A maps to NM_013227.3 T2232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr15:89398749 T>A maps to NM_013227.3 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr15:89417255 G>C did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:7251468 C>G maps to NM_014716.3 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr3:195028030 C>A maps to NM_012287.5 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:195012436 T>A maps to NM_012287.5 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:1229510 G>A maps to NM_030649.2 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:1233784 G>A maps to NM_030649.2 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr6:160199707 G>A maps to NM_005891.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:43216410 G>T maps to NM_001135706.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr17:43220989 G>A maps to NM_001135706.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:27529293 A>G maps to ENST00000375888 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr1:180399398 T>A did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:180471272 G>A maps to NM_032360.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:15120600 C>A maps to NM_001039844.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr17:31439076 T>C maps to NM_183377.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr17:32483503 G>A maps to NM_001094.4 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr17:31618635 G>A maps to NM_183377.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:50473824 G>T maps to NM_020039.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:156784709 C>T maps to NM_017419.2 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr4:156775227 C>T did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr11:44073207 G>A maps to NM_001031854.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:44073225 C>T maps to NM_001031854.2 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr11:44073267 C>T maps to NM_001031854.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr16:67692698 G>A maps to NM_001082486.1 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr16:67693459 G>A maps to NM_001082486.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr16:67693882 C>A maps to NM_001082486.1 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:61557821 C>T maps to NM_000789.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr17:61571741 C>G maps to NM_000789.3 Y1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr17:61566338 C>G maps to NM_000789.3 Y829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:61574233 C>T maps to NM_000789.3 S1193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr17:61574510 G>A maps to NM_000789.3 G1235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:15603611 C>T did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr23:15584407 G>C did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:15619007 G>A did not map to a codon.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr23:15613094 A>G did not map to a codon.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr19:6309769 G>A maps to NM_133492.2 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr11:76709866 T>C did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:100488802 C>T maps to NM_000665.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr14:23564342 C>T maps to NM_014977.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr17:40042497 G>A maps to ENST00000401700 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:40034449 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:40063715 G>A maps to ENST00000401700 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr17:40058021 C>T maps to ENST00000401700 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:40035066 C>T maps to ENST00000401700 E836E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:40061859 C>T maps to ENST00000401700 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:135659428 G>C maps to NM_138326.2 *337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:96747112 C>T maps to NM_020186.2 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr22:41922357 C>T maps to ENST00000396512 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr22:41919935 G>A maps to ENST00000396512 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr14:74004391 C>T maps to NM_001037161.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr14:74008366 G>T maps to NM_001037161.1 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr1:55072842 C>T maps to NM_015547.3 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:55059687 C>T maps to NM_015547.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:80640769 G>A maps to NM_130767.2 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:24698241 T>C maps to NM_018473.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr14:74061757 A>G maps to NM_152331.3 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr14:74060509 C>T maps to NM_152331.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr14:74086218 G>A maps to NM_001037162.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:23723191 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:23749057 G>A did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr23:23724803 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:23723707 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:73945809 G>A maps to NM_004035.6 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr3:58508312 T>C maps to NM_003500.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr3:58514634 G>C maps to NM_003500.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:58516344 G>A maps to NM_003500.3 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr4:8383248 G>A maps to NM_003501.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr2:111666364 G>A did not map to a codon.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr2:111666437 G>A maps to NM_001142807.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr11:47270243 G>A maps to NM_001610.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr19:11687261 G>A maps to NM_001111036.1 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:147131782 T>C maps to NM_016361.3 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr3:140998226 C>T maps to NM_001037172.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr3:132086632 C>G maps to NM_001134194.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:51293712 C>T maps to NM_033068.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr12:6753640 C>T maps to NM_032489.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr23:70814204 G>C did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr23:70823702 C>T did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:70830640 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:70824219 G>C did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:70824231 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:70823982 G>A did not map to a codon.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr23:70823684 G>C did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:70823737 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr23:70824045 G>C did not map to a codon.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr23:70823899 G>A did not map to a codon.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr15:78474319 G>A maps to NM_015162.4 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr15:78472019 C>T maps to NM_015162.4 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr19:6187795 C>T maps to NM_030924.3 Q623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:6177295 G>A maps to NM_030924.3 E265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr19:6166025 C>T maps to NM_030924.3 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr16:89169064 C>T maps to NM_174917.2 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr4:185681654 C>T did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:108904859 G>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:108921235 G>A did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr23:108926544 A>G did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:108926453 A>T did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr23:108902622 T>A did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr23:108904778 T>C did not map to a codon.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr23:108912327 G>C did not map to a codon.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr10:114177677 C>T maps to NM_016234.3 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr10:114136093 C>T maps to NM_016234.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr5:131329908 G>A maps to NM_001009185.1 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr16:20673129 C>T maps to NM_052956.2 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr16:20693762 G>A maps to NM_052956.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr16:20682932 G>A maps to NM_052956.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:20497918 C>A maps to NM_001010845.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr16:20497951 G>A maps to NM_001010845.2 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr16:20486733 C>T maps to NM_001010845.2 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:20476885 G>A maps to NM_001010845.2 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr16:20487095 G>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:20487016 C>T maps to NM_001010845.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr16:20565100 A>C maps to NM_182617.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:20570613 C>G maps to NM_182617.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr16:20566637 C>T maps to NM_182617.3 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:20570721 C>T maps to NM_182617.3 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr16:20559464 C>T maps to NM_182617.3 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:20787220 C>A maps to NM_005622.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr16:20781490 C>T maps to NM_005622.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:20781559 G>A maps to NM_005622.3 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr16:20797458 T>G maps to NM_005622.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:7469735 C>T maps to NM_001080454.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr12:7469846 C>T maps to NM_001080454.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr16:20442540 G>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr16:20430565 G>T maps to NM_017888.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:20439172 C>T maps to NM_017888.2 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr16:20439132 C>A maps to NM_017888.2 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:20442555 G>A maps to NM_017888.2 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:20451747 G>C maps to NM_017888.2 *580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr20:24989981 G>C maps to NM_032501.2 S605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr20:24993468 G>A maps to NM_032501.2 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr20:25011401 G>A maps to NM_032501.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:25004173 C>T maps to NM_032501.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr20:33508831 G>A maps to NM_001076552.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:81472118 G>T maps to NM_024560.2 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:81627153 T>C maps to NM_024560.2 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:81613829 C>A maps to NM_024560.2 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:81545668 C>A maps to NM_024560.2 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:81503350 A>G maps to NM_024560.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr12:81528728 C>G maps to NM_024560.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:90707104 C>G maps to NM_001141945.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr7:5569270 G>A maps to NM_001101.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:56778021 G>A maps to NM_001017992.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr15:35086907 C>A maps to NM_005159.4 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr17:79478102 G>T maps to NM_001614.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr17:79478625 C>A maps to NM_001614.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr17:79479039 C>T maps to NM_001614.2 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr3:179298934 C>A maps to NM_004301.3 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:100253068 G>A maps to NM_016188.4 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:100246280 G>A maps to NM_016188.4 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:111625708 C>T maps to NM_006687.2 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr9:111624685 C>G maps to NM_006687.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr9:111625060 C>G maps to NM_006687.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr9:111617802 G>A maps to NM_006686.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:111617355 G>A maps to NM_006686.3 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr9:111618174 C>T maps to NM_006686.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr9:111617532 C>T maps to NM_006686.3 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr1:18149578 C>T maps to NM_030812.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr19:8807821 G>A maps to NM_178525.3 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr1:236924421 C>T maps to NM_001103.2 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:236911017 T>C maps to NM_001103.2 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:236906323 G>A maps to NM_001103.2 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr1:236912509 C>T maps to NM_001103.2 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr11:66322612 C>A maps to NM_001104.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:66319002 G>A maps to NM_001104.1 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr19:39200968 C>G maps to NM_004924.3 S269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr14:58701145 T>A maps to NM_018477.2 Y377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr10:104250322 T>C maps to NM_005736.3 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr2:98274979 G>A maps to NM_005735.3 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:98275415 C>T maps to NM_005735.3 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:65492282 T>C maps to NM_001005386.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:65482680 A>C maps to NM_001005386.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:65480895 T>C maps to NM_001005386.2 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr20:37395020 G>A did not map to a codon.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr20:37396226 G>T maps to NM_024855.3 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr3:53914079 A>T maps to NM_022899.4 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:127185944 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:127185185 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:127185830 G>A did not map to a codon.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr23:127185369 G>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:127185997 T>C did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:2938693 C>T maps to NM_080431.4 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr1:2939014 G>A maps to NM_080431.4 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr1:2938390 C>A maps to NM_080431.4 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr1:2939272 C>A maps to NM_080431.4 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:158617404 C>T maps to NM_001111067.2 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:52378995 C>T maps to NM_020328.3 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr12:52370216 C>T maps to NM_020328.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:158399268 G>C maps to NM_145259.2 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:158443738 G>A maps to NM_145259.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr3:38524630 C>T maps to NM_001106.3 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr12:52307463 G>A maps to NM_001077401.1 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:52309042 G>A maps to NM_001077401.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:52314579 G>A maps to NM_001077401.1 W472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr12:52314549 C>G maps to NM_001077401.1 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr3:52018112 A>T maps to ENST00000458031 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr11:67412540 C>T maps to NM_080658.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:43251499 G>A maps to NM_000022.2 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr20:43251532 G>A maps to NM_000022.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr4:123305080 A>G maps to NM_139243.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:123314742 G>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:123301397 T>C did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr16:84229195 C>T maps to NM_139174.3 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr15:43641113 C>T maps to ENST00000422466 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr15:58925415 A>G maps to NM_001110.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr15:58889781 G>A maps to NM_001110.2 P737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:42852064 G>T did not map to a codon.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr17:42855360 G>A maps to NM_002390.4 W704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr10:127843861 G>T maps to NM_003474.4 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:127731633 T>C maps to NM_003474.4 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr10:127782639 G>A maps to NM_003474.4 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:155034447 G>A maps to NM_207197.1 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:155030887 C>T maps to NM_207197.1 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr2:9666272 G>A maps to NM_003183.4 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:9661433 G>A maps to NM_003183.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr2:9637327 A>T maps to NM_003183.4 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr8:39496008 G>T maps to NM_014237.2 G285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:39564394 T>C maps to NM_014237.2 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:156929849 A>T maps to ENST00000430702 Y425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:156915443 G>T maps to ENST00000430702 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:156957824 G>A maps to ENST00000430702 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr8:39624563 T>C did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:39682335 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:39682393 T>A maps to NM_001464.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr8:39624379 G>A maps to NM_001464.3 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr14:70990092 G>C maps to NM_003814.4 S511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:70925889 C>G maps to NM_003813.2 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:87765301 T>A maps to NM_021723.3 C392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr7:87785301 G>T maps to NM_021723.3 G630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr2:207345996 C>T maps to NM_003812.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:24168891 G>T maps to NM_014265.4 G109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr8:24167433 A>T maps to NM_014265.4 K60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr4:175896742 G>T maps to NM_014269.4 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:175896750 C>T maps to NM_014269.4 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:175896768 G>T maps to NM_014269.4 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:175897134 C>T maps to NM_014269.4 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:175896993 G>T maps to NM_014269.4 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:175897605 C>T maps to NM_014269.4 H310H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:175897974 T>C maps to NM_014269.4 D433D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr4:175897719 T>C maps to NM_014269.4 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr4:175899048 G>A maps to NM_014269.4 T791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr1:120437243 C>A maps to NM_021794.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:120437447 A>G maps to NM_021794.2 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr1:120438119 T>C maps to NM_021794.2 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr8:39068689 C>T maps to NM_145004.5 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr8:39089555 T>C maps to NM_145004.5 N512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:24356804 C>T maps to ENST00000380789 C633C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr8:24339680 G>T maps to ENST00000380789 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:24358342 C>T maps to ENST00000380789 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr8:24333984 C>T maps to ENST00000380789 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:135084730 C>T maps to NM_001109.4 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr8:38871555 T>C maps to NM_003816.2 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr21:28210182 A>G maps to NM_006988.3 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:28210879 T>C maps to NM_006988.3 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:8661980 G>A maps to NM_030957.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:33588884 G>T maps to NM_030955.2 S895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:33881450 C>A maps to NM_030955.2 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr5:33576200 G>A maps to NM_030955.2 N1310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr5:33576464 G>T maps to NM_030955.2 P1222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr5:33624345 C>T maps to NM_030955.2 K711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:33643536 A>G maps to NM_030955.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:33616117 C>A maps to NM_030955.2 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr5:33549374 G>A maps to NM_030955.2 P1413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:33576386 C>A maps to NM_030955.2 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:33684160 C>A did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr5:33576944 C>T maps to NM_030955.2 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr5:33637754 C>T maps to NM_030955.2 Q605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:136324142 G>A maps to NM_139025.3 Q1375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:136323095 G>A maps to NM_139025.3 T1319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr9:136307840 C>T maps to NM_139025.3 C737C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:136323071 G>A maps to NM_139025.3 V1311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr9:136323122 C>T maps to NM_139025.3 F1328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:72496542 C>A maps to NM_139155.2 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr10:72489915 G>A maps to NM_139155.2 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr10:72511851 G>T maps to NM_139155.2 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:72489105 C>T maps to NM_139155.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr10:72511361 G>C maps to NM_139155.2 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:130318900 C>T maps to NM_139055.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:130319056 C>T maps to NM_139055.2 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr5:5319208 C>T maps to NM_139056.2 Y1211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:5186270 G>C maps to NM_139056.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr5:5237175 G>A maps to NM_139056.2 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:5306807 G>A maps to NM_139056.2 S1126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr5:5235207 T>C maps to NM_139056.2 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr5:5318251 G>T maps to NM_139056.2 T1139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr15:100801715 C>A maps to NM_139057.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr15:100821559 C>T maps to NM_139057.2 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr16:77465452 G>A maps to NM_199355.2 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr16:77387770 C>A maps to NM_199355.2 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr16:77327095 G>C maps to NM_199355.2 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:77465452 G>A maps to NM_199355.2 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr16:77375633 G>C maps to NM_199355.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr16:77465452 G>A maps to NM_199355.2 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr16:77353778 C>G maps to NM_199355.2 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:77401512 T>C maps to NM_199355.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr16:77465342 G>T maps to NM_199355.2 S115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr5:128796152 C>T maps to NM_133638.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:128958004 T>C maps to NM_133638.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:129070696 G>T maps to NM_133638.3 G1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr5:128983576 C>T maps to NM_133638.3 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr5:129019946 C>T maps to NM_133638.3 C927C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:128957965 A>C maps to NM_133638.3 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr5:128977611 C>T maps to NM_133638.3 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:178557034 G>A maps to NM_014244.4 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:178770806 G>A maps to NM_014244.4 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr5:178552066 G>A maps to NM_014244.4 H955H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr12:43748065 G>A maps to ENST00000389420 Y1893Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr12:43944861 G>A maps to ENST00000389420 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr12:43769221 G>A maps to ENST00000389420 F1802F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:43846362 G>A maps to ENST00000389420 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr12:43822058 G>A maps to ENST00000389420 T1310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:43769236 A>G maps to ENST00000389420 A1797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:43847819 C>T maps to ENST00000389420 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr12:43777689 G>A maps to ENST00000389420 Q1515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:43777494 G>A maps to ENST00000389420 R1555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:43777746 T>G maps to ENST00000389420 R1496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr12:43823482 G>A maps to ENST00000389420 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:73149385 G>A maps to NM_014243.1 Q1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr4:73205405 C>A maps to NM_014243.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr4:73414353 C>G maps to NM_014243.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr4:73148853 C>G maps to NM_014243.1 *1206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:161163958 G>A maps to NM_005099.4 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr1:161167832 G>A maps to NM_005099.4 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:28338536 G>A maps to NM_007038.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr21:28338239 C>A maps to NM_007038.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr21:28296445 G>T maps to NM_007038.3 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr21:28338236 G>A maps to NM_007038.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr21:28338152 G>A maps to NM_007038.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr15:79092833 G>A maps to ENST00000258883 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr15:79092701 G>A maps to ENST00000258883 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr15:79058841 G>A maps to ENST00000258883 A1137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr15:79089015 C>T maps to ENST00000258883 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr15:79059198 C>T maps to ENST00000258883 E1018E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr11:130297716 G>C maps to NM_007037.4 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr11:130275559 G>A maps to NM_007037.4 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:130275887 G>A maps to NM_007037.4 N745N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr11:130278480 G>A maps to NM_007037.4 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr11:130275689 G>A maps to NM_007037.4 D811D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr11:130275911 C>T maps to NM_007037.4 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:64587787 G>A maps to NM_182920.1 I1283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:18474229 C>A did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr9:18777190 G>A maps to NM_001040272.4 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr9:18753313 G>A maps to NM_001040272.4 W675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr9:18504909 C>T maps to NM_001040272.4 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr9:18721645 G>A maps to NM_001040272.4 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr15:84651067 G>T maps to NM_207517.2 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr15:84657463 G>T maps to NM_207517.2 G1246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:84506851 C>A maps to NM_207517.2 C204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr15:84639318 C>T maps to NM_207517.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr15:84694058 G>T maps to NM_207517.2 T1509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:150529139 G>A maps to ENST00000369039 W563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:150529725 G>A maps to ENST00000369039 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:150528771 G>A maps to ENST00000369039 K525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:150529265 C>G maps to ENST00000369039 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:1506028 C>T maps to NM_213604.2 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr17:29253864 C>T maps to ENST00000394782 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:29283365 C>T maps to ENST00000394782 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr17:29272067 G>A maps to ENST00000394782 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:154573539 C>T maps to ENST00000292205 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:154561028 G>A maps to ENST00000292205 I1004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr21:46596173 G>A maps to NM_015833.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:46596323 C>T maps to NM_015833.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr10:1405855 C>A maps to NM_018702.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr10:1230935 G>C maps to NM_018702.2 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:78374174 G>A maps to NM_020421.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:140394569 C>T maps to NM_052853.3 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:41198103 T>A maps to NM_024876.3 K491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:41198104 G>A maps to NM_024876.3 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr7:45614711 G>A maps to NM_021116.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr7:45632417 C>T maps to NM_021116.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr7:45662326 C>T maps to NM_021116.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:45743069 C>T maps to NM_021116.2 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr7:45750163 C>T maps to NM_021116.2 G990G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:167865863 G>A maps to NM_018417.4 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr1:167798633 C>T maps to NM_018417.4 R1207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr1:167823633 C>G maps to NM_018417.4 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr5:7698430 C>G maps to NM_020546.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr5:7802383 G>A maps to NM_020546.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:7521005 C>A maps to NM_020546.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:7717277 C>A maps to NM_020546.2 S544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr5:7789837 G>C maps to NM_020546.2 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr5:7709415 G>A maps to NM_020546.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr5:7766897 G>A maps to NM_020546.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr2:25062773 T>A maps to NM_004036.3 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:25050955 C>T maps to NM_004036.3 E749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr2:25059787 G>A maps to NM_004036.3 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:25043594 G>A maps to NM_004036.3 Q1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr2:25042881 G>A maps to NM_004036.3 F1118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr14:24789047 G>C maps to NM_139247.3 S878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:24791325 G>A maps to NM_139247.3 N844N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr14:24789007 G>T maps to NM_139247.3 I891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr14:24789034 G>A maps to NM_139247.3 F882F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr3:123018977 G>A maps to NM_183357.2 T963T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:123023003 G>C maps to NM_183357.2 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:123019031 G>A maps to NM_183357.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr12:49176995 G>A maps to NM_015270.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr16:50332900 G>C maps to NM_001114.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:50325657 C>T maps to NM_001114.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:50347891 C>T maps to NM_001114.3 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr16:50348222 C>A maps to NM_001114.3 A959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:50332906 C>A maps to NM_001114.3 C347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr8:131862049 C>T did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr8:132051982 T>G maps to NM_001115.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr8:131861906 G>T maps to NM_001115.2 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:131861991 G>C maps to NM_001115.2 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr8:132052291 C>T maps to NM_001115.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:131792968 C>T maps to NM_001115.2 K1141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:131792677 A>G maps to NM_001115.2 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr8:131792907 C>A maps to NM_001115.2 E1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr8:132002725 C>T maps to NM_001115.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr8:131793004 C>T maps to NM_001115.2 R1129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr8:131826439 G>A maps to NM_001115.2 R930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr16:4164291 A>G maps to NM_001116.3 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr16:4165374 C>T maps to NM_001116.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr18:908353 C>A maps to NM_001117.3 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr18:909476 C>T maps to NM_001117.3 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr18:908271 C>G maps to NM_001117.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr4:2899999 G>A maps to NM_014189.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr2:70933501 C>T maps to NM_001185054.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:70901924 G>A maps to NM_001185054.1 D542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:70900405 G>A maps to NM_017488.3 F598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr2:70900121 G>T maps to NM_001185054.1 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr2:70903954 G>A maps to NM_001185054.1 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr4:100205589 G>C maps to NM_000667.3 S178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:100232741 C>T maps to NM_000668.4 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr4:100237445 G>A maps to NM_000668.4 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr4:100062704 G>T maps to ENST00000505590 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr4:99997691 G>A maps to NM_000671.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr4:100131355 G>T maps to NM_001102470.1 Y150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr4:100131635 G>A maps to NM_001102470.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr4:100341897 G>C maps to NM_000673.4 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:3504680 C>T maps to NM_018269.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:3502802 C>T maps to NM_018269.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr20:37209994 G>A maps to ENST00000416116 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr11:10327877 G>A did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:10327306 C>T maps to NM_001124.1 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr22:50921172 G>A maps to NM_024866.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr18:77895632 C>T maps to NM_014913.3 F779F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr18:77896154 G>C maps to NM_014913.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr10:64564962 C>T maps to NM_032804.5 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr22:24836655 C>T maps to NM_000675.4 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr22:24837219 C>T maps to NM_000675.4 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:112028407 T>G maps to NM_020683.6 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:112042928 G>A maps to NM_000677.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:112033365 G>A maps to NM_020683.6 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:119301304 C>A maps to NM_001125.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr3:119305354 G>A maps to NM_001125.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr3:119306397 C>T maps to NM_001125.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr8:26722303 C>T maps to ENST00000356368 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:26721955 C>T maps to ENST00000356368 Q177Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:96780850 C>A maps to NM_000682.5 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:3768875 C>T maps to NM_000683.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:3768938 C>T maps to NM_000683.3 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr4:3768966 C>T maps to NM_000683.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr4:3768923 C>T maps to NM_000683.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr10:115804436 G>A maps to NM_000684.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr10:115804439 G>A maps to NM_000684.2 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:148206507 C>T maps to NM_000024.5 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr5:148207020 C>T maps to NM_000024.5 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:67049152 G>T maps to NM_001619.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:67050603 G>A maps to NM_001619.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr11:67044772 G>A maps to NM_001619.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:67051731 G>A maps to NM_001619.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr22:26040616 G>A maps to NM_005160.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr20:60883182 G>A maps to NM_175573.1 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr22:40742708 C>G maps to NM_000026.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:40754969 C>T maps to ENST00000428371 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:40759035 G>A maps to NM_000026.2 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr22:40745954 C>T maps to ENST00000428371 H518H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr1:244614998 C>A maps to NM_001126.3 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:244587319 G>C maps to NM_001126.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr14:105208278 C>T maps to NM_199165.1 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr14:105196288 G>A maps to NM_199165.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:44151817 C>T maps to NM_001129.3 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr7:44151907 G>A maps to NM_001129.3 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr7:44144369 G>T maps to NM_001129.3 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr7:44151107 C>T maps to NM_001129.3 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr15:89173492 G>T maps to NM_022767.3 G316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr15:89169568 G>A maps to NM_022767.3 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr19:3054132 C>T maps to NM_198969.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr19:3053999 G>C maps to NM_198969.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr19:3054016 G>A maps to NM_198969.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr4:7795474 G>A maps to NM_001134647.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:7780603 C>A did not map to a codon.
Sequencing variant TCGA-DQ-7596-01A-11D-2229-08 chr5:148687052 G>A maps to NM_152406.2 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr10:116057014 G>A maps to NM_001001936.1 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr10:116057053 C>G maps to NM_001001936.1 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr10:116067593 C>A maps to NM_001001936.1 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:116059061 C>G maps to NM_001001936.1 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr4:88035994 G>A maps to NM_001166693.1 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr4:87968605 C>T maps to NM_001166693.1 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr4:88046197 G>T maps to NM_001166693.1 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:148048357 C>G did not map to a codon.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr23:147582652 G>C did not map to a codon.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr23:147743549 C>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:148037157 G>A did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr23:148048567 C>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:147743455 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:148037549 G>C did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr23:148059933 G>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr23:148037567 G>C did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr23:147924494 G>A did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr23:148072768 G>T did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr23:147733536 G>T did not map to a codon.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr23:148055021 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:147744216 C>T did not map to a codon.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr23:148037674 T>A did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr23:148048584 G>T did not map to a codon.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr23:147985763 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr23:148039926 A>G did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:100203725 G>A maps to NM_001025108.1 D852D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr2:100209884 G>A maps to NM_001025108.1 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr2:100623781 C>T maps to NM_001025108.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr2:100210747 C>A maps to NM_001025108.1 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:100623730 G>A maps to NM_001025108.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:100210205 C>T maps to NM_001025108.1 K664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:100266104 G>A maps to NM_001025108.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:100623132 C>T maps to NM_001025108.1 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:100210322 G>T maps to NM_001025108.1 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr2:100185339 G>A maps to NM_001025108.1 R1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr5:132228811 T>C did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr5:132222031 C>T maps to NM_014423.3 K1023K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr5:132270025 G>C maps to NM_014423.3 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr4:74351713 C>T maps to NM_001133.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr4:74364894 G>T maps to NM_001133.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:74318194 T>A maps to NM_001134.1 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr4:178358643 G>A maps to NM_000027.3 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:236877175 G>C maps to NM_001037131.1 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr2:237032609 G>T maps to NM_001037131.1 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:236708048 C>T maps to NM_001037131.1 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr2:236957874 C>A maps to NM_001037131.1 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr2:236659079 C>T maps to NM_001037131.1 Y207Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:58125674 G>T maps to NM_001122772.1 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:58125675 G>T maps to NM_001122772.1 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr12:58131111 G>A maps to NM_001122772.1 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr12:58124353 G>A maps to NM_001122772.1 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr7:150817138 C>T maps to NM_031946.4 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:150784094 G>T maps to NM_031946.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:150814820 C>T maps to NM_031946.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr10:46322370 G>A maps to ENST00000355953 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:46322016 C>T maps to ENST00000355953 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr10:51748543 G>T maps to NM_001077665.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr10:51465225 T>G maps to ENST00000416142 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr10:51464880 G>A maps to ENST00000416142 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr15:87097593 T>C maps to NM_152336.2 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr15:86807623 G>T maps to NM_152336.2 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr15:86800202 G>T maps to NM_152336.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr11:47681868 G>T maps to ENST00000357610 C857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:27278586 C>T maps to NM_021831.5 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:27276858 C>A maps to NM_021831.5 Y161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr2:27278918 C>T maps to NM_021831.5 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr6:32148966 G>A maps to ENST00000375070 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr7:100161550 C>T maps to NM_006076.4 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr5:76349812 C>T maps to NM_018046.4 Y497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr5:76332494 G>T maps to NM_018046.4 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:141315362 C>A maps to NM_018238.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr7:141333765 C>T maps to NM_018238.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr7:141333735 C>T maps to NM_018238.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr1:100349944 C>T maps to ENST00000311030 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:100357190 C>T maps to ENST00000311030 F994F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:100387119 C>A maps to ENST00000311030 T1505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr1:100358104 T>G maps to ENST00000311030 P1068P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:100343221 A>G maps to ENST00000311030 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:32138237 G>A maps to NM_032741.4 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr21:45389027 G>T maps to NM_001037553.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr21:45397972 C>T maps to NM_001037553.1 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:161587366 C>T maps to NM_020133.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr8:6566209 C>G maps to NM_018361.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr15:78807439 G>A maps to NM_001013619.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr2:178305724 C>T maps to NM_003659.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:985676 G>C maps to NM_198576.2 L1648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:981867 C>T maps to NM_198576.2 P1001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr1:982023 G>A maps to NM_198576.2 V1053V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:978799 C>T maps to NM_198576.2 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr1:981637 G>A maps to NM_198576.2 P968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:230845930 C>T maps to NM_000029.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:230846410 G>C maps to NM_000029.3 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:230841941 C>T maps to NM_000029.3 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:230838922 G>A maps to NM_000029.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:88247623 C>T maps to ENST00000395847 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr9:88293286 A>T maps to ENST00000395847 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:88272526 T>C maps to ENST00000395847 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr9:88270060 C>A maps to ENST00000395847 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr3:148458872 T>C maps to NM_032049.2 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:115303581 G>T did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr23:115304381 G>C did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:11807586 C>T maps to NM_001040196.1 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:11808622 A>G maps to NM_001040196.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:35037088 T>C maps to NM_031900.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:35010166 C>A maps to NM_031900.3 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:35039553 C>T maps to NM_031900.3 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr5:35037139 G>A maps to NM_031900.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:35035324 A>G did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr5:35010176 C>G maps to NM_031900.3 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr4:109681434 C>T maps to NM_031279.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr4:109667915 A>C did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr4:109669201 C>T maps to NM_031279.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:247051785 A>G maps to ENST00000428671 D764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:247031020 T>A maps to ENST00000428671 K1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:247014459 T>C maps to ENST00000428671 K1654K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:247025260 C>A maps to ENST00000428671 G1283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:247040555 C>T maps to ENST00000428671 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr1:247027357 C>T maps to ENST00000428671 Q1174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr20:32880203 G>A maps to NM_000687.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr1:27878170 C>T maps to NM_001029882.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:27874900 G>A maps to NM_001029882.2 F1242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr1:27876246 G>A maps to NM_001029882.2 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:27878365 C>T maps to NM_001029882.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr1:27874637 G>T maps to NM_001029882.2 S1330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:135787270 C>A maps to NM_017651.4 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr11:62294808 T>C maps to NM_001620.1 V2360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr11:62300565 T>C maps to NM_001620.1 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:62301180 G>C maps to NM_001620.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:62297925 G>T maps to NM_001620.1 P1321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:62287083 C>T maps to NM_001620.1 P4935P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr11:62293149 T>C maps to NM_001620.1 E2913E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:62289229 G>C maps to NM_001620.1 S4220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr11:62292957 C>T maps to NM_001620.1 V2977V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr11:62289613 G>C maps to NM_001620.1 S4092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr11:62294493 G>A maps to NM_001620.1 P2465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:62296992 T>C maps to NM_001620.1 P1632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:62285787 T>C maps to NM_001620.1 G5367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:62298957 G>A maps to NM_001620.1 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:62286411 C>G maps to NM_001620.1 L5159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:62297748 C>T maps to NM_001620.1 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:62284988 C>A maps to NM_001620.1 G5634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr11:62291337 G>A maps to NM_001620.1 L3517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr11:62291088 C>G maps to NM_001620.1 L3600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr11:62287509 G>A maps to NM_001620.1 F4793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr11:62284338 C>G maps to NM_001620.1 G5850G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr11:62291748 T>A maps to NM_001620.1 I3380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr11:62295104 C>A maps to NM_001620.1 E2262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:62287461 G>A maps to NM_001620.1 I4809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr11:62259276 T>C maps to NM_024060.2 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr11:62293275 G>C maps to NM_001620.1 L2871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr11:62293495 G>C maps to NM_001620.1 S2798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr14:105419117 C>A maps to NM_138420.2 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr14:105410834 C>A maps to NM_138420.2 S3651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr14:105409976 G>A maps to NM_138420.2 D3937D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr14:105410636 G>C maps to NM_138420.2 L3717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr14:105412487 G>A maps to NM_138420.2 P3100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr14:105415895 C>T maps to NM_138420.2 K1964K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:105414034 G>A maps to NM_138420.2 Q2585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr14:105418064 G>A maps to NM_138420.2 G1241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr14:105412106 G>C maps to NM_138420.2 P3227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr14:105411953 G>A maps to NM_138420.2 V3278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr14:105410213 G>A maps to NM_138420.2 A3858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr14:105416846 G>A maps to NM_138420.2 A1647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:105418940 C>T maps to NM_138420.2 K949K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr14:105420854 C>T maps to NM_138420.2 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr14:105411722 G>A maps to NM_138420.2 D3355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr14:105406586 G>A maps to NM_138420.2 D5067D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr14:105406784 G>A maps to NM_138420.2 I5001I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr14:105420815 G>A maps to NM_138420.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:105408932 G>A maps to NM_138420.2 S4285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:105414530 G>A maps to NM_138420.2 P2419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:105417194 G>A maps to NM_138420.2 S1531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:105418184 G>A maps to NM_138420.2 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:105415982 C>T maps to NM_138420.2 L1935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:105408302 G>A maps to NM_138420.2 A4495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:105418136 G>A maps to NM_138420.2 S1217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr14:105409646 G>C maps to NM_138420.2 L4047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr14:105406037 G>T maps to NM_138420.2 L5250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr14:105410722 G>A maps to NM_138420.2 Q3689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr14:105414044 G>A maps to NM_138420.2 L2581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr14:105419159 G>A maps to NM_138420.2 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr14:105419468 G>C maps to NM_138420.2 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr14:105420225 G>C maps to NM_138420.2 S521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:105410276 C>G maps to NM_138420.2 V3837V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:105411032 C>G maps to NM_138420.2 L3585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr14:105409426 G>A maps to NM_138420.2 L4121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr14:105411704 A>G maps to NM_138420.2 P3361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr14:105406955 A>C maps to NM_138420.2 A4944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr14:105413126 G>A maps to NM_138420.2 P2887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr5:423992 G>A maps to NM_020731.3 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr5:422959 G>A maps to NM_020731.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr5:422968 G>A maps to NM_020731.3 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr14:77926054 G>A maps to NM_012111.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:61411928 C>A maps to ENST00000389584 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:31584616 G>A maps to NM_001623.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:133993217 C>G maps to NM_001185095.1 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr23:129281540 C>G did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr23:129272622 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:129272622 C>G did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr22:21331012 C>T maps to NM_144704.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:143486274 G>A maps to NM_016108.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:106987307 G>A maps to NM_001624.2 Q1175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:106973168 C>T maps to NM_001624.2 V1032V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:26648787 C>G maps to NM_001039775.3 V1588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:26658051 G>A maps to NM_001039775.3 G1414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:26664048 G>A maps to NM_001039775.3 S1208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr1:159035749 G>A maps to NM_004833.1 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:6049119 C>T maps to NM_006303.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:6329145 G>A maps to NM_014336.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr21:45709684 C>T maps to NM_000383.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr1:4829976 C>T maps to NM_018836.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:4772085 C>T maps to NM_018836.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:4772199 C>T maps to NM_018836.3 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:33502360 A>G maps to NM_001625.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr9:4718522 C>G maps to NM_016282.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:77763625 G>A maps to NM_174858.1 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:77984358 G>T maps to NM_174858.1 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:77806201 G>A maps to NM_174858.1 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr14:96937851 A>G maps to NM_152327.2 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:55195782 G>T maps to ENST00000427138 E890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:55182884 C>A maps to ENST00000427138 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:55183031 C>T maps to ENST00000427138 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr17:55184347 C>G maps to ENST00000427138 S550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:19835243 C>T maps to NM_007202.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr17:19844262 G>A maps to NM_007202.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:19861846 T>C maps to NM_007202.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr13:42891736 A>G maps to NM_016248.2 L1826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr13:42876730 C>T maps to NM_016248.2 F1283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr13:42877786 C>T maps to NM_016248.2 L1635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr6:151671463 C>T maps to NM_005100.3 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr6:151672231 A>G maps to NM_005100.3 A902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr6:151669885 C>T maps to NM_005100.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr6:151671661 G>A maps to NM_005100.3 Q712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr15:86189093 C>G maps to NM_006738.4 S1428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr15:86259037 T>C maps to NM_006738.4 R1877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr23:119037535 A>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:119054533 C>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:119037468 C>G did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:119054500 G>T did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:112899401 C>G maps to NM_007203.4 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:112898558 T>G maps to NM_007203.4 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:112899251 G>T maps to NM_007203.4 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr9:112898858 C>T maps to NM_007203.4 H345H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:112899837 C>A maps to NM_007203.4 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:112899230 A>G maps to NM_007203.4 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:112900743 T>C maps to NM_007203.4 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr12:4736093 G>A maps to NM_006422.2 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr12:4737713 C>T maps to NM_006422.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr23:49957553 G>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:49958927 C>A did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:49958506 A>G did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:49958649 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:49961629 G>C did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr23:49957376 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:49959014 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr23:49957166 T>C did not map to a codon.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr23:49957772 C>A did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr23:49958169 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:49957581 T>C did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:49958757 C>G did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:49957066 G>C did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr14:64936394 G>C maps to NM_004857.3 *428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr14:33293222 G>A maps to NM_004274.4 S2068S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr14:33293955 C>T maps to NM_004274.4 R2313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:33147557 T>G maps to NM_004274.4 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr14:33292160 G>A maps to NM_004274.4 S1714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr14:33165312 C>A maps to NM_004274.4 Y999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:131520610 T>C maps to ENST00000431975 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr6:131602680 G>T maps to ENST00000431975 G282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr6:131571735 C>G maps to NM_138633.1 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr19:15483733 C>G maps to NM_005858.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr19:15514302 G>A maps to NM_014371.2 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:91695763 T>C maps to NM_005751.4 H2078H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr7:91735019 C>T maps to NM_005751.4 R3787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr7:91643573 A>T maps to NM_005751.4 K1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr7:91682105 C>G maps to NM_005751.4 S1812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr7:91659266 G>T maps to NM_005751.4 G1403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:91691799 C>T maps to NM_005751.4 Q1993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:91724386 T>G maps to NM_005751.4 L3210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:91631453 T>G maps to NM_005751.4 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:91630491 C>A maps to NM_005751.4 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:91632537 A>T maps to NM_005751.4 K1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:91622236 A>G maps to NM_005751.4 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr7:91708995 C>T maps to NM_005751.4 Q2517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr7:91737897 T>C maps to NM_005751.4 Y3879Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr7:91682140 C>T maps to NM_005751.4 R1824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr7:91729011 G>A maps to NM_005751.4 V3575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr6:109978084 T>C maps to NM_001145128.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:39463963 C>G maps to NM_024595.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr6:88387535 C>A maps to NM_018064.3 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr9:117143418 G>A maps to NM_030767.4 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr7:134223688 C>G maps to NM_020299.4 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:137790054 G>T maps to NM_005989.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:4889383 C>T maps to NM_001040177.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:19632583 G>A maps to NM_003689.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:19630781 G>A maps to NM_003689.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr1:19596119 G>A maps to NM_201252.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr1:19596155 G>T maps to NM_201252.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:105241316 G>A maps to NM_001014432.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr14:105238728 G>A maps to NM_001014432.1 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr14:105239674 G>A maps to NM_001014432.1 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:50374956 C>T maps to ENST00000391835 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:40762854 G>A maps to NM_001626.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:243778439 A>C maps to NM_005465.3 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:243727051 G>A maps to NM_005465.3 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr9:116150609 C>T maps to ENST00000277315 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:52240615 C>T maps to ENST00000441729 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr3:52245380 C>T maps to ENST00000441729 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:55039984 C>G did not map to a codon.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr23:55054213 T>A did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr23:55042038 A>C did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:55042055 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr23:55047575 C>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:55041390 A>G did not map to a codon.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr4:74284001 G>A maps to NM_000477.5 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:74274381 C>A maps to NM_000477.5 C114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:105258903 G>A maps to NM_001627.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:49962337 G>A maps to NM_153329.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr9:75531988 C>T maps to NM_000689.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:58287337 C>A did not map to a codon.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr15:58306119 G>C maps to NM_003888.2 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr15:58254323 C>G maps to NM_003888.2 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr15:101445831 C>G maps to NM_000693.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr15:101447333 G>T maps to NM_000693.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr15:101448627 C>T maps to NM_000693.2 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr9:38396722 C>T maps to NM_000692.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr9:38396908 A>G maps to NM_000692.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:38396325 G>A maps to NM_000692.3 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:125828901 G>A maps to ENST00000273450 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:125833453 C>T maps to ENST00000273450 G686G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-7402-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:125872404 G>C maps to ENST00000273450 S257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:125855666 C>T maps to ENST00000273450 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr3:125824635 C>T maps to ENST00000273450 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr3:125826018 G>A maps to ENST00000273450 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr12:105440678 G>A maps to NM_001034173.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:105420515 G>A maps to NM_001034173.3 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr12:112227668 C>A maps to NM_000690.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr17:19641683 C>T maps to NM_000691.4 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr17:19645911 C>T maps to NM_000691.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:19555869 G>C maps to NM_001031806.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr11:67787206 C>T maps to NM_001161473.1 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr11:67789311 C>T maps to NM_001161473.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:67433602 G>A maps to NM_001031615.1 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:67431899 G>A maps to NM_001031615.1 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:19209671 C>A maps to NM_003748.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr6:24523068 C>T maps to NM_170740.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:24533786 G>A maps to NM_170740.1 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr14:74538941 G>C maps to NM_005589.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:135239567 G>T maps to NM_022568.3 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:165667714 A>G maps to NM_000696.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr16:30081229 G>A maps to ENST00000395248 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr16:30080250 C>T maps to ENST00000395248 I218I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-F7-7848-01A-11D-2129-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr17:26901250 A>G maps to NM_005165.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:26902185 G>A maps to NM_005165.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr12:34175677 C>T maps to NM_032834.3 Y48Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr12:34179306 C>T maps to NM_032834.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr12:38714761 C>G maps to NM_001013620.3 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr13:52586580 C>T maps to NM_001004127.2 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:52593180 G>A maps to NM_001004127.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr13:52586553 G>A did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:52598681 G>A maps to NM_001004127.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:50298024 G>A maps to NM_024105.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr23:110924493 C>T did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:110979970 T>C did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr23:110951258 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:110966070 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:111000959 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:95538322 C>G maps to NM_144988.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:125651538 A>C maps to NM_001195223.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr9:101980620 C>T maps to NM_033087.3 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr3:183963044 G>A maps to NM_005787.5 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr3:183963098 G>A maps to NM_005787.5 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr13:37569652 G>T maps to NM_013338.4 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:111708981 T>A maps to ENST00000428306 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:111731282 A>G maps to ENST00000428306 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:29456499 A>T maps to NM_004304.3 R806R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr2:30143170 C>A maps to NM_004304.3 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr2:30143410 G>A maps to NM_004304.3 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:29543629 G>A maps to NM_004304.3 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr2:29451852 A>G maps to NM_004304.3 H904H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:78161200 C>T maps to NM_006020.2 W112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr12:109526160 C>T maps to NM_001145375.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr11:43941466 G>A did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:102100193 C>A maps to NM_017621.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr7:102097842 A>T maps to NM_017621.3 *303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr7:102098317 C>G maps to NM_017621.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr17:18098326 C>T maps to ENST00000261650 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr19:6374914 C>G maps to NM_032306.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:107427561 G>A maps to ENST00000417449 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr2:3726068 G>A maps to ENST00000403787 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr2:73717188 A>G maps to NM_015120.4 Q2700Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:73651681 C>T maps to NM_015120.4 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:73676155 T>A maps to NM_015120.4 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr2:73826529 A>G maps to NM_015120.4 V3849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:73717131 A>G maps to NM_015120.4 E2681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:73651782 G>C maps to NM_015120.4 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr2:73676803 C>G maps to NM_015120.4 Y1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr2:73675675 C>T maps to NM_015120.4 D673D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:6913396 T>C maps to NM_000697.2 C588C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr17:6900304 G>A maps to NM_000697.2 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr17:6909232 G>A maps to NM_000697.2 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr17:6905054 G>A maps to NM_000697.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr17:7983185 C>G maps to NM_001139.2 L276L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-UF-A7JA-01A-12D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:4542785 G>A maps to NM_001140.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr17:4535216 G>A maps to NM_001140.3 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr17:7951078 G>A maps to NM_001141.2 W566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr17:7948605 C>T maps to NM_001141.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:45938938 C>T maps to NM_000698.2 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr17:8020223 G>A maps to ENST00000380149 Y230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:8017843 G>C maps to ENST00000380149 S369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:8021161 C>T maps to ENST00000380149 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr4:113353309 C>T maps to NM_025144.3 H869H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr4:113353567 G>C maps to NM_025144.3 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr4:113347689 G>T maps to NM_025144.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:113356373 G>T maps to NM_025144.3 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:113352353 C>T maps to NM_025144.3 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr4:113352757 C>T maps to NM_025144.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:113352353 C>T maps to NM_025144.3 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr18:56203583 G>A maps to NM_052947.3 L1279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr18:56202140 T>A maps to NM_052947.3 K1760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr18:56184166 G>T maps to NM_052947.3 I1971I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr18:56171232 C>T maps to NM_052947.3 Q2059Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr18:56247485 G>C maps to NM_052947.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr18:56202446 C>A maps to NM_052947.3 G1658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr18:56203185 C>G maps to NM_052947.3 V1411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr18:56246909 G>A maps to NM_052947.3 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr15:85399942 G>A maps to NM_020778.4 Q860Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:85360148 G>T maps to NM_020778.4 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr15:85384097 C>A maps to NM_020778.4 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:85399942 G>A maps to NM_020778.4 Q860Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:85407690 G>A maps to NM_020778.4 L1708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr15:85401043 G>A maps to NM_020778.4 Q1227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:85382229 G>T maps to NM_020778.4 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:85400611 G>A maps to NM_020778.4 A1083A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr15:85383934 T>G maps to NM_020778.4 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:21903030 G>A maps to NM_000478.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:21889727 C>A maps to NM_000478.4 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:233246045 C>T maps to NM_001632.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr2:233243765 C>T maps to NM_001632.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr2:233246270 C>T maps to NM_001632.3 D458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr2:233245429 G>A maps to NM_001632.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr2:233274347 C>T maps to NM_031313.2 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:202625888 G>A maps to NM_020919.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr2:202593825 C>T maps to NM_020919.3 K887K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr2:202626248 C>T maps to NM_020919.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr3:46728523 G>A maps to NM_147129.3 H161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:46719880 T>C did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr2:202483820 G>A maps to NM_001168221.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr2:202469363 C>T maps to NM_001168221.1 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr2:203807530 C>T maps to NM_024744.14 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:203839199 C>G maps to NM_024744.14 S492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:85680629 G>C did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr12:85677392 C>G maps to NM_006982.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr12:85674212 C>T maps to NM_006982.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:44297070 A>G maps to NM_021926.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr11:44286712 G>T maps to NM_021926.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:44286553 C>T maps to NM_021926.3 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:33521248 G>A maps to NM_152462.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:33520507 C>T maps to NM_152462.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:11188897 C>T maps to NM_054028.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr8:11188845 C>T maps to NM_054028.1 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:11189364 C>T maps to NM_054028.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr5:34005990 T>C maps to NM_001167595.1 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr4:71467196 A>G maps to NM_016519.4 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:71468990 C>T maps to NM_016519.4 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr9:116823280 G>A maps to NM_001633.3 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:116823770 G>A maps to NM_001633.3 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr9:116838906 C>T maps to NM_001633.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr11:46567251 G>C maps to ENST00000458649 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:46564068 G>A maps to ENST00000458649 Q500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:46564191 G>A maps to ENST00000458649 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:46565584 C>T maps to ENST00000458649 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr11:46564147 C>T maps to ENST00000458649 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr6:111210178 C>G maps to NM_001634.4 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr16:2579488 C>A maps to NM_001145815.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr16:2579488 C>T maps to NM_001145815.1 L415L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HL-7533-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:2580408 G>T maps to NM_001145815.1 V478V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-WA-A7GZ-01A-11D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr23:11314927 T>C did not map to a codon.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr23:11316947 C>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr24:6736362 G>T did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr12:53823689 C>T maps to NM_020547.2 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:110051360 G>A maps to NM_020703.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr12:47472578 C>T maps to NM_001143668.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:49755533 G>A maps to NM_198722.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:109441840 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:109560967 G>A did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:112058640 C>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:112033889 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:112025793 A>G did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr23:112048304 C>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr23:112033826 C>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:112054478 C>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:112022392 C>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:112021851 A>G did not map to a codon.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr23:112054573 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:112058608 C>G did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr11:94533289 G>T maps to NM_130847.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:134086482 G>A maps to ENST00000514516 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr3:134086461 C>T maps to ENST00000514516 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:110170414 C>A maps to ENST00000393689 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr1:110168330 G>A maps to ENST00000393689 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:38530703 C>G maps to NM_001635.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr7:38505846 G>A maps to NM_001635.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:38530745 C>G did not map to a codon.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:38431513 G>A maps to NM_001635.3 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr7:38433622 G>T maps to NM_001635.3 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:38462074 G>A maps to NM_001635.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:38471786 A>G did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:49455118 G>A maps to NM_000481.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:49455119 A>G maps to NM_000481.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:104115821 T>C maps to ENST00000305865 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr7:2752118 C>A maps to NM_133463.1 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr17:66246327 G>C did not map to a codon.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr2:112621424 C>T maps to NM_022662.2 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:140078133 G>A maps to NM_013366.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr9:140082435 C>T maps to NM_013366.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr14:21162088 G>A maps to NM_001097577.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:77269771 G>A maps to NM_015305.3 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr14:77269771 G>A maps to NM_015305.3 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:77274327 G>A maps to NM_015305.3 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr8:108334193 G>T maps to NM_001146.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr8:6372250 G>A maps to NM_001147.2 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:6378819 G>A maps to NM_001147.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr8:6366504 C>T maps to NM_001147.2 K426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr20:870885 C>T maps to NM_015985.2 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr20:853761 C>G maps to NM_015985.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr20:869079 G>A maps to NM_015985.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:178834725 C>T maps to NM_004673.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr1:178834308 C>T maps to NM_004673.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:129851243 G>A maps to NM_012098.2 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr1:63064453 C>T maps to NM_014495.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:8436123 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr19:10204169 G>A maps to NM_031917.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:10206705 G>A maps to NM_031917.2 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:11249655 C>G maps to NM_021146.2 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr8:41525934 C>T maps to ENST00000415018 Q1748Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:41545689 G>C maps to ENST00000415018 L1414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr8:41529900 C>G maps to ENST00000415018 V1689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr8:41530293 G>A maps to ENST00000415018 D1558D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr8:41555569 C>T maps to ENST00000415018 E876E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr8:41581096 G>T maps to ENST00000415018 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr8:41552253 C>T maps to ENST00000415018 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr8:41572571 G>A maps to ENST00000415018 H541H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr8:41519417 G>A maps to ENST00000415018 A1840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr8:41577279 G>A maps to ENST00000415018 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr8:41550657 G>A maps to ENST00000415018 N1198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:114275821 A>G maps to NM_001148.4 A2016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr4:114264271 G>T maps to NM_001148.4 E1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr4:114290864 G>A maps to NM_001148.4 E3838E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:114278086 C>T maps to NM_001148.4 I2771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr4:114279448 C>T maps to NM_001148.4 L3225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:114209629 C>T maps to NM_001148.4 N755N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:114274327 C>A maps to NM_001148.4 T1518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr4:114257134 G>A maps to NM_001148.4 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr4:114095603 C>A maps to NM_001148.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr4:114254239 G>A maps to NM_001148.4 A1085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr4:114294538 G>A maps to NM_001148.4 E3931E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:114179510 T>C maps to NM_001148.4 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr4:114262918 C>T maps to NM_001148.4 C1323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr4:114251400 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:61832870 C>A maps to NM_020987.2 E2590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:61822995 C>T maps to NM_020987.2 S4156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:61819456 C>G maps to ENST00000503366 L1689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:61840376 C>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:62039398 T>G did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr10:61832597 G>A maps to NM_020987.2 Q2681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:61830609 T>C maps to NM_020987.2 Q3343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr10:61834986 G>T maps to NM_020987.2 P1884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr10:61898789 C>T maps to NM_020987.2 K890K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr10:61833594 T>C maps to NM_020987.2 R2348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr10:61830996 C>T maps to NM_020987.2 K3214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:190554268 A>G maps to NM_144708.3 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr2:190571720 A>G maps to NM_144708.3 Q656Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr2:190584296 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:190611140 C>T maps to NM_144708.3 Q1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr17:54534294 G>C maps to NM_153228.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr17:54428210 C>T maps to NM_153228.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr17:54535255 G>A maps to NM_153228.2 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:4085589 G>A maps to NM_016376.3 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:14758586 A>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr5:14713735 C>A maps to NM_054027.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr5:139876312 A>G maps to ENST00000253810 E818E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr5:139918551 C>T maps to ENST00000253810 Q2502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr5:139908267 C>T maps to ENST00000253810 L1913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:139781713 G>A maps to ENST00000253810 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr5:139903728 G>T maps to ENST00000253810 E1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:91948720 A>G maps to NM_019004.1 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:113270781 C>T maps to NM_178510.1 H697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:113270782 C>T maps to NM_178510.1 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:17394534 G>A maps to NM_152363.4 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:133327232 C>T maps to NM_015114.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr12:133331318 C>T maps to NM_015114.1 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:241494414 C>T maps to ENST00000401804 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr2:241492384 G>A maps to ENST00000401804 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:241465801 G>A maps to ENST00000401804 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr2:241492399 G>A maps to ENST00000401804 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr2:241451334 C>T maps to ENST00000401804 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:16640448 T>C maps to NM_020319.2 E421E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr10:92675320 C>T maps to NM_014391.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:92675592 A>G maps to NM_014391.2 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr10:92675631 G>C maps to NM_014391.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr13:111558411 G>A maps to NM_017664.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr16:89351116 G>A maps to NM_013275.4 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:89350643 G>C maps to NM_013275.4 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr16:89349565 G>A maps to NM_013275.4 D1128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:89348956 G>A maps to NM_013275.4 D1331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr16:89348248 C>T maps to NM_013275.4 R1567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr16:89357576 C>A maps to NM_013275.4 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr16:89346490 C>T maps to NM_013275.4 A2153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr16:89350233 G>A maps to NM_013275.4 R906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr16:89350643 G>C maps to NM_013275.4 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr16:89341311 C>T maps to NM_013275.4 A2541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr18:9211768 G>A maps to NM_015208.3 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr18:9254482 C>T maps to NM_015208.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr18:9257920 A>T maps to NM_015208.3 G1552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr18:9257170 A>G maps to NM_015208.3 R1302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr18:9256147 G>A maps to NM_015208.3 K961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr18:9256443 C>G maps to NM_015208.3 S1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:9258556 C>T maps to NM_015208.3 S1764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:9275634 C>T maps to NM_015208.3 A1959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr18:9257776 G>T maps to NM_015208.3 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr18:9204503 G>A maps to NM_015208.3 W89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr17:27937743 G>A maps to NM_152345.4 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:70819808 G>A maps to NM_030816.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr4:73990773 A>G maps to NM_032217.3 G1116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr4:74005791 C>T maps to NM_032217.3 K847K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr4:74010531 A>C maps to NM_032217.3 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:99343355 G>C maps to NM_020349.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:99340626 C>T maps to NM_020349.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr9:67951985 G>T maps to NM_001012419.1 G317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:69423575 G>C maps to NM_001098805.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:4200160 C>T maps to ENST00000262970 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:4216578 G>A maps to ENST00000262970 Q564Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr19:4219649 A>T maps to ENST00000262970 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr10:27324645 C>T maps to NM_014915.2 S911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr10:27366290 C>T maps to NM_014915.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:33110270 G>A maps to NM_032139.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:33131244 T>C maps to NM_032139.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr19:33113489 C>T maps to NM_032139.2 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr18:21214077 G>A maps to NM_173505.2 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr10:37442497 A>C did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr10:37421250 G>C maps to ENST00000374660 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr10:37431033 T>G maps to ENST00000374660 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:37419230 T>G maps to ENST00000374660 Y89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:37419290 C>T maps to ENST00000374660 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr10:37430688 G>A maps to ENST00000374660 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr10:37419269 G>T maps to ENST00000374660 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr10:37418910 C>T maps to ENST00000374660 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr10:37506718 G>A maps to ENST00000374660 R1123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr10:37508302 T>C maps to ENST00000374660 P1284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr18:14787089 G>A maps to NM_001145029.1 W575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr18:14797797 A>G maps to NM_001145029.1 K658K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr18:14851926 T>A maps to NM_001145029.1 A1209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr18:14851602 G>A maps to NM_001145029.1 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr5:94024257 T>C maps to NM_032290.3 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr12:52282463 C>A maps to NM_182608.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr12:52284806 G>T maps to NM_182608.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr5:79855682 C>T maps to NM_001004441.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:79854711 G>C maps to NM_001004441.2 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr5:79854711 G>C maps to NM_001004441.2 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:145558912 C>T maps to NM_144698.3 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:145562414 C>T maps to NM_144698.3 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr1:145561562 T>C maps to NM_144698.3 H417H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:97779625 C>G maps to NM_001164315.1 Y50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:97779538 C>T maps to NM_001164315.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:97866191 C>T maps to NM_001164315.1 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr2:97808555 A>G maps to NM_001164315.1 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:186318368 G>A maps to NM_181726.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:197943432 C>A maps to NM_001195144.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr2:197990617 G>A maps to NM_001195144.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr2:197990623 G>A maps to NM_001195144.1 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr2:197990662 G>A maps to NM_001195144.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr2:197990751 G>A maps to NM_001195144.1 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:197866544 C>T maps to NM_001195144.1 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:173628227 A>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:94230097 G>A maps to NM_017704.2 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr20:10018978 C>T maps to NM_198798.1 N10N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr20:10030800 G>T maps to NM_198798.1 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr4:125592803 G>C maps to NM_020337.2 S543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:56641849 G>A maps to NM_173595.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56638204 G>A maps to NM_173595.3 R913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:71211739 G>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:71206394 C>T maps to NM_001115116.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr2:71206792 C>T maps to NM_001115116.1 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:77817742 T>C maps to NM_001029870.1 E420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr2:110373217 G>T maps to NM_023016.3 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr23:118893449 G>A did not map to a codon.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr23:118893113 G>A did not map to a codon.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr6:35053631 G>A maps to NM_015245.2 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:99548222 G>T maps to NM_181670.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:99194840 G>T maps to NM_152788.3 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:99793502 T>A maps to NM_152788.3 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr12:100173679 C>T maps to NM_152788.3 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:99223029 C>T maps to NM_152788.3 Q996Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr12:100200409 G>A maps to NM_152788.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr16:4774825 C>T maps to NM_133450.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr16:4777096 G>A maps to NM_133450.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:21262062 G>A maps to NM_145865.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:101540675 G>A maps to ENST00000375018 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr9:101552737 C>A maps to ENST00000375018 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr9:101552848 G>A maps to ENST00000375018 H133H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr2:220100548 T>A maps to NM_001042410.1 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr2:220098636 C>T maps to NM_001042410.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:220101165 G>A maps to NM_001042410.1 *727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr2:220098106 C>T maps to NM_001042410.1 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr7:36462272 G>A maps to NM_018685.2 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr7:36462395 C>G maps to NM_018685.2 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:36459870 C>T maps to NM_018685.2 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:70028646 C>T maps to NM_018043.5 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr11:69933943 C>T maps to NM_018043.5 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr11:69954472 G>A maps to NM_018043.5 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr11:69934123 C>G maps to NM_018043.5 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:43596800 G>C maps to NM_018075.3 S546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:5941700 C>T maps to ENST00000356134 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr12:6031928 G>A maps to ENST00000356134 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:5842043 C>T did not map to a codon.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr12:5744498 G>A maps to ENST00000356134 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr12:6030358 G>A maps to ENST00000356134 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr12:5744414 C>G maps to ENST00000356134 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:26681843 C>T maps to NM_031418.2 Y933Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:26529698 A>T maps to NM_031418.2 K161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:26563573 C>T maps to NM_031418.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr12:101480442 C>T maps to ENST00000392977 C514C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr12:101491681 G>T maps to ENST00000392977 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr12:101365181 C>T maps to ENST00000392977 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:101510519 A>C maps to ENST00000392977 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:101442141 A>T maps to ENST00000392977 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:22249036 G>T maps to NM_213599.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:22296149 C>A maps to NM_213599.2 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:22294480 A>T maps to NM_213599.2 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr11:22296275 A>T maps to NM_213599.2 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr11:22257771 G>T maps to NM_213599.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr11:22257815 C>A maps to NM_213599.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr11:22281075 C>T maps to NM_213599.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:242135325 C>T maps to NM_001001666.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr19:17436102 G>A maps to NM_020959.2 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr19:17436108 G>A maps to NM_020959.2 H916H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr11:419730 T>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:432044 G>A maps to NM_001012302.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:428113 G>A maps to NM_001012302.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr15:69113048 C>T maps to NM_006305.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr15:90328693 G>A maps to NM_001150.2 F930F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr15:90347555 G>A maps to NM_001150.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr15:90348579 C>T maps to NM_001150.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr15:90335530 G>C maps to NM_001150.2 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:90346714 G>T maps to NM_001150.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr2:69302733 C>T maps to NM_032208.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr4:80993705 C>T maps to NM_001145794.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr10:46121635 C>T maps to NM_001128324.1 E545E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr10:46121830 T>C maps to NM_001128324.1 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:75775271 G>T maps to NM_000700.1 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr9:75777731 A>G maps to NM_000700.1 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:81921760 G>A maps to NM_145869.1 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:81930561 C>T maps to NM_145869.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:81925935 C>G maps to NM_145869.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr8:124693563 C>T maps to NM_001003954.1 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:122605899 G>A maps to NM_001154.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr5:150497393 A>C maps to NM_001155.4 Y481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:75138724 T>A maps to NM_004034.2 K430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:75139820 G>A maps to NM_004034.2 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:150967078 G>A maps to NM_003568.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:150956842 C>T maps to NM_003568.2 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr7:36677510 T>C maps to NM_001177506.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:36580097 C>T did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr17:40997731 A>T maps to NM_009590.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:201507511 A>G maps to NM_001159.3 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:201515836 C>T maps to NM_001159.3 F996F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr2:201468753 C>G maps to NM_001159.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr2:201499610 G>A maps to NM_001159.3 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:113189559 C>T maps to NM_018569.4 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr22:29747174 G>A maps to NM_001127.3 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr22:29730293 G>A maps to NM_001127.3 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr22:29738275 G>A maps to NM_001127.3 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45T-01A-11D-A24D-08 chr22:29750745 G>T maps to NM_001127.3 Y277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr22:29736731 G>A maps to NM_001127.3 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr16:71779056 G>A maps to ENST00000423132 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr16:71798595 G>A maps to ENST00000423132 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr16:71823312 G>A maps to ENST00000423132 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr16:71805056 A>G did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr14:24030797 G>A maps to NM_003917.2 Q594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:16314373 C>T maps to NM_001130524.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:10689576 G>A maps to ENST00000453102 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:15863568 C>A did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:50285912 C>T maps to NM_014203.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:50305112 C>T maps to NM_014203.2 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:50302995 G>A maps to NM_014203.2 T415T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-A45O-01A-21D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:988625 A>T maps to ENST00000332231 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:972222 C>T maps to ENST00000332231 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr17:34001259 G>A maps to NM_001030006.1 G748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:34050651 G>A maps to NM_001030006.1 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr17:34050651 G>A maps to NM_001030006.1 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr17:33977577 G>C maps to NM_001030006.1 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:183900580 C>T maps to ENST00000411763 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr3:183896749 G>A maps to ENST00000411763 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr5:77298845 C>T maps to NM_003664.3 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:83335613 C>A maps to NM_004644.3 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:83328415 G>A maps to NM_004644.3 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:83328416 G>T maps to NM_004644.3 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:83331551 G>A maps to NM_004644.3 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:2121202 G>A maps to ENST00000355272 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:2109207 T>C did not map to a codon.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr19:2120997 C>T maps to ENST00000355272 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:2109957 C>G did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr19:2121735 C>T maps to ENST00000355272 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:2121211 G>A maps to ENST00000355272 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:2110167 C>T maps to ENST00000355272 Q1077Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:2110820 G>A maps to ENST00000355272 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr19:2110191 G>C maps to ENST00000355272 T1069T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:2110167 C>T maps to ENST00000355272 Q1077Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:114442907 G>C maps to NM_006594.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:51221215 C>T maps to NM_007347.3 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr15:51233738 T>G maps to NM_007347.3 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:99701069 G>A maps to ENST00000429084 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr7:99704399 C>G maps to ENST00000429084 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr7:99703603 C>T maps to ENST00000429084 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr7:99699578 C>A maps to ENST00000429084 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr7:99700567 C>G maps to ENST00000429084 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr12:99065372 C>T maps to NM_181861.1 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:99077024 C>A maps to NM_181861.1 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr9:72086605 T>C maps to NM_001163.3 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:72131979 G>A maps to NM_001163.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr9:72131430 G>A maps to NM_001163.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:72067079 G>A maps to NM_001163.3 N642N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr9:72073069 A>C did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr15:29346506 G>A maps to NM_005503.3 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr15:29386516 G>T did not map to a codon.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr15:29346704 C>T maps to NM_005503.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr15:29346998 C>T maps to NM_005503.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr15:29346521 G>A maps to NM_005503.3 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr19:3759728 C>T maps to NM_004886.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr19:3752700 C>G maps to NM_004886.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr11:6425032 G>A maps to ENST00000389906 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:26849702 G>A maps to NM_019043.3 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr10:26789883 A>G maps to NM_019043.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:41016113 G>A maps to NM_004307.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:41016053 G>A maps to NM_004307.1 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr4:40936490 G>A maps to NM_004307.1 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr4:40818227 G>A maps to NM_004307.1 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:139938223 G>C maps to ENST00000354402 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:112178923 G>T maps to NM_001127510.2 G2545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:112175214 A>G maps to NM_001127510.2 K1308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:112175990 C>G maps to NM_001127510.2 S1567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:112177569 C>T maps to NM_001127510.2 S2093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:112103072 A>G maps to NM_001127510.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:1462152 C>T maps to NM_005883.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr18:10471670 C>A maps to ENST00000423585 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr18:10471913 G>A maps to ENST00000423585 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:159558170 G>C maps to NM_001639.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:55033052 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:150241168 G>A maps to NM_001077628.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:150241156 G>A maps to NM_001077628.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr11:43333734 C>T maps to NM_001142930.1 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:68772423 C>G maps to NM_173545.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:57003608 G>T maps to NM_005161.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:36362533 C>T maps to NM_001024807.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:36369998 C>T maps to NM_001024807.1 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr1:156563321 C>T maps to ENST00000446584 P231P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BB-7871-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr11:116692026 G>A maps to NM_000482.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr11:116692566 C>T maps to NM_000482.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr11:116661545 C>T maps to NM_052968.4 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr11:116661094 G>A maps to NM_052968.4 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr2:21228714 G>T maps to NM_000384.2 I3675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:21231537 A>G maps to NM_000384.2 P2734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr2:21232629 C>T maps to NM_000384.2 L2370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:21255245 C>T maps to NM_000384.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:21233457 G>A maps to NM_000384.2 N2094N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:21231101 G>A maps to NM_000384.2 Q2880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr2:21234135 G>T maps to NM_000384.2 L1868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:21231327 G>A maps to NM_000384.2 L2804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:21224688 G>T maps to NM_000384.2 I4535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr2:21231801 G>T maps to NM_000384.2 S2646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr2:21233486 G>A maps to NM_000384.2 R2085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:21265244 C>T maps to NM_000384.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:21231270 A>T maps to NM_000384.2 A2823A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:21234731 C>A maps to NM_000384.2 E1670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr2:21245908 C>T maps to NM_000384.2 Q870Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr2:21247864 G>C maps to NM_000384.2 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr2:21232376 G>A maps to NM_000384.2 Q2455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr2:21234387 A>C maps to NM_000384.2 V1784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr2:21252781 A>G maps to NM_000384.2 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr16:28508716 G>C maps to NM_018690.2 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr6:41029193 C>A maps to NM_006789.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr22:39387521 G>C maps to ENST00000402182 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr22:39387497 G>A maps to ENST00000402182 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr22:39411611 G>A maps to ENST00000396762 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr22:39421331 T>C maps to NM_152426.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr22:39482339 C>T maps to NM_021822.3 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr22:39497504 C>T maps to NM_001166003.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr12:56755863 C>T maps to NM_001638.2 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr17:64225440 T>A maps to NM_000042.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:64222174 G>A maps to NM_000042.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr22:36657699 G>A maps to NM_145343.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr22:36661940 G>T maps to NM_145343.2 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr22:36662063 G>A maps to NM_145343.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr22:36541543 G>A maps to NM_145640.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr22:36124943 G>A maps to NM_030642.1 *434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:12940237 G>A maps to NM_001130415.1 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:12940570 A>T maps to NM_001130415.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr6:31625864 G>C maps to NM_019101.2 *189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr23:23897087 C>G did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr21:27269977 C>T maps to NM_000484.3 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:57291321 A>G maps to NM_012096.2 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr12:105569860 C>T did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr12:105568150 G>A maps to NM_018171.3 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr12:105593154 T>G maps to NM_018171.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr16:88876923 G>A maps to NM_000485.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr9:32973633 T>A maps to NM_001195248.1 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr7:30951586 G>T maps to NM_198098.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:154295467 G>A maps to NM_080429.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:77301378 C>A maps to NM_173039.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr2:241631600 C>A maps to ENST00000429564 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr12:50367219 C>T maps to NM_001652.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr12:50369452 G>A maps to NM_001652.3 *283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr9:33385822 G>A maps to NM_001170.1 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr16:25228595 G>A maps to NM_001169.2 W30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr15:58458910 C>T maps to NM_020980.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr15:58471424 C>T maps to NM_020980.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:115361748 G>A maps to NM_173800.4 K969K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr5:115298652 G>A maps to NM_173800.4 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:115336168 G>T maps to NM_173800.4 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:115350197 A>G maps to NM_173800.4 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr15:35224629 C>T maps to NM_014691.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr15:35185890 C>T maps to NM_014691.2 R848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr15:35168165 C>T maps to NM_014691.2 E1069E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:66905880 A>T did not map to a codon.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr23:66943630 T>C did not map to a codon.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr23:66765157 T>A did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:66905871 G>T did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr23:66905871 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr23:66765954 G>C did not map to a codon.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr23:66765122 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr23:66765024 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:47429394 C>T did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:72409007 G>A maps to NM_001040118.2 F895F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr11:72410571 A>G maps to NM_001040118.2 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr4:36230304 C>G maps to NM_015230.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:36162101 G>A maps to NM_015230.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:141059693 G>A maps to NM_022481.5 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:143695305 G>C maps to NM_015193.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr8:143695620 G>A maps to NM_015193.3 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr3:57561385 T>C maps to NM_001660.3 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr7:127231135 C>T maps to NM_001662.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:47197399 A>T did not map to a codon.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr22:43195056 C>T maps to NM_014570.4 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:68208740 G>A maps to NM_006421.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:68123820 A>G maps to NM_006421.3 I1572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr8:68130078 T>C maps to NM_006421.3 L1517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr8:68184171 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:68145180 C>T did not map to a codon.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr8:68111169 C>T maps to NM_006421.3 *1850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr8:68178421 G>A maps to NM_006421.3 Q648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr20:47633820 T>C maps to NM_006420.2 L1451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:47587686 C>T maps to NM_006420.2 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr20:47591349 C>T maps to NM_006420.2 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr20:47567891 C>T maps to NM_006420.2 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr20:47592668 C>T maps to NM_006420.2 Q631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr4:153784810 A>G maps to NM_001025595.1 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr11:6500027 C>T maps to NM_012402.2 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:68086771 G>A maps to NM_001172.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr14:68113730 G>A maps to NM_001172.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr14:68113731 C>T maps to NM_001172.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr13:107196397 C>A maps to NM_018011.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K0-01B-21D-A31L-08 chr11:46703668 G>A maps to NM_004308.2 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:148944412 G>C did not map to a codon.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr4:148800392 G>A maps to NM_024605.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr15:32921800 C>T maps to NM_014783.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:32921914 G>T maps to NM_014783.3 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr15:32926131 A>G did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:32128564 T>C maps to NM_018287.5 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:32197131 C>A maps to NM_018287.5 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:143913224 G>C did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr2:143913202 T>C maps to NM_018460.3 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr2:144314010 C>A maps to NM_018460.3 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr2:144381700 G>A did not map to a codon.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr16:24988543 T>G maps to NM_001006634.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr16:24990292 T>C maps to NM_001006634.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr16:24942603 G>T maps to NM_001006634.1 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:24955122 G>A maps to NM_001006634.1 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr6:129950551 T>C maps to NM_033515.2 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:99003901 G>C maps to NM_032900.4 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:24884721 T>C maps to NM_020824.3 K1212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr10:24874615 C>T maps to NM_020824.3 Q1534Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:24884717 G>A maps to NM_020824.3 R1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr10:24955939 T>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr10:24896475 G>C maps to NM_020824.3 S879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:24896426 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:24874384 C>T maps to NM_020824.3 V1611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:24908777 G>A maps to NM_020824.3 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr10:24874494 C>A maps to NM_020824.3 E1575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr10:24883911 C>T maps to NM_020824.3 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr10:49667776 C>T maps to ENST00000417912 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr10:49658866 C>T maps to ENST00000417912 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:86915781 T>C maps to NM_001025616.2 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:69002482 G>A maps to NM_001007231.2 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:69043494 G>T did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:142283206 G>T maps to NM_015071.4 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr5:142416770 G>A maps to NM_015071.4 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr5:142513632 C>G maps to NM_015071.4 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr5:142264900 T>C maps to NM_015071.4 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr18:6882170 T>G maps to ENST00000400091 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr18:6890050 C>T maps to ENST00000400091 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:94697029 C>T maps to NM_004815.3 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:94650454 C>T maps to NM_004815.3 E694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:94669494 A>G maps to NM_004815.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:161018683 A>G maps to NM_001025598.1 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:161022563 G>A maps to NM_001025598.1 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr1:161017687 G>A maps to NM_001025598.1 A1041A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr3:119121026 G>A maps to NM_020754.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:119133481 G>A maps to NM_020754.2 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr3:119133478 C>A maps to NM_020754.2 G901G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr3:119112314 C>T maps to NM_020754.2 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:128844700 C>T maps to NM_001142685.1 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr11:128993379 C>A maps to NM_001142685.1 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:128851368 C>T maps to NM_001142685.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:128840370 G>A maps to NM_001142685.1 V1565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:128839215 T>C maps to NM_001142685.1 R1950R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:36278703 C>T maps to ENST00000007510 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr23:130215771 C>G did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr23:130217855 A>G did not map to a codon.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr23:130218230 G>T did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr23:130218938 A>C did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:130220338 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:130215645 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:130220537 C>T did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:130220634 T>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:130217752 T>G did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:130217854 G>A did not map to a codon.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr23:130220373 C>G did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:130218247 C>A did not map to a codon.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr23:130220640 T>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:145773626 G>A maps to NM_025251.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr8:145770918 C>T maps to NM_025251.1 E745E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:145771071 G>A maps to NM_025251.1 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:145772612 C>T maps to NM_025251.1 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr8:145758700 C>T maps to NM_025251.1 K899K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr8:145806378 C>T maps to NM_025251.1 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:153178173 C>T did not map to a codon.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr23:153178905 C>T did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr23:153175296 T>C did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:153178183 G>C did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:153178993 C>T did not map to a codon.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr23:153186903 T>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153178232 A>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153184377 G>A did not map to a codon.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr23:153176045 C>G did not map to a codon.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr23:153184626 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr23:153184448 G>T did not map to a codon.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr14:32586345 C>T maps to NM_001030055.1 Q1240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr14:32561107 A>G maps to NM_001030055.1 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr14:32561641 T>C maps to NM_001030055.1 D589D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:11187735 C>G did not map to a codon.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr23:11204463 C>A did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr23:11204460 G>C did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr23:11207006 T>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:11272775 C>G did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:11197433 T>C did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:11187647 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:11682603 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr23:11197557 A>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:11682446 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr23:11206868 C>G did not map to a codon.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr22:45244836 C>T maps to ENST00000352766 Y468Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:57870383 C>T maps to ENST00000393797 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr12:57866397 G>T maps to ENST00000393797 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr12:57871046 A>T maps to ENST00000393797 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr12:57867439 G>C maps to ENST00000393797 S747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr12:57869284 G>C maps to ENST00000393797 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr17:79827208 G>A maps to NM_004309.4 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:15103493 C>A maps to NM_001175.4 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:42409914 C>T maps to NM_199002.1 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr19:42406035 G>C did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:1876768 G>C maps to ENST00000398564 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:1808225 C>T maps to ENST00000398564 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:1808168 C>T maps to ENST00000398564 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr8:1905419 G>A maps to ENST00000398564 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:17990993 C>T maps to NM_018125.3 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:156950258 G>A maps to NM_198236.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr1:156926232 C>T maps to NM_198236.1 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:120352146 C>T maps to NM_015313.2 P1472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr11:120329911 C>T maps to NM_015313.2 R804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:120347992 T>A maps to NM_015313.2 L1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr11:120322293 A>G maps to NM_015313.2 E639E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr17:8216366 G>A maps to NM_173728.3 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:3386049 C>T maps to NM_014448.3 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:3395014 C>T maps to NM_014448.3 Y551Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr11:73071381 G>A maps to NM_014786.3 L1408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:73074383 G>C maps to NM_014786.3 G1710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr11:73067755 C>G maps to NM_014786.3 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:73073651 C>T maps to NM_014786.3 L1623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr11:73064047 C>T maps to NM_014786.3 L1148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:73021299 C>T maps to NM_014786.3 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:73021728 C>T maps to NM_014786.3 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr11:73021440 C>T maps to NM_014786.3 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:73021623 C>T maps to NM_014786.3 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:7506610 G>T maps to NM_001130955.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:7531841 C>T maps to NM_001130955.1 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:7529458 G>A maps to NM_001130955.1 K741K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr1:16532080 G>A maps to NM_153213.3 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:16532754 G>A maps to NM_153213.3 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr1:155920658 G>A maps to NM_001162383.1 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:155924707 G>A maps to NM_001162383.1 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr3:56766329 G>A maps to NM_001128615.1 D420D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:56771215 G>A maps to NM_001128615.1 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr5:148977394 G>A maps to NM_001001669.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:106473960 C>A maps to ENST00000420470 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr4:106474092 G>A maps to ENST00000420470 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:144060359 G>T maps to NM_005435.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:135764127 C>A did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:135757210 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr23:135764978 A>C did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr23:135795498 C>T did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr23:135862906 G>A did not map to a codon.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr23:135754233 C>A did not map to a codon.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr23:135814306 A>G did not map to a codon.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr23:135750259 C>T did not map to a codon.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr23:135862939 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:111927982 C>T maps to NM_001113511.1 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr13:111919972 T>C maps to NM_001113511.1 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr13:111919900 C>G maps to NM_001113511.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr23:62917012 G>C did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr23:62875462 A>G did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:62917153 C>G did not map to a codon.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr23:62917121 G>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:62885894 G>A did not map to a codon.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr23:62898399 C>T did not map to a codon.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr1:27089710 C>T maps to NM_006015.4 G889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:27099912 C>T maps to NM_006015.4 A1264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:27057873 C>T maps to NM_006015.4 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr1:27106259 C>T maps to NM_006015.4 D1957D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr1:27099012 G>C maps to NM_006015.4 G1143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr1:27100151 G>A maps to NM_006015.4 S1316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:27106227 C>T maps to NM_006015.4 Q1947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr1:27102149 C>T maps to NM_006015.4 N1692N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:27088728 C>T maps to NM_006015.4 Q780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:27100150 C>A maps to NM_006015.4 S1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr1:27059231 A>G maps to NM_006015.4 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr1:27101098 C>T maps to NM_006015.4 R1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr6:157528079 G>A maps to ENST00000367148 A1975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr6:157522506 C>T maps to ENST00000367148 T1633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr6:157150435 C>T maps to ENST00000367148 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr6:157528757 C>T maps to ENST00000367148 S2201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr6:157528520 G>T maps to ENST00000367148 V2122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:157150435 C>T maps to ENST00000367148 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:157521837 G>A did not map to a codon.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr6:157522597 C>T maps to ENST00000367148 R1664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr12:46245424 C>A maps to NM_152641.2 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:46244777 C>T maps to NM_152641.2 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr12:46233254 C>T maps to NM_152641.2 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr12:46245722 C>T maps to NM_152641.2 R1273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:46233279 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:46285668 C>T maps to NM_152641.2 R1677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr12:46244615 C>T maps to NM_152641.2 Q904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:46245638 C>T maps to NM_152641.2 Q1245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:46245163 C>T maps to NM_152641.2 P1086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr12:46245857 C>T maps to NM_152641.2 Q1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr12:46245683 G>T maps to NM_152641.2 E1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr12:46245375 C>G maps to NM_152641.2 S1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr12:46123886 C>T maps to NM_152641.2 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr12:46231437 G>A maps to NM_152641.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr19:964395 G>A maps to NM_005224.2 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr15:74836399 G>A maps to ENST00000395077 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr9:34621455 C>T maps to NM_001017363.1 *413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr14:58827629 T>C maps to NM_002892.3 D650D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:235345583 C>A maps to NM_016374.5 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:235403678 A>G maps to NM_016374.5 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr2:97218001 C>A maps to NM_212481.1 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:97217884 C>T maps to NM_212481.1 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr10:63829550 T>C maps to NM_032199.2 Y398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr10:63661488 G>A maps to NM_032199.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:63852351 G>T maps to NM_032199.2 E1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:49020699 C>G maps to NM_006321.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:101794927 G>C maps to NM_001177.3 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr12:101790180 C>A maps to NM_001177.3 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr23:100243213 A>G did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:100240807 G>A did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr23:100240774 A>T did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:100240717 T>C did not map to a codon.
Alternatively spliced codon TCGA-CN-5364-01A-01D-1434-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr3:160395541 C>T maps to NM_025047.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:160395578 C>A maps to NM_025047.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:235404768 G>A maps to ENST00000339728 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:97503852 T>A maps to NM_177976.1 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr12:123467100 C>T maps to NM_001002252.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr1:202104632 G>A maps to NM_138795.2 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr7:102727177 G>C maps to NM_031905.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:109285455 C>T maps to NM_032131.4 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:23321900 G>A maps to NM_173081.3 P786P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:28284016 C>A maps to NM_018076.2 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr10:28272786 T>A maps to NM_018076.2 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:28149712 C>T maps to NM_018076.2 R954R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr10:28250519 G>A maps to NM_018076.2 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr10:28283900 A>T maps to NM_018076.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr16:31470892 C>T maps to ENST00000408912 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:31477645 C>T maps to ENST00000408912 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr16:31473900 C>T maps to ENST00000408912 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr16:31477789 G>A maps to ENST00000408912 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr19:19165127 C>T maps to ENST00000392336 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:19166616 C>A maps to ENST00000392336 C391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr3:137940803 G>A maps to ENST00000469044 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr3:137964057 G>T maps to ENST00000470821 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:232143098 G>A maps to ENST00000359743 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:232146797 G>A maps to ENST00000359743 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr2:232123815 G>A did not map to a codon.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr2:232079576 C>T maps to ENST00000359743 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr2:232141378 C>T maps to ENST00000359743 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr23:100911936 G>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:100911055 C>G did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr23:100911436 C>G did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:100912387 T>C did not map to a codon.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr23:100911660 T>C did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:100911313 G>A did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:100911995 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:100912203 C>T did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:100879978 G>A did not map to a codon.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr23:100880788 C>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:101858707 G>T did not map to a codon.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr23:101858253 A>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:101857874 C>T did not map to a codon.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr23:101857875 T>G did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr23:101857638 A>T did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr23:101857288 A>T did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr23:101857798 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr23:100871294 G>C did not map to a codon.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr1:150785758 C>T maps to NM_001668.3 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr15:80845045 G>A maps to NM_014862.3 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr15:80845024 G>A maps to NM_014862.3 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr15:80884000 G>T maps to NM_014862.3 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr15:80872757 A>T maps to NM_014862.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr11:13391306 G>A maps to ENST00000403290 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr12:27533230 G>A maps to NM_020183.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr7:98931011 C>T maps to NM_006409.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr7:98961222 C>T maps to NM_006409.3 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:98951627 T>C maps to NM_006409.3 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:98988656 G>A maps to NM_005720.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr7:98988875 G>A maps to NM_005720.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:98984356 C>T maps to NM_005720.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr7:98988689 C>T maps to NM_005720.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr2:219099115 A>G maps to NM_005731.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr3:9839365 G>C maps to NM_001198793.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr3:169486047 C>G maps to NM_032487.4 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr3:35732404 T>A maps to ENST00000458225 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr3:35732492 A>T maps to ENST00000458225 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr23:69496304 C>G did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:69489242 A>C did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr23:69496003 A>T did not map to a codon.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr17:4619833 G>C maps to ENST00000412477 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:4620534 C>T maps to ENST00000412477 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:4623744 C>T maps to ENST00000412477 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr19:18121447 G>A maps to NM_015683.1 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:4896811 G>A maps to NM_001080523.1 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr5:78181426 G>A maps to NM_000046.3 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr23:2838723 G>A did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr23:2825394 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:2827948 G>A did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:2825334 C>T did not map to a codon.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr23:2828810 C>G did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:2878421 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:2873521 G>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:3002412 G>A did not map to a codon.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr23:3030220 C>T did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr23:3021855 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr23:2998963 C>T did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr23:3002434 G>C did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr17:66366597 G>A maps to NM_014960.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:66352843 C>T maps to NM_014960.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr23:2947378 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:2951408 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr5:149677913 G>A maps to NM_001012301.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr5:149677007 G>A maps to NM_001012301.2 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:149678015 A>G maps to NM_001012301.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr4:114823651 G>A maps to NM_024590.3 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr4:114823766 G>C maps to NM_024590.3 S488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr11:3681096 G>A maps to NM_004314.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:3681447 C>T maps to NM_004314.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:77003500 C>T maps to NM_001130016.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:77003167 T>C maps to NM_001130016.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr22:19960525 G>A maps to NM_001670.2 H824H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr22:19960652 G>A maps to NM_001670.2 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr22:19967758 G>A maps to NM_001670.2 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr23:25028383 C>G did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:25033719 T>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:25033815 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:122944442 G>C maps to NM_024769.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr8:131073298 T>C maps to NM_018482.2 T906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:131149239 T>C maps to NM_018482.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr2:9484910 G>C maps to NM_003887.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr2:9437558 A>G maps to NM_003887.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr1:23769116 G>A maps to NM_001143778.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr1:23760010 C>T maps to NM_017707.3 Q678Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr1:23782675 T>C maps to NM_017707.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:239342303 C>T maps to NM_001040445.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:239344390 C>T maps to NM_001040445.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr2:239342261 G>A maps to NM_001040445.1 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr7:150878412 T>C maps to ENST00000422024 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr7:150878271 G>A maps to ENST00000422024 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr23:63445186 C>G did not map to a codon.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr23:63444271 G>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:123270162 C>A maps to NM_080928.3 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:42248417 G>A maps to NM_080863.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr17:42248180 C>T maps to NM_080863.4 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr17:42248324 C>T maps to NM_080863.4 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:76397846 C>A maps to NM_080868.2 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr2:237172796 G>A maps to NM_212556.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr14:94404062 G>C maps to ENST00000434324 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr14:94417435 C>T maps to ENST00000434324 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr14:94405552 G>A maps to ENST00000434324 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr14:94405624 G>A maps to ENST00000434324 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:94405723 G>A maps to ENST00000434324 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr7:95157464 C>A maps to NM_016116.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr7:95157167 G>A maps to NM_016116.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr4:177146430 C>T maps to NM_080874.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr4:177136849 G>A maps to NM_080874.3 C297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr4:177146411 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr9:132400245 G>A maps to NM_017873.2 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr12:48545076 C>G maps to NM_024095.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr12:48543325 C>T maps to NM_024095.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:48543151 T>C maps to NM_024095.3 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr23:15268557 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:15262663 G>A did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr23:15266982 C>A did not map to a codon.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr23:15270436 G>A did not map to a codon.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr10:73892813 C>G did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr6:100964150 C>A maps to NM_006828.2 E1994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr6:101098481 G>A maps to NM_006828.2 Q1062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:103352675 T>C maps to NM_004316.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IF-01A-11D-A31L-08 chr12:103352384 G>A maps to NM_004316.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:108169093 G>A maps to NM_203436.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr1:155408357 G>C maps to ENST00000368346 S1863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr1:155309119 G>A maps to ENST00000368346 R2839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:155313464 G>A maps to ENST00000368346 R2689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr8:37986387 G>A maps to NM_004674.3 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr23:1748782 G>A did not map to a codon.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr23:1755397 G>C did not map to a codon.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr23:1752051 G>C did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:1742147 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:1743189 C>T did not map to a codon.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr23:1742088 C>T did not map to a codon.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr23:1752131 G>A did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:1546742 C>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:1546871 C>G did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr23:1551171 C>A did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:1554651 C>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr23:1538001 C>T did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:12848399 A>C maps to NM_004317.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr19:12856228 C>T maps to NM_004317.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr2:190532560 G>A maps to NM_019048.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:190531560 C>T maps to NM_019048.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr14:104561974 C>T maps to NM_001080464.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr8:62430205 G>A maps to NM_004318.3 I669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr8:62438566 C>T maps to NM_004318.3 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:62430611 T>C maps to NM_004318.3 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:62496583 C>T maps to NM_004318.3 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:62555449 G>A maps to NM_004318.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr8:62475422 G>A maps to NM_004318.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr22:26830195 C>T maps to NM_020437.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr1:197072272 C>A maps to NM_018136.4 V2036V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr1:197091046 G>A maps to NM_018136.4 Q1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:197070879 G>A maps to NM_018136.4 Q2501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:197070946 T>C maps to NM_018136.4 Q2478Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:197115444 G>C maps to NM_018136.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:197072674 C>T maps to NM_018136.4 L1902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:197087023 G>A maps to NM_018136.4 L1320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr1:197070907 G>A maps to NM_018136.4 F2491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr9:95236913 G>C maps to NM_017680.4 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:70188033 G>A maps to NM_152792.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr2:70188049 C>T maps to NM_152792.2 W257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:79954343 G>C maps to ENST00000306729 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:62159698 C>T maps to NM_025080.3 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:62124475 G>A maps to NM_025080.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:133333931 C>T maps to NM_000050.4 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr3:130737545 C>T maps to ENST00000514044 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr2:96803344 G>A maps to NM_001002036.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:176833524 G>A maps to ENST00000281881 P1268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr1:177001736 G>A maps to ENST00000281881 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:176998824 G>A maps to ENST00000281881 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:176983946 G>A maps to ENST00000281881 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:176853474 C>A maps to ENST00000281881 E1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:176903327 G>C maps to ENST00000281881 V885V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:176993767 A>T maps to ENST00000281881 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr1:176918379 G>A maps to ENST00000281881 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:176983993 C>A maps to ENST00000281881 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr1:176833487 T>G maps to ENST00000281881 R1281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:119202970 C>A maps to ENST00000313400 L1233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr9:119976895 G>T maps to ENST00000313400 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr9:119770527 G>A maps to ENST00000313400 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr9:119976973 C>A maps to ENST00000313400 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:119567938 G>A maps to ENST00000313400 Q790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr9:119495732 C>T maps to ENST00000313400 E822E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr9:119738467 C>G did not map to a codon.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr20:31022344 C>T maps to ENST00000375687 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr20:31022591 C>T maps to ENST00000375687 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr20:31023530 G>T maps to ENST00000375687 E1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:31022344 C>T maps to ENST00000375687 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr20:31022591 C>T maps to ENST00000375687 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr20:31023207 G>A maps to ENST00000375687 W898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr20:31019453 T>C maps to ENST00000375687 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr20:31021383 G>C maps to ENST00000375687 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr2:26022287 G>A maps to NM_018263.4 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:25978929 G>A maps to NM_018263.4 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:26029097 C>T maps to NM_018263.4 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr2:25982411 G>C maps to NM_018263.4 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr18:31224902 C>T maps to NM_030632.1 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr18:31325739 T>C maps to NM_030632.1 S1976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr18:31314317 G>T maps to NM_030632.1 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr18:31323160 C>T maps to NM_030632.1 R1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:31323687 C>A maps to NM_030632.1 C1292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr18:31226288 G>A maps to NM_030632.1 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:31324488 C>T maps to NM_030632.1 L1559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:31324489 C>T maps to NM_030632.1 R1560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr18:31318978 A>G maps to NM_030632.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr18:31324831 G>T maps to NM_030632.1 E1674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr18:31319575 C>G maps to NM_030632.1 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:117060269 C>T maps to NM_130768.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr8:124346145 C>T maps to NM_014109.3 P1150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr8:124359413 T>C maps to NM_014109.3 Q710Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:23980729 G>A maps to NM_017552.1 I1212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:24009038 A>T maps to NM_017552.1 L944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr2:24046266 G>A maps to NM_017552.1 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr2:24111243 A>G maps to NM_017552.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:1455560 G>A maps to NM_018188.3 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:1417590 C>T maps to NM_031921.4 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:1430869 G>A maps to NM_031921.4 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:1390859 C>T maps to NM_001039211.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:29220739 G>A maps to NM_024857.3 K1623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr17:29219775 C>T maps to NM_024857.3 S1470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr17:29185321 C>T maps to NM_024857.3 S979S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:29162130 G>A maps to NM_024857.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:29162271 G>A maps to NM_024857.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:29162893 A>C maps to NM_024857.3 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:51203319 C>T maps to NM_005171.4 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:212788548 G>T maps to NM_001674.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr22:39918603 C>A maps to NM_182810.1 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr22:39917518 G>C maps to NM_182810.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr22:39917916 C>G maps to NM_182810.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr19:50434166 G>A maps to NM_001193646.1 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:161736176 C>A maps to NM_007348.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr6:32085105 C>T maps to NM_004381.4 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr12:53911087 G>A maps to NM_001130059.1 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr12:14650640 G>A maps to NM_018179.3 Q1149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:10524588 C>T maps to NM_024997.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:10524743 A>G maps to NM_024997.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr5:81549159 G>C maps to NM_031482.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr2:234198585 G>A maps to ENST00000392018 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:64679356 G>A maps to ENST00000421419 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:64662528 C>G maps to ENST00000421419 L1913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:64678742 C>T maps to ENST00000421419 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr11:64665372 C>T maps to ENST00000421419 S1646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr14:96772062 G>C maps to NM_018036.5 T1532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr14:96783633 C>A maps to NM_018036.5 E1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:96783493 G>A maps to NM_018036.5 F1066F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr14:96783565 G>A maps to NM_018036.5 D1042D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:96797951 T>C maps to NM_018036.5 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr14:96757160 T>C maps to NM_018036.5 L1897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr14:96829295 C>G maps to NM_018036.5 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr23:107393408 A>G did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:107377333 A>C did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:63282340 A>T maps to NM_032852.2 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:10663622 T>A maps to NM_032885.4 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:10663601 C>T maps to NM_032885.4 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr3:11389502 C>T maps to NM_006395.2 P426P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-A4C6-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr7:150721006 G>A maps to NM_173681.5 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:294140 C>T maps to ENST00000409479 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:294724 C>G maps to ENST00000409479 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:38570427 A>G maps to NM_001135673.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr2:38537547 C>T maps to NM_001135673.1 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:108213983 A>G maps to NM_000051.3 E2768E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr11:108160405 T>C maps to NM_000051.3 I1438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:108106436 C>T maps to NM_000051.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:81078337 C>G maps to NM_015251.2 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr16:81075962 G>A maps to NM_015251.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:7045483 C>T maps to NM_001940.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:7046364 C>G maps to NM_001940.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr12:7046046 G>C maps to NM_001940.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr12:7046136 T>A maps to NM_001940.3 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:7046508 A>G maps to NM_001940.3 G693G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr10:69991146 C>T maps to NM_145178.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr15:25924781 G>T maps to NM_024490.3 V1402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr15:25953177 G>A maps to NM_024490.3 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:25959217 G>A maps to NM_024490.3 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr15:25924904 G>T maps to NM_024490.3 V1361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr15:25962005 G>T maps to NM_024490.3 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr15:25961900 C>T maps to NM_024490.3 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr15:25959361 G>T maps to NM_024490.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr15:25924661 G>C maps to NM_024490.3 S1442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr15:25924961 C>T maps to NM_024490.3 R1342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:25925039 C>T maps to NM_024490.3 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:25953189 G>A maps to NM_024490.3 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr15:25953376 C>T maps to NM_024490.3 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr15:25947158 G>A maps to NM_024490.3 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:160044981 T>G did not map to a codon.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr5:159992485 G>T maps to NM_025153.2 R1454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr5:160059204 G>T maps to NM_025153.2 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:160029628 G>A maps to NM_025153.2 Y1106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:160033897 C>A maps to NM_025153.2 E1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:160071163 A>G maps to NM_025153.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr5:160063200 G>T maps to NM_025153.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr5:160033922 C>T maps to NM_025153.2 L1003L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7596-01A-11D-2229-08 chr5:159992576 G>A maps to NM_025153.2 S1423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:160044885 T>C maps to NM_025153.2 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:47559988 C>T maps to NM_020453.3 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:47538839 G>A maps to NM_020453.3 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr13:113530143 C>T maps to NM_032189.3 S1072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr13:113508637 C>T maps to NM_032189.3 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr13:113479842 G>A maps to NM_032189.3 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr13:113481012 C>G maps to NM_032189.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:182605424 C>T maps to NM_014616.1 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:182631659 A>G maps to NM_014616.1 T1110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:138880487 T>C did not map to a codon.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr23:138864753 T>A did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr23:138880467 T>C did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr23:138886712 C>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:138840004 G>A did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:138871516 C>T did not map to a codon.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr23:138832232 C>A did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr23:138899027 G>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:138844237 G>T did not map to a codon.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr23:138869397 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:138825760 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:138820218 G>C did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr13:25265202 G>T maps to NM_001185085.1 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr13:25265210 G>A maps to NM_001185085.1 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr13:25266964 A>G maps to NM_001185085.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr13:25263407 G>A maps to NM_001185085.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr13:25265102 A>G maps to NM_001185085.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:19766740 C>G maps to NM_020410.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:19765409 G>A maps to NM_020410.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:17312617 G>A maps to NM_001141974.1 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr3:194171000 T>G maps to NM_024524.3 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:194140609 G>A maps to NM_024524.3 Q1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr3:194167832 C>T maps to NM_024524.3 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:194149601 C>T maps to NM_024524.3 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:194169312 C>T maps to NM_024524.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr3:193166097 C>G maps to NM_032279.2 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr3:193185177 G>T maps to NM_032279.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr3:193120554 T>C maps to NM_032279.2 A1159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr3:193185104 C>A maps to NM_032279.2 G372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:193185237 C>T maps to NM_032279.2 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr3:193166023 G>C maps to NM_032279.2 S708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr3:193132480 G>T maps to NM_032279.2 I967I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr3:193232585 G>T maps to NM_032279.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr3:193201785 T>A maps to NM_032279.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr3:193125104 G>A maps to NM_032279.2 A1125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr3:193007776 G>A maps to NM_198505.2 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr3:192997177 G>A maps to NM_198505.2 Q1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:193068903 G>A maps to NM_198505.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr3:193068948 A>T maps to NM_198505.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:193039578 C>T maps to NM_198505.2 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:116946584 C>A maps to NM_000701.7 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:160104994 C>T maps to NM_000702.3 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:160098578 C>A maps to NM_000702.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:160099963 C>T maps to NM_000702.3 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:160093058 C>G maps to NM_000702.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr19:42489282 G>T maps to ENST00000441343 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:42482829 G>A maps to ENST00000441343 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr19:42471440 G>A maps to ENST00000441343 Y991Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:42489171 G>A maps to ENST00000441343 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:160134054 C>T maps to NM_144699.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:160128898 C>G maps to NM_144699.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr1:160124905 C>A maps to NM_144699.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:160156137 C>T maps to NM_144699.3 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr1:160143990 C>T maps to NM_144699.3 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr17:7557556 C>G maps to NM_001678.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr17:7557505 C>T maps to NM_001678.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:141622515 C>G maps to NM_001679.2 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:119504589 T>C did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr23:119509288 C>A did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr23:119509240 C>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:119513342 C>T did not map to a codon.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr16:28906159 G>A maps to NM_173201.3 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:28895896 G>T maps to NM_173201.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr16:28913311 C>T maps to NM_173201.3 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:110783811 C>T maps to NM_170665.3 S916S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:110783051 A>G did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:3844429 C>T maps to NM_174953.1 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr17:3850834 G>A maps to NM_174953.1 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:10392201 G>A maps to NM_001001331.2 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr3:10417305 C>T maps to NM_001001331.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr3:10384544 C>T maps to NM_001001331.2 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:152814262 C>A did not map to a codon.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr23:152813446 C>T did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:152845712 C>G did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:152821579 C>T did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr23:152825276 G>A did not map to a codon.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr23:152808590 C>G did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:152845455 C>T did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr23:152807329 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:152830498 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:152823748 C>G did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:152813320 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:152806878 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:152807133 G>T did not map to a codon.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr23:152801883 G>T did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:152845572 C>T did not map to a codon.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr23:152813366 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:152814276 C>G did not map to a codon.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr23:152815067 C>T did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:152818724 G>A did not map to a codon.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr23:152807231 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:152823652 C>T did not map to a codon.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr23:152815727 G>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:203708792 A>G maps to NM_001684.3 P1143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:203696680 G>A maps to NM_001001396.1 L1097L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:203708957 A>G maps to NM_001684.3 L1198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:130686023 G>C maps to NM_001001486.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:130683849 T>A maps to NM_001001486.1 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr3:130715583 C>G maps to NM_001001486.1 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr3:130683877 C>T maps to NM_001001486.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr3:130682856 C>T maps to NM_001001486.1 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr16:84488473 C>T maps to ENST00000416219 N677N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:84444202 C>T maps to ENST00000416219 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr16:84492911 C>T maps to ENST00000416219 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr16:84432169 G>A maps to ENST00000416219 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:84495408 C>T maps to ENST00000416219 C886C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr16:84438771 G>A maps to ENST00000416219 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:36051331 G>A maps to NM_000704.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr19:36041994 G>A maps to NM_000704.2 I968I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:36048662 G>T maps to NM_000704.2 C529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:36050967 C>T maps to NM_000704.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr18:43666160 G>A maps to NM_001001937.1 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:7841764 C>T maps to NM_001001973.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:1244102 C>T maps to NM_001687.4 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:46973028 C>G maps to NM_005175.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr12:54063125 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:54063663 C>T maps to NM_005176.5 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr2:176043849 T>C maps to NM_001689.4 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:176043861 A>G maps to NM_001689.4 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:73038631 G>C maps to NM_006356.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr22:43036196 G>A maps to NM_001165877.1 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr14:50792425 A>G maps to NM_001003803.2 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr23:153663827 C>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:153660715 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:153662659 C>T did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:81613992 C>T maps to NM_001017971.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr23:40456518 G>C did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr23:40456554 G>C did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:40456554 G>C did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:40456835 C>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:124221736 G>T maps to NM_012463.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:124221631 G>A maps to NM_012463.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:124242529 C>G maps to NM_012463.3 S841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr7:138418933 G>A maps to NM_130840.2 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:138455986 C>T maps to NM_130840.2 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:138417792 C>T maps to NM_130840.2 E579E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr16:2569562 C>T maps to NM_001694.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr16:2569363 C>G maps to NM_001694.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:67487538 G>A maps to NM_004691.4 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:87126073 C>A maps to NM_152565.1 S89S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BA-A6DA-01A-31D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr7:149575775 C>T maps to ENST00000479613 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:71185207 C>A maps to NM_001692.3 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:71189954 C>T maps to NM_001692.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr8:20074762 A>G maps to NM_001693.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:10923307 G>A maps to NM_001039362.1 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:18111366 A>G did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:198492685 G>A maps to ENST00000489986 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:54669196 C>A maps to NM_015941.2 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr8:54682245 C>T maps to NM_015941.2 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr23:77294476 G>T did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:77254134 C>T did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr23:77243872 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:77271302 G>T did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr23:77301811 G>C did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:77267138 T>G did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr23:77245060 A>T did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr23:77245123 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:77258709 G>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:77286939 G>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:77286940 G>A did not map to a codon.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr23:77275823 G>A did not map to a codon.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr23:77287020 A>G did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr13:52536025 C>T maps to NM_000053.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr13:52542594 G>A maps to NM_000053.2 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr13:52509014 G>A maps to NM_000053.2 V1425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:42602536 T>A did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr4:42416642 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:42466778 G>A maps to NM_006095.2 A849A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr4:42445653 G>C maps to NM_006095.2 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr4:42590347 T>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:42554537 A>T maps to NM_006095.2 Y501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr4:42580324 C>T maps to NM_006095.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr4:42553226 C>T maps to NM_006095.2 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr13:26127955 C>T maps to NM_016529.4 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr13:26535777 G>A maps to NM_016529.4 L1083L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr13:26125579 G>T maps to NM_016529.4 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr18:55368509 G>A maps to NM_005603.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:154309987 C>A maps to NM_020452.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr1:154303597 T>A maps to NM_020452.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:154306628 C>T maps to NM_020452.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:154313341 C>T maps to NM_020452.3 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:1800000 C>A maps to NM_138813.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:1800406 G>A maps to NM_138813.2 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr19:1784855 G>A maps to NM_138813.2 R1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45T-01A-11D-A24D-08 chr19:1811702 G>A maps to NM_138813.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr15:50211035 C>A maps to NM_024837.2 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr15:50264848 G>T maps to NM_024837.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr15:50152429 G>C maps to NM_024837.2 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr15:50215662 A>C maps to NM_024837.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr20:50346509 C>A maps to NM_006045.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr20:50244147 C>T maps to NM_006045.1 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr20:50234076 G>A maps to NM_006045.1 D789D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:50255950 G>A maps to NM_006045.1 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:50292703 C>G maps to NM_006045.1 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr18:77108130 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr18:77107888 C>T maps to NM_198531.3 F934F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:17921886 G>C maps to NM_145691.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr15:35834662 A>G maps to NM_080650.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:142241602 G>A maps to NM_001184.3 S1411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr3:142176528 A>T maps to NM_001184.3 G2524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:48505261 C>T maps to NM_130384.1 Q622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:3529963 C>G maps to NM_139321.2 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:3581668 C>G maps to NM_139321.2 S1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:3553416 C>T maps to NM_139321.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr20:3605204 C>T maps to NM_139321.2 F1283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:117045742 G>T maps to NM_207303.2 G751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:117061410 G>T maps to NM_207303.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:117486769 G>T maps to NM_207303.2 E1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:117226685 G>T maps to NM_207303.2 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:116889157 A>G maps to NM_207303.2 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:116975563 G>A maps to NM_207303.2 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:116853720 C>A maps to NM_207303.2 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr10:117061461 C>T maps to NM_207303.2 C909C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:76814234 C>T did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:76939408 C>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:76778861 C>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:76891447 G>C did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:76872191 C>G did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:76937130 G>C did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:76776375 G>A did not map to a codon.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr23:76890139 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr23:76937545 T>C did not map to a codon.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr23:76776327 G>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:76939150 C>G did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:76874426 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:76854950 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:76938633 T>C did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr23:76875968 A>G did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:76938249 G>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:76944408 G>T did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:76937978 C>A did not map to a codon.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr23:76776334 T>C did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr23:76907827 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:76874399 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:76889052 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:76889053 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:76920139 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:76938405 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:76938081 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:76890176 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr23:76944322 A>T did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr23:76938208 A>T did not map to a codon.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr23:76890119 G>A did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:76938923 A>T did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:76939595 A>T did not map to a codon.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr23:76814256 A>G did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:76872080 C>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr6:16327554 C>T maps to NM_000332.3 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:16327464 C>T maps to NM_000332.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr6:16327206 C>T maps to NM_000332.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr6:16307060 A>G maps to NM_000332.3 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr22:46114313 C>T maps to NM_013236.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr22:46125409 C>T maps to NM_013236.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr12:111895023 A>G maps to NM_002973.3 P1170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:111923528 G>A maps to NM_002973.3 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr12:111956092 G>A maps to NM_002973.3 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:111948252 A>T maps to NM_002973.3 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr12:111993686 C>A maps to NM_002973.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr16:28846985 C>T maps to NM_148414.1 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr16:28844639 C>T maps to NM_148414.1 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:28847378 G>A maps to NM_148414.1 Q1007Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:28847704 C>T maps to NM_148414.1 V1066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr16:28848064 C>T maps to NM_148415.1 S1034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr14:92563178 C>A maps to ENST00000359819 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr14:92563015 A>G did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr23:13337978 T>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:63982083 G>A maps to NM_001177387.1 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:63981378 A>G maps to NM_001177387.1 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:63982053 A>G maps to NM_001177387.1 K852K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr1:110034335 G>A maps to NM_153340.4 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:110033786 A>G maps to NM_153340.4 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:42272026 G>C maps to NM_020218.1 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:93983200 G>A maps to NM_001698.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:74756405 G>A maps to ENST00000258081 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:74755570 C>A maps to ENST00000258081 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr1:1309520 G>A maps to NM_001127230.1 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr19:57743152 C>A maps to NM_001015878.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr19:57746746 C>T maps to NM_001015878.1 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr19:57746757 G>T maps to NM_001015878.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:57746377 A>G maps to NM_001015878.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:70227854 G>T did not map to a codon.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr7:69364471 G>A maps to NM_015570.2 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:70255075 G>T maps to NM_015570.2 S958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:70252203 C>G maps to NM_015570.2 S773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:70255919 C>T maps to NM_015570.2 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr7:70236611 A>G maps to NM_015570.2 Q604Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:70255696 G>A maps to NM_015570.2 T1165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:70227907 G>T maps to NM_015570.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr7:70228013 C>T maps to NM_015570.2 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr15:34295411 T>A did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:32598670 A>T maps to NM_015060.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr10:99437757 C>T maps to NM_021732.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr12:63543950 G>A maps to NM_000706.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:63543950 G>T maps to NM_000706.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr12:63544544 G>A maps to NM_000706.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:206224959 C>T maps to NM_000707.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr23:153172114 G>C did not map to a codon.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr23:153171134 C>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:69459588 C>T did not map to a codon.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr23:69455942 G>A did not map to a codon.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr23:69458122 C>T did not map to a codon.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr23:69455617 G>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:69458110 C>A did not map to a codon.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr23:69456944 C>G did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:69262101 T>C did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr23:69264202 T>A did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr16:364683 C>T did not map to a codon.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr16:396962 G>A maps to NM_003502.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr16:396884 C>A maps to NM_003502.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr16:347825 G>A maps to NM_003502.3 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr17:63554318 C>T maps to NM_004655.3 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:63533162 G>A maps to NM_004655.3 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr17:63526138 C>T maps to NM_004655.3 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:63533089 C>A maps to NM_004655.3 G602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr19:41726661 G>A maps to NM_021913.3 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:41743858 C>G maps to NM_021913.3 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:41745208 C>A maps to NM_021913.3 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr19:41759571 C>G maps to NM_021913.3 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:99565808 C>A maps to NM_001185.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:99565929 C>T maps to NM_001185.3 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr17:79163625 G>A maps to ENST00000269392 A1065A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr8:103851014 C>A maps to NM_148174.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr15:45007751 G>T maps to NM_004048.2 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:235643459 G>A maps to ENST00000366599 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:235618983 T>C maps to ENST00000366599 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:193150248 C>T maps to NM_003783.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:33246188 C>T maps to NM_003782.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr21:41033130 C>T maps to NM_033172.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr21:41033142 C>T maps to NM_033172.1 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr13:31891810 G>A maps to NM_194318.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr11:134253870 C>T maps to NM_054025.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:71571433 G>T maps to NM_080742.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr11:62384202 G>T maps to NM_012200.2 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr19:17918901 C>T maps to NM_014256.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr19:17918690 C>T maps to NM_014256.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:17922447 C>T maps to NM_014256.3 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:122691148 T>C maps to NM_030765.2 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:182987804 C>T maps to NM_032047.4 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr2:232263353 C>T maps to NM_145236.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:232262648 C>T maps to NM_145236.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:232262573 C>A maps to NM_145236.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:41932173 C>T maps to NM_198540.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr19:41931831 C>T maps to NM_198540.2 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr12:58021970 G>A maps to NM_001478.3 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr12:58021629 C>T maps to NM_001478.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:47243540 C>T maps to NM_153446.2 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr17:47219489 G>A maps to NM_153446.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr12:661642 C>T maps to NM_173593.3 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr12:645454 C>T maps to NM_173593.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr12:666882 G>A maps to NM_173593.3 E830E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr12:653524 G>A maps to NM_173593.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr11:376087 C>T maps to NM_178537.4 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:44456111 C>A maps to ENST00000309519 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:118942966 G>A maps to NM_212543.1 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:118945718 C>T maps to NM_212543.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr5:177036572 G>A maps to NM_007255.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:117186310 C>G maps to NM_012104.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr11:117161342 C>T maps to NM_012104.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr21:42647328 C>T maps to NM_012105.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr21:30693735 C>T maps to NM_206866.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr21:30699036 C>T maps to NM_206866.1 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr6:90660198 G>C maps to NM_001170794.1 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:90660480 A>G maps to NM_001170794.1 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr9:33264311 C>A maps to NM_004323.5 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr6:57048921 A>G maps to NM_004282.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:57048774 A>G maps to NM_004282.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:121436716 C>T maps to NM_004281.3 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:121436442 C>T maps to NM_004281.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr10:121411303 C>T maps to NM_004281.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:38066592 A>G maps to NM_004874.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr21:11049618 T>A maps to NM_182482.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr21:11058237 G>A maps to NM_182482.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr21:11058205 T>C maps to NM_182482.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr17:79418799 G>A maps to ENST00000436173 A1361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr17:79410354 C>T maps to ENST00000436173 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr17:79409646 C>T maps to ENST00000436173 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:40754429 T>C maps to NM_014952.3 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr15:40750962 C>G maps to NM_014952.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr15:40756082 A>G maps to NM_014952.3 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:40751118 C>T maps to NM_014952.3 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr8:143566045 G>T maps to NM_001702.2 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:32210288 C>T maps to NM_001703.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr1:32207756 C>T maps to NM_001703.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:32221927 C>T maps to NM_001703.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:32206007 C>T maps to NM_001703.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr1:32205186 C>T maps to NM_001703.2 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:69666696 C>A maps to NM_001704.2 C507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:70048837 G>C maps to NM_001704.2 T1073T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:69646436 C>T maps to NM_001704.2 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr6:69349298 G>A maps to NM_001704.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr6:69703850 C>A maps to NM_001704.2 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr6:70040461 C>T maps to NM_001704.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr6:69684691 G>T maps to NM_001704.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:69349245 G>T maps to NM_001704.2 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr6:70049223 G>T did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr6:70048881 C>A maps to NM_001704.2 S1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr6:70070995 G>A maps to NM_001704.2 L1277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr17:79058641 C>T maps to NM_017451.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr17:79080652 G>T maps to NM_017451.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr17:79073792 C>T maps to NM_017451.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr7:97941555 G>T maps to NM_018842.4 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:102951360 C>A maps to NM_017935.4 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr4:102984275 A>G maps to NM_017935.4 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr16:88052250 G>A maps to NM_001173543.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr16:88052148 G>A maps to NM_001173543.1 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr3:52437162 G>A maps to NM_004656.2 Y627Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:215610515 T>C maps to NM_000465.2 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr2:215646135 G>A maps to NM_000465.2 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:135462893 C>T maps to NM_020064.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr9:135462839 C>T maps to NM_020064.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr1:91182215 G>A maps to NM_020063.1 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr1:91180102 C>T maps to NM_020063.1 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr11:129245989 G>A maps to NM_003658.4 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:17275435 G>A maps to NM_006317.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:31508227 C>A maps to ENST00000417556 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:31597335 G>A maps to NM_080686.2 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr6:31605290 A>G maps to NM_080686.2 E2134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr6:31604565 G>A maps to NM_080686.2 P1997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr6:31601197 C>T maps to NM_080686.2 P1454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:31600742 G>A maps to NM_080686.2 R1431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr6:31601230 G>A maps to NM_080686.2 L1465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr9:134367623 C>T maps to NM_013318.3 P2150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:134308155 A>T maps to NM_013318.3 K90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr9:134321938 C>T maps to NM_013318.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:134351500 G>T maps to NM_013318.3 E1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:171560971 G>T maps to ENST00000392078 E2895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:171509613 A>G maps to ENST00000392078 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:171509617 G>T maps to ENST00000392078 E1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K0-01B-21D-A31L-08 chr6:31609354 T>C maps to ENST00000404765 T840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr6:31612822 C>T maps to ENST00000404765 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:31668717 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:31657448 G>A maps to ENST00000375842 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:64756792 C>T maps to NM_138456.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:49458946 C>T maps to NM_138761.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr14:35262043 G>A maps to NM_013448.2 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr14:35253083 T>C maps to NM_013448.2 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr7:72856542 G>A maps to NM_032408.3 R1479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr12:56995030 G>T maps to NM_013449.3 P1411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr12:56994037 C>T maps to NM_013449.3 E1615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57003657 G>A maps to NM_013449.3 R654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr12:56994064 G>A maps to NM_013449.3 L1606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr2:160243033 G>A maps to NM_013450.2 R1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:160194205 G>A maps to NM_013450.2 C1844C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:160257123 G>A maps to NM_013450.2 Q962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:160294954 C>G maps to NM_013450.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:160206344 T>C maps to NM_013450.2 S1579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:160194091 C>T maps to NM_013450.2 R1882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr2:160229586 C>T maps to NM_013450.2 G1394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:27147272 T>A maps to NM_003986.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr11:66278498 G>A maps to NM_024649.4 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr12:76740852 C>T maps to NM_024685.3 Q304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:123663244 G>T maps to NM_152618.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr16:56536339 C>T maps to NM_031885.3 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:73028231 C>A maps to NM_033028.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:73028237 C>T maps to NM_033028.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:122791434 G>A maps to NM_176824.1 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr4:122756430 G>C maps to NM_176824.1 S460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr4:122760788 G>C maps to NM_176824.1 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:33388765 C>T maps to NM_198428.2 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr7:33390924 C>G maps to NM_198428.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr7:33185887 T>C maps to NM_198428.2 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:33376100 G>A maps to NM_198428.2 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:33390829 G>A did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:107492190 G>A maps to NM_001142568.1 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:107520041 G>C maps to NM_001142568.1 R884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr3:107497344 G>T maps to NM_001142568.1 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:45316586 C>G maps to NM_005581.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr1:156618414 G>A maps to NM_021948.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:156628470 C>T maps to NM_021948.3 C858C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:156621473 G>A maps to NM_021948.3 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:156621404 C>T maps to NM_021948.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:156616599 C>T maps to NM_021948.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr1:156622193 C>T maps to NM_021948.3 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156622556 G>A maps to NM_021948.3 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr7:107224423 C>T maps to NM_001008405.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:107234421 A>G maps to NM_001008405.2 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr23:152988621 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:152981080 G>A did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:152967529 T>A did not map to a codon.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr23:152968411 G>A did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:75269449 C>A maps to NM_001170714.1 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr16:75263549 G>T maps to NM_001170714.1 R870R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:75276925 G>T maps to NM_001170714.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:75276934 G>A maps to NM_001170714.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr1:94140189 G>A maps to NM_003567.2 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:94037257 G>C maps to NM_003567.2 S648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr1:94033377 G>A maps to NM_003567.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr20:52611550 C>A maps to NM_003657.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr20:52561466 G>A maps to NM_003657.2 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr20:52570171 C>T maps to NM_003657.2 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:115110827 G>A maps to NM_005872.2 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:115110807 A>C maps to NM_005872.2 Y207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:59115301 C>A maps to ENST00000407086 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr17:58967053 A>G did not map to a codon.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr17:59115268 A>G maps to ENST00000407086 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:58988026 C>A maps to ENST00000407086 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr12:25047337 T>G maps to NM_001178093.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:24995058 C>T maps to NM_001178093.1 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr19:49303333 C>T maps to NM_001190.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:49310268 G>A maps to NM_001190.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr10:127512149 T>A maps to NM_016567.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr3:165547360 G>A maps to NM_000055.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:165547585 G>A maps to NM_000055.2 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:165548245 C>T maps to NM_000055.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:165503941 C>A maps to NM_000055.2 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr3:165548002 G>A maps to NM_000055.2 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr6:80878707 G>A maps to NM_183050.2 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:80838881 A>T maps to NM_183050.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr16:31120603 C>A maps to NM_005881.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr1:85733453 G>A maps to NM_003921.4 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:85733495 C>T maps to NM_003921.4 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr2:60688816 G>A maps to NM_022893.3 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:60689545 G>A maps to NM_022893.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr2:60688663 G>A maps to NM_022893.3 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr2:60688600 G>A maps to NM_022893.3 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:99641174 G>A maps to NM_138576.2 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr14:99641459 A>C maps to NM_138576.2 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr14:99642173 C>T maps to NM_138576.2 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:52404617 G>T maps to NM_020396.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:50169079 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr19:50176977 C>T maps to NM_138639.1 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:12232293 C>T maps to NM_138722.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr19:45262844 C>A maps to NM_005178.4 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr19:45259539 G>A maps to NM_005178.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:187447043 G>A maps to NM_001706.4 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr3:187447583 G>A maps to NM_001706.4 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr17:6927485 C>G maps to NM_181844.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr16:30904176 G>A maps to NM_004765.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr16:30899218 G>C maps to NM_004765.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:147091475 C>T maps to NM_004326.2 H505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:147092753 T>A maps to NM_004326.2 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:147096738 C>T maps to NM_004326.2 N1420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:147091316 C>T maps to NM_004326.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:147096414 C>T maps to NM_004326.2 G1312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr1:147090755 C>A maps to NM_004326.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:118772309 C>A maps to NM_182557.2 A714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr11:118769636 G>T maps to NM_182557.2 I1329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr11:118769942 G>A maps to NM_182557.2 P1227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr11:118774060 G>A maps to NM_182557.2 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr6:136597186 T>C maps to NM_014739.2 K492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:136593165 C>T maps to NM_014739.2 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:136597447 T>A maps to NM_014739.2 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr6:136599799 G>T maps to NM_014739.2 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr6:136597546 C>T maps to NM_014739.2 E372E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr6:136597105 C>G maps to NM_014739.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:136597401 T>A maps to NM_014739.2 K421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr16:81298333 C>T maps to NM_017429.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:81320957 G>A maps to NM_017429.2 W454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr11:112065458 G>T maps to NM_031938.4 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:112071360 C>T maps to NM_031938.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr11:112064602 C>A maps to NM_031938.4 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr23:39930339 C>T did not map to a codon.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr23:39922006 C>A did not map to a codon.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr23:39923016 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:39932750 G>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr23:39933956 T>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:39913235 C>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:39913586 C>T did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:39933795 G>T did not map to a codon.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr23:39932419 G>T did not map to a codon.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr23:39937100 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:39923688 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:39933388 G>A did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:39921469 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr23:39934149 T>C did not map to a codon.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr23:39934189 C>T did not map to a codon.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr23:39933062 G>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:129184757 G>T did not map to a codon.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr23:129147515 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:129147429 C>T did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:129171508 G>A did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr23:129147535 C>T did not map to a codon.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr23:129190057 G>A did not map to a codon.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr23:129148035 A>G did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:129149412 C>T did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:129159270 G>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:129149303 G>T did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr23:129154963 G>T did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr23:129149171 G>A did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr23:129146961 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:129171505 G>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:129156916 C>T did not map to a codon.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr23:129147296 C>A did not map to a codon.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr23:129171429 C>T did not map to a codon.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr23:129171430 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:129156924 C>G did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:129148457 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:129150169 G>A did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr22:23523320 C>T maps to NM_004327.3 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr22:23596157 C>T maps to NM_004327.3 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr22:23523167 C>T maps to NM_004327.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr22:23603612 C>A maps to NM_004327.3 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr2:219527642 C>T maps to NM_004328.4 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr3:197241273 G>A maps to NM_203315.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr4:104017354 G>C maps to NM_020139.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr4:104016381 A>C maps to NM_020139.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr14:96730570 G>C maps to NM_000710.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr14:96730783 C>T maps to NM_000710.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:96730396 C>T maps to NM_000710.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:96707405 C>T maps to NM_000623.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr14:96706959 C>T maps to NM_000623.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:27679628 G>T maps to NM_001143810.1 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:70798482 A>G maps to NM_018429.2 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:70786859 G>A maps to NM_018429.2 K514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:70835390 T>C maps to NM_018429.2 N1979N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:70858307 T>C maps to NM_018429.2 I2568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:40970593 G>C maps to NM_003766.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr17:40967927 G>A maps to NM_003766.3 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr23:18189126 G>A did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr23:18234752 T>A did not map to a codon.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr23:18195819 G>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:18220018 C>T did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr23:18221632 G>T did not map to a codon.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr23:18192181 G>T did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr23:18183157 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:18221662 G>T did not map to a codon.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr23:18195874 G>A did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr23:18192279 A>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:18183238 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:18213471 C>T did not map to a codon.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr23:18220054 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr23:18221818 T>C did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr23:18183226 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr6:107390513 G>A maps to NM_001080450.2 N627N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:107390675 G>A maps to NM_001080450.2 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr4:42145871 G>A maps to NM_207406.3 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr4:42122293 C>T maps to NM_207406.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:49202064 G>C maps to NM_024603.2 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:49208438 G>A maps to NM_024603.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr10:13481366 G>C maps to ENST00000396900 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr10:13522935 C>T maps to ENST00000396900 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr10:13538827 G>C maps to ENST00000396900 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:12866478 C>T maps to NM_017682.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:12864085 C>T maps to NM_017682.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:70065251 A>C maps to NM_032735.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:70049560 C>T maps to NM_032735.2 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr12:70087538 G>A maps to NM_032735.2 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:93628606 C>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr11:205337 G>A maps to NM_001098787.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr23:102471380 G>A did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr23:102471103 C>A did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr23:101408933 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:14755858 C>T maps to NM_016561.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:17475390 C>T maps to NM_001195.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr3:133119064 C>A maps to NM_003571.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr3:133119349 G>A maps to NM_003571.2 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr3:133193814 G>T maps to NM_003571.2 *416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:152772637 C>T did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:152771514 C>T did not map to a codon.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr23:102004644 C>A did not map to a codon.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr23:102005358 G>T did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:102004118 G>A did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:102004985 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr23:102004841 A>G did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr23:102005205 T>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:102005444 G>A did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr20:61637637 G>A maps to NM_080606.3 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr12:26276084 T>C maps to NM_030762.2 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:78426857 C>A maps to NM_001713.2 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:78373341 G>T maps to NM_017614.4 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr10:60546841 G>C did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr10:60558320 G>A did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:60461889 C>A maps to NM_001080512.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:32260339 G>C maps to NM_001714.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr9:95526891 C>T maps to NM_001003800.1 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr22:18222144 C>A maps to NM_197966.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr12:51693065 C>A maps to NM_016293.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:22494438 G>A maps to NM_018688.4 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:102195710 G>A maps to NM_182962.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:102195383 G>A maps to NM_182962.1 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr17:76212843 A>G maps to NM_001012271.1 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:76212112 G>A maps to NM_001012271.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:32832520 G>T did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:32730181 G>T maps to NM_016252.3 E3204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:32688440 C>T maps to NM_016252.3 Q1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:32724765 C>G maps to NM_016252.3 S2874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:32667174 G>A maps to NM_016252.3 E1329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:32605288 C>T maps to NM_016252.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr2:32733226 C>G maps to NM_016252.3 S3294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr2:32640715 C>A maps to NM_016252.3 S786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:32750696 T>C did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr20:61869949 C>G maps to NM_139317.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr19:53793207 C>T maps to NM_033341.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr8:11412839 G>C did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr15:91346817 C>T maps to NM_000057.2 A1142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:28601108 A>T maps to NM_000386.2 L251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr17:28598378 G>C maps to NM_000386.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr17:28618497 C>T maps to NM_000386.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:97987323 T>G did not map to a codon.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr10:97987175 G>A maps to NM_013314.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr10:97956811 G>C maps to NM_013314.3 S368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56109966 C>T maps to NM_001487.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr10:102039976 G>A maps to NM_173809.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr10:102045959 G>C maps to NM_173809.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:43832355 C>T maps to NM_000712.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr7:43827504 C>T maps to NM_000712.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:43827604 C>T maps to NM_000712.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr19:40971541 G>A maps to NM_000713.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:40953924 T>C maps to NM_000713.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr15:40398125 G>A maps to NM_001003940.1 H54H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr8:22066961 C>T maps to NM_006129.4 C860C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr2:69093521 C>T maps to NM_014482.1 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr2:69093550 G>T maps to NM_014482.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:50659549 G>T did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:50659550 A>T did not map to a codon.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr23:50658861 G>T did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr23:50654064 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:50659223 A>C did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr4:79763572 A>G maps to NM_198892.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr4:79792102 G>A maps to NM_198892.1 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr4:79833123 C>A maps to NM_198892.1 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr4:81967327 G>A maps to NM_001201.2 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:54418850 C>T maps to NM_130850.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr6:7845404 C>T maps to NM_001718.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr20:55777624 G>A maps to NM_001719.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr20:55750063 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:55803322 C>T maps to NM_001719.2 R191R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-4739-01A-02D-1512-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:40229410 G>T maps to NM_203456.2 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr7:34118793 A>G maps to NM_133468.3 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:34118697 C>G maps to NM_133468.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:34009963 G>A maps to NM_133468.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr7:34125425 C>G maps to NM_133468.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:34125524 T>C maps to NM_133468.3 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr10:88649930 G>A maps to NM_004329.2 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr4:96036834 G>T did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:96046262 C>G maps to ENST00000440890 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr4:96025718 G>A did not map to a codon.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr2:203420619 T>G maps to NM_001204.6 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr2:203383546 G>C maps to NM_001204.6 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr10:43318579 T>A maps to NM_014753.3 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr23:15567987 C>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:15543444 C>G did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:15555262 G>T did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:15560112 G>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:15548115 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr23:15568080 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr9:16552614 G>A maps to NM_017637.5 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr9:16419592 G>A maps to NM_017637.5 D898D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:16437493 C>T maps to NM_017637.5 W233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr5:172586981 G>T maps to NM_013979.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:112999436 C>A maps to ENST00000273395 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:112991947 C>T maps to ENST00000273395 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr4:13606483 T>C maps to NM_148894.2 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:13601054 G>T maps to NM_148894.2 S2490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:13605782 G>T maps to NM_148894.2 S914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr4:13603426 T>C maps to NM_148894.2 A1699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr4:13602127 G>T maps to NM_148894.2 A2132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr4:13604616 G>A maps to NM_148894.2 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr2:198636707 T>G did not map to a codon.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr2:198646520 C>T maps to NM_197970.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr6:3140674 C>T maps to NM_004332.2 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr20:36954719 C>A maps to NM_001725.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:36952336 C>T maps to NM_001725.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr20:31607531 C>T maps to NM_025227.1 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr20:31604855 G>C maps to NM_025227.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:31601614 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:31601639 G>C maps to NM_025227.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr20:31606866 G>A did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr22:32831729 G>A maps to NM_174932.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr20:31620829 G>A maps to NM_174897.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:65907894 C>T maps to ENST00000321892 Q1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:140482831 T>G maps to NM_004333.4 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr12:112097071 C>T maps to NM_006768.3 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr12:112082287 T>C maps to NM_006768.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr12:112110579 T>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:112097134 A>G maps to NM_006768.3 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:41246659 T>C maps to ENST00000471181 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:41256888 C>T maps to ENST00000471181 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:41276071 G>A maps to ENST00000471181 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr17:41256882 A>C did not map to a codon.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr13:32936726 A>T maps to NM_000059.3 R2625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr13:32950825 T>A maps to NM_000059.3 Y2884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr13:32971099 C>A maps to NM_000059.3 P3189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr13:32910543 G>A maps to NM_000059.3 Q684Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr13:32903577 A>C did not map to a codon.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr13:32893409 G>A maps to NM_000059.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr13:32912649 T>C maps to NM_000059.3 D1386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr13:32930697 G>A maps to NM_000059.3 L2523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr13:32937583 C>T maps to NM_000059.3 Q2749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:154305514 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr22:50191665 C>A maps to ENST00000342989 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:32942322 C>T maps to ENST00000395289 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:32947815 G>T maps to ENST00000395289 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:136906944 C>T maps to NM_007371.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:15350542 G>A maps to NM_058243.2 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr19:15355573 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:15367071 G>C maps to NM_058243.2 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:15349768 G>A maps to NM_058243.2 L1269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:15350614 G>A maps to NM_058243.2 S1100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:15350584 C>T maps to NM_058243.2 V1110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr19:15383895 G>A maps to NM_058243.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr16:50383953 G>A maps to NM_001173984.2 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:137496707 G>A maps to NM_139199.1 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:137507795 G>A maps to NM_139199.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr5:137488416 T>C maps to NM_139199.1 E870E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr5:870639 C>T maps to NM_001009877.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr5:878567 C>T maps to NM_001009877.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr5:881267 C>G maps to NM_001009877.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr5:878553 G>T maps to NM_001009877.2 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr1:92447252 C>G maps to ENST00000347608 S660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr1:92459806 C>A maps to ENST00000347608 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:92446707 C>T maps to ENST00000347608 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr14:105692445 C>T maps to NM_001519.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr8:37702007 T>C maps to NM_018310.3 *420W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:37704451 A>G maps to NM_018310.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:125509699 C>T maps to NM_080626.5 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr17:59857703 G>C maps to NM_032043.2 S618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr17:59770873 C>G did not map to a codon.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr5:34925419 G>A maps to NM_018321.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr11:66108785 C>A maps to NM_001024957.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr3:9775847 G>A maps to NM_001003694.1 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:9786776 G>C maps to NM_001003694.1 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:9782626 T>C did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:135574474 G>A did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr23:135572632 C>T did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:135574490 C>T did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr19:55805722 A>C maps to NM_032430.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr19:55798462 G>A maps to NM_032430.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr11:1464608 C>T maps to NM_003957.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr11:1475729 C>T maps to NM_003957.2 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:40574318 G>C maps to NM_018963.3 S1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr21:40558960 A>G maps to NM_018963.3 N2318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr21:40568319 A>G maps to NM_033656.2 Y2225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr21:40650699 G>A maps to NM_018963.3 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr21:40559106 G>A maps to NM_018963.3 R2270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr21:40571182 G>C maps to NM_018963.3 S1720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:79932625 T>A did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr23:79975056 C>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:79990690 C>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:79999662 G>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:79999616 C>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:79999688 G>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:80049246 G>C did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:79947377 G>A did not map to a codon.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr23:79932684 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:79946659 G>C did not map to a codon.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr23:79979295 T>C did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr23:79988993 T>C did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:79980559 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:79989633 C>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:79999596 C>G did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr23:79999655 C>A did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr23:79980466 C>T did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:79975137 C>T did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr23:79978123 C>T did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr23:79960223 T>A did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr23:80001188 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:79955509 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:79991558 C>T did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:79938021 G>A did not map to a codon.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr23:79932673 A>G did not map to a codon.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr23:80001090 G>A did not map to a codon.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr23:79990683 C>T did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:79945533 G>A did not map to a codon.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr23:79939568 A>T did not map to a codon.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:62457909 G>A maps to NM_001130702.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:62458141 C>T maps to NM_001130702.1 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr1:32841953 C>T maps to NM_001143888.1 E372E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:571570 C>T maps to NM_198591.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:579569 C>T maps to NM_001728.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:49692475 C>G maps to NM_003458.3 L1829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr3:49690315 G>A maps to NM_003458.3 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr3:49697989 G>A maps to NM_003458.3 E2904E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr3:49689518 C>T maps to NM_003458.3 R844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:49702265 C>T maps to NM_003458.3 F3925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:49699341 C>G maps to NM_003458.3 S3355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr9:116122897 C>A maps to NM_017688.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:15716966 A>C maps to ENST00000382346 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:122848578 G>A maps to NM_001098169.1 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr11:122848357 C>A maps to NM_001098169.1 *234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr11:122848392 G>A maps to NM_001098169.1 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr11:122852271 C>T maps to NM_001098169.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr11:122848401 G>A maps to NM_001098169.1 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr10:93744028 C>T maps to NM_003972.2 D765D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:83698894 G>A maps to NM_025238.3 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:83687527 G>A maps to NM_025238.3 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr15:83710627 A>G maps to NM_025238.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:13427227 C>T maps to NM_032320.5 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:108051314 T>A maps to NM_001018072.1 Y1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:108029159 G>C maps to NM_001018072.1 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr16:3639180 C>T maps to NM_032444.2 R1486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr16:3639416 G>A maps to NM_032444.2 Q1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr16:3646277 C>T maps to NM_032444.2 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:3639183 C>T maps to NM_032444.2 Q1485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr16:3656526 C>T maps to NM_032444.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:124036331 C>A maps to ENST00000368994 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:124050610 G>A maps to ENST00000368994 L165L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-7099-01A-41D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:1993165 G>C maps to NM_017797.3 Y179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:1993105 C>T maps to NM_017797.3 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:1990033 G>A maps to NM_017797.3 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr20:11899748 C>T maps to NM_014962.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:105716078 C>T maps to NM_033271.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr14:105715747 C>T maps to NM_033271.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr14:93709137 G>A maps to NM_001002860.2 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr14:93708888 G>A maps to NM_001002860.2 A1043A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr14:93712181 C>A maps to NM_001002860.2 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr1:92568215 C>T maps to NM_183242.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:92568215 C>T maps to NM_183242.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:75673328 C>T maps to NM_001729.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr4:75681109 C>T maps to NM_001729.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:15686311 C>T maps to NM_000060.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:15677116 C>T maps to NM_000060.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr3:15686776 G>T maps to NM_000060.2 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:72798853 G>C maps to NM_001037637.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:92539206 T>C maps to NM_001731.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:203276430 G>A maps to NM_006763.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:100615598 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:100604913 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:100608906 T>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:100608292 C>G did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr23:100617675 T>A did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr23:100617677 C>A did not map to a codon.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr23:100617200 T>C did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:100608881 T>A did not map to a codon.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr23:100630176 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr23:100630194 C>T did not map to a codon.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr3:112198457 C>A maps to NM_181780.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr6:26468368 G>T maps to NM_007049.3 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr6:26393158 G>A maps to NM_001197237.1 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr6:26392972 G>A maps to NM_001197237.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr6:26409842 C>T maps to NM_007048.5 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr6:26373230 G>A maps to NM_001197246.1 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr6:26448954 G>A did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:26451999 A>T maps to NM_006994.4 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr6:32372948 C>T maps to ENST00000468270 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:180429672 G>A maps to NM_197975.2 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr5:180424309 C>T maps to NM_197975.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr5:180338420 C>T maps to NM_001040462.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:180472572 C>T maps to NM_152547.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:180483001 T>G maps to NM_152547.4 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr10:103291077 A>T maps to NM_033637.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr2:111419370 C>G maps to NM_004336.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr2:111416239 C>T maps to NM_004336.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:111419370 C>T maps to NM_004336.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr2:111398995 G>A maps to NM_004336.3 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr15:40494808 C>T maps to ENST00000412359 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:40488919 C>T maps to ENST00000412359 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr15:40462758 G>A maps to ENST00000412359 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:105563585 C>T maps to NM_007073.4 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr6:105577361 G>T maps to NM_007073.4 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr6:41897914 G>A maps to NM_004053.3 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:41900356 C>T maps to NM_004053.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:41899232 C>T maps to NM_004053.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr17:56385248 G>C maps to NM_004758.2 P1595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr17:56387405 C>T maps to NM_004758.2 E1271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:56403659 C>T maps to NM_004758.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:56397484 G>T maps to NM_004758.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:56382995 T>A maps to NM_004758.2 K1756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr10:45473429 C>A maps to NM_007021.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr10:45473231 G>A maps to NM_007021.3 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr10:63450357 A>G maps to NM_173554.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr10:77818490 C>T maps to NM_032024.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr10:15138709 C>T maps to NM_153244.1 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr10:15138577 C>G maps to NM_153244.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:115895717 T>A maps to NM_018017.2 K482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:121618669 G>T maps to NM_024834.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:98743186 T>A maps to NM_015652.2 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr10:98742211 C>T maps to NM_015652.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:127414361 C>T maps to ENST00000356792 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr10:127412502 C>T maps to ENST00000356792 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr10:127438082 C>T maps to ENST00000356792 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr10:127429585 C>G maps to ENST00000356792 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr10:127429568 G>C did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr10:5804549 T>C maps to NM_017782.4 D2410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr10:5799598 G>A maps to NM_017782.4 V2283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr10:5789367 G>A maps to NM_017782.4 E1328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:5789009 C>G maps to NM_017782.4 S1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:5790609 G>A maps to NM_017782.4 K1742K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:5782358 C>T maps to NM_017782.4 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr10:5772855 A>C maps to NM_017782.4 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr10:5791143 G>C maps to NM_017782.4 G1920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:102749398 A>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:102748695 C>A maps to NM_021830.4 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr10:102749196 G>A maps to NM_021830.4 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:99968791 C>T maps to ENST00000314594 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr10:99969385 G>A maps to ENST00000314594 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr10:120513992 G>A maps to NM_153810.4 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr10:50902582 G>T did not map to a codon.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr10:73521631 G>T maps to NM_022153.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:82187165 C>T maps to NM_032333.4 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr10:82187155 C>G maps to NM_032333.4 Y160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr10:99349662 G>A maps to NM_001009997.2 W3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr10:23633574 G>T maps to NM_153714.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:50532656 G>A maps to NM_001135196.1 Q689Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:50531537 T>C maps to NM_001135196.1 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:50255050 T>A maps to NM_001031746.3 K272*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-T2-A6WX-01A-12D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr10:50272779 C>T maps to NM_001031746.3 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr10:105893539 A>G maps to ENST00000389588 T1479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr10:105956619 C>G maps to ENST00000389588 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr10:105905259 G>C maps to ENST00000389588 L1307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr10:115535550 G>A maps to NM_182601.1 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:118425269 G>T maps to ENST00000388884 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:120094624 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr10:134751106 C>T maps to ENST00000368586 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr10:118100358 C>A maps to NM_198515.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:85944464 C>A maps to NM_207373.2 C63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr11:8942973 C>G maps to NM_020643.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr11:64876852 G>A maps to NM_013265.2 K515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:68029520 G>A maps to NM_022338.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr11:76253278 C>T maps to ENST00000393457 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr11:76237520 C>T maps to ENST00000393457 Q614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr11:76255466 G>A maps to ENST00000393457 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr11:76234274 A>G maps to ENST00000393457 K588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:556880 G>A maps to NM_173573.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr11:558217 C>T maps to NM_173573.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr11:555111 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr11:557946 G>A maps to NM_173573.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:33566370 G>A maps to ENST00000389726 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:33564818 G>A maps to ENST00000389726 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:33682489 C>G maps to ENST00000389726 S1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:33565124 G>A maps to ENST00000389726 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:33565763 A>G maps to ENST00000389726 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:33631335 T>G maps to ENST00000389726 Y1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr11:33596354 G>A maps to ENST00000389726 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:6231256 C>T maps to NM_173525.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:30354490 A>T maps to NM_152316.1 K169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:62437248 C>G maps to ENST00000431002 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:47176812 G>A did not map to a codon.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:71822258 G>T maps to NM_014042.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr11:111796826 G>T maps to NM_080659.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:111155056 G>A maps to NM_198498.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr11:93483548 C>A maps to ENST00000354421 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:124637134 G>A maps to ENST00000374979 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr11:124637179 T>C maps to ENST00000374979 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr11:124670230 T>A maps to ENST00000374979 K16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr11:122817445 C>T maps to NM_024806.2 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr11:61254048 C>T maps to NM_145017.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr11:65685262 G>A maps to NM_001135635.1 H183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr11:101951963 A>G maps to NM_032930.2 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr11:86056625 G>A maps to NM_016401.3 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:82644764 T>A maps to NM_145018.3 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr11:111385712 G>C maps to NM_207430.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:61539101 C>T maps to NM_001127392.1 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr11:61533489 G>A maps to NM_001127392.1 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:61543820 G>A maps to NM_001127392.1 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:61548769 C>T maps to NM_001127392.1 S911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr11:61551036 C>T maps to NM_001127392.1 I1028I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:82792638 A>G maps to NM_032230.2 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:88440659 G>A maps to NM_001009894.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr12:110206654 G>T maps to NM_032829.2 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:32135422 A>T maps to NM_018169.3 K512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr12:32134254 A>G maps to NM_018169.3 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr12:32138777 C>G maps to NM_018169.3 S1630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr12:32136679 C>T maps to NM_018169.3 Q931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr12:32135922 C>T maps to NM_018169.3 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr12:13526326 C>T maps to ENST00000318426 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:21680691 G>C maps to NM_030572.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr12:4609472 G>C maps to NM_020374.2 S424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr12:4639057 C>T maps to NM_020374.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr12:4645270 C>T maps to NM_020374.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr12:4639178 C>T maps to NM_020374.2 W121*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CN-A63U-01A-11D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:40041679 G>T maps to NM_001031748.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:49075373 C>A maps to NM_017822.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:103699897 C>T maps to NM_001099336.1 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:103695915 A>G maps to NM_001099336.1 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:121448688 G>A maps to NM_022895.1 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr12:121442192 C>T maps to NM_022895.1 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:105381945 T>G maps to NM_152318.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr12:102569389 C>T maps to NM_017915.3 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr12:117175615 G>A maps to NM_024738.1 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:4430448 C>T maps to NM_020375.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr12:4430448 C>T maps to NM_020375.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr12:88379765 C>T maps to NM_152589.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:88381701 G>A maps to NM_152589.1 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr12:88420319 G>T maps to NM_152589.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:88379795 A>G maps to NM_152589.1 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:112699140 G>A maps to NM_001109662.2 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:112684765 G>C maps to NM_001109662.2 V1312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:112711539 G>A maps to NM_001109662.2 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr12:112605213 G>A maps to NM_001109662.2 F3975F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr12:112602001 G>A maps to NM_001109662.2 S4032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:112605282 G>A maps to NM_001109662.2 F3952F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:112711556 G>C maps to NM_001109662.2 S433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr12:112622227 G>A maps to NM_001109662.2 A3342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr12:112665942 C>T maps to NM_001109662.2 G2096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:112605240 C>G maps to NM_001109662.2 P3966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:112681212 G>A maps to NM_001109662.2 V1462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr12:112667558 G>A maps to NM_001109662.2 A1982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr12:112650350 G>C maps to NM_001109662.2 L2351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr12:112681769 G>T maps to NM_001109662.2 V1347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:112608227 G>A maps to NM_001109662.2 T3815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:112665918 A>G maps to NM_001109662.2 V2104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr12:112703749 C>G maps to NM_001109662.2 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr12:112622356 G>A maps to NM_001109662.2 V3299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:113629588 G>A maps to NM_032848.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr12:113629195 G>A maps to NM_032848.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr12:113624688 G>A maps to NM_032848.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:48888676 G>A maps to NM_152319.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:48888619 G>A maps to NM_152319.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr12:48888658 A>G maps to NM_152319.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:64784225 G>T maps to NM_001170633.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr12:64678477 C>A maps to NM_001170633.1 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:7054985 G>A maps to NM_138425.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr12:14976228 G>A maps to NM_175874.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:14976372 C>T maps to NM_175874.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr12:14976228 G>A maps to NM_175874.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:14976312 C>T maps to NM_175874.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr12:97093834 A>G maps to ENST00000342887 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr12:97112263 A>G maps to ENST00000342887 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr12:97087579 C>T maps to ENST00000342887 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr12:97078469 T>C maps to ENST00000342887 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:97084907 T>C maps to ENST00000342887 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:80632730 G>C maps to NM_173591.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:80735782 T>A maps to NM_173591.3 I1693I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr12:80658859 C>G maps to NM_173591.3 Y689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:80699365 C>G maps to NM_173591.3 S1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr12:80752448 A>C did not map to a codon.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr12:80658871 C>T maps to NM_173591.3 C693C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr12:80651656 A>T maps to NM_173591.3 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr12:48578121 C>T maps to NM_001013635.3 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:14959574 T>G maps to NM_001013698.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:14959194 G>A maps to NM_001013698.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr12:27235254 C>G maps to ENST00000398815 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr12:31815159 T>C maps to NM_001135864.1 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr12:31820645 C>T maps to NM_001135864.1 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr12:93100818 C>T maps to NM_001037671.3 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:93101489 G>T maps to NM_001037671.3 *191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr13:111980539 T>C maps to NM_152324.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr13:111973248 G>T maps to NM_152324.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr13:111996451 C>T maps to NM_152324.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr13:39597213 G>A maps to NM_025138.3 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:39588613 C>G did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr13:113086836 T>A did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr13:73320741 G>A maps to ENST00000377815 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr13:103338494 G>A maps to NM_001010977.1 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr14:57082693 C>A maps to NM_017799.3 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:57052605 C>G maps to NM_017799.3 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:57092098 G>C did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr14:90770701 G>A maps to NM_017970.2 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr14:90759043 T>C maps to NM_017970.2 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr14:90783140 G>C maps to NM_017970.2 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr14:50092738 G>A maps to NM_018139.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:50092538 T>C maps to NM_018139.2 Q745Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr14:57938206 G>A maps to NM_018168.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr14:45686254 G>A maps to NM_018353.4 F990F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr14:45711964 G>A maps to NM_018353.4 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:74825000 C>T maps to NM_018228.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:74825105 C>T maps to NM_018228.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr14:74824427 C>T maps to NM_018228.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr14:76642982 T>G maps to NM_017926.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:76621244 C>G maps to NM_017926.2 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:76621146 G>A maps to NM_017926.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:23567115 T>C maps to NM_017924.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr14:23567288 G>C maps to NM_017924.2 *141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:96848582 G>A did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr14:96851861 G>A maps to NM_016472.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr14:96851942 C>G maps to NM_016472.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr14:60592507 A>T maps to ENST00000404681 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr14:60582437 A>G maps to ENST00000404681 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr14:60591151 G>T maps to ENST00000404681 E755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:81209425 C>T maps to NM_152446.3 E933E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr14:77873010 T>A maps to NM_138791.1 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:59946013 G>A maps to NM_144581.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr14:59950998 C>T maps to NM_144581.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr14:77327046 G>T maps to NM_194287.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr14:77294656 C>T maps to NM_194287.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr14:77844480 T>A maps to NM_001010860.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:99182605 G>A maps to NM_182560.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr14:76549918 G>C maps to NM_052873.2 *214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr14:76452139 T>A maps to NM_052873.2 L4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr14:76549007 C>G maps to NM_052873.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr14:50472358 G>A maps to NM_001012706.1 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:24769252 C>G maps to NM_174913.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr14:45373696 G>A maps to NM_001017923.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr14:58605803 C>T maps to ENST00000438670 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr14:58605874 G>A maps to ENST00000438670 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr14:58471867 T>G maps to ENST00000438670 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr14:74523882 C>T maps to NM_025057.2 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:74516715 C>T maps to NM_025057.2 H368H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:74516716 C>T maps to NM_025057.2 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr14:95921872 C>A maps to NM_152592.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr14:95921869 G>C maps to NM_152592.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:65041171 G>C did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr14:100793679 C>G maps to NM_207117.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr14:100789774 C>T maps to NM_207117.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:100795097 C>T maps to NM_207117.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr14:103573993 C>T maps to NM_001077594.1 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:103566783 C>T maps to NM_001077594.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:105452938 C>T maps to NM_174891.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:23456765 T>C maps to NM_021944.2 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:24922339 T>G maps to NM_018958.2 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr15:24923845 T>C maps to NM_018958.2 G944G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr15:24923161 C>A maps to NM_018958.2 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr15:24924385 G>C maps to NM_018958.2 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr15:24921115 G>T maps to NM_018958.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr15:24921688 C>T maps to NM_018958.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:24923323 T>A maps to NM_018958.2 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr15:24921061 C>A maps to NM_018958.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:24922336 C>T maps to NM_018958.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:24922762 A>G maps to NM_018958.2 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr15:24921553 T>A maps to NM_018958.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr15:24923770 A>T maps to NM_018958.2 P919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:40675131 G>A maps to NM_033286.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:34380294 G>A maps to NM_020154.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:76496184 C>G maps to NM_152335.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:76467993 G>A maps to NM_152335.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr15:76496313 G>A maps to NM_152335.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr15:93015668 G>A maps to NM_153040.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr15:93016180 A>G did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr15:49663514 G>C maps to NM_152647.2 S365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr15:49880218 C>T maps to NM_152647.2 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:49833957 C>A maps to NM_152647.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:49903432 T>C maps to NM_152647.2 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr15:75498856 T>C maps to NM_015492.4 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr15:75499828 C>T maps to NM_015492.4 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:83679040 G>A maps to NM_144597.2 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr15:90168260 C>T maps to NM_152259.3 R1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr15:90143869 C>T maps to NM_152259.3 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr15:90168445 C>A maps to NM_152259.3 G1635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:45723008 A>G maps to NM_197955.1 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr15:40630981 C>T maps to NM_207380.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:40627526 C>T maps to NM_207380.2 Q479Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr15:39544746 T>G maps to NM_207445.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr15:34648620 A>G maps to ENST00000438749 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:34648776 C>T maps to ENST00000438749 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:34640392 C>T maps to ENST00000438749 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:34646692 G>C maps to ENST00000438749 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr15:34649145 G>A maps to ENST00000438749 E969E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr15:34648089 C>A maps to ENST00000438749 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr15:34648290 T>G maps to ENST00000438749 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:90784557 C>A maps to NM_001013657.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr15:90784880 C>T maps to NM_001013657.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:74032914 C>T maps to NM_001039614.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:615180 C>G maps to ENST00000293874 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr16:1399475 C>A maps to NM_001001410.2 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:1399438 C>T maps to NM_001001410.2 *313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:15661908 C>T maps to NM_033201.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:81094969 C>T maps to NM_152337.2 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr16:81087677 A>G maps to NM_001100873.1 *389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr16:67700070 G>A maps to NM_032140.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr16:67700076 G>A maps to NM_032140.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:67700133 C>T maps to NM_032140.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr16:29827929 C>G maps to NM_024516.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr16:31510703 G>A maps to NM_022744.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr16:2510988 G>A maps to NM_025108.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:19612992 C>G maps to NM_020314.5 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:19659192 C>T maps to NM_020314.5 Q762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:19586418 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:19576214 C>T maps to NM_020314.5 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr16:19628031 C>T maps to NM_020314.5 Q465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr16:8719530 G>A maps to NM_024109.2 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:67168321 C>T maps to NM_025187.3 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:67173917 G>A maps to NM_025187.3 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:67154022 C>T maps to NM_025187.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:4797505 C>G maps to NM_139170.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:9210766 T>A maps to NM_014117.2 *276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr16:9186808 C>G maps to NM_014117.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:1891861 G>C maps to NM_001163560.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr16:49430550 C>T maps to NM_144602.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr16:49407996 C>T maps to NM_144602.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:2260001 C>G maps to NM_182563.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr16:67702163 C>T maps to NM_001012984.2 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr16:19718477 G>C maps to NM_001012991.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:5112510 G>A maps to ENST00000350219 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr16:1470387 G>A maps to NM_001010878.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr16:30770422 C>T did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr17:80363225 G>A maps to NM_175902.4 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr17:72951929 G>A maps to NM_030630.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr17:72954849 G>C maps to NM_030630.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:29226354 G>A maps to NM_024683.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:56620308 C>T maps to NM_001038704.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:56620419 G>C maps to NM_001038704.1 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:56620818 G>A maps to NM_001038704.1 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:10608830 G>A maps to NM_020233.4 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr17:42228330 G>A maps to NM_024032.3 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:42232287 A>G maps to NM_024032.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr17:79203021 G>A maps to NM_144679.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:45481246 T>A maps to NM_152347.4 L674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr17:45452135 A>G maps to NM_152347.4 K392K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr17:45490283 T>A did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:45479496 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr17:45451888 C>G maps to NM_152347.4 S310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr17:65988154 G>C maps to NM_181655.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr17:34185927 C>T maps to NM_152781.2 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr17:34192400 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr17:34190055 C>T maps to NM_152781.2 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr17:8131623 T>C maps to NM_025099.5 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr17:8141730 G>A maps to NM_025099.5 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:79517286 G>T maps to NM_025161.5 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr17:79516277 G>A maps to NM_025161.5 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr17:57287433 C>T maps to NM_018149.6 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr17:57288114 C>T maps to NM_018149.6 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr17:57287808 C>T maps to NM_018149.6 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr17:7330241 G>A maps to NM_175734.4 W311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:7329024 G>A maps to NM_175734.4 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr17:7330659 G>T maps to NM_175734.4 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr17:30668272 G>A maps to NM_022344.2 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr17:30666950 G>A maps to NM_022344.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:72588217 A>T maps to NM_152460.2 T11T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-7071-01A-12D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:72588199 G>A maps to NM_152460.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:72588682 C>T maps to NM_152460.2 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:72588511 G>A maps to NM_152460.2 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:59489602 C>T maps to NM_203425.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:3724645 C>T maps to NM_001114118.1 W299*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-T2-A6WX-01A-12D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:79632427 C>A maps to NM_001039842.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr17:36997561 G>A maps to NM_001080465.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr18:13645457 C>G maps to NM_181481.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr18:13645526 C>T maps to NM_181481.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr18:13645286 G>A maps to NM_181481.3 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr18:13681842 T>A maps to NM_152352.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr18:43795986 G>T maps to NM_145055.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr18:52258569 G>A maps to NM_173629.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr18:30969507 A>C maps to NM_001105528.1 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr18:30791982 A>G maps to NM_001105528.1 H705H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:21001408 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr18:51892103 C>T maps to ENST00000382911 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr18:21098935 C>T maps to NM_013326.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr19:30193699 C>T maps to NM_001031726.2 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr19:58472908 G>A maps to NM_152474.4 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:30496289 C>T maps to NM_003796.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:30498455 G>A maps to NM_003796.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:900135 G>C maps to NM_138774.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr19:1235875 C>T maps to ENST00000382477 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr19:1235905 G>A maps to ENST00000382477 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr19:1231185 G>A maps to ENST00000382477 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:3557191 C>A maps to NM_021731.2 G70G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-5977-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:3623946 G>A maps to NM_021231.1 P127P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DQ-5625-01A-01D-1870-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-F7-A624-01A-22D-A30E-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-KU-A66S-01A-21D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:2096976 G>T maps to NM_001039846.1 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:2096976 G>T maps to NM_001039846.1 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:11485523 C>T maps to NM_175871.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:50666223 T>C maps to NM_152358.2 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:16611791 C>G maps to NM_032207.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:16614077 C>G maps to NM_032207.2 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:16613910 C>T maps to NM_032207.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr19:7569252 G>A maps to NM_198534.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr19:18675831 G>A did not map to a codon.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:55670430 C>G maps to ENST00000301249 *609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:55670684 G>A maps to ENST00000301249 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:55672074 C>T maps to ENST00000301249 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr19:14001122 C>T maps to ENST00000454313 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:14000823 G>C maps to ENST00000454313 S282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:14000434 G>A maps to ENST00000454313 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:14000435 G>A maps to ENST00000454313 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:14003598 C>T maps to ENST00000454313 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:1011794 C>T maps to NM_001033026.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr19:17389760 G>C maps to NM_014173.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr19:10202782 G>A maps to NM_018381.2 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:51770668 G>A maps to NM_173635.1 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:7278537 T>A maps to NM_020156.3 Y291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr23:119760994 C>T did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr23:119760089 G>A did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:119760658 C>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:22987521 C>A maps to NM_000491.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr17:5337060 G>A maps to NM_001212.3 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:22973834 C>A maps to NM_172369.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr2:119914518 G>A maps to NM_182528.3 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:16562731 G>A maps to NM_001010908.1 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr10:16563016 G>A maps to NM_001010908.1 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:159781810 C>A maps to NM_031908.4 G115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr5:159781982 G>A maps to NM_031908.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr5:159776735 G>A maps to NM_031908.4 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr5:34033476 G>A maps to NM_181435.4 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:34035785 G>T maps to NM_181435.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:47611621 C>T maps to NM_031909.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:47611714 C>T maps to NM_031909.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:1143808 G>A maps to NM_207419.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr16:1144796 C>T maps to NM_207419.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr13:24890209 C>T maps to NM_178540.3 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr13:24465688 C>A maps to NM_001007537.1 G247G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-P3-A5QF-01A-11D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr13:24465586 C>T maps to NM_001135816.1 L10L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-P3-A5QF-01A-11D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr13:24466093 T>C maps to NM_001007537.1 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr12:7244098 G>A maps to ENST00000290575 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:7241887 C>T did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:7260990 C>T maps to NM_016546.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:7177303 G>T maps to NM_001734.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:7169970 G>A maps to NM_001734.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:7177492 G>A maps to NM_001734.3 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:111490595 C>T maps to NM_018372.3 K765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:111492685 T>C maps to NM_018372.3 K552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:172414283 C>T maps to NM_139240.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr1:200867569 C>T maps to NM_018265.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:200880919 G>A maps to NM_018265.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr1:200869305 C>T maps to NM_018265.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:210006692 A>G maps to NM_014388.6 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:162824617 G>A maps to NM_178550.4 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:169798415 C>G maps to NM_018186.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:36785433 C>T maps to NM_001162530.1 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:36785373 C>T maps to NM_001162530.1 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:169391452 C>T maps to ENST00000367806 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:169390783 T>G maps to ENST00000367806 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:169390780 G>C maps to ENST00000367806 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:169364285 C>T maps to ENST00000367806 *510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:169390627 T>C maps to ENST00000367806 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr1:169390948 A>C maps to ENST00000367806 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:220864028 G>A maps to NM_024709.4 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr1:207200886 G>T maps to NM_023938.5 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr1:179363132 T>A maps to NM_144696.4 L320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:179452355 C>T maps to NM_144696.4 H697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:179398720 C>T maps to NM_144696.4 Y433Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:179354443 A>G maps to NM_144696.4 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:11007908 C>T maps to NM_001170754.1 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:170965782 T>C maps to NM_001163629.1 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:170961322 G>A maps to NM_001163629.1 W349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:170941011 C>A maps to NM_001163629.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr1:170961469 G>A maps to NM_001163629.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:182869252 G>C maps to ENST00000287709 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:67558948 G>C maps to NM_001013674.1 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:67558778 G>C maps to NM_001013674.1 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:16719857 C>T maps to NM_001114600.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr1:19923550 G>T maps to ENST00000433528 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:169761756 C>T maps to NM_033418.1 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr1:12819313 C>T maps to NM_152290.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr1:116675766 G>A maps to NM_152367.2 W290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:57258098 T>C maps to NM_001004303.4 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:57254661 G>A maps to NM_001004303.4 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:57258320 G>C maps to NM_001004303.4 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:57257876 G>T maps to NM_001004303.4 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:57257987 G>T maps to NM_001004303.4 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:57209832 C>T maps to NM_001004303.4 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr1:57254644 C>A did not map to a codon.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:27276604 G>A maps to NM_152365.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr1:27278034 G>A maps to NM_152365.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:75078364 C>A maps to NM_001002912.4 G377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:75038605 C>A maps to NM_001002912.4 E930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:75038327 G>C maps to NM_001002912.4 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:75037805 C>T maps to NM_001002912.4 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:75072414 T>A maps to NM_001002912.4 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:75039017 T>C maps to NM_001002912.4 K792K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:75038327 G>T maps to NM_001002912.4 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:75072530 C>A maps to NM_001002912.4 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr1:75072309 G>A maps to NM_001002912.4 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:75038708 C>T maps to NM_001002912.4 G895G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:75072543 C>T maps to NM_001002912.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr1:75072552 C>T maps to NM_001002912.4 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:75036914 C>A maps to NM_001002912.4 A1493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:75038684 C>A maps to NM_001002912.4 V903V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr1:75055745 G>T maps to NM_001002912.4 S582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr1:75038819 G>T maps to NM_001002912.4 P858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr1:75038609 C>A maps to NM_001002912.4 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr1:55175808 C>T maps to ENST00000454855 R1336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:55145694 C>T maps to ENST00000454855 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:55144427 G>A maps to ENST00000454855 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:55118985 G>A maps to ENST00000454855 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:55148400 G>T maps to ENST00000454855 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:55118865 C>A maps to ENST00000454855 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:55139798 C>G maps to ENST00000454855 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:55282672 T>A maps to NM_001110533.1 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:11775203 C>G maps to NM_198545.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:230979404 G>A maps to NM_032800.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr1:185094239 G>C maps to NM_030934.4 S532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:185114664 G>A maps to NM_030934.4 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:185143908 A>G maps to NM_001105518.1 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr1:28208650 C>G maps to NM_001105556.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:154179929 C>G maps to NM_001098616.1 *254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr1:154180095 G>A maps to NM_001098616.1 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr1:178491562 T>A maps to NM_032126.4 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr1:226173191 C>T maps to NM_152608.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:233113937 G>A maps to NM_032324.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:233105695 C>T maps to NM_032324.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:233105722 C>T maps to NM_032324.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:222903000 A>T maps to NM_144695.2 K266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr1:222892302 G>A maps to NM_144695.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:109191449 G>C maps to ENST00000370031 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr1:109191449 G>C maps to ENST00000370031 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:25571721 C>T maps to NM_020317.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:223568028 C>G maps to NM_152610.2 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr1:223567416 C>T maps to NM_152610.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr1:156704057 G>A maps to NM_015997.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:228362982 C>T maps to NM_001010867.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:209956454 G>A maps to NM_152485.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr1:153617663 A>G maps to NM_015607.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr1:2125496 C>A maps to ENST00000359030 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr1:60505606 C>T maps to NM_152377.2 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:60503710 T>C maps to NM_152377.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr1:16559456 G>A maps to NM_030907.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:172539801 G>C did not map to a codon.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr1:172558355 T>C maps to ENST00000367723 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr1:172555025 T>G maps to ENST00000367723 T684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr1:172546683 C>T maps to NM_014283.3 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr1:172558718 A>G maps to ENST00000367723 P978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:172520756 C>T maps to ENST00000367723 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr1:172526903 A>G maps to ENST00000367723 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:156897320 C>T maps to NM_144702.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:156901814 C>T maps to NM_144702.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr1:156897771 A>G maps to NM_144702.2 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr1:156897443 G>A maps to NM_144702.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:34666532 C>T maps to NM_001134734.1 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:34667793 C>G maps to NM_001134734.1 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:34667769 C>T maps to NM_001134734.1 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:229462742 C>A maps to NM_145257.3 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:31910823 C>T maps to ENST00000437789 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:9498786 T>C maps to NM_012261.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr20:9510311 C>A maps to NM_012261.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr20:9510394 C>T maps to NM_012261.3 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr20:42825778 C>T maps to NM_016470.6 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr20:42825850 C>T maps to NM_016470.6 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr20:31877738 G>T maps to NM_033197.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr20:35444080 C>T maps to NM_080627.2 K588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr20:35441118 G>A maps to NM_080627.2 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr20:35443717 G>C maps to NM_080627.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr20:35467697 G>A maps to NM_080627.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr20:35444092 G>A maps to NM_080627.2 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr20:18379175 C>T maps to NM_001099407.1 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr20:18440912 G>T maps to NM_001099407.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr20:35757570 C>G did not map to a codon.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr20:35748154 G>C maps to ENST00000343811 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr20:62493606 C>G maps to NM_080622.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr20:62493541 C>T maps to NM_080622.3 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:62493543 G>A maps to NM_080622.3 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:2796270 T>C maps to NM_080739.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr20:60989011 G>C maps to NM_080833.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:60987713 C>T maps to NM_080833.2 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr20:34611648 C>T maps to ENST00000373973 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:30602762 C>T maps to ENST00000300415 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr20:30602816 C>T maps to ENST00000300415 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr20:44515722 C>T maps to NM_080608.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr20:44515634 G>A maps to NM_080608.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr20:44516181 G>A maps to NM_080608.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:58519669 T>C maps to NM_022106.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:31647252 G>A maps to NM_182658.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr20:31657704 G>T maps to NM_182658.1 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr20:31652344 G>T maps to NM_182658.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:31652272 C>T maps to NM_182658.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr20:31671215 C>A maps to NM_182519.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:31685547 C>A maps to NM_182519.2 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:31671443 T>C maps to NM_182519.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:31676816 C>T maps to NM_182519.2 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr20:3295767 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr20:3262361 G>C maps to NM_001009984.1 S846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr20:62187168 C>T maps to NM_024059.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr20:5753648 G>A maps to NM_152504.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:20150021 C>T maps to ENST00000389655 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:20208963 C>T maps to ENST00000389655 I671I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr20:20177326 G>A maps to ENST00000389655 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr20:20278850 G>A maps to ENST00000389655 A1084A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr20:20257900 C>T maps to ENST00000389655 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr20:3739185 G>C maps to NM_001039140.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:24954319 C>A maps to NM_020531.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:5081502 G>A maps to NM_001009923.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr20:1161908 C>T maps to NM_018354.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr20:1161731 G>A maps to NM_018354.1 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr20:746094 G>A maps to NM_033409.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr20:31812909 C>T maps to NM_178466.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr20:31813053 G>T did not map to a codon.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr20:18794839 G>A maps to NM_178483.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr20:18794792 G>T maps to NM_178483.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr20:10603801 G>A maps to NM_001009608.1 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr21:45949753 C>A maps to ENST00000443468 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr21:45948374 C>T maps to ENST00000443468 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr21:45553590 G>A maps to NM_004649.6 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr21:45553635 G>A maps to NM_004649.6 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:47711252 G>C maps to NM_058181.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr21:47716086 C>T maps to NM_058181.1 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:46387036 C>A maps to NM_058190.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:24939876 G>A maps to ENST00000266155 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr22:20049074 G>A maps to NM_152906.4 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr22:20041041 C>T maps to NM_152906.4 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr22:19839544 A>T maps to NM_024627.5 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr22:29456408 G>A maps to NM_015370.1 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr22:42477981 C>T maps to NM_033318.3 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr22:24982182 G>A maps to NM_207644.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr22:24982180 C>T maps to NM_207644.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr22:46644181 C>A did not map to a codon.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr22:32548590 C>T maps to NM_001010859.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr22:23974144 G>A maps to NM_016449.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr21:43309400 C>T maps to NM_015500.1 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr21:43327242 G>C maps to NM_015500.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:73785529 G>A maps to ENST00000334126 S1573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:73814403 C>A maps to ENST00000334126 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:73795938 C>T maps to ENST00000334126 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr11:73803465 G>C maps to ENST00000334126 S1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr2:99763937 C>G maps to ENST00000424491 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr2:27803324 C>T maps to NM_032266.3 R1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:27800114 G>T maps to NM_032266.3 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:27804811 C>T maps to NM_032266.3 H1791H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr2:27804892 G>A maps to NM_032266.3 L1818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:27804295 G>A maps to NM_032266.3 E1619E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:27804509 G>T maps to NM_032266.3 E1691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:27800371 C>T maps to NM_032266.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr2:27804460 C>T maps to NM_032266.3 S1674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr2:26998434 G>T maps to NM_017877.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:101881352 T>C maps to NM_017546.4 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:101881466 C>T maps to NM_017546.4 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr2:101874385 G>T maps to NM_017546.4 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:75921516 C>T maps to NM_003203.4 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr2:26667761 C>T maps to NM_145038.2 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:26667170 C>T maps to NM_145038.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:26667098 T>C maps to NM_145038.2 D346D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr2:26667092 G>A maps to NM_145038.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr2:106690369 C>T maps to NM_032411.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:70406676 C>T maps to NM_017880.1 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:70408541 T>C maps to NM_017880.1 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr2:70408754 C>G maps to NM_017880.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:24255768 G>A maps to NM_025203.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr2:24261334 G>A maps to NM_025203.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr2:24261746 G>C maps to NM_025203.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:11284116 G>A maps to NM_182500.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr2:88828763 C>T maps to NM_152670.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:27360066 A>G maps to NM_178553.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:27360921 T>C maps to NM_178553.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:241831031 G>T maps to NM_001085437.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr2:241835039 G>A maps to NM_001085437.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr2:241835204 G>A maps to NM_001085437.1 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:99439550 G>T maps to NM_207362.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr2:99448809 C>A did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr2:99438683 G>C maps to NM_207362.2 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:37473322 G>A maps to NM_144736.4 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr2:47378588 C>T maps to NM_001163561.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:219222440 C>T maps to NM_198559.1 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:219229376 G>A maps to NM_198559.1 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:74867186 C>T maps to NM_138804.3 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr2:74802647 T>A maps to NM_138804.3 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr2:210962877 G>A maps to NM_152519.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:211018890 G>C maps to NM_152519.2 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr2:210993801 T>A maps to NM_152519.2 K395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:29294901 C>T maps to NM_001029883.1 E742E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:29296560 G>T maps to NM_001029883.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr2:54558136 C>T maps to NM_001100396.1 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:74043890 C>A maps to NM_001080474.1 I847I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr2:209036778 G>A maps to NM_001099334.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:228476325 C>T maps to NM_020161.3 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:242814993 C>A maps to NM_173821.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr2:242815329 C>T maps to NM_173821.2 Y541Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:63661027 C>A maps to NM_015910.4 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:191064815 G>A maps to NM_032321.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr2:85051171 A>G maps to ENST00000409520 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr2:85066402 G>A maps to ENST00000409520 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr2:85051177 C>T maps to ENST00000409520 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr2:85097546 G>A maps to ENST00000409520 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:6696607 G>A maps to NM_000064.2 G953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:6686811 G>A maps to NM_000064.2 A1197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:6714451 C>T maps to NM_000064.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr19:6697748 G>A maps to NM_000064.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:6709692 A>T did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:6684803 T>C maps to NM_000064.2 K1337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr12:8212397 G>A maps to NM_004054.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:8211439 G>A maps to NM_004054.2 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr12:8212706 G>A maps to NM_004054.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr12:8212580 C>T maps to NM_004054.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr12:8211881 A>T maps to NM_004054.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:8212049 C>T maps to NM_004054.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:119236072 G>A maps to NM_016589.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:119236159 G>A maps to NM_016589.3 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:119217735 A>G maps to NM_016589.3 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr3:119458166 G>A maps to NM_033364.3 Q509Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr3:119459394 G>T did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr3:119428694 C>G maps to NM_033364.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:14755663 C>A maps to NM_032137.4 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr3:14769944 G>T did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:14799081 C>T maps to NM_032137.4 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr3:14798937 G>A maps to NM_032137.4 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr3:194790785 C>T maps to NM_152531.4 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:194947465 C>T maps to NM_152531.4 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr3:194947477 G>A maps to NM_152531.4 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:194991444 G>A maps to NM_152531.4 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:44437945 C>T maps to NM_173826.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr3:44442040 C>T maps to NM_173826.3 H360H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:44409182 A>G maps to NM_173826.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr3:44448932 G>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:10146170 G>A maps to NM_001164839.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:99881148 G>A maps to NM_032359.3 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr3:118865681 A>T maps to NM_152539.2 K216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr3:118866241 C>T maps to NM_152539.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:118865465 G>T maps to NM_152539.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr3:118865965 G>C maps to NM_152539.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr3:118865484 T>A maps to NM_152539.2 L150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:11885622 C>T maps to ENST00000444133 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr3:196434582 T>A maps to NM_032898.3 K115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr3:133647531 G>C maps to NM_025041.2 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr3:129023504 C>G maps to NM_001006109.1 S301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr3:129023601 C>G maps to NM_001006109.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr3:88199219 C>G maps to NM_173824.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr3:88205751 G>A maps to NM_173824.3 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr3:88202408 C>T maps to NM_173824.3 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7596-01A-11D-2229-08 chr3:43121308 G>A maps to NM_032806.4 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr3:157289046 C>T maps to NM_001130002.1 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:143691431 C>G maps to NM_173552.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:143691743 C>T maps to NM_173552.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr3:143691329 C>T maps to NM_173552.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:192516653 G>T maps to NM_178496.3 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr3:192516359 G>A maps to NM_178496.3 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr3:56681251 C>A did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr3:56657517 T>C maps to ENST00000447900 V1520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:56681003 G>A maps to ENST00000447900 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:138669185 C>A maps to NM_001040061.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:47545863 G>A maps to NM_001031703.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:31962427 C>T maps to NM_007293.2 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr4:57843127 C>G maps to NM_032313.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:57842905 G>A maps to NM_032313.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr4:113533742 C>G maps to NM_018392.4 V868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr4:113483597 C>T maps to NM_018392.4 L1542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:113483554 G>A maps to NM_018392.4 L1557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr4:113462063 T>A maps to NM_018392.4 T1941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr4:8456492 C>T maps to NM_152544.2 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr4:8472842 C>T maps to NM_152544.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr4:8465767 C>T maps to NM_152544.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:76489444 C>T maps to NM_178497.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:170671805 C>T maps to NM_017867.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:170663145 C>A maps to NM_017867.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:128949869 A>T maps to ENST00000454347 K314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr4:128938656 G>A did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:120221510 G>C maps to NM_001170330.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr4:120221570 G>A maps to NM_001170330.1 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:121958384 G>A maps to NM_024574.3 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr4:121957685 G>A maps to NM_024574.3 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr4:121957930 G>A maps to NM_024574.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr4:121958732 A>G maps to NM_024574.3 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:121961082 A>T did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr4:113107861 C>G maps to NM_152400.2 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr4:130027802 G>A did not map to a codon.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr4:98480262 G>T maps to NM_174952.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr4:98893487 C>T maps to NM_174952.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr4:165878635 A>G maps to NM_153027.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr4:71024145 C>A maps to NM_214711.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:71020139 G>A maps to NM_214711.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr4:71024189 C>A maps to NM_214711.3 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr4:71024298 G>A maps to NM_214711.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr4:184595925 G>A maps to NM_021942.4 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr4:184626158 C>A maps to NM_021942.4 I997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr4:184629642 A>G maps to NM_021942.4 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr4:159894345 G>C maps to NM_152543.2 S61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr4:140196469 G>A maps to ENST00000260011 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr4:5975388 T>C maps to ENST00000324058 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr4:5961119 C>T maps to ENST00000324058 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:5527952 C>T maps to NM_005750.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:5528038 C>G maps to NM_005750.2 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:71096931 G>A maps to NM_152997.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:71096925 C>T maps to NM_152997.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:123797115 G>A maps to NM_001735.2 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:123737101 A>G maps to NM_001735.2 H1324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:47823720 G>A maps to ENST00000355085 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr5:134782554 G>A maps to NM_130848.2 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr5:31538723 G>C maps to NM_018356.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:43453837 T>A maps to NM_022483.4 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr5:102612012 A>G maps to NM_033211.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr5:43506487 G>A maps to NM_198566.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr5:56212662 T>G maps to NM_153706.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:93856568 A>C maps to ENST00000513200 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:2752748 A>T maps to NM_178569.2 K72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr5:43040043 C>A maps to NM_001014279.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr5:43040112 A>C maps to NM_001014279.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr5:154214194 G>A maps to NM_032385.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:156770190 G>A maps to NM_001001343.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:156770491 G>T maps to NM_001001343.3 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:37181061 C>A maps to NM_023073.3 E1823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr5:37169104 G>A maps to NM_023073.3 L2341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr5:37162627 G>A maps to NM_023073.3 F2543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr5:64946651 G>A maps to NM_001093755.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr5:64931137 G>A maps to NM_001093755.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr5:41904483 C>G maps to NM_175921.4 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr5:41917316 G>A maps to NM_175921.4 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr5:41911178 G>T maps to NM_175921.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr5:139508126 C>T maps to NM_001007189.1 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr5:159821392 C>A maps to NM_022090.3 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:159821206 C>A maps to NM_022090.3 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:159821612 C>G maps to NM_022090.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr5:159821579 T>G maps to NM_022090.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr5:131796261 C>T maps to NM_001013717.1 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:41160244 G>T maps to NM_001115131.1 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr5:41159287 C>A maps to NM_001115131.1 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr5:41199908 C>A maps to NM_001115131.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr5:41159280 G>A maps to NM_001115131.1 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:41160390 C>A maps to NM_001115131.1 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr5:41158814 C>A maps to NM_001115131.1 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr5:41149486 G>A maps to NM_001115131.1 Q827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr6:11723675 G>C maps to NM_001143948.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:139363854 G>C did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:139363992 C>T maps to NM_021243.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr6:165715501 C>T maps to NM_144980.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr6:165715309 G>A maps to NM_144980.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr6:165715171 G>A maps to NM_144980.3 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:165715438 C>T maps to NM_144980.3 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr6:165715177 G>A maps to NM_144980.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr6:165711542 C>T maps to NM_144980.3 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:33679328 G>A maps to NM_032340.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:48036040 G>A maps to NM_001013732.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr6:47846395 G>A maps to NM_001013732.3 H728H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr6:48036106 G>A maps to NM_001013732.3 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:54025220 A>T maps to ENST00000502396 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr6:4073711 C>T maps to NM_173563.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr6:31079538 G>A maps to NM_014070.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr6:74161324 G>A maps to NM_138441.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr6:43476147 C>T maps to NM_001012974.1 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr6:88127959 C>T maps to NM_001031743.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:88144768 C>T maps to NM_001031743.2 Q498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:88127993 C>A maps to NM_001031743.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr6:88126411 G>A maps to NM_001031743.2 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr6:97694536 T>C maps to NM_198468.2 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr6:97677199 G>A maps to NM_198468.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr6:97677101 G>C maps to NM_198468.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr6:97621032 G>A maps to NM_198468.2 S915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr6:121615731 T>C maps to ENST00000275159 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr6:121526219 C>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:121562641 T>A maps to ENST00000275159 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr6:121544495 A>C maps to ENST00000275159 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr6:127796905 G>A maps to NM_001012279.2 S755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:127797100 C>T maps to NM_001012279.2 A690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr6:109481811 G>T maps to NM_173830.4 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr6:110636639 A>G maps to NM_001123364.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:110567451 G>A maps to NM_001123364.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:110567268 C>T maps to NM_001123364.1 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr6:2623873 G>A maps to NM_152554.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr6:118790379 T>C maps to NM_001042475.2 K703K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr6:118790382 G>C maps to NM_001042475.2 S702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:118887219 G>C maps to NM_001042475.2 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:74073397 C>T maps to NM_001017361.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:36285133 C>T maps to NM_001010903.4 *653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:36294356 C>T maps to NM_001010903.4 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:31691749 C>T maps to NM_138272.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr6:31692647 T>G maps to NM_138277.1 *223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr6:31691641 C>G maps to NM_138272.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr6:31736951 G>C maps to NM_025258.2 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:31743182 C>T maps to NM_025258.2 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr6:127911330 A>G maps to NM_001010905.1 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr6:127899829 G>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:24718800 G>A maps to NM_030939.4 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:39082852 A>G maps to NM_018322.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr6:170156466 C>T maps to NM_018341.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:35706177 G>A maps to NM_145028.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr6:35715211 G>A did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr6:151859253 C>G maps to ENST00000367290 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr6:151936745 G>T maps to ENST00000367290 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:151939224 A>G maps to ENST00000367290 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:151939128 G>A maps to ENST00000367290 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr6:151936669 C>A maps to ENST00000367290 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr5:40958325 G>A maps to NM_000587.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:40723653 G>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:40498770 A>G maps to NM_001193311.1 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:40228094 A>G maps to NM_001193311.1 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr7:86826066 C>T maps to NM_024315.2 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr7:42950073 G>A maps to NM_001099858.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:6639934 G>T maps to NM_024067.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr7:23339006 C>T maps to NM_138446.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr7:25191213 C>G did not map to a codon.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:148288031 T>G maps to NM_145304.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr7:148288040 C>G maps to NM_145304.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr7:39606029 C>T maps to NM_020192.3 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:39606100 C>G maps to NM_020192.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:99753353 C>T maps to NM_018275.3 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:99754718 G>A maps to NM_018275.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:100033361 G>A maps to NM_145030.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr7:100033540 C>T maps to NM_145030.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr7:134852540 A>G maps to NM_024033.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:1040141 C>T maps to NM_032350.5 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr7:1037376 C>A maps to NM_032350.5 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr7:100084785 G>A maps to ENST00000423930 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:100816657 C>A maps to NM_198571.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr7:100817863 G>A maps to NM_198571.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr7:100815521 G>A maps to NM_198571.2 H316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:112124969 C>T maps to NM_182597.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:139030440 G>A maps to NM_197964.3 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr7:120906435 C>T maps to NM_024913.4 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:120629788 G>C maps to NM_024913.4 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:120740126 G>A maps to NM_024913.4 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:112555358 A>G did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:89939441 C>T maps to NM_001039706.2 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr7:89915650 G>T maps to NM_001039706.2 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr7:89915640 C>G maps to NM_001039706.2 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr7:89917651 A>G maps to NM_001039706.2 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:89887456 C>T maps to NM_001039706.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr7:89939465 A>T maps to NM_001039706.2 K914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr7:108524577 C>G maps to NM_001024607.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr1:57340683 C>A maps to NM_000562.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:57351626 A>T maps to NM_000562.2 K295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:57399014 G>A maps to NM_000066.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:57420404 G>A maps to NM_000066.2 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:57422502 A>G maps to NM_000066.2 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:57415425 C>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:57411575 C>G maps to NM_000066.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr1:57425788 T>C maps to NM_000066.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr9:139840947 G>C maps to NM_000606.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr9:139839825 G>A maps to NM_000606.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr8:144124444 C>G maps to NM_173687.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:144124660 G>A maps to NM_173687.2 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:144124661 G>T maps to NM_173687.2 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:144124505 T>C did not map to a codon.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr8:146278030 G>T maps to ENST00000444534 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:33369603 G>A maps to NM_001102401.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr8:33357859 G>A maps to NM_001102401.1 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:33361333 G>A maps to NM_001102401.1 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:444570 C>T maps to NM_175075.3 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:67796028 C>T maps to NM_173518.4 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr8:67808487 C>T maps to NM_173518.4 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr8:67408706 C>T maps to NM_152765.3 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:144654309 A>G maps to NM_001100878.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr8:144650813 G>A maps to NM_001100878.1 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr8:144652141 C>T maps to NM_001100878.1 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr8:124253496 G>C maps to NM_032847.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr8:12878577 C>T maps to NM_020844.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr8:12878805 G>A maps to NM_020844.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:12870298 C>A maps to NM_020844.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:117954795 G>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:39306835 G>C maps to NM_001737.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr5:39341763 A>G maps to NM_001737.3 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr5:39364512 G>T maps to NM_001737.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr9:35664476 G>C maps to NM_032818.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr9:35665130 C>A maps to NM_032818.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:98678716 G>A did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:138391607 C>G maps to NM_001048265.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:131038471 C>T maps to NM_001040011.1 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr9:104239326 C>T maps to NM_032342.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr9:104238219 C>T maps to NM_032342.1 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr9:35043436 C>T maps to NM_203299.2 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr9:35042304 C>G maps to NM_203299.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:35045472 G>A maps to NM_203299.2 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:72459431 G>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:72435948 T>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr9:112963680 C>G maps to NM_001012993.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:100672659 C>T maps to NM_016481.3 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr9:140173371 C>T maps to NM_017723.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr9:89771558 T>C maps to NM_001001709.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:135357755 G>A maps to NM_207417.1 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:135447845 G>A maps to NM_207417.1 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr9:135374894 C>G maps to NM_207417.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:34611110 G>A maps to NM_148179.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr9:97717509 C>A maps to NM_001193329.1 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr9:97823002 C>T maps to NM_001193329.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr9:140510166 G>C maps to NM_032937.4 S162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:111903625 G>A maps to NM_014334.2 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr9:111903701 C>T maps to NM_014334.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr9:111903626 A>G maps to NM_014334.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr9:116185749 G>T maps to ENST00000451722 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:91606128 G>A maps to NM_001001938.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr9:111795699 A>G maps to NM_032012.3 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr9:214661 G>A maps to NM_152569.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:4605409 C>T maps to ENST00000454239 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr9:4604232 T>A maps to ENST00000454239 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:4625425 A>G maps to ENST00000454239 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:90502038 C>T maps to NM_178828.4 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr9:90500019 G>A maps to NM_178828.4 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr9:90500808 A>C maps to NM_178828.4 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr9:90499866 G>T maps to NM_178828.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr9:90501078 C>T maps to NM_178828.4 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:90501483 C>T maps to NM_178828.4 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr9:115456513 C>T did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr9:26861106 G>A maps to NM_024828.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr9:114500746 T>A maps to NM_173521.3 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr9:114538158 G>A maps to NM_173521.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr9:114470139 T>C maps to NM_173521.3 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr9:139734267 C>T maps to NM_001173988.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr9:139734270 C>T maps to NM_001173988.1 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr9:117399280 C>G maps to ENST00000374049 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr9:117389235 A>T maps to ENST00000374049 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr9:117400876 G>T maps to ENST00000374049 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr9:15778998 G>T maps to NM_173550.2 G978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr9:15695294 G>C maps to NM_173550.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:15777661 C>G maps to NM_173550.2 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:15971755 C>T maps to NM_173550.2 P1301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:136260785 C>A maps to NM_153710.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr9:136253247 C>G maps to NM_153710.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:135602854 T>A maps to NM_152572.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:135698628 C>T maps to NM_152572.2 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr8:86240820 G>A maps to NM_001738.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr17:49825157 G>A maps to NM_001082534.1 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr17:49713311 A>G maps to NM_001082534.1 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:49143423 C>G maps to NM_001217.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr15:63637702 G>A maps to NM_001218.3 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr15:63620321 G>C maps to NM_001218.3 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:150235225 T>G maps to NM_012113.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr8:86389458 G>A maps to NM_000067.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:86386584 G>T maps to NM_000067.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:86386566 C>T maps to NM_000067.2 H122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr8:86392936 T>C maps to NM_000067.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr8:86388067 G>A maps to NM_000067.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr8:86360301 G>T maps to NM_005181.3 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr8:86358381 G>A maps to NM_005181.3 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr16:87960540 G>C maps to NM_001739.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr23:15792451 A>T did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:9022704 C>T maps to ENST00000413627 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:66881110 T>C maps to NM_005182.2 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr8:61178600 C>T maps to NM_004056.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr8:61192398 T>C maps to NM_004056.4 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr13:49924926 C>A maps to NM_001079670.1 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr13:49957000 C>A maps to NM_001079670.1 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:227170662 C>T maps to NM_020247.4 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr22:24447310 G>T maps to NM_012295.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr22:24463126 C>T maps to NM_012295.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr22:24483644 G>A maps to NM_012295.3 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr22:24463008 C>G maps to NM_012295.3 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr22:24563211 G>A maps to NM_012295.3 Q1871Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr22:24480530 G>T did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr22:24432586 A>G maps to NM_012295.3 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:24573697 C>T maps to NM_012295.3 F2144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:24515340 C>T maps to NM_012295.3 N1436N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr18:20833899 C>T maps to NM_001100619.2 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr18:20833869 C>G maps to NM_001100619.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:67223245 C>T maps to NM_145200.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:67225047 C>T maps to NM_145200.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr19:48543883 G>A maps to NM_019855.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr22:30125449 C>T maps to NM_182527.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr22:30125494 C>T maps to NM_182527.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr18:21735866 G>C maps to NM_138644.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:64936609 G>A maps to ENST00000371073 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr19:13411422 C>T maps to NM_023035.2 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr19:13470440 C>G maps to NM_023035.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr19:13366019 C>A maps to NM_023035.2 P1552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr19:13346064 C>T maps to NM_023035.2 L1701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:13411467 G>A maps to NM_023035.2 D729D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:13368241 G>T maps to NM_023035.2 I1508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr19:13414686 G>A maps to NM_023035.2 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:13395973 C>T maps to NM_023035.2 E1204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:13446696 C>T maps to NM_023035.2 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr19:13476248 C>T maps to NM_023035.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr19:13446717 G>A maps to NM_023035.2 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr9:140919616 C>T maps to ENST00000277549 V1094V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr9:141006848 G>A did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:140946542 G>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:140901298 G>A maps to ENST00000277549 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr9:140811747 C>T maps to ENST00000277549 C277C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-F7-A624-01A-22D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:140938226 T>C maps to ENST00000277549 S1097S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr9:140772597 C>G maps to ENST00000277549 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr9:140807637 T>C maps to ENST00000277549 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:2613672 C>T maps to ENST00000399634 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr12:2614033 G>A maps to NM_199460.2 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr12:2659196 G>T maps to NM_199460.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr12:2778130 C>T maps to NM_199460.2 S1600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr12:2602464 C>A maps to NM_199460.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr12:2690863 G>T maps to NM_199460.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr12:2760858 C>A maps to NM_199460.2 V1381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:2566792 G>A maps to NM_199460.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr12:2721073 C>T maps to NM_199460.2 Y1261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr12:2694583 G>T maps to NM_199460.2 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:2786305 G>A maps to NM_199460.2 Q1673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:2797905 G>A maps to NM_199460.2 G2109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr12:2602461 C>T maps to NM_199460.2 H341H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr12:2714951 G>A maps to NM_199460.2 K1072K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr3:53844074 G>A maps to NM_001128840.1 W1981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:53699744 C>A maps to NM_001128840.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr3:53834347 G>T maps to NM_001128840.1 E1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:53834388 C>T maps to NM_001128840.1 F1679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:53785837 C>T maps to NM_001128840.1 P1193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr3:53837488 G>T maps to NM_001128840.1 R1825R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:181767768 G>A maps to ENST00000357570 E2247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:181690997 C>A maps to ENST00000357570 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:181702848 C>T maps to ENST00000357570 P1075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr1:181479696 G>A maps to ENST00000357570 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:181690907 G>A maps to ENST00000357570 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr1:181702069 G>T maps to ENST00000357570 E950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:181701837 C>T maps to ENST00000357570 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:181702878 G>T maps to ENST00000357570 V1085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:181767619 C>T maps to ENST00000357570 Q2198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:181731777 C>A maps to ENST00000357570 I1558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr23:49089766 G>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:49075888 G>T did not map to a codon.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr23:49065125 G>A did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr23:49066461 G>T did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:49076129 C>T did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:49067780 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:49065124 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:49084738 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:49083522 C>A did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:49070717 C>G did not map to a codon.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr23:49087677 C>T did not map to a codon.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr23:49065817 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:48649386 G>A maps to NM_018896.3 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr17:48649308 C>T maps to NM_018896.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:48685318 G>A maps to NM_018896.3 E1548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr16:1250444 C>T maps to NM_021098.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr16:1265003 C>T maps to NM_021098.2 Y1654Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr22:40075137 C>T maps to NM_021096.3 D1694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr22:40060148 C>T maps to NM_021096.3 G1217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr22:40060133 G>A maps to NM_021096.3 T1212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr22:40066098 C>A maps to NM_021096.3 I1417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr22:40061517 G>A maps to NM_021096.3 A1289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr1:201012530 G>T maps to NM_000069.2 V1642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:201046134 G>C maps to NM_000069.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:201021713 G>A maps to NM_000069.2 T1308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:201009438 C>A maps to NM_000069.2 E1764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr1:201061190 G>A maps to NM_000069.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr1:201008964 C>T maps to NM_000069.2 R1872R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:81620520 A>T maps to NM_000722.2 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:81693670 C>G did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr7:81714096 G>A maps to NM_000722.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:81620502 G>C maps to NM_000722.2 Y598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr7:81589060 T>C maps to NM_000722.2 R1017R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:81579767 G>T maps to NM_000722.2 I1072I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:81978943 C>T maps to NM_000722.2 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr7:81593572 C>A maps to NM_000722.2 E893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr7:81589081 C>G maps to NM_000722.2 G1010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:50421636 G>A maps to ENST00000435965 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr3:50402369 C>T maps to ENST00000435965 Q1090Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr3:50418477 T>C maps to ENST00000435965 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:54604085 C>T maps to NM_018398.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:1995442 G>T maps to NM_172364.4 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:2027516 G>A maps to NM_172364.4 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr12:1902907 G>A maps to NM_172364.4 C1109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:2016672 G>A maps to NM_172364.4 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:2019089 T>C maps to NM_172364.4 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:18807303 C>A maps to NM_201596.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr10:18827230 C>G maps to NM_201596.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr10:18827253 C>G maps to NM_201596.2 S483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr12:49219231 C>T maps to NM_000725.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr12:49220821 C>T maps to NM_000725.2 Y352Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr2:152954849 G>C maps to NM_000726.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr22:36960637 C>A maps to NM_006078.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr22:37098537 C>A maps to NM_006078.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr22:36960514 G>A maps to NM_006078.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr16:24372923 C>A maps to NM_006539.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr16:24366277 C>T maps to NM_006539.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr16:24366271 G>A maps to NM_006539.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr16:24373117 C>T maps to NM_006539.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr17:65026798 C>T maps to NM_014405.3 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr17:65026897 C>G maps to NM_014405.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr17:64961155 C>T maps to NM_014405.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:64881044 G>A maps to NM_014404.1 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr17:64881203 C>T maps to NM_145811.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:54496184 G>A maps to NM_145814.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr19:54515286 G>T maps to NM_145814.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:54445348 C>G maps to NM_031896.4 Y210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:54445545 G>A maps to NM_031896.4 *276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:54418658 C>A maps to NM_031896.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:54416118 C>T maps to NM_031896.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:54444856 C>T maps to NM_031896.4 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr19:54416153 G>C maps to NM_031896.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr19:54416162 C>T maps to NM_031896.4 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr19:54483235 C>T maps to NM_031895.5 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:54466452 G>A maps to NM_031895.5 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr2:27459688 C>T maps to NM_004341.3 R1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:27463929 G>A maps to NM_004341.3 L1881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:27457393 G>A maps to NM_004341.3 Q1209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr2:27446490 G>C maps to NM_004341.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:115049406 C>G maps to NM_014333.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr11:115102136 G>A maps to NM_014333.3 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr11:115088673 T>C maps to NM_014333.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr3:85961649 C>T maps to NM_153184.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:85932570 C>G maps to NM_153184.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:85961534 T>G maps to NM_153184.3 L174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr3:86114797 C>T maps to NM_153184.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr3:86028419 C>A maps to NM_153184.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr1:159162469 C>G maps to NM_021189.3 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr3:62459952 T>C maps to ENST00000383709 R1124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:62467453 G>A maps to ENST00000383709 I1039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:122033248 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr7:121960382 T>G maps to NM_001167940.1 R1247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr6:7365750 C>A maps to NM_001170692.1 G715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:71418696 G>A maps to NM_001740.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr16:71406096 C>T maps to NM_001740.4 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:14990470 G>A maps to NM_001741.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr11:14989342 T>G maps to NM_001033953.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr11:14991581 G>A maps to NM_001741.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:15098957 C>A maps to NM_000728.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:15098969 C>G maps to NM_000728.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:54110136 C>T maps to NM_020898.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr12:54115807 C>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:54115879 G>A maps to NM_020898.2 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:46926687 C>A maps to ENST00000448105 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr17:46939665 G>A maps to ENST00000448105 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr17:46929947 G>A maps to ENST00000448105 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr7:93055793 C>T maps to NM_001164737.1 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:93106954 A>G maps to NM_001164737.1 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:93098028 G>A maps to NM_001164737.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:93108689 G>A maps to NM_001164737.1 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:93055849 G>A maps to NM_001164737.1 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:188247908 G>A maps to NM_005795.4 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:188225463 C>T maps to NM_005795.4 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:134635183 A>G maps to NM_033138.3 K618K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:105218106 G>A maps to NM_001001412.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr10:105218229 G>A maps to NM_001001412.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:105209671 G>A maps to NM_015916.4 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr10:105207025 G>C maps to NM_015916.4 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:71571223 C>T maps to NM_031468.3 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:71743728 C>T maps to NM_031468.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:71252798 C>G maps to NM_031468.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:71488752 C>T maps to NM_031468.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr7:128407639 C>T maps to ENST00000342367 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr3:9807480 C>T maps to NM_003656.3 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:12866499 C>T maps to NM_153498.2 H290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:209781227 C>A maps to NM_020439.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr1:209786147 C>A maps to NM_020439.2 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr5:149636339 C>T maps to NM_015981.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:149602273 C>G maps to NM_015981.3 *490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:114376955 C>T maps to ENST00000515496 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr4:114469878 A>G maps to ENST00000515496 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr5:110819998 G>A maps to NM_001744.4 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr17:3775882 C>T maps to ENST00000381771 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr12:121687598 C>T maps to NM_006549.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:138719359 G>A maps to ENST00000409386 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr9:138714637 G>A maps to ENST00000409386 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr9:138712792 G>A maps to ENST00000409386 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr9:138714832 C>T maps to ENST00000409386 E569E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:200801915 G>A maps to ENST00000236925 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:200826432 G>C did not map to a codon.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr1:7798136 G>A maps to NM_015215.2 K1259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr1:7798137 C>T maps to NM_015215.2 L1260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:6880242 C>T maps to NM_015215.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:7724544 G>C maps to NM_015215.2 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:7737773 C>T maps to NM_015215.2 H965H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:7724811 C>T maps to NM_015215.2 I735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:7725000 G>A maps to NM_015215.2 G798G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:7797325 T>C maps to NM_015215.2 C1118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr1:7724490 G>A maps to NM_015215.2 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr1:7724553 G>A maps to NM_015215.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr1:7812555 C>T maps to NM_015215.2 R1641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr1:7724086 C>T maps to NM_015215.2 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:7797458 C>T maps to NM_015215.2 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:7796588 C>T maps to NM_015215.2 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr17:4883248 G>A maps to NM_015099.3 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:4883213 G>T maps to NM_015099.3 S468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr12:67706498 G>A maps to NM_018448.3 L1194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:67699869 C>T maps to NM_018448.3 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr12:67699817 T>C maps to NM_018448.3 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr3:12861600 G>A maps to NM_001162499.1 R987R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:76989754 G>C maps to NM_138793.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:76991154 C>T maps to NM_138793.3 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:76993494 G>A maps to NM_138793.3 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr5:179143226 C>T maps to ENST00000415618 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr1:40536135 C>T maps to NM_001105530.1 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:17539516 A>G maps to NM_006366.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:17551729 G>A maps to NM_006366.2 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr6:17426914 G>A maps to NM_006366.2 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:85628365 C>T maps to NM_001747.2 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr11:64978755 G>A maps to NM_005186.3 *715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:64954684 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:241534073 C>G maps to NM_023083.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:241535794 C>T maps to NM_023083.3 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:241534550 C>A maps to NM_023083.3 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr2:241535884 C>T maps to NM_023083.3 D476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr2:30961323 C>T did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr2:30965218 C>T maps to ENST00000295055 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:223933089 C>G maps to NM_001748.4 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr15:42701995 C>T maps to NM_000070.2 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr15:42678428 C>T maps to NM_000070.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr11:76834876 C>T maps to ENST00000360841 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr23:110496307 C>G did not map to a codon.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr23:110492171 C>T did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr23:110491845 T>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:110494249 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:110494327 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr23:110495671 C>A did not map to a codon.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr23:110491149 G>C did not map to a codon.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr23:110491850 C>G did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:110495608 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:15274051 T>C maps to NM_014296.2 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr3:15287139 C>T maps to NM_014296.2 Q658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:230883367 G>A maps to NM_006615.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:36637119 C>A maps to NM_001749.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr16:55601231 A>G maps to NM_032330.1 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:30881779 T>C maps to NM_001002259.1 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:30876221 G>A maps to NM_001002259.1 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr12:30878928 G>A maps to NM_001002259.1 Q626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr12:30872090 A>C maps to NM_001002259.1 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:30878974 C>T maps to NM_001002259.1 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:5914739 C>A maps to ENST00000394521 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr12:75706696 T>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:35910093 G>A maps to NM_144647.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:113212163 G>T did not map to a codon.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:113189887 A>C maps to NM_006135.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr7:116546360 C>T maps to NM_006136.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr1:19705095 C>T maps to ENST00000375145 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr1:19670880 T>A maps to ENST00000375145 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:37888525 G>A maps to NM_014550.3 S889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr22:37892474 G>A maps to NM_014550.3 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr22:37892522 G>A maps to NM_014550.3 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr22:37891879 C>T maps to NM_014550.3 E730E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr7:2984094 C>T maps to NM_032415.4 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr7:2946385 G>A maps to NM_032415.4 Y1117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:2951811 G>A maps to NM_032415.4 A1046A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr7:2987214 G>A maps to NM_032415.4 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:78182029 C>T maps to NM_024110.2 Y967Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:78156548 C>T maps to NM_024110.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:78165219 C>T maps to NM_024110.2 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:78164613 G>A maps to NM_024110.2 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:40853725 G>A maps to NM_032587.3 K764K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr9:139264311 C>A maps to NM_052813.4 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr16:8952229 G>A maps to NM_014316.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:111290822 C>T maps to NM_018210.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:11031563 G>C maps to NM_199141.1 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:11030597 C>T maps to NM_199141.1 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr19:11032327 G>T maps to NM_199141.1 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr19:11027110 C>T maps to NM_199141.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:67191489 G>C maps to NM_001166222.1 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr11:3028177 G>A maps to NM_001014437.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr13:111340149 C>T maps to NM_024537.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr13:111299461 C>T maps to NM_024537.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr12:25308246 G>A maps to NM_018272.3 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:25297595 T>C maps to NM_018272.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:40914963 G>A maps to NM_170589.3 Q860Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr15:40954308 C>T maps to NM_170589.3 L2318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:40915395 C>T maps to NM_170589.3 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:40917520 C>T maps to NM_170589.3 Q1713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr15:40915623 G>A maps to NM_170589.3 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:41401989 C>G did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr23:41390288 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:41390336 T>G did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:41469158 C>T did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:41379815 C>G did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr16:2235117 G>T maps to NM_020764.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr16:2235156 C>G maps to NM_020764.3 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:2228625 G>A maps to NM_020764.3 S1407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr16:2237365 C>T maps to NM_020764.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr16:2231475 G>A maps to NM_020764.3 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:73498199 C>A maps to NM_020753.3 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr17:73500709 C>T maps to NM_020753.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr17:73499572 C>T maps to NM_020753.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr17:73498127 G>A maps to NM_020753.3 F1009F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr17:73498433 C>T maps to NM_020753.3 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr17:73498856 C>T maps to NM_020753.3 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr11:104900410 G>T maps to NM_033292.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr2:202050585 C>G maps to NM_032977.3 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:15164408 C>T maps to NM_012114.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr4:185550590 C>T maps to NM_032991.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:104819392 C>A maps to NM_001225.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:104869610 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:104878061 C>T did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr4:110612107 G>A maps to NM_001226.3 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr4:110610528 G>C maps to NM_001226.3 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr2:202149859 C>G maps to NM_001080125.1 S434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr2:202131410 C>T maps to NM_001080125.1 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr2:202151269 C>T maps to NM_001080125.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr2:202131410 C>T maps to NM_001080125.1 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr2:202149537 G>C did not map to a codon.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr2:202151269 C>T maps to NM_001080125.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:202137619 G>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:202137358 A>G did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr2:202131497 C>T maps to NM_001080125.1 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr2:202150038 C>T maps to NM_001080125.1 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:202151269 C>T maps to NM_001080125.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:202150029 C>T maps to NM_001080125.1 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr2:202136251 C>T maps to NM_001080125.1 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr2:202149972 C>T maps to NM_001080125.1 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr2:202149750 C>T maps to NM_001080125.1 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr2:202136241 C>A maps to NM_001080125.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr2:202137500 T>C did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:202151260 C>T maps to NM_001080125.1 Q521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr2:202151269 C>T maps to NM_001080125.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr2:202149972 C>T maps to NM_001080125.1 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr2:202137500 T>C did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr2:202149972 C>T maps to NM_001080125.1 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr2:202150038 C>T maps to NM_001080125.1 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr2:202136276 C>A maps to NM_001080125.1 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr2:202150038 C>T maps to NM_001080125.1 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr6:90578309 A>T maps to NM_012115.3 I1767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr1:160165805 G>A maps to NM_001231.4 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr3:122003854 C>T maps to NM_001178065.1 C1028C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:122003857 G>A maps to NM_001178065.1 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:122003884 G>A maps to NM_001178065.1 Q1038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr3:121973188 C>G maps to NM_001178065.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr20:55012463 C>A maps to NM_020356.3 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr20:55020993 G>A maps to NM_020356.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr20:55027485 C>T maps to NM_020356.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:10715870 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:10703258 C>T maps to NM_001079843.1 R1326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:10713621 G>C maps to NM_001079843.1 S831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr1:10715870 C>A did not map to a codon.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr11:65792842 G>A maps to NM_053054.3 H336H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr11:65793517 G>A maps to NM_053054.3 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr11:65788060 G>A maps to NM_053054.3 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:65789073 C>G maps to NM_053054.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr15:43927950 G>A maps to NM_172095.1 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:43940127 G>A maps to NM_172095.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr15:43924463 T>C maps to NM_172095.1 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr15:43927556 C>G did not map to a codon.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr15:43931100 C>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:134343828 G>A maps to NM_178019.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:134345141 C>A maps to NM_178019.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:26527433 G>A maps to NM_198137.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr1:26524862 C>T maps to NM_198137.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr14:92136189 G>A maps to NM_024764.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:38853161 C>T maps to NM_021185.4 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr19:38860882 C>A maps to NM_021185.4 A1066A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:38847128 C>T maps to NM_021185.4 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:38861430 G>C maps to NM_021185.4 *1160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr7:116166688 G>A maps to NM_001753.4 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr3:8787387 C>T maps to NM_001234.3 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr10:74234890 C>T maps to NM_006077.3 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr20:32212734 C>T maps to NM_005093.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr20:32232450 G>A maps to NM_005093.3 *605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr20:32217676 C>T maps to NM_005093.3 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr20:32212723 C>T maps to NM_005093.3 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr20:32212680 C>G maps to NM_005093.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr16:88945791 C>A maps to NM_005187.5 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:119103213 C>T maps to NM_005188.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr3:105421036 T>A maps to NM_170662.3 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr3:105572429 G>A maps to NM_170662.3 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:105586265 G>C maps to NM_170662.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr19:45296735 G>A maps to NM_012116.3 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:45284577 C>T maps to NM_012116.3 H205H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr18:70205524 G>A maps to NM_182511.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:169927999 A>T maps to NM_032783.4 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr21:44474013 G>A maps to ENST00000398168 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr17:46152375 C>G maps to ENST00000442683 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:46153469 G>A maps to ENST00000442683 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr17:77758351 C>T maps to NM_005189.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr17:77758171 G>A maps to NM_005189.2 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr17:77753182 G>T maps to NM_005189.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:77757829 G>A maps to NM_005189.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:77758180 C>T maps to NM_005189.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:26251376 G>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:39262786 T>C maps to NM_014292.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr22:39530550 G>C maps to NM_175709.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:77768667 G>T maps to NM_020649.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr17:77769024 C>T maps to NM_020649.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:14020718 C>T maps to NM_017721.4 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr19:14024039 C>G maps to NM_017721.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr19:14024410 A>G maps to NM_017721.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:52826197 G>A maps to NM_032449.2 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr4:15529186 C>T maps to NM_001080522.2 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr10:70531027 A>G maps to NM_018237.2 K788K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr10:70514523 T>A maps to NM_018237.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:70520822 C>T maps to NM_018237.2 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr10:70549468 G>T maps to NM_018237.2 E1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:89418757 T>A maps to NM_001008661.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr3:42906308 C>G maps to NM_001296.4 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr16:28596280 C>T maps to NM_138414.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr18:66504329 A>T maps to NM_024781.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr17:42979941 G>A maps to NM_213607.1 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:15132718 G>A maps to NM_173482.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr19:15131271 G>A did not map to a codon.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr19:56160924 C>T maps to NM_013301.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:35661157 C>T maps to NM_174923.2 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr9:35658693 C>G maps to NM_174923.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:219873819 G>A maps to NM_194302.2 D1541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:219900383 G>A maps to NM_194302.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:219903261 C>T maps to NM_194302.2 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr2:219892530 G>T maps to NM_194302.2 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:219878633 C>G maps to NM_194302.2 G1245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr10:74645513 C>T maps to NM_138357.1 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr18:47788586 T>C maps to NM_145020.3 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr18:47769416 G>A maps to NM_145020.3 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr5:114611170 A>T maps to NM_001040440.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:58301438 G>T maps to NM_014157.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:48801463 G>T maps to NM_144577.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr19:48800481 G>A maps to NM_144577.3 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr22:21989392 G>A maps to NM_152612.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr22:21989382 C>G maps to NM_152612.2 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr22:21989428 C>T maps to NM_152612.2 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr23:48925108 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:48921430 C>A did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:48921912 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:48924781 C>A did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:33370187 G>A maps to NM_032816.3 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:33444519 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr19:33390876 G>C maps to NM_032816.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:33444522 G>A maps to NM_032816.3 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr19:18054451 C>G maps to NM_001136203.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr5:68581235 A>G maps to NM_176816.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:23682550 G>T maps to NM_138771.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:31683299 G>A maps to NM_194300.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:31682744 C>A maps to NM_194300.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:31614169 G>T maps to NM_194300.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr7:31682831 C>A maps to NM_194300.2 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:42793454 C>T maps to NM_144719.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:13869956 G>T maps to NM_030818.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr19:13873752 G>C maps to NM_030818.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr19:13873431 G>A maps to NM_030818.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr7:92902041 A>G maps to NM_017667.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr7:92979233 A>T maps to NM_017667.2 V784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr7:92987684 C>T maps to NM_017667.2 I944I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr7:92926148 G>A did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:57761224 G>A maps to NM_032269.5 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr16:57760011 G>A maps to NM_032269.5 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:128446881 G>A maps to NM_022742.3 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr7:128446755 G>A maps to NM_022742.3 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr7:128445931 C>T maps to NM_022742.3 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr7:128441259 G>T maps to NM_022742.3 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:79637312 C>T maps to NM_199287.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:109408220 G>A maps to NM_144978.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:109405344 A>T maps to NM_144978.1 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr2:109463282 G>A maps to NM_144978.1 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:109473415 G>T maps to NM_144978.1 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr3:123633808 C>T maps to NM_022757.4 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr2:179732806 G>T maps to NM_173648.3 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr2:179730505 G>A maps to NM_173648.3 D904D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr2:179718335 C>A maps to NM_173648.3 E1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:74709691 G>A maps to ENST00000393965 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:74702466 A>G maps to ENST00000393965 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr2:74709079 G>A maps to ENST00000393965 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr17:16593776 C>T maps to NM_014695.1 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr17:16638737 G>A maps to NM_014695.1 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr7:76871151 C>G maps to NM_020879.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr7:76891593 T>C maps to NM_020879.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:106152106 G>C maps to NM_001008723.1 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr10:106139932 G>A maps to NM_001008723.1 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr10:106153148 A>G maps to NM_001008723.1 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr10:106113660 T>A maps to NM_001008723.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:106118283 A>G maps to NM_001008723.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:159196816 C>T maps to NM_138803.3 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:124845048 A>T maps to NM_025004.2 K192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:124829769 G>A maps to NM_025004.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr11:124857972 C>T maps to NM_025004.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:197534572 C>G maps to NM_001080539.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr2:197565897 A>G maps to NM_001080539.1 K563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:11545747 C>T maps to NM_145045.4 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr19:11537571 C>T maps to NM_145045.4 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:11532485 G>A maps to NM_145045.4 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:49912473 G>A maps to NM_144688.4 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:77283401 C>A maps to NM_001042784.1 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:11464485 G>T maps to ENST00000427879 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:133378998 G>A did not map to a codon.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr1:93698027 C>T maps to NM_206886.2 Q898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:159850409 T>C maps to NM_012337.2 K326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:159850453 G>A maps to NM_012337.2 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr1:159842918 C>T maps to NM_012337.2 E464E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:159857774 G>T maps to NM_012337.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:49099870 C>T did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:49104138 C>G did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:49104912 C>T did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:44461304 C>T maps to NM_152499.1 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:3683958 C>T maps to NM_152492.2 Q565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:139106385 G>A maps to NM_015439.2 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr6:139101030 C>T maps to NM_015439.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:74559049 G>A maps to ENST00000321288 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:74536423 C>T maps to ENST00000321288 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr15:74536342 G>A maps to NM_025055.3 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:27384411 C>T maps to NM_030771.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr3:49292910 G>A maps to NM_178173.3 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr3:49278822 G>T did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:126138593 C>T maps to ENST00000505024 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr12:96288807 G>T maps to NM_182496.2 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:96312653 C>A maps to NM_182496.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr12:96310925 C>T maps to NM_182496.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:180349271 G>T maps to NM_181426.1 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr3:180377523 C>A maps to NM_181426.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr3:180372657 C>A maps to NM_181426.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:180381720 A>T maps to NM_181426.1 Y48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr3:180397108 C>G maps to NM_181426.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr17:78063684 T>G did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr17:78073372 G>A maps to NM_017950.2 Q1076Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr12:94761951 G>C maps to NM_001042399.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr17:8638908 C>A maps to NM_144681.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr17:8638890 C>A maps to NM_144681.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr17:62533806 T>C maps to NM_138363.1 D792D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:62521961 C>T maps to NM_138363.1 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:63898392 G>A maps to NM_145036.3 N680N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr17:64062992 A>G maps to NM_145036.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr17:63848086 C>T maps to NM_145036.3 Q743Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr17:61830157 C>A maps to NM_020198.2 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:61843412 T>C maps to NM_020198.2 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr17:61843400 G>T maps to NM_020198.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:128755857 G>A maps to NM_024768.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr3:128755944 G>A maps to NM_024768.2 Q525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr3:191098614 A>C did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr3:191098614 A>C did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr3:48476324 G>A maps to NM_024661.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr3:113172486 C>T maps to NM_144718.3 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:113172676 G>C maps to NM_144718.3 S593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr3:107097119 C>A maps to NM_032600.2 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:107097153 C>T maps to NM_032600.2 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr17:80156246 T>C maps to ENST00000445854 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr17:80130727 G>A maps to ENST00000445854 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:122090638 G>C maps to NM_001017928.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:61592412 T>A did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:111336786 C>T maps to NM_152591.1 Y400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr12:111311765 G>A did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:111296482 G>A maps to NM_152591.1 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:111318960 G>A maps to NM_152591.1 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:111342494 C>T maps to NM_152591.1 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:120530922 C>T maps to NM_207311.2 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr12:120510421 C>T maps to NM_207311.2 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:3079403 C>T maps to NM_001103175.1 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:49312667 G>C maps to NM_033124.4 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:49312667 G>A maps to NM_033124.4 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:56651599 G>A maps to NM_001141947.1 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr3:56649287 A>T maps to NM_001141947.1 K567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:93088642 C>T maps to NM_181645.3 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr11:93141394 A>G did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr18:52571633 G>A maps to NM_025214.2 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:32676498 G>C maps to NM_001008391.2 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr11:32635160 G>T maps to NM_001008391.2 Y901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr11:32635517 C>T maps to NM_001008391.2 E782E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr12:550056 C>T maps to NM_032358.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:547672 T>C maps to NM_032358.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:774144 G>T maps to NM_001031737.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:774150 T>C maps to NM_001031737.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:46914603 C>T maps to NM_032040.3 W488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:46915887 C>T maps to NM_032040.3 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr19:46915758 G>A maps to NM_032040.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:46914993 G>A maps to NM_032040.3 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr19:46914993 G>A maps to NM_032040.3 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr19:46915422 C>G maps to NM_032040.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:46914651 C>T maps to NM_032040.3 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr3:112324347 G>A maps to ENST00000447230 Y934Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr3:112358038 C>T maps to ENST00000447230 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:112358404 C>T maps to ENST00000447230 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:86108779 C>T maps to NM_001156474.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr11:96117452 T>C maps to NM_024725.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:56602976 T>A maps to NM_001080433.1 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:56419778 G>A maps to NM_001080433.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:56420318 C>T maps to NM_001080433.1 H328H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:56419697 G>A maps to NM_001080433.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr2:56420051 G>A maps to NM_001080433.1 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:56599549 C>T maps to NM_001080433.1 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr11:65658861 G>A maps to NM_006848.2 *203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr11:60609626 G>T maps to NM_024098.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr11:66359151 G>A maps to NM_018219.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:66358521 C>T maps to NM_018219.2 W655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:66359328 G>A maps to NM_018219.2 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:55561401 A>T maps to ENST00000436346 L852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:55570924 G>A maps to ENST00000436346 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr2:55549804 G>A maps to ENST00000436346 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr11:64109500 C>T maps to NM_032251.5 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr11:64112191 C>T maps to NM_032251.5 Q727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:64109473 T>C maps to NM_032251.5 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:64109584 T>A maps to NM_032251.5 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr11:64108645 C>G maps to NM_032251.5 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr14:91772192 G>A maps to NM_001080414.2 S1091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:91780145 G>A maps to NM_001080414.2 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:91787564 G>A maps to NM_001080414.2 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:91770130 G>A maps to NM_001080414.2 A1183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:91738969 C>G maps to NM_001080414.2 *2029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr14:91749740 G>C maps to NM_001080414.2 S1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr19:47763904 A>T maps to NM_015603.2 K91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:47761886 G>T maps to NM_015603.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:82985035 C>G did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr12:28702084 G>A maps to NM_018318.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:118758499 G>C maps to NM_019044.4 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:118698846 A>G maps to NM_019044.4 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr19:4267628 G>A maps to NM_018074.4 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr4:7043918 C>T maps to NM_153376.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:41828508 C>T maps to NM_052848.1 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr19:41825479 G>A maps to NM_052848.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr19:41828538 C>T maps to NM_052848.1 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:41828523 C>T maps to NM_052848.1 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:169031116 C>G maps to NM_017785.4 S575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:31110479 G>A maps to NM_001105564.1 V835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr6:31122386 T>A maps to NM_001105564.1 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr6:31118255 C>T maps to NM_001105564.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr9:36170587 C>T maps to NM_005893.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:36170743 C>T maps to NM_005893.2 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr9:36169708 C>T maps to NM_005893.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:6291977 C>T maps to NM_176875.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr11:6290926 T>G maps to NM_176875.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:34308414 G>A maps to NM_004590.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr17:34304697 C>T maps to NM_004590.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr17:34398364 C>A maps to NM_002988.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr9:34691100 G>C maps to NM_006274.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr17:32582400 G>T maps to NM_002982.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:228680243 C>A maps to NM_004591.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr17:34340341 G>T maps to NM_005064.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:8122781 C>T maps to NM_005624.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr5:43388546 C>T maps to NM_148672.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:43382138 G>T maps to NM_148672.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:32647333 G>A maps to ENST00000394620 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr17:32647354 G>A maps to ENST00000394620 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr13:37011962 C>T maps to NM_003914.3 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr13:37011779 C>A maps to NM_003914.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr13:37011902 G>A maps to NM_003914.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr4:122740556 A>T maps to NM_001237.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:68473451 G>A maps to NM_031966.2 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr14:20781878 G>A maps to NM_182849.1 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:50089688 C>T did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:50094304 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:50053262 G>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:50052940 A>T did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:50052897 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:50052791 G>T did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:50053213 A>G did not map to a codon.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr23:50053853 T>G did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr23:50028248 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:50089706 G>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:50052854 T>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:50053221 A>C did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr23:50051786 T>A did not map to a codon.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr23:50052073 C>G did not map to a codon.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr23:50052862 T>C did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:50054109 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr23:50054267 A>G did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:50053731 C>G did not map to a codon.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr23:50052278 G>A did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr11:69462870 C>T maps to NM_053056.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr11:69457890 C>T maps to NM_053056.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr11:69462816 C>T maps to NM_053056.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr12:4409144 C>T maps to NM_001759.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:4398026 C>G maps to NM_001759.3 Y197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr19:30314570 C>T maps to NM_001238.1 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr19:30312986 G>T maps to NM_001238.1 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr8:95897702 G>C maps to NM_057749.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:95893860 T>C maps to NM_057749.1 *405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:2495572 G>A maps to NM_001761.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr4:78079684 G>C did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:78079753 C>G maps to NM_004354.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:159680600 G>A maps to NM_024565.5 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr14:99961944 C>T maps to ENST00000437596 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:1325616 G>A maps to NM_030937.4 P333P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CN-A641-01A-11D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr1:1334479 G>A maps to NM_030937.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:1323209 G>A maps to NM_030937.4 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:208576751 G>T maps to ENST00000295414 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:55669216 T>C maps to ENST00000442196 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr15:55657498 G>A maps to ENST00000442196 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr15:55677907 G>T maps to ENST00000442196 S22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr15:55681564 C>A maps to ENST00000442196 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:40832611 C>T maps to NM_016602.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:46399947 G>A maps to NM_001123041.2 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr3:46307686 A>T maps to NM_178328.1 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr3:46307075 C>T maps to NM_178328.1 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr3:32995556 T>C maps to NM_005508.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:32995561 G>A maps to NM_005508.4 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr17:38711203 G>A maps to NM_001838.3 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr3:39374085 C>T maps to NM_005201.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:39374448 C>T maps to NM_005201.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr3:39374724 T>G maps to NM_005201.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:45942753 G>A maps to NM_031200.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr3:132319325 C>T maps to NM_178445.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:132319824 C>G maps to NM_178445.1 S195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr4:139966006 A>C maps to NM_012118.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr4:139965865 C>T maps to NM_012118.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:139966177 C>T maps to NM_012118.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr12:69993769 C>T maps to NM_006431.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr2:62096645 G>A maps to NM_006430.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:62096655 A>G maps to NM_006430.2 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr2:62104183 C>T maps to NM_006430.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:10256235 G>A maps to NM_012073.3 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:10258520 A>G maps to NM_012073.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:56120138 C>T maps to NM_001762.3 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr7:56129469 C>T maps to NM_001762.3 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr17:33288391 G>C maps to NM_006584.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:33269643 G>A maps to NM_006584.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:73470150 C>G maps to NM_006429.3 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr22:17072996 G>A maps to NM_014406.4 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr22:17072822 G>A maps to NM_014406.4 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr22:17073428 T>A maps to NM_014406.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr22:17071880 G>A maps to NM_014406.4 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr22:17072849 G>A maps to NM_014406.4 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:117560847 C>T maps to NM_004258.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr6:74524816 C>G maps to NM_133493.3 L1294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr6:74492436 G>A maps to NM_133493.3 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:7640426 T>G maps to NM_004244.4 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:7653981 C>T maps to NM_004244.4 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:7649407 C>G did not map to a codon.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr12:7639149 G>A maps to NM_004244.4 H801H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr12:7651746 C>T maps to NM_004244.4 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:7556293 G>A maps to ENST00000416109 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr12:7559176 G>A maps to ENST00000416109 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:7548985 C>T maps to ENST00000416109 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:7548991 C>G maps to ENST00000416109 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr5:66492457 G>A maps to NM_005582.2 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr16:28943928 C>A maps to NM_001178098.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:158227271 A>T maps to NM_001763.2 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:158226597 C>G maps to NM_001763.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:158225911 G>A maps to NM_001763.2 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr1:158299852 C>T maps to NM_001764.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:158262650 C>T maps to NM_001765.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:158151353 C>T maps to NM_001766.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:158151870 C>T maps to NM_001766.3 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:158153925 C>T maps to NM_001766.3 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr1:158323795 C>T maps to NM_030893.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr1:117297442 T>A maps to NM_001767.3 Y84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr3:112064024 C>G maps to NM_001004196.2 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:112647681 C>A maps to NM_138806.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:112648187 A>G maps to NM_138806.3 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr3:112548232 T>C did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr19:7809919 G>A maps to NM_021155.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:7810692 C>T maps to NM_021155.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr19:35832024 C>T maps to NM_001771.3 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:35828817 G>A maps to NM_001771.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr19:35832794 G>A maps to NM_001771.3 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr18:67614186 G>A maps to NM_006566.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:167408591 G>A maps to NM_198053.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr1:167409930 G>C maps to NM_198053.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:167400950 G>A maps to NM_198053.2 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:66083526 C>T maps to NM_020404.2 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:66083844 C>T maps to NM_020404.2 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:6554305 G>A maps to NM_001242.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr2:204571442 C>T maps to NM_006139.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr6:47563618 G>A maps to NM_012120.2 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr16:30364371 C>T maps to NM_006110.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:72469963 C>T maps to NM_007261.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr17:72619722 G>C maps to ENST00000426295 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr17:72613587 C>T maps to ENST00000426295 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr17:72613476 C>T maps to ENST00000426295 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:72691917 G>A maps to ENST00000412086 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr17:72691255 G>T maps to ENST00000412086 Y299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr2:160639927 G>C maps to NM_001198759.1 L1681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr19:8367859 G>A maps to NM_016579.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:8367820 C>A maps to NM_016579.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:8369978 C>T maps to NM_016579.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:51742807 T>A maps to NM_001772.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:51729134 G>T maps to NM_001772.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:208061163 A>T maps to NM_001025109.1 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:208062191 C>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:80285971 C>T maps to NM_001127444.1 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr4:15835918 C>A maps to NM_001775.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:15850160 G>C did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:15850185 G>C maps to NM_001775.2 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:118184488 C>T maps to NM_000733.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:45910391 G>A maps to ENST00000423698 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:45910388 G>A maps to ENST00000423698 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:6909312 G>A maps to NM_000616.4 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr23:135741548 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr23:135741435 A>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:135741391 G>C did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:135741518 C>A did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:135741429 C>T did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:35222734 G>A maps to NM_000610.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:35218338 G>A maps to NM_000610.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:207966939 G>C maps to ENST00000441839 *374Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:111435055 G>T maps to NM_000560.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr1:207504537 G>A maps to NM_001114752.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:157805733 G>T maps to NM_005894.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:157804401 G>A maps to NM_005894.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr11:60780907 A>T maps to NM_006725.3 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr17:7483024 C>T maps to NM_001251.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr19:6586077 G>T maps to NM_001252.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:149782188 C>T did not map to a codon.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr19:42383228 G>A maps to NM_001783.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:2411679 C>T maps to NM_004356.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:44640600 C>A maps to NM_002231.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:160523209 G>A maps to NM_001184879.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:121838296 T>C maps to NM_175862.3 H302H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr2:87013079 G>T maps to ENST00000456996 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr2:87016464 G>T maps to ENST00000456996 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:87042813 G>A maps to NM_172213.3 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr20:23065974 G>A maps to NM_012072.3 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr20:23066031 G>A maps to NM_012072.3 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr3:111316965 G>C did not map to a codon.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr19:14517887 G>A maps to NM_078481.2 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr19:14512332 C>T maps to NM_078481.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:14513675 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:14513433 C>T maps to NM_078481.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:14508887 C>T maps to NM_078481.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr19:14507205 C>T maps to NM_078481.2 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:14507943 C>T maps to NM_078481.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:2644346 C>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:149963726 G>A did not map to a codon.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr13:49823088 G>A maps to NM_030911.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr13:49823101 G>T did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:43020962 G>C maps to NM_138477.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr15:43020902 G>T maps to NM_138477.2 I917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:43022881 C>T maps to NM_138477.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr10:12277055 C>T maps to NM_006023.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:12238300 A>T maps to NM_006023.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr10:12277091 C>T maps to NM_006023.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr9:99329077 C>T maps to NM_001077181.1 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:99285990 C>A maps to NM_033331.2 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr9:99314079 G>A maps to NM_033331.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:115002174 G>T did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr13:115007714 C>T maps to NM_003903.3 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr13:115004937 C>A maps to NM_003903.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:43825056 C>T maps to NM_001255.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:137666819 G>T maps to NM_001790.3 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr5:137626345 C>G maps to NM_001790.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr17:45219296 T>G maps to NM_001114091.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:45235605 G>A maps to NM_001114091.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:541374 T>C maps to NM_004359.1 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:10505717 C>A maps to NM_007065.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr9:4679815 G>T maps to NM_017913.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr9:4697875 C>T maps to NM_017913.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr1:22413013 A>G maps to NM_001039802.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:227300479 C>T maps to ENST00000366766 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr1:227261647 C>T maps to ENST00000366766 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:103416153 C>A maps to NM_006035.3 E1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr14:103438344 G>A maps to NM_006035.3 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr14:103410645 G>C maps to NM_006035.3 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr14:103410675 G>A maps to NM_006035.3 I1320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr11:64602836 C>T maps to NM_017525.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr11:64602887 C>G maps to NM_017525.2 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:64603994 C>G maps to NM_017525.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr11:64606236 T>C maps to NM_017525.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:64595053 C>T maps to NM_017525.2 L1365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr11:64602359 C>T maps to NM_017525.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:64597447 G>A maps to NM_017525.2 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:64603284 C>A maps to NM_017525.2 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:64599130 G>A maps to NM_017525.2 S1050S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr11:65088449 G>A maps to NM_006779.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr17:71282258 G>A maps to NM_012121.4 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:71281967 G>A maps to NM_012121.4 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr17:71281755 G>C maps to NM_012121.4 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr17:71281907 G>A maps to NM_012121.4 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr22:19470229 C>T maps to NM_001178010.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr17:38450240 A>G maps to NM_001254.3 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr17:38451699 T>C maps to NM_001254.3 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:91978659 G>A maps to NM_001134420.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr8:25346198 G>A maps to ENST00000434814 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:25325856 A>G maps to ENST00000434814 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:25365242 A>C maps to ENST00000434814 R1022R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr8:25319724 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:6958257 T>C maps to NM_031299.4 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:105477873 T>A maps to NM_145701.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr7:21956455 A>G maps to NM_018719.4 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:38161589 G>T maps to NM_018101.2 G78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr1:38158640 C>T maps to NM_018101.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:45127377 G>A maps to NM_022842.3 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr1:54607035 C>T maps to NM_201546.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:54610232 C>G maps to NM_201546.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr1:54606861 G>C maps to NM_201546.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr16:68849488 C>T maps to NM_004360.3 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:68867194 T>C maps to NM_004360.3 N814N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:24537585 C>T maps to NM_006727.3 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr5:24488014 C>A maps to NM_006727.3 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr5:24537630 G>A maps to NM_006727.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:24492956 G>C maps to NM_006727.3 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr5:24537630 G>A maps to NM_006727.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr5:24487860 G>A maps to NM_006727.3 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:24488014 C>T maps to NM_006727.3 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:24488038 C>T maps to NM_006727.3 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:24535388 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr5:24537717 A>G maps to NM_006727.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr5:24491934 A>G maps to NM_006727.3 D542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr5:24487948 G>A maps to NM_006727.3 Y730Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr16:64984724 G>A maps to NM_001797.2 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr16:65022109 C>A maps to NM_001797.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr16:64984855 G>A maps to NM_001797.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr16:65026866 C>A maps to NM_001797.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr16:65016075 A>G maps to NM_001797.2 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr16:65005484 G>A maps to NM_001797.2 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr16:65016141 G>A maps to NM_001797.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr16:65006888 C>T maps to NM_001797.2 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr16:65032723 A>G maps to NM_001797.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr16:64984709 G>A maps to NM_001797.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr16:65038543 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:65022212 G>A maps to NM_001797.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr16:64984718 C>A maps to NM_001797.2 L615L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-A6K1-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:65006864 T>C maps to NM_001797.2 K444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr16:65032648 G>A maps to NM_001797.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr5:21752112 G>T maps to NM_004061.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr16:83520130 C>T maps to ENST00000268613 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr16:83813621 C>T maps to ENST00000268613 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr16:83712012 G>T maps to ENST00000268613 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr16:83711848 C>T maps to ENST00000268613 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:89257809 C>T maps to NM_004933.2 H435H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:89254678 C>T maps to NM_004933.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr16:89251623 C>A maps to NM_004933.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr16:89261436 C>T maps to NM_004933.2 F773F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr16:66945109 C>G maps to NM_004062.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:95161032 C>T maps to NM_001144663.1 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:95174379 G>T maps to NM_001144663.1 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr8:95172203 T>A maps to NM_001144663.1 K516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr8:95182706 T>C maps to NM_001144663.1 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr5:19571722 C>T maps to NM_004934.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr5:19483428 G>A maps to NM_004934.3 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr5:19473363 C>A maps to NM_004934.3 G782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:19839080 G>A maps to NM_004934.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr5:19721468 G>A maps to NM_004934.3 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr5:19473640 C>T maps to NM_004934.3 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr5:19483517 C>A maps to NM_004934.3 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr5:19483610 G>A maps to NM_004934.3 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr18:64239252 G>T maps to NM_021153.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr18:64239323 T>A maps to NM_021153.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr18:64176483 C>G did not map to a codon.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr18:64172066 T>A maps to NM_021153.2 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr18:64178907 G>A maps to NM_021153.2 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr18:64172338 C>A maps to NM_021153.2 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr18:64178850 A>T maps to NM_021153.2 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr18:64202256 A>T maps to NM_021153.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr18:64172126 A>G maps to NM_021153.2 Y747Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr18:25585918 C>T maps to NM_001792.3 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr18:25589800 C>A maps to NM_001792.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr18:25593760 G>C maps to NM_001792.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:25570167 A>G maps to NM_001792.3 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr18:59221720 C>T maps to NM_031891.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr18:59221474 C>A maps to NM_031891.2 I651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr18:59195438 C>G maps to NM_031891.2 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr20:44839175 G>T maps to NM_021248.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr20:44839166 G>C maps to NM_021248.1 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:44803672 G>A maps to NM_021248.1 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr10:73553320 C>A maps to ENST00000398860 V2217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr10:73405727 C>T maps to ENST00000398860 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr10:73572553 C>G maps to ENST00000398860 V3185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr10:73537540 C>T maps to ENST00000398860 L1655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr10:73326582 C>T maps to ENST00000398860 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr10:73569778 C>T maps to ENST00000398860 F2980F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:73539196 C>T maps to ENST00000398860 D1792D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:73570314 G>A maps to ENST00000398860 L3027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr10:73406418 G>A maps to NM_052836.3 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr14:23518341 C>T maps to NM_022478.3 Q618Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:23523751 G>C maps to NM_022478.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:58571731 G>A maps to NM_177980.2 K645K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr20:58587739 G>A maps to NM_177980.2 A818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:58569539 T>C maps to NM_177980.2 N554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:68712541 G>T maps to NM_001793.4 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:68729191 G>A maps to NM_001793.4 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr16:68716357 G>T maps to NM_001793.4 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:68721544 C>T maps to NM_001793.4 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr16:68729735 C>T maps to NM_001793.4 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr16:68710360 C>T maps to NM_001793.4 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr20:60503416 C>T maps to NM_001794.2 Y647Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr20:60485512 C>T maps to NM_001794.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr20:60508097 G>A maps to NM_001794.2 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr20:60511841 C>T maps to NM_001794.2 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:66436579 G>A maps to NM_001795.3 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr16:66426223 G>A maps to NM_001795.3 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:31323024 C>T maps to NM_004932.2 D661D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:31323141 C>A maps to NM_004932.2 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:31316321 A>G maps to NM_004932.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:31302365 C>T maps to NM_004932.2 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr5:31323358 C>T maps to NM_004932.2 R773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr5:31317852 G>T maps to NM_004932.2 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr18:63547682 C>A maps to NM_004361.2 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr18:63547694 C>T maps to NM_004361.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr18:63526185 C>T maps to NM_004361.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr18:63489455 C>G maps to NM_004361.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr18:63491991 G>A maps to NM_004361.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr16:61935157 G>A maps to NM_001796.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr16:61687978 G>T maps to NM_001796.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr16:61859021 A>T maps to NM_001796.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:26885966 T>C maps to NM_016279.3 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:26885786 G>T maps to NM_016279.3 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:26890581 C>A maps to NM_016279.3 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:26906876 G>C maps to NM_016279.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr5:26885872 G>A maps to NM_016279.3 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr5:26885960 T>C maps to NM_016279.3 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr5:26885756 G>A maps to NM_016279.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr5:26988326 C>A maps to NM_016279.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr5:26881604 T>C maps to NM_016279.3 Q670Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr5:26906903 G>T maps to NM_016279.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:85961612 C>T maps to NM_033100.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:85961613 C>T maps to NM_033100.2 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr5:176018403 G>A did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:176005488 G>A maps to NM_001171976.1 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:176017685 G>A maps to NM_001171976.1 K1179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr5:176018455 C>A maps to NM_001171976.1 L1235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr5:176012979 C>T maps to NM_001171976.1 D920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:105624677 C>T maps to NM_152750.4 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr7:105664840 T>A maps to NM_152750.4 Y697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:621850 G>A maps to NM_021924.4 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr11:621407 C>T maps to NM_021924.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:1572345 C>T maps to ENST00000401097 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr1:1572326 G>A maps to ENST00000401097 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:40134275 C>T maps to NM_003718.4 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr7:40134009 C>T maps to NM_003718.4 Q1324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:90419959 C>T maps to NM_012395.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IF-01A-11D-A31L-08 chr2:202687544 G>A maps to ENST00000450471 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr2:202677238 C>T maps to ENST00000450471 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr12:96728557 A>G maps to NM_002595.4 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr12:96688774 A>C did not map to a codon.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr1:205495567 C>T maps to NM_212503.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:67275065 C>A maps to NM_005851.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:73998156 C>T maps to NM_001258.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr17:74001437 G>A maps to NM_001258.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr7:150752370 G>A maps to NM_004935.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr17:30815309 C>T maps to NM_003885.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr17:30815063 C>T maps to NM_003885.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:31967482 C>T maps to ENST00000357886 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:31967497 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr9:123210238 G>A maps to NM_018249.4 Q987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:123169395 G>C maps to NM_018249.4 L1619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr9:123239728 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:123313138 G>A maps to NM_018249.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:46051294 A>G did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr17:46053297 C>T maps to NM_176096.1 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr17:46053297 C>T maps to NM_176096.1 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:92300835 C>T maps to NM_001145306.1 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr7:92355094 G>A maps to NM_001145306.1 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr13:26975691 G>A maps to NM_001260.1 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr6:21000492 C>T maps to NM_017774.3 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr5:133644118 G>A maps to NM_001113575.1 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:18646648 G>A did not map to a codon.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr23:18646533 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:18622161 G>T did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:18602397 T>G did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr23:18626934 G>A did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr23:18593591 G>C did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:18622488 A>G did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:18638052 G>T did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:18631352 C>A did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr23:18668576 G>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:18616686 G>T did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr23:18606256 G>T did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr23:18622106 C>T did not map to a codon.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr12:12870949 G>A maps to NM_004064.3 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr12:12871105 G>A maps to NM_004064.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:21971208 T>A did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:21968241 C>T did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr9:21970970 G>T maps to NM_001195132.1 Y129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr9:21971095 C>A maps to NM_001195132.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr9:21968241 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr9:21968241 C>T did not map to a codon.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr9:21971095 C>A maps to NM_001195132.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr9:21971095 C>A maps to NM_001195132.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr9:21971207 C>T did not map to a codon.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr9:21971095 C>A maps to NM_001195132.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr9:21971152 C>A maps to NM_001195132.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr9:21968242 T>C did not map to a codon.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr9:21968241 C>T did not map to a codon.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:21970899 C>T did not map to a codon.
Alternatively spliced codon TCGA-CV-5444-01A-02D-1512-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr9:21970899 C>A did not map to a codon.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr9:21971207 C>T did not map to a codon.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr9:21971120 G>A maps to NM_001195132.1 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr9:21968241 C>T did not map to a codon.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr9:21971152 C>A maps to NM_001195132.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr9:21974798 C>A maps to NM_001195132.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:184367347 C>T maps to NM_017632.2 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr4:184366789 G>A maps to NM_017632.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:51439743 G>C maps to NM_078626.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr14:54868292 T>A maps to NM_005192.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr10:14867592 G>A maps to NM_001029954.2 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr5:115151944 G>A maps to NM_001801.2 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:125830979 C>A maps to ENST00000392693 E1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:139866495 G>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:139866413 G>T did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr23:139866349 G>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:139866429 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr23:139866461 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:139865976 C>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:139865994 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr23:139865844 C>G did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr23:139865949 C>G did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:139865919 C>T did not map to a codon.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr16:22358366 C>T maps to NM_001802.1 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr4:85525493 C>A maps to NM_001263.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr4:85538788 C>T maps to NM_001263.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:85562098 C>T maps to NM_001263.3 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:85530593 G>A maps to NM_001263.3 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:5166472 G>A did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:31084821 G>T maps to NM_001264.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr16:88874607 C>G maps to NM_030928.3 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr16:88873831 C>G maps to NM_030928.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:149562338 C>A maps to NM_001804.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:149562460 G>A maps to NM_001804.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:72667340 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:72667519 C>T did not map to a codon.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:4935983 G>A maps to ENST00000328908 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:4937971 G>A did not map to a codon.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr16:80718468 G>A maps to NM_152342.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:43026181 G>A maps to NM_001712.4 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:43031508 G>C maps to NM_001712.4 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr19:45206847 C>T maps to ENST00000396750 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:51983644 C>T maps to NM_001080405.1 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr19:45175994 G>A maps to NM_020219.3 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr19:45024568 G>T maps to NM_001102597.1 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:42128133 G>A maps to NM_001817.2 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:42224050 C>T maps to NM_004363.2 D565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:42221506 G>A maps to NM_004363.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:42224890 G>A maps to NM_004363.2 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:42221416 C>T maps to NM_004363.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr19:42223994 C>T maps to NM_004363.2 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr19:42260734 C>T maps to NM_002483.4 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:42260721 C>T maps to NM_002483.4 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:42260760 C>T maps to NM_002483.4 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr19:42265997 G>C maps to NM_002483.4 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr19:42260721 C>A maps to NM_002483.4 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:42270106 C>T maps to NM_002483.4 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:42181429 A>T maps to NM_006890.3 Y236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr19:42187737 G>A maps to NM_006890.3 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:42187950 C>A maps to NM_006890.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr19:42187953 A>G maps to NM_006890.3 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:33792384 C>T maps to NM_004364.3 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr8:48649938 C>A maps to NM_005195.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:48650424 G>A maps to NM_005195.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:33870421 A>T maps to NM_001806.2 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr2:37455846 T>C maps to NM_005760.2 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr22:18022153 G>A maps to ENST00000400579 W753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr22:18022013 C>T maps to ENST00000400579 Q707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr22:17619606 C>A maps to NM_033070.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:17601078 G>A maps to NM_031890.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:17601354 G>T maps to NM_031890.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr9:135941932 G>A maps to NM_001807.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr9:135947075 T>C maps to NM_001807.3 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr9:135946436 C>T maps to NM_001807.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr1:15793936 C>T maps to ENST00000375924 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr1:15812462 C>A maps to ENST00000442979 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:22329568 C>T maps to NM_005747.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:22313043 C>T maps to NM_007352.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:22313088 C>G maps to NM_007352.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr11:47510569 C>T maps to NM_001172639.1 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr10:11308600 G>A maps to NM_006561.3 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr10:11370982 G>A maps to NM_006561.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr1:151688427 C>G maps to NM_007185.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr18:34855108 G>T maps to NM_020180.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:34850863 C>T maps to NM_020180.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:72582345 C>T maps to NM_052840.4 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:72582527 G>A maps to NM_052840.4 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr15:72608203 C>T maps to NM_052840.4 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:46795747 C>A maps to NM_014246.1 E1760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr22:46760505 G>A maps to NM_014246.1 R2894R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr22:46859979 G>A maps to NM_014246.1 G1269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr22:46776785 C>T maps to NM_014246.1 P2385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr22:46931726 G>T maps to NM_014246.1 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr22:46759999 G>A maps to NM_014246.1 C2976C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr22:46774556 C>A maps to NM_014246.1 R2438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr22:46785345 C>T maps to NM_014246.1 L2132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:46787170 G>A maps to NM_014246.1 G2054G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr22:46859706 G>A maps to NM_014246.1 C1360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr22:46773074 G>T maps to NM_014246.1 L2489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:109795730 C>T maps to NM_001408.2 H1010H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:109794494 G>C maps to NM_001408.2 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:109810497 C>G maps to NM_001408.2 S2045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr1:109801081 C>T maps to NM_001408.2 C1113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr1:109806317 C>T maps to NM_001408.2 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:109812162 G>A maps to NM_001408.2 E2310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:109801498 C>T maps to NM_001408.2 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr1:109810194 G>A maps to NM_001408.2 E2013E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr1:109794267 C>T maps to NM_001408.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:109801624 G>A maps to NM_001408.2 S1294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:109804949 G>A maps to NM_001408.2 E1476E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:109814241 C>A maps to NM_001408.2 S2608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr1:109794500 C>T maps to NM_001408.2 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:109793607 G>T maps to NM_001408.2 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:109812411 C>T maps to NM_001408.2 F2359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:48689418 C>T maps to NM_001407.2 V1938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr3:48694602 G>A maps to NM_001407.2 D1309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:48677666 C>T maps to NM_001407.2 R3117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:48696554 G>A maps to NM_001407.2 N1171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr3:48683173 C>G did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:27015012 C>T maps to NM_001809.3 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:27016145 G>A maps to NM_001809.3 *141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:3766500 C>A maps to NM_001810.5 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr20:3766554 G>A maps to NM_001810.5 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:104054925 G>A maps to NM_001813.2 Q2216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr4:104062021 G>C maps to NM_001813.2 L1901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:104035709 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr4:104054932 C>T maps to NM_001813.2 Q2213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr1:214825108 C>T maps to NM_016343.3 C2680C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:214816432 C>A maps to NM_016343.3 L1584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr1:214816111 A>G maps to NM_016343.3 S1477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr1:214813370 G>T maps to NM_016343.3 E564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:100417905 C>T did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:100403042 A>T did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:100382651 G>C did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr5:64824347 G>C maps to NM_022145.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:81045654 G>A maps to NM_001100624.1 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:81045702 C>T maps to NM_001100624.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr16:81053754 T>C maps to NM_001100624.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:25038609 G>A maps to NM_024322.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:67862384 C>T maps to NM_025082.3 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr16:67863713 G>A maps to NM_025082.3 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr17:16247995 G>A maps to NM_181716.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:16256480 C>T maps to NM_181716.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr17:16253306 G>A maps to NM_181716.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr6:126661542 T>C maps to ENST00000368325 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr9:123914806 A>G maps to NM_007018.4 K1336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:123930379 C>T maps to NM_007018.4 Q1951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:123904512 A>C maps to NM_007018.4 R946R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr9:123852643 G>C maps to NM_007018.4 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:123880718 G>C maps to NM_007018.4 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:123912682 G>A maps to NM_007018.4 G1295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr5:122725741 C>T maps to NM_153223.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:122725653 A>G maps to NM_153223.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:56830507 C>A maps to NM_025009.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr4:56823518 G>A maps to NM_025009.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr15:49052435 G>A maps to NM_001194998.1 Q864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr15:49059303 A>G maps to NM_001194998.1 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr15:49064752 G>T maps to NM_001194998.1 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:117282543 G>A maps to NM_014956.4 S1399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr11:117222547 C>T maps to NM_014956.4 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:117263264 C>T maps to NM_014956.4 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:117222547 C>T maps to NM_014956.4 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr11:117267962 G>T maps to NM_014956.4 A1145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:243362359 A>G did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:243354557 C>G maps to NM_014812.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:243349133 C>A maps to NM_014812.2 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:243289828 T>C maps to NM_014812.2 E1559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:243328084 T>C maps to NM_014812.2 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr18:13069787 A>T maps to NM_032142.3 K1703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:13087591 A>G maps to NM_032142.3 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr18:13056572 C>T maps to NM_032142.3 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr18:13053022 G>T maps to NM_032142.3 T1041T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr18:13042230 G>A maps to NM_032142.3 Q655Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr18:13055882 T>C maps to NM_032142.3 N1098N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr18:13095537 C>G maps to NM_032142.3 V2097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr18:13068893 C>T maps to NM_032142.3 I1622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:34067177 G>A maps to NM_007186.3 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr20:34091851 G>A maps to NM_007186.3 L1885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr20:34089670 G>C did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:34054792 C>T maps to NM_007186.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr20:34078579 C>T maps to NM_007186.3 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr20:34090745 C>A maps to NM_007186.3 R1517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:88487639 C>A maps to NM_025114.3 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:88478551 C>G maps to NM_025114.3 L1505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:180006139 G>T maps to NM_014810.4 S1342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:180012228 C>T maps to NM_014810.4 V1467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:180022903 C>G maps to NM_014810.4 S1670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr1:180061878 G>A maps to NM_014810.4 R2213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr1:180022216 A>G maps to NM_014810.4 R1635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr1:180053304 C>T maps to NM_014810.4 Q2093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr10:95287807 T>C maps to NM_018131.4 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:95564302 G>A maps to NM_014679.3 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr3:134265046 C>G maps to NM_025180.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr2:65300089 A>G maps to NM_015147.2 K620K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:65299048 C>A maps to NM_015147.2 Y273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr5:637679 C>G maps to NM_018140.3 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr5:635559 G>A maps to NM_018140.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr18:12697407 C>T did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr9:80856705 G>A maps to NM_001098802.1 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr9:80880326 A>C maps to NM_001098802.1 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr3:101446255 G>T maps to ENST00000327230 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr3:101476832 G>A maps to ENST00000327230 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:111702063 T>C maps to NM_001007794.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr9:14720105 G>A maps to NM_005454.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr9:131190587 C>T maps to NM_016174.4 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:47095334 G>T maps to NM_022766.5 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr2:182423401 G>A maps to NM_001030311.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr16:55846956 T>A did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr16:55844471 C>G maps to NM_001025195.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:55846877 A>G maps to NM_001025195.1 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:66975678 G>A maps to NM_003869.5 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr16:66974468 G>A maps to NM_003869.5 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr16:66977253 G>A maps to NM_003869.5 W555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:67005130 G>T maps to NM_024922.5 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:55899898 C>T maps to NM_001143685.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr16:55895398 G>A maps to NM_001143685.1 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:67042972 C>G maps to ENST00000326686 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr18:580885 G>T maps to NM_004066.1 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr18:580650 G>T maps to NM_004066.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr18:580761 C>T maps to NM_004066.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr18:580869 C>T maps to NM_004066.1 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:151997741 G>C did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr5:89695348 C>A maps to NM_004365.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:56996943 G>C maps to NM_000078.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr16:57016141 C>T maps to NM_000078.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr16:57007304 G>A maps to NM_000078.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:57015125 C>G maps to NM_000078.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:31917212 G>A maps to ENST00000437789 G931G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:31919770 G>A maps to ENST00000437789 K1255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr6:31917332 C>T maps to ENST00000437789 I971I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr2:131356269 G>A maps to NM_032545.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:196658547 A>T did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:196658598 G>A maps to NM_000186.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:196697551 C>T maps to NM_000186.3 F771F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr1:196712600 G>A maps to NM_000186.3 P1051P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:196697649 C>A maps to NM_000186.3 S804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:196709851 T>A maps to NM_000186.3 G962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:196694374 T>C maps to NM_000186.3 N607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr1:196684846 T>A maps to NM_000186.3 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr1:196706755 C>T maps to NM_000186.3 Y916Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:196796098 C>A maps to NM_002113.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:196796105 G>A maps to NM_002113.2 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:196794653 G>T maps to NM_002113.2 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:196928026 A>G maps to ENST00000367421 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr1:196918741 C>T maps to ENST00000367421 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:196920099 G>A maps to ENST00000367421 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr1:196918741 C>T maps to ENST00000367421 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:196871596 T>C maps to NM_006684.2 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:196971750 T>A maps to ENST00000367414 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:196967389 C>G maps to ENST00000367414 S392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:196964874 T>C maps to ENST00000367414 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:196953184 A>T maps to ENST00000367414 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:196977704 G>A maps to ENST00000367414 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr4:110667594 A>G maps to ENST00000394635 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr11:65623572 G>A maps to NM_005507.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr11:65623575 G>A maps to NM_005507.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:65623194 G>T maps to NM_005507.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:202005137 C>T maps to NM_001127183.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:47486636 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:47486250 A>G did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:47485838 G>A did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr23:47486680 A>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:47486605 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:47487640 G>T did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:117232002 G>A maps to NM_000492.3 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:117243762 G>A maps to NM_000492.3 S945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:117251689 T>A maps to NM_000492.3 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr7:117149099 A>G maps to NM_000492.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr7:117230488 G>T maps to NM_000492.3 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:87797906 G>A maps to NM_000735.2 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:49539416 G>A maps to ENST00000391869 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:151491281 C>G maps to NM_020770.2 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:151491339 G>A maps to NM_020770.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr15:57815715 G>A maps to NM_032866.3 Q915Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr15:57732648 C>T maps to NM_032866.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr15:57730853 C>T maps to NM_032866.3 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr15:57837889 A>T maps to NM_032866.3 K1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr15:41246008 G>A maps to NM_024111.3 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr15:41245816 C>T maps to NM_024111.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr17:48545766 A>C maps to NM_001267.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr19:4418036 A>G maps to NM_005483.2 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:4442303 C>T maps to NM_005483.2 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr19:4432044 C>T maps to NM_005483.2 Q682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr21:37788585 C>T maps to NM_005441.2 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr21:37769776 G>A maps to NM_005441.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr21:37781743 G>T maps to NM_005441.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr10:75542189 G>C maps to NM_203298.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:126633571 C>G maps to ENST00000508789 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr11:73584273 G>A maps to NM_016565.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr5:98233024 C>T did not map to a codon.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr5:98218908 T>C maps to NM_001270.2 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr5:98233987 G>T maps to NM_001270.2 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:146763162 G>C did not map to a codon.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr1:146736115 T>A maps to NM_004284.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr15:93540503 C>G maps to NM_001271.3 V1252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr15:93518122 C>A maps to NM_001271.3 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr15:93563369 C>T maps to NM_001271.3 R1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:93527663 G>A maps to NM_001271.3 E1057E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr15:93528730 C>T maps to NM_001271.3 Q1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr15:93547974 C>T maps to NM_001271.3 F1469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:7806007 G>A maps to NM_001005271.2 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr17:7802767 G>A maps to NM_001005271.2 T876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr17:7809900 G>T maps to NM_001005271.2 L1522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:7813773 C>T maps to NM_001005271.2 S1932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr17:7800528 G>A maps to NM_001005271.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr17:7797865 C>T maps to NM_001005271.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr17:7793094 G>T did not map to a codon.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr12:6691341 G>C maps to ENST00000309577 V1520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:6690554 C>G did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:6709457 G>T maps to ENST00000309577 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr12:6692097 G>A maps to ENST00000309577 P1412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:6680032 A>G did not map to a codon.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr12:6707159 G>A maps to ENST00000309577 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:6196850 G>A maps to NM_015557.2 G837G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:6195443 C>A maps to NM_015557.2 E906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr20:40068725 G>A maps to NM_032221.3 C1307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr20:40045304 G>A maps to NM_032221.3 R2137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr20:40162086 A>G maps to NM_032221.3 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr20:40065913 C>T maps to NM_032221.3 T1356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr20:40050615 G>C maps to NM_032221.3 L1553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr20:40076561 C>A maps to NM_032221.3 G1245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr20:40076562 C>G maps to NM_032221.3 L1244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:40065974 C>G did not map to a codon.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr20:40041962 C>G did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr8:61778179 C>T maps to NM_017780.2 L2894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:61749498 A>G maps to NM_017780.2 L1371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr8:61765871 C>T maps to NM_017780.2 T2196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:61769308 G>A maps to NM_017780.2 S2490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr8:61736505 C>T maps to NM_017780.2 V1103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr8:61764695 G>A maps to NM_017780.2 Q1928Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:61741253 C>T maps to NM_017780.2 L1137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr8:61778054 G>T maps to NM_017780.2 E2853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:61765574 C>T maps to NM_017780.2 D2097D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr14:21874022 C>A maps to NM_001170629.1 E970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr14:21881156 T>C did not map to a codon.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr14:21863098 C>A maps to NM_001170629.1 E1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr14:21873942 C>T maps to NM_001170629.1 P996P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:53191363 C>T maps to ENST00000219084 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:53857423 C>T maps to NM_018397.4 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:125525181 G>C maps to NM_001274.4 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr11:125514439 C>T maps to NM_001274.4 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr22:29130640 G>T maps to NM_001005735.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr22:29090105 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr22:29107974 G>A maps to NM_001005735.1 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:16638947 T>C maps to NM_006387.5 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr19:16638962 G>A maps to NM_006387.5 H411H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:16630504 A>T maps to NM_006387.5 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:133433062 G>C maps to NM_001161344.1 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:133423716 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:133438053 T>A maps to NM_001161344.1 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr14:93393910 C>A maps to NM_001275.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr20:5897557 G>A maps to NM_001819.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:203150382 G>A maps to NM_001276.2 Y206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:203149597 C>T maps to NM_001276.2 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr1:111778657 C>T maps to NM_004000.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:111778260 G>T maps to NM_004000.2 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr1:111862862 G>A maps to NM_201653.2 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:111861133 G>A maps to NM_201653.2 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr1:111857200 G>A maps to NM_201653.2 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr23:72797281 C>G did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:72797281 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:902273 G>A maps to NM_001142676.1 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr11:870489 C>T maps to NM_001142676.1 Q348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr1:203188950 C>T maps to NM_003465.2 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:203186207 G>A maps to NM_003465.2 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:203194942 C>T maps to NM_003465.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:203192646 C>T maps to NM_003465.2 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr11:67821472 C>T maps to NM_001277.2 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:51018495 C>G maps to NM_005198.4 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:384664 A>T did not map to a codon.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr3:447202 G>T maps to NM_006614.2 G1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr3:369939 C>T maps to NM_006614.2 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:367720 T>A maps to NM_006614.2 C57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr3:439979 G>A maps to NM_006614.2 P1055P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:383652 C>T maps to NM_006614.2 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr3:440040 C>T maps to NM_006614.2 Q1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:85119735 A>T did not map to a codon.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr23:85302516 G>A did not map to a codon.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr23:85218988 G>T did not map to a codon.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr23:85211359 C>T did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:241798756 G>A maps to NM_001821.3 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr1:241798407 G>A maps to NM_001821.3 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:241797419 C>T maps to NM_001821.3 W550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:241798316 G>C maps to NM_001821.3 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr1:241797268 G>A maps to NM_001821.3 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr19:59063498 C>T maps to NM_014453.2 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr14:24679886 A>G maps to NM_014169.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr14:24682633 G>A maps to NM_014169.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr8:23114103 G>A maps to NM_152272.3 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr2:175742726 T>A maps to NM_001822.4 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:175742856 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr2:175677210 C>G did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr2:175689186 G>C maps to NM_001822.4 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr7:29519926 A>G maps to NM_004067.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:29440185 G>A maps to NM_004067.2 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:29544358 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr11:89935703 G>A maps to NM_012124.2 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr15:41549176 C>T maps to NM_007236.4 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr16:23767218 C>T maps to NM_022097.2 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:220404982 G>A maps to NM_024536.5 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:150934782 C>T maps to NM_019015.1 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:150931159 T>G maps to NM_019015.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr8:141521630 C>A maps to NM_017444.4 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7596-01A-11D-2229-08 chr8:141525223 G>A did not map to a codon.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:184101431 T>C did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr3:184104640 G>A maps to NM_003741.2 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr3:184100494 C>T maps to NM_003741.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr3:184100716 C>G maps to NM_003741.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr3:184105821 G>C did not map to a codon.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr23:109943934 A>T did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr23:109919482 C>A did not map to a codon.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr23:109943926 T>C did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:109922600 C>T did not map to a codon.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr23:110002959 C>A did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr23:109919582 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr23:109937529 A>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:74414542 G>A maps to NM_015424.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr11:62677312 G>C maps to NM_000738.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr7:136699800 C>T maps to NM_001006628.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:136700235 C>T maps to NM_001006628.1 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:240072484 G>A maps to NM_000740.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:240071197 C>A maps to NM_000740.2 Y149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr11:46406909 G>A maps to NM_000741.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr11:46407894 G>C maps to NM_000741.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr2:175614730 G>T maps to NM_001039523.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr8:27327421 C>T maps to NM_000742.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr15:78894290 G>T maps to NM_000743.4 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:78893978 T>C maps to NM_000743.4 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr20:61982207 G>A maps to NM_000744.5 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr20:61978194 G>A maps to NM_000744.5 Y593Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:61978200 C>T maps to NM_000744.5 W591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:61981709 G>A maps to NM_000744.5 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr20:61981274 G>A maps to NM_000744.5 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr20:61981079 C>T maps to NM_000744.5 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr4:40356014 G>C maps to NM_017581.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr4:40339348 C>T maps to NM_017581.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:40351345 G>T maps to NM_017581.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr4:40356179 G>A maps to NM_017581.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr4:40351153 C>T maps to NM_017581.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:7350421 C>T maps to NM_000747.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr17:7360040 G>A maps to NM_000747.2 *502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:154544327 G>T maps to NM_000748.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr8:42552688 G>A did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr8:42563959 T>C maps to NM_000749.3 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr8:42586939 C>T maps to NM_000749.3 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr8:42587133 C>G maps to NM_000749.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr8:42587172 C>A maps to NM_000749.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:4802765 G>A maps to NM_000080.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:233406215 G>A maps to NM_005199.4 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr2:233408063 G>T maps to NM_005199.4 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr2:233410350 C>T maps to NM_005199.4 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr11:45672188 G>A maps to NM_003654.4 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr11:45672335 C>A maps to NM_003654.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:101011993 G>A maps to NM_004854.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr12:105150836 C>T maps to NM_018413.5 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr7:2472568 G>T maps to NM_018641.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr3:126255197 T>C did not map to a codon.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr15:40764194 C>G maps to NM_130468.3 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr10:125769718 G>A maps to NM_015892.3 N544N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr3:142840968 G>C maps to NM_004267.3 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:142840275 G>C maps to NM_004267.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:73767556 C>T maps to NM_004273.4 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:75563208 C>T maps to NM_024533.3 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr16:75564111 G>A maps to NM_024533.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:75563190 G>A maps to NM_024533.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr16:75563730 C>G maps to NM_024533.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr16:75563436 C>T maps to NM_024533.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr16:75512967 G>A maps to NM_021615.4 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr16:75512868 C>T maps to NM_021615.4 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr16:75513582 C>T maps to NM_021615.4 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr16:75513162 G>C maps to NM_021615.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr16:75512886 C>T maps to NM_021615.4 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr16:75513141 T>C maps to NM_021615.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr16:75513528 G>C maps to NM_021615.4 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:75512862 G>A maps to NM_021615.4 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr16:75512583 G>A maps to NM_021615.4 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr23:46433850 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:46434413 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:34262944 G>A maps to NM_022467.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr18:24497257 G>C maps to NM_031422.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr15:101719014 A>G maps to NM_014918.4 H329H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr15:101791397 G>A maps to NM_014918.4 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr5:129241115 C>T maps to NM_175856.4 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:129520043 C>A maps to NM_175856.4 Y403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr5:129521408 C>T maps to NM_175856.4 F858F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr10:101961843 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:101969540 T>C maps to NM_001278.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:16275695 C>A maps to NM_054113.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:26852279 G>T maps to NM_001029881.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:42799109 G>T maps to NM_015125.3 E1532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr19:42793502 G>A maps to NM_015125.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:42794461 C>T maps to NM_015125.3 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr19:42793355 C>G maps to NM_015125.3 Y386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:42795872 G>A maps to NM_015125.3 Q954Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr18:12264383 G>T maps to ENST00000342845 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr18:12277157 G>A maps to ENST00000342845 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr16:10995907 T>A maps to NM_000246.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr16:11004075 G>T maps to NM_000246.3 E950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr16:11016080 G>A maps to NM_000246.3 P1069P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:11000926 G>A maps to NM_000246.3 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:10989223 C>T maps to NM_000246.3 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:65499132 G>A maps to NM_003613.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr15:65491099 G>A maps to NM_003613.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr15:65490838 T>C maps to NM_003613.3 E595E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr15:65491006 G>C maps to NM_003613.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr15:65489296 G>A maps to NM_003613.3 S1109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:19656360 C>A maps to NM_153221.2 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:19656684 C>T maps to NM_153221.2 R1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr19:19655207 G>A maps to NM_153221.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr19:19655255 G>A maps to NM_153221.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7593-01A-11D-2229-08 chr19:19651097 C>T maps to NM_153221.2 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:175213788 G>A maps to NM_004882.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr2:175252491 G>A maps to NM_004882.3 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr19:1271982 G>A maps to ENST00000413636 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:69184785 C>T maps to NM_032830.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr12:120195318 G>C maps to ENST00000392521 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr12:120139471 C>T maps to ENST00000392521 V1833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr12:120166408 G>C maps to ENST00000392521 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr12:120172976 G>A maps to ENST00000392521 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:120128039 C>G maps to ENST00000392521 R2034R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr23:71521738 G>T did not map to a codon.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr9:130941636 C>T maps to NM_012127.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr9:130941369 C>T maps to NM_012127.2 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr13:53036053 G>T maps to NM_001098525.1 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr2:113514029 A>G maps to NM_152515.3 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr12:106633143 C>T maps to NM_006825.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:46801863 C>G maps to ENST00000415402 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr11:46771968 T>C maps to ENST00000415402 L1860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:46772904 T>C maps to ENST00000415402 K1771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:46842733 C>A maps to ENST00000415402 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr5:80555066 C>A maps to NM_001825.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:91930189 T>C maps to NM_001827.1 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:122104658 G>A maps to NM_015282.2 I1495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:122125365 G>A maps to NM_015282.2 G1228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr2:122202538 C>A did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:33585010 C>T maps to ENST00000359576 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:86961315 C>T maps to NM_001285.3 Q691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:86919184 G>T maps to NM_006536.5 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr1:86913312 A>G maps to NM_006536.5 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:87043753 C>T maps to ENST00000263723 N708N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr11:67134939 A>T maps to NM_013246.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr11:67132765 A>T maps to NM_013246.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:143028712 G>A maps to NM_000083.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr3:184074821 C>T maps to NM_004366.4 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:184071989 C>T maps to NM_004366.4 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:184072049 G>A maps to NM_004366.4 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr23:10201607 C>A did not map to a codon.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr23:10176319 G>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:10176391 C>G did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:10188915 G>T did not map to a codon.
Sequencing variant TCGA-CV-7100-01A-11D-2012-08 chr23:10201602 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:10188787 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:49855410 C>G did not map to a codon.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr23:49840629 C>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:49853387 G>A did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:49854986 G>A did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:11896102 C>T maps to ENST00000376496 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr1:11883822 G>A maps to ENST00000376496 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:11887265 C>T maps to ENST00000376496 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:11893657 G>A maps to ENST00000376496 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr1:11900210 C>T maps to NM_001286.2 I847I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr16:1501639 G>A maps to ENST00000382745 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr16:1510883 G>A maps to ENST00000382745 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:16353262 C>A maps to NM_004070.3 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr1:16357046 C>T maps to NM_004070.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr1:16378295 A>C maps to NM_000085.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:16380199 A>G maps to NM_000085.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:16383002 G>A maps to NM_000085.3 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:16383003 G>A did not map to a codon.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:190026160 G>A maps to NM_021101.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr3:170150426 C>T maps to NM_005602.5 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:100876195 C>A did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr3:190122680 C>T maps to NM_006580.3 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:190122650 C>T maps to NM_006580.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:190106201 T>C maps to NM_006580.3 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr21:31538875 C>T maps to NM_012131.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr21:31538656 G>A maps to NM_012131.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:43201676 G>A maps to NM_148960.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr23:106171759 G>C did not map to a codon.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr23:106171510 T>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:8560294 C>A maps to NM_194284.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr8:8559961 C>G maps to NM_194284.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:113650822 T>A maps to NM_001101389.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr7:73183872 G>T maps to NM_001306.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:73184250 C>T maps to NM_001306.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr22:19511490 G>A maps to NM_003277.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr16:3063470 C>T maps to NM_020982.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:51227676 G>C maps to NM_002975.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr12:10124194 A>C maps to ENST00000355690 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr12:10167882 C>T maps to NM_001129998.1 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr12:10167140 C>T maps to NM_001129998.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr12:10167980 G>A maps to NM_001129998.1 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr14:38724914 G>A maps to NM_175060.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr14:38724165 C>A maps to NM_175060.1 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:11114116 G>A maps to ENST00000409790 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:11118683 C>T maps to ENST00000409790 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr16:11071201 G>A maps to ENST00000409790 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:14707911 C>T maps to ENST00000417570 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:14710933 C>T maps to ENST00000417570 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr19:14710994 G>T did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr19:14705356 G>A maps to ENST00000417570 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr16:74455116 G>A maps to NM_001011880.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr16:74447557 G>C maps to NM_001011880.2 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr16:74447537 G>T maps to NM_001011880.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr16:74447538 C>T maps to NM_001011880.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr16:70211271 G>A maps to NM_173619.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr16:70211271 G>A maps to NM_173619.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr12:10241821 C>T did not map to a codon.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr12:10149468 C>T maps to NM_016509.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:10147806 G>T maps to NM_016509.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr12:10149792 A>G maps to NM_016509.3 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr12:9840538 C>T maps to NM_001004419.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr12:9845687 C>T maps to NM_001004419.3 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr16:78064471 G>T maps to NM_005752.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr12:8278193 C>T maps to NM_016184.3 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr12:8673785 A>G maps to NM_080387.4 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr12:8691818 C>A maps to NM_014358.2 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:8693385 G>T maps to NM_014358.2 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:71046979 C>T maps to NM_173535.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:7830110 C>T maps to NM_014257.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:7831596 C>G maps to NM_014257.4 Y280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr19:7828325 C>T maps to NM_014257.4 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:141635613 C>T maps to NM_013252.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:8630045 A>T maps to NM_001007033.1 K206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:8608727 T>A maps to NM_001007033.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:8628755 T>C maps to NM_001007033.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:10279170 T>A maps to NM_197947.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:141310458 C>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:31700050 A>G maps to NM_001288.4 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:154528135 T>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:139889997 G>A maps to NM_004669.2 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:25153551 C>T maps to NM_013943.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr1:25167424 G>A maps to NM_013943.2 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr6:45870950 C>T maps to NM_001114086.1 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr21:36042976 G>C maps to ENST00000360731 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr5:157218919 C>A maps to NM_001195555.1 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:157218824 G>A maps to NM_001195555.1 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr12:122839066 G>A maps to ENST00000302528 R414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:122794384 G>T maps to ENST00000302528 S1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:122825410 C>T maps to ENST00000302528 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:122825884 T>A maps to ENST00000302528 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr12:122825751 T>G maps to ENST00000302528 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr12:122862211 C>T maps to ENST00000302528 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr12:122825428 C>T maps to ENST00000302528 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr19:36508624 G>A maps to NM_015526.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr19:36507074 C>T maps to NM_015526.2 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr1:155240699 C>T maps to ENST00000368361 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:155238103 T>C maps to ENST00000368361 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:155240768 C>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:155236561 G>A maps to ENST00000368361 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:155236562 G>A maps to ENST00000368361 H265H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr1:155238538 G>A maps to ENST00000368361 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:155239299 C>T maps to ENST00000368361 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:155240680 G>A maps to ENST00000368361 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr1:155234037 G>A maps to ENST00000368361 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr15:74922108 T>G maps to NM_001130028.1 L601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr15:74918244 C>T maps to NM_001130028.1 N399N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:95670572 C>T maps to NM_024734.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr14:95677034 G>A maps to NM_024734.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr14:95670175 G>A maps to NM_024734.3 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr14:95669936 A>G maps to NM_024734.3 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr14:95670746 G>A maps to NM_024734.3 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr16:28502857 G>T maps to NM_000086.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr16:28497942 G>A maps to NM_000086.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr13:77566262 C>T maps to NM_006493.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr15:68504042 G>A maps to NM_017882.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:1719414 C>T maps to NM_018941.3 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr4:10533897 G>A maps to NM_052964.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr4:56316288 T>C maps to NM_004898.2 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr4:56301652 G>A maps to NM_004898.2 Q824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr11:72145269 G>T maps to NM_030813.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:72013355 G>A maps to NM_030813.3 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:72114047 C>T maps to NM_030813.3 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr11:72012909 G>C maps to NM_030813.3 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr6:35765035 G>A maps to NM_001832.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr19:45490455 G>A maps to NM_001294.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:45491405 C>G maps to NM_001294.2 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr19:45494629 C>T maps to NM_001294.2 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:1321748 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:1330448 G>A maps to NM_030782.3 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr15:65447146 C>T maps to NM_006660.3 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr15:65456380 G>C maps to NM_006660.3 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:150659510 G>T maps to NM_001195794.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:150690258 C>T maps to NM_001195794.1 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr4:17524556 C>G maps to NM_001079827.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:9804037 G>C maps to NM_001009566.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:9794123 C>G maps to NM_001009566.1 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:9795144 C>G maps to NM_001009566.1 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:140178480 C>G maps to NM_022131.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:140281732 C>A maps to NM_022131.2 R765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr3:140251221 C>A maps to NM_022131.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr3:140178486 C>A maps to NM_022131.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr3:140277532 G>C maps to NM_022131.2 V625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr3:140281752 C>A maps to NM_022131.2 C771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr3:140251314 C>A maps to NM_022131.2 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:140285007 G>A maps to NM_022131.2 E927E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:140282028 C>T maps to NM_022131.2 S822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:7302137 G>T maps to NM_014718.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:7286259 C>T maps to NM_014718.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:7288934 C>T maps to NM_014718.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr12:7293929 C>T maps to NM_014718.3 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:57756759 T>G maps to NM_004859.3 V933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:57758311 G>T maps to NM_004859.3 E987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:19183839 G>A maps to NM_007098.3 L1376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr16:3586201 C>G maps to NM_015041.1 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr18:641462 G>A maps to NM_199167.1 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:645094 C>A maps to NM_199167.1 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr8:62212793 C>T maps to NM_173519.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr8:62212793 C>A maps to NM_173519.2 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:62212799 G>A maps to NM_173519.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr6:123377031 C>T maps to NM_001010852.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr6:123319156 C>A maps to NM_001010852.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr6:123332280 C>T maps to NM_001010852.2 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:123332246 C>T maps to NM_001010852.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr13:100518603 C>A maps to NM_206808.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr14:24976686 G>A maps to NM_001836.2 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:22218160 T>C maps to NM_018686.3 C407C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr5:10280583 C>T maps to NM_138809.3 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr16:81740625 G>A maps to NM_198390.2 K735K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr16:81726768 C>T maps to NM_198390.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr12:108685629 G>A maps to NM_001142344.1 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:47840884 C>T maps to NM_016308.2 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr16:66603836 A>T did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr16:66642246 G>A maps to NM_181553.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:23848307 G>A maps to ENST00000339180 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:79034790 C>T maps to NM_153610.3 I3401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:79029871 A>T maps to NM_153610.3 K1762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:79031361 C>T maps to NM_153610.3 D2258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr5:79032925 G>T maps to NM_153610.3 E2780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr5:79026748 T>C maps to NM_153610.3 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:79095240 G>A maps to NM_153610.3 E4004E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr5:79027401 T>C maps to NM_153610.3 D938D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:79029811 C>T maps to NM_153610.3 Q1742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr5:79028658 T>C maps to NM_153610.3 S1357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:88363946 G>T maps to NM_173538.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr8:87917338 C>T maps to NM_173538.2 H63H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr18:72180809 G>A maps to NM_018235.2 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr18:72167226 C>T maps to NM_018235.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr18:72183551 G>A maps to NM_018235.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:72185801 C>T maps to NM_018235.2 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr23:150911735 C>T did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr23:150912244 G>A did not map to a codon.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr23:150911101 C>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:150912138 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:150908081 C>T did not map to a codon.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr23:150912369 G>C did not map to a codon.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr23:150912150 G>A did not map to a codon.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr23:150912214 G>C did not map to a codon.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr23:150912535 G>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:98999859 C>T maps to NM_001298.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:98986449 C>A maps to NM_001298.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr2:99012565 C>T maps to NM_001298.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr2:99013495 G>A maps to NM_001298.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr2:99013276 G>A maps to NM_001298.2 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr2:99013474 G>A maps to NM_001298.2 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr2:99013492 C>T maps to NM_001298.2 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:99013660 C>T maps to NM_001298.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:99013681 C>T maps to NM_001298.2 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr2:99013651 G>T maps to NM_001298.2 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr11:6261425 G>A maps to NM_001037329.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:6262987 G>A maps to NM_001037329.2 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr16:57994803 C>T maps to NM_001297.4 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:57954369 G>C maps to NM_001297.4 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr16:57994741 A>G did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr16:57938670 C>T maps to NM_001297.4 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr8:87641147 T>C maps to NM_019098.4 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr8:87638273 C>T maps to NM_019098.4 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:87738775 C>T maps to NM_019098.4 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:87638234 G>T maps to NM_019098.4 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr8:87679199 G>A maps to NM_019098.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:224804896 G>A maps to NM_152495.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:26510928 C>T maps to ENST00000374253 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:26504061 C>G maps to ENST00000374253 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:26510593 G>A maps to ENST00000374253 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr1:26510919 G>A maps to ENST00000374253 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr1:26513908 C>T maps to ENST00000374253 Q471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr23:21609139 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:21670528 G>A did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr23:21627261 C>G did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:21545079 C>T did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr23:21515964 G>A did not map to a codon.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr23:21534661 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:21581439 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:21609286 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:21609287 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:21627284 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:21627269 G>T did not map to a codon.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr23:21627481 G>T did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr23:21550064 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:21581469 G>C did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr23:21550080 G>A did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr6:154763229 C>T maps to NM_173515.2 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:154727610 G>A maps to NM_173515.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:154763421 A>G maps to NM_173515.2 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:11657660 C>A maps to NM_001299.4 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:101090474 C>G maps to NM_020348.2 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr10:104831529 G>C did not map to a codon.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr10:104835933 G>A maps to NM_017649.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:97490843 C>T maps to NM_017623.4 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:97427041 C>G maps to NM_020184.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:58608532 G>C maps to NM_016284.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr16:58577498 T>C maps to NM_206999.1 L1482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr16:58572082 C>T maps to NM_016284.3 Q1741Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr12:70747680 C>T maps to NM_014515.5 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr19:54653381 G>C maps to NM_014516.3 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr19:54646739 G>T did not map to a codon.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr19:54652229 C>T maps to NM_014516.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:135078967 A>T maps to NM_001190850.1 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr7:135106924 G>A maps to NM_001190850.1 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr7:135080594 G>C maps to NM_001190850.1 S307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr5:179998329 G>A maps to NM_015455.3 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr5:179976991 G>A maps to NM_015455.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr4:78697452 T>C maps to ENST00000512485 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr6:88854381 C>T maps to NM_016083.4 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:88854006 C>T maps to NM_016083.4 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr6:88854285 C>T maps to NM_016083.4 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:24202068 G>C maps to NM_001841.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr1:24201771 G>A maps to NM_001841.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:24201677 G>A maps to NM_001841.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:68521023 C>A maps to NM_015463.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:246810954 G>C maps to NM_152609.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:246810955 C>T maps to NM_152609.2 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:246810609 C>T maps to NM_152609.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:246784752 A>G maps to NM_152609.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr17:40958809 G>A maps to NM_173478.2 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:17388166 C>G maps to NM_017738.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr9:17394893 G>A maps to NM_017738.2 V814V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:17340895 C>T maps to NM_017738.2 N572N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:41422959 T>A maps to NM_001843.2 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr12:41374735 G>C maps to NM_001843.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr12:41421671 T>A maps to NM_001843.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr12:41330594 G>A maps to NM_001843.2 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr12:41463812 C>T maps to NM_001843.2 G1011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:205038983 C>T maps to NM_005076.3 D742D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:205039106 C>A maps to NM_005076.3 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:205034930 G>A maps to NM_005076.3 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:205042323 G>A maps to NM_005076.3 G991G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:205027163 C>T maps to NM_005076.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:74334567 G>C maps to NM_020872.1 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:74315640 G>A maps to NM_020872.1 R993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:74350692 C>A maps to NM_020872.1 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:74350576 G>A maps to NM_020872.1 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:74411123 G>T maps to NM_020872.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:74350819 C>A maps to NM_020872.1 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr3:74350657 T>A maps to NM_020872.1 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:74315788 C>T maps to NM_020872.1 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr3:74418523 A>G maps to NM_020872.1 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr3:74535778 C>T maps to NM_020872.1 W62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:2778010 A>T maps to NM_175607.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:2777986 C>G maps to NM_175607.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr3:2928745 C>T maps to NM_175607.1 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:2777998 T>A maps to NM_175607.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:99715884 C>A maps to NM_014361.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:99786822 C>T maps to NM_014361.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:99690440 G>A maps to NM_014361.2 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:99827583 G>T maps to NM_014361.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr11:100126550 C>T maps to NM_014361.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:100061930 C>T maps to NM_014361.2 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr11:100141897 C>T maps to NM_014361.2 R747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr11:100126555 C>A maps to NM_014361.2 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr3:1414631 T>C maps to NM_014461.2 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr3:1320175 A>G maps to NM_014461.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr3:1363507 C>G maps to NM_014461.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:1269677 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:1414580 C>T maps to NM_014461.2 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr3:1418743 C>T maps to NM_014461.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:1424825 G>A maps to NM_014461.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:40842781 G>A maps to NM_003632.2 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr17:40842781 G>A maps to NM_003632.2 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr17:40839867 G>A maps to NM_003632.2 W392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr17:40839805 C>T maps to NM_003632.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr7:147183110 C>G maps to NM_014141.5 Y585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr7:147914378 G>C did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr7:147844613 G>T maps to NM_014141.5 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:146536830 C>T maps to NM_014141.5 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr7:146829389 C>T maps to NM_014141.5 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:146829567 C>T maps to NM_014141.5 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:147259326 G>T maps to NM_014141.5 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:148112632 G>A maps to NM_014141.5 A1307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:147815306 C>T maps to NM_014141.5 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr7:147600792 C>T maps to NM_014141.5 C745C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr7:147600792 C>T maps to NM_014141.5 C745C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr7:146829380 C>G maps to NM_014141.5 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:147869370 C>A maps to NM_014141.5 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr7:146741039 C>T maps to NM_014141.5 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr16:76556035 G>A maps to NM_033401.3 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr16:76501309 T>A maps to NM_033401.3 C514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr16:76389224 C>A maps to NM_033401.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:76482787 C>T maps to NM_033401.3 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr16:76496002 G>A did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr16:76555133 T>C maps to NM_033401.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr16:76501401 C>G maps to NM_033401.3 S545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr16:76486631 C>A maps to NM_033401.3 Y432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr16:76556014 C>T maps to NM_033401.3 N871N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr16:76482035 C>G maps to NM_033401.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr16:76486616 T>A maps to NM_033401.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr16:76528819 G>A maps to NM_033401.3 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:125555769 T>A maps to NM_130773.2 I1029I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr2:125261981 G>A maps to NM_130773.2 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:124783247 G>A maps to NM_130773.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr2:125284859 A>G did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:125671690 C>T maps to NM_130773.2 F1249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr2:125530439 T>A maps to NM_130773.2 S865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:7851509 C>T maps to NM_001037144.4 Q749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:7849044 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr17:7843415 G>A maps to NM_001037144.4 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr17:40716510 C>G maps to NM_001042532.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr7:51203959 C>T maps to ENST00000395542 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr7:51203859 C>A maps to ENST00000395542 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:51096581 C>A maps to ENST00000395542 G819G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr7:51251896 C>T did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr7:51096986 G>T maps to ENST00000395542 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr2:165551666 C>A maps to ENST00000392717 S821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr2:165551420 G>T maps to ENST00000392717 P903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr2:165551293 G>A maps to ENST00000392717 Q946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr2:165555990 T>C maps to ENST00000392717 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr9:140150357 G>C did not map to a codon.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr14:31349791 G>A did not map to a codon.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr14:31355513 T>C maps to NM_004086.2 D491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:31346826 G>A maps to NM_004086.2 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:230827171 G>A maps to NM_007357.2 K659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr1:230795360 C>G maps to NM_007357.2 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr13:46092894 A>G did not map to a codon.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr16:70557287 G>C maps to NM_015386.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:70515273 G>C maps to NM_015386.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr16:70514945 G>A maps to NM_015386.2 F779F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:107198558 C>T maps to NM_006348.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr7:106898717 C>T maps to NM_006348.3 K593K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr16:23415098 C>T maps to NM_153603.3 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr16:23436184 G>A maps to NM_153603.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr16:69373326 C>T maps to NM_032382.4 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr16:69370548 C>T maps to NM_032382.4 R148R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-6225-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:103548501 G>A maps to NM_080629.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:103474058 G>T maps to NM_080629.2 S560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:103381185 C>G did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr1:103345283 G>A maps to NM_080629.2 S1755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr1:103348753 C>G did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:103364317 A>G maps to NM_080629.2 G1396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:103462680 C>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:103440440 T>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:103343705 C>A maps to NM_080629.2 E1776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:103480095 G>A maps to NM_080629.2 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:103345448 T>C maps to NM_080629.2 G1700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr1:103354186 C>A did not map to a codon.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr1:103471420 C>T maps to NM_080629.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:103405900 A>T maps to NM_080629.2 P1134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:103453202 G>A maps to NM_080629.2 Q842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:103481223 C>T maps to NM_080629.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr1:103491397 C>T maps to NM_080629.2 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr1:103352613 T>A did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr1:103444278 G>A maps to NM_080629.2 G925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:103354180 G>T maps to NM_080629.2 P1532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr1:103548388 G>T maps to NM_080629.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr1:103483408 G>A maps to NM_080629.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr1:103364277 G>A maps to NM_080629.2 Q1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr1:103428219 C>A maps to NM_080629.2 E1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:103364260 C>T maps to NM_080629.2 K1415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:33135223 C>G maps to NM_080680.2 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:33133581 G>T maps to NM_080680.2 G1498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:33146750 C>A did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:33148773 G>A maps to NM_080680.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:33145003 T>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:33139528 C>T maps to NM_080680.2 P1037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr6:75829168 G>A maps to ENST00000322507 S2369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:75893060 C>T maps to ENST00000322507 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:75843069 C>A maps to ENST00000322507 V1911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr6:75851808 G>A maps to ENST00000322507 V1632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr6:75875235 A>G maps to ENST00000322507 D990D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:75806968 C>T maps to ENST00000322507 P2859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr6:75818863 G>C maps to ENST00000322507 S2657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr6:75865510 G>A maps to ENST00000322507 R1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr10:71707079 C>T maps to ENST00000356340 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H8-01A-21D-A34J-08 chr10:71690202 C>A maps to ENST00000356340 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:121240970 A>T maps to NM_021110.1 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr8:121220600 G>A did not map to a codon.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:121216035 G>A maps to NM_021110.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr8:121174683 G>A maps to NM_021110.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr8:121256221 C>T maps to NM_021110.1 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr8:121290785 G>C maps to NM_021110.1 V1150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:121290347 A>T did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:121267541 G>A maps to NM_021110.1 W939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr8:121357677 T>G maps to NM_021110.1 T1651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:121222115 G>A maps to NM_021110.1 E481E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:121292243 C>T maps to NM_021110.1 P1184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr8:121282322 G>A maps to NM_021110.1 W1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr8:121222050 C>T maps to NM_021110.1 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr9:101748162 G>A maps to NM_001855.3 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:101765754 G>C maps to NM_001855.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:32163680 G>T maps to NM_001856.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr1:32154662 G>T maps to NM_001856.3 I548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:32165442 C>T maps to NM_001856.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:32134423 C>T maps to NM_001856.3 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:32164197 G>A maps to NM_001856.3 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:32157017 C>T maps to NM_001856.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr1:32148955 G>A maps to NM_001856.3 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr10:105821184 G>A maps to NM_000494.3 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr10:105799373 G>C maps to NM_000494.3 S938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:105819883 G>A maps to NM_000494.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:105807536 G>A maps to NM_000494.3 I765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr10:105821187 C>G maps to NM_000494.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr10:105836187 C>T did not map to a codon.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr21:46875806 C>T maps to ENST00000359759 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:46912602 C>A maps to ENST00000359759 G1145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr21:46925145 C>T maps to ENST00000359759 P1404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr21:46899994 G>A maps to ENST00000359759 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr21:46875458 C>T maps to ENST00000359759 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr21:46888623 C>G maps to ENST00000359759 S607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr21:46888525 C>T maps to ENST00000359759 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr21:46930060 G>A maps to ENST00000359759 A1608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:70639471 C>T maps to NM_001858.4 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr6:70856591 A>T maps to NM_001858.4 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr6:70778325 G>T maps to NM_001858.4 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:70840115 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr6:70642745 A>G maps to NM_001858.4 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:70639565 C>T maps to NM_001858.4 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr6:70637858 C>T maps to NM_001858.4 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr17:48273001 G>A maps to NM_000088.3 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:48273983 A>T maps to NM_000088.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr17:48278777 C>A maps to NM_000088.3 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr17:48268761 T>C maps to NM_000088.3 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:48278808 G>A maps to NM_000088.3 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr7:94052390 C>T maps to NM_000089.3 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:94058729 A>G maps to NM_000089.3 V1314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr7:94057677 C>T maps to NM_000089.3 G1200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr7:94056510 T>C maps to NM_000089.3 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:94054508 C>T maps to NM_000089.3 N918N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:94053706 C>T maps to NM_000089.3 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:94034998 C>T maps to NM_000089.3 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr7:94052414 A>T maps to NM_000089.3 G850G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr7:94049929 C>A maps to NM_000089.3 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr20:61950908 G>A maps to ENST00000326996 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr20:61929271 C>T maps to ENST00000326996 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr20:61943053 G>A maps to ENST00000326996 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:56044742 G>A maps to NM_030820.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr6:56006597 C>T maps to NM_030820.3 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:56033059 G>A maps to NM_030820.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr8:139601675 G>A maps to NM_152888.1 P1567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:139691865 A>T maps to NM_152888.1 C1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr8:139706750 C>A maps to NM_152888.1 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr8:139890086 G>A maps to NM_152888.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:139614356 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:139729091 G>A maps to NM_152888.1 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:139649039 T>G did not map to a codon.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr8:139606418 G>A maps to NM_152888.1 Q1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr8:139620233 T>G did not map to a codon.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr8:139601579 G>A maps to NM_152888.1 P1599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:139824101 T>A maps to NM_152888.1 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr8:139728520 G>T maps to NM_152888.1 G804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr8:139696688 G>A maps to NM_152888.1 L997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:139611072 G>A maps to NM_152888.1 I1418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr8:139672720 A>T maps to NM_152888.1 G1081G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr8:139790649 C>A did not map to a codon.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr8:139674287 G>A maps to NM_152888.1 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr8:139610997 T>G maps to NM_152888.1 P1443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:139890020 C>T maps to NM_152888.1 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr8:139793187 G>A maps to NM_152888.1 D544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr8:139707100 C>A maps to NM_152888.1 E872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr8:139611101 C>A maps to NM_152888.1 G1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:177694328 T>C maps to ENST00000390654 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:86340370 A>T maps to NM_152890.5 T1033T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:86200452 T>C maps to NM_152890.5 K1659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:86289269 G>T maps to NM_152890.5 G1246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:86361733 A>G maps to NM_152890.5 D949D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr4:110222986 G>A maps to ENST00000333642 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:109822295 C>T maps to ENST00000333642 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:109895697 T>C maps to ENST00000333642 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr4:109805339 C>T maps to ENST00000333642 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr4:109861733 G>A maps to ENST00000333642 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr4:110223070 G>A maps to ENST00000333642 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:117071685 C>T maps to NM_032888.2 F1788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr9:116930230 C>T maps to NM_032888.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:116931742 G>T maps to NM_032888.2 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:116931124 G>A maps to NM_032888.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr9:117062951 G>T maps to NM_032888.2 G1562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr7:7412995 C>T maps to NM_001037763.2 E847E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr7:7413145 T>C maps to NM_001037763.2 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr12:48388218 C>T maps to NM_001844.4 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:48372457 G>A maps to NM_001844.4 G939G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:48383558 G>A maps to NM_001844.4 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:48369217 A>G maps to NM_001844.4 D1256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr2:189854842 C>T maps to NM_000090.3 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr2:189876409 G>A maps to NM_000090.3 V1437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr2:189855055 A>T maps to NM_000090.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:189873852 A>G maps to NM_000090.3 G1243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:189854842 C>A maps to NM_000090.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:189870119 T>A maps to NM_000090.3 R992R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:189873732 T>G maps to NM_000090.3 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr13:110813612 C>T maps to NM_001845.4 W1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr13:110827072 G>A maps to NM_001845.4 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:110831732 A>G maps to NM_001845.4 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr13:110815840 C>T maps to NM_001845.4 Q1406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr13:110831645 G>A maps to NM_001845.4 I772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:110831717 G>A maps to NM_001845.4 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr13:111102706 C>G maps to NM_001846.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr13:111142100 G>A maps to NM_001846.2 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr13:111160474 G>T maps to NM_001846.2 P1596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:228128541 G>C maps to NM_000091.4 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:228153932 C>G maps to NM_000091.4 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr2:228173693 A>T maps to NM_000091.4 A1514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:228159767 G>A maps to NM_000091.4 K1169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr2:228148996 A>G maps to NM_000091.4 K939K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr2:228169767 A>G maps to NM_000091.4 E1407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:74722219 A>T maps to NM_001130105.1 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:74696050 C>G maps to NM_001130105.1 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:227973310 G>A maps to ENST00000396625 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr2:227920691 A>G maps to ENST00000396625 D895D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr2:227983387 T>C maps to ENST00000396625 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:227922251 C>T maps to ENST00000396625 G816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:227985822 G>A maps to ENST00000396625 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr2:228009237 T>A maps to ENST00000396625 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr2:227924262 G>A maps to ENST00000396625 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr23:107930714 C>T did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr23:107834352 G>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:107802346 A>C did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:107844631 G>T did not map to a codon.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr23:107920731 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:107834329 G>A did not map to a codon.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr23:107829871 A>G did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr23:107909816 T>C did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr23:107865910 G>A did not map to a codon.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr23:107924155 G>T did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:107925059 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:107823794 T>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:107823795 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:107834371 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:107920798 C>T did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:107923959 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr23:107925106 A>T did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:107403882 T>G did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr23:107553985 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:107433637 G>A did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr23:107413936 C>G did not map to a codon.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr23:107417816 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:107430381 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr23:107408110 C>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:107403861 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr23:107400292 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr23:107449789 T>A did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr9:137715308 C>A maps to NM_000093.3 G1564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr9:137650127 G>T maps to NM_000093.3 E641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:137653805 G>C maps to NM_000093.3 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr9:137591782 C>A maps to NM_000093.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr9:137734076 C>T maps to NM_000093.3 I1815I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr9:137716558 C>T maps to NM_000093.3 Y1604Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:189962025 C>A maps to NM_000393.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr2:189932827 A>T maps to NM_000393.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:189909939 C>A maps to NM_000393.3 G1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:10071182 C>T maps to NM_015719.3 A1714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:10090690 G>A maps to NM_015719.3 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:10090710 G>A maps to NM_015719.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:10080262 G>A maps to NM_015719.3 I1362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr19:10077031 C>T maps to NM_015719.3 A1580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr19:10108061 G>A maps to NM_015719.3 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:10102490 C>T maps to NM_015719.3 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:10079144 G>A maps to NM_015719.3 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:10090690 G>A maps to NM_015719.3 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr21:47410317 C>T maps to NM_001848.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr21:47422130 G>C did not map to a codon.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr21:47409673 A>G maps to NM_001848.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr21:47404293 C>G maps to NM_001848.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr21:47412127 C>T maps to NM_001848.2 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr21:47422151 G>A maps to NM_001848.2 W696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr21:47422152 G>A maps to NM_001848.2 W696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr21:47532716 G>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr21:47549386 C>A maps to NM_058174.2 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr21:47537348 G>A maps to NM_001849.3 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr21:47549242 C>T maps to NM_058174.2 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr21:47546044 C>G maps to NM_001849.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr21:47535817 G>A maps to NM_001849.3 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:238255175 C>T maps to NM_004369.3 Q2354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:238267207 C>A maps to NM_004369.3 G2143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr2:238267676 C>T did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr2:238253406 G>A maps to NM_004369.3 F2418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:238296330 G>T maps to NM_004369.3 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr2:238253400 C>G maps to NM_004369.3 R2420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:238285727 C>T maps to NM_004369.3 A919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:238242091 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:238287555 A>G maps to NM_004369.3 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:238249122 G>A maps to NM_004369.3 F2812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:238275605 G>T maps to NM_004369.3 R1742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:238296309 C>T maps to NM_004369.3 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr2:238283538 G>A maps to NM_004369.3 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr2:238275792 C>A maps to NM_004369.3 G1679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:238244937 C>T maps to NM_004369.3 A2935A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:238274457 C>T maps to NM_004369.3 Q1907Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr3:130159095 C>A maps to ENST00000312481 R1972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr3:130095260 T>C maps to ENST00000312481 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:130361867 G>A did not map to a codon.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:130292956 C>T maps to NM_001102608.1 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:130300642 G>C maps to NM_001102608.1 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:130293226 G>A maps to NM_001102608.1 V1135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:130281984 G>A maps to NM_001102608.1 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:130285859 C>A maps to NM_001102608.1 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:130327808 G>T did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:130293196 G>A maps to NM_001102608.1 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr3:130287206 C>A maps to NM_001102608.1 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr3:130368270 C>A maps to NM_001102608.1 I1866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr3:130368003 G>A maps to NM_001102608.1 K1777K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:130285900 T>C maps to NM_001102608.1 N546N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr3:130282221 G>T maps to NM_001102608.1 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:48625736 G>A maps to NM_000094.3 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:48626387 G>A maps to NM_000094.3 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr3:48625823 C>T maps to NM_000094.3 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:48626387 G>A maps to NM_000094.3 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr3:48626134 G>A maps to NM_000094.3 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr3:48617462 C>A did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr3:48605584 C>A maps to NM_000094.3 G2605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr3:48610944 C>A did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr3:48612945 G>A maps to NM_000094.3 R2002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:99514874 C>A maps to ENST00000429802 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr1:36564393 C>T maps to NM_005202.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:70993475 C>T maps to NM_001851.4 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:71009789 C>T maps to NM_001851.4 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr1:40775612 G>A maps to NM_001852.3 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:61451327 G>A maps to NM_001853.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr20:61461170 G>A maps to NM_001853.3 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr8:120103454 G>A maps to NM_006438.3 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr2:3691422 G>T maps to ENST00000418971 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr2:3691473 G>T maps to ENST00000418971 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr2:3691386 C>T maps to ENST00000418971 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:334985 C>T maps to NM_130386.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr18:480722 G>A maps to NM_130386.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr18:347015 G>A maps to NM_130386.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr18:346847 C>T maps to NM_130386.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr18:357514 C>T maps to NM_130386.2 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr18:346751 G>T maps to NM_130386.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr10:22606901 C>T maps to NM_012071.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr22:19950330 C>T maps to NM_001135162.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr1:160261695 G>A maps to NM_001098398.1 C1066C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:160276192 G>A maps to NM_001098398.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr1:160276271 C>T maps to NM_001098398.1 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:160312933 G>A maps to NM_001098398.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:160303418 C>T maps to NM_001098398.1 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:160281695 G>A maps to NM_001098398.1 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:160260440 G>A maps to NM_001098398.1 P1161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr1:160309983 A>G maps to NM_001098398.1 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:14490303 G>A maps to NM_001144061.1 Q690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:14486568 C>T maps to NM_001144061.1 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:14502568 T>G maps to NM_001144061.1 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:139090584 T>C maps to NM_004766.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:139093346 G>A maps to NM_004766.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr3:139092254 C>A did not map to a codon.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr19:19014115 C>T maps to NM_007263.3 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr3:128993712 C>T maps to NM_016128.3 H763H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:128979528 C>G maps to NM_016128.3 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:128976644 C>T maps to NM_016128.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr3:128986827 C>T maps to NM_016128.3 Y531Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr7:130295822 C>A maps to ENST00000445977 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:49436469 C>T maps to NM_001143887.1 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr17:17150426 T>A maps to NM_003653.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:17163628 G>A maps to NM_003653.3 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:6833911 C>T maps to NM_001164093.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:46103841 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:198318313 G>A maps to NM_025147.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr6:99817631 C>T maps to NM_017421.3 W318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr9:131088087 C>G maps to NM_016035.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr9:131085367 G>A maps to NM_016035.3 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:120947834 G>C maps to NM_032314.3 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr12:120960069 C>T maps to NM_032314.3 W100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr14:74426167 A>C maps to NM_182476.1 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:19087179 C>T maps to NM_016138.4 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr16:19085307 C>G maps to NM_016138.4 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr16:19087046 G>A maps to NM_016138.4 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr4:47605459 A>G maps to NM_006587.2 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:47765466 A>G maps to NM_006587.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr4:47597911 G>A maps to NM_006587.2 S985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:67206198 G>T maps to NM_020441.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:67207898 C>T maps to NM_020441.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:67206255 G>A maps to NM_020441.2 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:67209949 C>A maps to NM_020441.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:109042421 G>A maps to ENST00000420959 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr12:109051079 C>T maps to ENST00000420959 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr9:100895439 A>G maps to NM_052820.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:100893278 G>A maps to NM_052820.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr15:69011052 C>T maps to NM_006091.3 H328H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr17:27943184 G>A maps to ENST00000345068 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr17:14110157 C>A maps to NM_001303.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:14110528 G>A maps to NM_001303.3 *444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:53042128 T>A maps to NM_004375.3 K151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:70795899 C>T maps to NM_016468.5 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:73923917 G>A maps to NM_173827.2 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr7:1015139 C>G maps to NM_001031617.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:85822626 G>A maps to NM_006067.4 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:120876215 G>T maps to NM_004373.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr12:120876251 C>T maps to NM_004373.2 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr6:75950912 C>T maps to NM_001865.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:42580402 C>A maps to NM_004718.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr3:148916151 A>C did not map to a codon.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr16:19557136 A>G did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr16:19553368 C>G maps to NM_014711.4 S737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:129910534 C>G maps to NM_001869.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:129950684 G>T maps to NM_016352.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr7:129950639 C>T maps to NM_016352.3 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:130008365 C>A maps to NM_080385.4 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr8:68419034 C>T maps to NM_020361.4 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:68419111 T>C maps to NM_020361.4 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:17015050 G>T maps to ENST00000443236 G1469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:17039835 G>A maps to ENST00000443236 P1077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr19:17038879 G>A maps to ENST00000443236 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr19:17010308 G>A maps to ENST00000443236 R1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:17057902 C>T maps to ENST00000443236 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:17122306 G>A maps to ENST00000443236 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr19:17008586 G>A maps to ENST00000443236 N1717N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:148558762 G>T did not map to a codon.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr13:46641510 G>A maps to NM_001872.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr13:46627850 G>A maps to NM_001872.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr13:46661881 C>A maps to NM_001872.3 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr13:46679069 C>T did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr13:46656635 G>A maps to NM_001872.3 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:46632472 T>C maps to NM_001872.3 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr13:46629915 G>A maps to NM_001872.3 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:28788938 G>A maps to NM_001304.4 K1225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:83221345 C>A maps to ENST00000261723 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:83226686 G>A maps to ENST00000261723 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr15:83296033 G>A maps to ENST00000261723 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:15054113 A>G maps to NM_001177382.1 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr5:173359490 C>T maps to NM_030627.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:173317389 T>C maps to NM_030627.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr4:786391 G>A maps to NM_006651.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:56985658 C>T maps to NM_181654.3 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr12:69250399 C>T maps to NM_001874.4 Q383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr12:69260745 C>T maps to NM_001874.4 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:69265655 C>G maps to NM_001874.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr10:101829593 C>T maps to NM_001308.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr10:101816847 G>A maps to NM_001308.2 C311C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:101816814 C>T maps to NM_001308.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:101824950 G>A maps to NM_001308.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr10:101802264 C>T maps to NM_001308.2 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:194063362 G>T maps to NM_001080513.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:194062678 G>A maps to NM_001080513.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:194062540 G>A maps to NM_001080513.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr3:194063383 G>A maps to NM_001080513.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:194061982 G>A maps to NM_001080513.2 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr3:194061796 G>T maps to NM_001080513.2 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr20:34215282 G>A maps to NM_003915.5 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr16:57149417 C>T maps to NM_152727.5 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr16:57147237 C>T maps to NM_152727.5 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:57151427 C>T maps to NM_152727.5 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:57153531 G>A maps to NM_152727.5 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr8:87567119 C>T maps to NM_003909.3 Q388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr8:87552513 G>A maps to NM_003909.3 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr3:131415427 G>A maps to ENST00000502818 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr3:131300470 C>T maps to ENST00000502818 K291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr3:131254047 T>C maps to ENST00000502818 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:36767802 G>A maps to NM_020939.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:36766230 C>A did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr14:24546187 G>A maps to NM_006032.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr14:24545395 G>A maps to NM_006032.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr14:24546881 C>T maps to NM_006032.2 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr16:89662998 C>A maps to NM_014427.4 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr16:89661965 G>A maps to NM_014427.4 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:39079365 A>C maps to NM_153634.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:39047851 A>G maps to NM_153634.2 Y509Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr3:9757197 C>T maps to ENST00000383832 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr2:207825637 C>A maps to NM_173077.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:211521292 C>A maps to NM_001122633.1 V1207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:211421498 G>A maps to NM_001122633.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr2:211441129 T>C maps to NM_001122633.1 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr2:211471659 C>T maps to NM_001122633.1 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr2:211539660 A>G maps to NM_001122633.1 E1385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr2:211454903 G>A maps to NM_001122633.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr2:211464275 C>T maps to NM_001122633.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:145621931 C>A maps to NM_013291.2 E903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:145626156 C>T maps to NM_013291.2 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr8:145623785 G>A maps to NM_013291.2 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr14:92628078 C>T maps to NM_017437.1 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr14:92625449 G>T maps to NM_017437.1 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr14:92601739 C>T maps to NM_017437.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr14:92625619 T>A maps to NM_017437.1 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:92600676 C>T maps to NM_017437.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr14:92609451 C>G maps to NM_017437.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:9580746 G>A maps to NM_016207.2 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:69652583 C>T maps to ENST00000266679 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:69656337 A>G maps to ENST00000266679 *589W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr12:69653875 A>G maps to ENST00000266679 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr11:61183737 G>A maps to NM_024811.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:68575045 C>G maps to NM_001876.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr11:68548197 C>T maps to NM_001876.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:68542816 G>A maps to NM_001876.3 Y514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr11:68566775 C>T maps to NM_001876.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:68540780 C>T maps to NM_001876.3 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:68527763 G>A maps to NM_001876.3 Q691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:68552320 G>A maps to NM_001876.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:68552335 G>A maps to NM_001876.3 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr11:68579924 G>T maps to NM_001876.3 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr11:68582882 G>A maps to NM_001876.3 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr11:68552416 G>A maps to NM_001876.3 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr22:51011395 G>T maps to NM_152245.2 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr19:50210774 C>T maps to NM_152359.2 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:50215190 C>T maps to NM_152359.2 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:50208328 C>T maps to NM_152359.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:50204809 C>A maps to NM_152359.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:50204036 G>A maps to NM_152359.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr1:53676584 G>A maps to NM_000098.2 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr1:53676522 C>T maps to NM_000098.2 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr7:29105713 G>A maps to NM_031311.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:29111997 G>A maps to NM_031311.3 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:29132251 G>T maps to NM_031311.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr7:29111496 G>A maps to NM_031311.3 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr7:29135785 C>T maps to NM_031311.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr23:88008676 G>C did not map to a codon.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr23:88008651 T>A did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:88009097 G>T did not map to a codon.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr23:88008564 C>A did not map to a codon.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr23:88008756 A>C did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr23:88008987 G>C did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr23:88008502 G>C did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:88009298 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:2779447 G>A maps to NM_019609.4 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr4:8602933 C>A maps to NM_001014447.2 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:207751507 C>A maps to NM_000651.4 A1632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr1:207679360 C>T maps to NM_000651.4 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:207741205 G>A maps to NM_000651.4 G1330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:207787830 G>T maps to NM_000651.4 E2220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:207753919 C>T maps to NM_000651.4 L1726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr1:207890872 T>C maps to NM_175710.1 D493D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr1:207857215 G>C did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:207649643 C>T maps to NM_001006658.2 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:207652614 T>A maps to NM_001006658.2 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr1:207646234 A>G maps to NM_001006658.2 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:207643211 G>A maps to NM_001006658.2 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:207653359 T>A maps to NM_001006658.2 I1050I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:207648544 A>G maps to NM_001006658.2 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr15:78640276 C>T maps to NM_004378.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr12:94072576 C>G maps to NM_003805.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr16:1718075 C>A maps to NM_020825.3 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr16:1706278 C>T maps to NM_020825.3 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:1720767 G>C maps to NM_020825.3 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:1716089 G>A maps to NM_020825.3 R923R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr9:131864309 A>G maps to NM_000755.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:131860426 C>T maps to NM_000755.3 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:197390577 C>A maps to NM_201253.2 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:197297663 T>C maps to NM_201253.2 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:197396746 T>A maps to NM_201253.2 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:197404460 C>T maps to NM_201253.2 D1156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:197298068 G>A maps to NM_201253.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:197396758 G>A maps to NM_201253.2 E768E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:197390385 C>T maps to NM_201253.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:197390562 G>A maps to NM_201253.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:197326132 T>C maps to NM_201253.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:197404337 T>C maps to NM_201253.2 G1115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr1:197390403 C>T maps to NM_201253.2 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr1:197404199 A>C maps to NM_201253.2 G1069G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr1:197390550 G>C maps to NM_201253.2 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr1:197398706 C>T maps to NM_201253.2 H935H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:126137516 C>T maps to NM_173689.5 P1176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr9:126136902 C>T maps to NM_173689.5 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:126137567 G>A maps to NM_173689.5 G1193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:126132736 C>T maps to NM_173689.5 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:126132585 G>A maps to NM_173689.5 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr9:35736715 C>G maps to NM_006368.4 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr9:35733424 G>A maps to NM_006368.4 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:46341830 C>G maps to ENST00000288400 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:4171168 C>T maps to NM_032607.1 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:4155014 C>T maps to NM_032607.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:4171732 C>T maps to NM_032607.1 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:28547349 A>T maps to NM_182898.2 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr7:28857686 G>C did not map to a codon.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr7:28609990 G>A maps to NM_182898.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:3778855 G>A maps to NM_004380.2 P2064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr16:3820843 G>C maps to NM_004380.2 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr16:3819188 C>A maps to NM_004380.2 E1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:3781252 G>C maps to NM_004380.2 V1704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:3779047 C>T maps to NM_004380.2 L2000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:3777766 G>A maps to NM_004380.2 V2427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr16:3779590 G>T maps to NM_004380.2 C1819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:3781357 G>A maps to NM_004380.2 T1669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr16:3819249 C>T maps to NM_004380.2 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr16:3832720 G>A maps to NM_004380.2 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr16:3820791 G>A maps to NM_004380.2 Q887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr16:3779446 C>T maps to NM_004380.2 R1867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr16:3779765 G>C maps to NM_004380.2 S1761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr16:3789615 G>A maps to NM_004380.2 Q1415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:85375814 C>G maps to NM_001039618.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:85375309 G>A maps to NM_001039618.2 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:102000149 T>C maps to NM_153836.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:9979743 C>T maps to NM_001077415.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:9979761 C>T maps to NM_001077415.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr22:50319134 G>A maps to NM_001135101.1 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr22:50315315 C>A maps to NM_001135101.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr8:67089289 G>C maps to NM_000756.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr5:76264638 C>T maps to NM_001882.3 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:43893832 G>A maps to NM_001145146.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr7:30702316 G>A maps to ENST00000348438 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:30695279 G>T maps to ENST00000348438 Y350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:36774271 A>G maps to NM_016441.2 K964K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr2:36691742 C>T maps to NM_016441.2 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr4:1388817 A>T maps to NM_175918.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:49803046 A>T maps to NM_001131.2 C244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr6:49803037 C>T maps to NM_001131.2 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:49704205 A>G maps to NM_001190986.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:49704109 C>T maps to NM_001190986.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr8:75928803 G>A maps to NM_031461.5 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr16:84906614 C>T maps to NM_031476.3 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:1340184 C>T maps to NM_016823.2 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:1317517 A>G did not map to a codon.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr23:1325402 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:1314913 C>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:1327713 A>G did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:1317427 C>T did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:5862864 G>A maps to NM_001014809.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr20:20023026 C>T maps to NM_016652.4 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr20:20029144 C>T maps to NM_016652.4 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:152382204 C>G maps to NM_016190.2 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:152383332 C>T maps to NM_016190.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr1:152384625 G>A maps to NM_016190.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:17275396 C>T maps to NM_014675.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:17263290 G>A maps to NM_014675.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:17295648 G>T maps to NM_014675.3 L1705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:17275396 C>T maps to NM_014675.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr1:17256381 G>T maps to NM_014675.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr1:17280764 G>A maps to NM_014675.3 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr1:17296410 G>A maps to NM_014675.3 Q1811Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr7:87027900 C>T maps to NM_001143935.1 Q622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:99655056 G>A maps to NM_018058.4 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr10:99683125 C>T maps to NM_018058.4 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr10:99696029 C>T maps to NM_018058.4 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:122724649 G>T did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:122720854 G>A maps to NM_019604.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:122709300 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:122726430 T>C maps to NM_019604.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:33155700 C>T maps to NM_006371.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr19:18853805 C>T maps to NM_001098482.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:18856673 C>T maps to NM_001098482.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr19:18856685 G>T maps to NM_001098482.1 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr15:91172508 C>T maps to NM_022769.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr15:91181739 G>A maps to NM_022769.3 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:48342675 A>T maps to NM_000554.4 K118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:48337741 C>T maps to NM_000554.4 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:107415888 T>C maps to NM_004075.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr11:45880358 G>A maps to NM_021117.3 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr22:27019316 G>A did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:27026411 G>A maps to NM_001886.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:27026340 C>T maps to NM_001886.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr22:27024265 G>A maps to NM_001886.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr22:26995606 G>A maps to NM_001887.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr22:26995537 C>T maps to NM_001887.3 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr22:25601218 G>A maps to NM_004076.3 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr22:25599780 G>A maps to NM_004076.3 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr22:25601254 G>A maps to NM_004076.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:97596760 G>T maps to ENST00000182096 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:97596631 G>C maps to ENST00000182096 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:151133381 G>A maps to NM_144727.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:21006354 G>A maps to NM_015974.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr1:75172794 G>A maps to NM_001889.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:75188945 G>A maps to NM_001889.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr21:34968062 G>C maps to ENST00000416217 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:53573577 C>T maps to NM_015989.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr12:53563910 C>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr22:41969736 C>T maps to NM_014460.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:115268983 T>C maps to NM_001130523.1 K511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:115275261 G>C maps to NM_001130523.1 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr20:47682984 T>C maps to NM_001316.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:110466424 C>G maps to NM_000757.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:110456909 C>T maps to NM_000757.4 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr5:149439333 C>T maps to NM_005211.3 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:131409632 C>A maps to NM_000758.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr5:131411511 C>T maps to NM_000758.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:1407467 C>T did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr23:1409268 C>T did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr23:1407733 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:1407735 C>T did not map to a codon.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr23:1428415 G>A did not map to a codon.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr22:37322076 G>A maps to ENST00000262825 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:37325495 C>T maps to ENST00000262825 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr22:37328805 G>A did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:19297417 C>T maps to NM_018371.4 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr8:19316070 G>A maps to NM_018371.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr8:19316148 G>T maps to NM_018371.4 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr8:19277992 C>T maps to NM_018371.4 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr8:19315938 G>A maps to NM_018371.4 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:19316154 T>C did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr8:19277938 C>T maps to NM_018371.4 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr10:43678750 C>T maps to NM_018590.3 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr10:43650761 G>A maps to NM_018590.3 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:61972820 C>A maps to NM_022640.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr17:61949684 T>A did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:61949590 G>C maps to NM_020991.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr15:75094369 C>T maps to NM_004383.2 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:2820915 G>T maps to NM_033225.5 A3094A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr8:3081279 C>T maps to NM_033225.5 P1485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr8:3245094 C>T maps to NM_033225.5 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr8:3059158 G>A maps to NM_033225.5 L1691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr8:3087642 G>A maps to NM_033225.5 Q1422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr8:2820153 G>A maps to NM_033225.5 F3154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr8:3611464 G>A maps to NM_033225.5 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:2855569 G>A maps to NM_033225.5 S2780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr8:2820009 G>A maps to NM_033225.5 S3202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:4494991 G>A maps to NM_033225.5 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr8:3059179 G>A maps to NM_033225.5 T1684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr8:2976017 G>A maps to NM_033225.5 F2111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:3165293 G>A maps to NM_033225.5 S1291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:2886889 G>T maps to NM_033225.5 C2602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr8:3046477 G>T maps to NM_033225.5 Y1818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:2813198 G>A maps to NM_033225.5 C3302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:3265496 G>A maps to NM_033225.5 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr8:2855701 G>A maps to NM_033225.5 I2736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr8:3046418 G>T maps to NM_033225.5 S1838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr8:2820897 C>T maps to NM_033225.5 P3100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr8:3216728 A>G maps to NM_033225.5 L1083L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:34180271 G>A maps to ENST00000373381 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:34066576 G>T maps to ENST00000373381 G2208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:34123660 G>T maps to ENST00000373381 G1404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:34383834 C>A maps to ENST00000373381 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:34276391 G>A maps to ENST00000373381 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:34066516 G>C maps to ENST00000373381 L2228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:34174730 C>T maps to ENST00000373381 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:34092181 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:34180271 G>C maps to ENST00000373381 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr1:34123603 G>T maps to ENST00000373381 I1423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr1:34192215 C>T maps to ENST00000373381 K773K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr1:34204888 G>T maps to ENST00000373381 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr1:34068081 C>T maps to ENST00000373381 P2159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr1:34035052 G>A maps to ENST00000373381 S2644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:113599422 G>A maps to NM_198123.1 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:113267586 G>T maps to NM_198123.1 S3311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr8:113317028 A>G maps to NM_198123.1 Y2729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr8:113569163 A>G maps to NM_198123.1 C1354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr8:113812445 C>A maps to NM_198123.1 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr8:114186128 A>G maps to NM_198123.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr8:113966913 G>T maps to NM_198123.1 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr8:113694783 G>T maps to NM_198123.1 S855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr8:113484818 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:113421232 C>T maps to NM_198123.1 Q1808Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:114111142 G>T maps to NM_198123.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr8:113529454 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr8:113420612 G>A maps to NM_198123.1 Q1847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr8:113668481 G>A maps to NM_198123.1 Q969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr8:113668482 G>T maps to NM_198123.1 T968T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr8:113402994 A>G maps to NM_198123.1 T1944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr8:113275943 G>C maps to NM_198123.1 G3262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:113249530 G>C maps to NM_198123.1 Y3505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:113277721 G>T maps to NM_198123.1 G3202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:113317076 G>A maps to NM_198123.1 S2713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:113668539 C>G maps to NM_198123.1 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:113562954 G>T maps to NM_198123.1 I1503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:113259247 C>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:113243842 C>A maps to NM_198123.1 G3587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:113585862 C>T maps to NM_198123.1 T1303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:113599378 G>T maps to NM_198123.1 C1267*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-6952-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr8:113267645 A>T maps to NM_198123.1 C3291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:113585855 G>A maps to NM_198123.1 L1306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:113694686 C>T maps to NM_198123.1 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:113326781 A>T maps to NM_198123.1 P2475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr8:113347672 G>A maps to NM_198123.1 I2350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:114031356 G>A maps to NM_198123.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:113585823 G>A maps to NM_198123.1 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:113277673 A>G maps to NM_198123.1 N3218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:113697682 G>A maps to NM_198123.1 Q812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:113697866 C>T maps to NM_198123.1 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr8:113326249 G>T maps to NM_198123.1 S2527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr8:113347647 A>G maps to NM_198123.1 L2359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr8:113241098 G>T maps to NM_198123.1 S3617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:114326861 T>C maps to NM_198123.1 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr8:113662432 G>T maps to NM_198123.1 C1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr8:113563055 G>A maps to NM_198123.1 R1470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr8:114111058 G>C maps to NM_198123.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:113353855 G>A maps to NM_198123.1 R2168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr8:113353842 G>T maps to NM_198123.1 S2172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr8:113259261 C>T maps to NM_198123.1 Q3403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr8:113293460 A>G maps to NM_198123.1 P3150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr8:113299437 G>T maps to NM_198123.1 P3062P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:70810587 A>G maps to NM_001890.1 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr4:70823387 G>T maps to NM_001891.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr5:148899952 T>C did not map to a codon.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr13:37679303 G>A maps to NM_145203.5 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr17:80211117 G>A maps to NM_001893.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr22:38698934 G>C maps to NM_001894.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr22:38690153 G>A maps to NM_001894.4 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr22:38698964 C>G maps to NM_001894.4 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:122930767 G>A maps to NM_001044723.1 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr20:485835 G>A maps to NM_177559.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr20:468205 G>A maps to NM_177559.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr20:468127 G>A maps to NM_177559.2 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr20:489117 G>T maps to NM_177559.2 Y26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr16:58202513 C>T maps to NM_001896.2 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:58220735 G>A maps to NM_001896.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:75982532 G>A maps to NM_001897.4 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr15:75981391 G>A maps to NM_001897.4 R672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr15:75977613 C>T maps to NM_001897.4 L1406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:75979624 G>A maps to NM_001897.4 Q1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:75981040 G>A maps to NM_001897.4 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr15:75981290 C>T maps to NM_001897.4 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr15:75981296 G>A maps to NM_001897.4 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr15:75974678 C>T maps to NM_001897.4 Q1635Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:47618789 C>T maps to ENST00000383738 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr3:47618420 C>T maps to ENST00000383738 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:68044263 G>A maps to ENST00000389042 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr8:68092139 G>T maps to ENST00000389042 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:39184824 G>C maps to NM_033027.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr12:51467695 G>A maps to NM_030809.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr2:166532980 G>T maps to ENST00000409420 G222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:166533060 C>T maps to ENST00000409420 C248C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr20:18143303 C>T maps to NM_020536.4 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr20:18163850 G>T maps to NM_020536.4 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr20:18165391 A>C maps to NM_020536.4 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr20:23731350 G>A maps to NM_001898.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr20:23614553 T>A maps to NM_000099.2 *147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:23860132 T>A maps to NM_001900.4 K61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr20:23860166 G>A maps to NM_001900.4 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr20:23860157 G>A maps to NM_001900.4 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr20:23586432 G>C maps to NM_001008693.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr20:23546667 C>G maps to NM_080610.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr20:23545617 G>C maps to NM_080610.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr20:23546709 A>T maps to NM_080610.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr21:45194586 G>T maps to NM_000100.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr23:100078982 G>A did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:100087824 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr23:100087837 C>A did not map to a codon.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr10:53459123 G>A maps to NM_015235.2 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr23:134947916 G>T did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr23:134947935 A>T did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:120008794 G>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:120009418 C>T did not map to a codon.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr23:120009316 C>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:120008942 C>A did not map to a codon.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr23:120008848 T>A did not map to a codon.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr23:120008849 C>G did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:120007814 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:120008875 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:120008972 G>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:120008749 C>T did not map to a codon.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr23:120008978 T>C did not map to a codon.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr23:120008773 A>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:120009410 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr23:120008939 C>T did not map to a codon.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr23:153880468 C>T did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr23:153880550 A>T did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr23:153880411 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr23:153880850 G>C did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:19995653 C>T maps to NM_172241.2 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr18:19995818 T>C maps to NM_172241.2 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr14:39769087 A>T maps to ENST00000396158 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:39815159 T>C maps to ENST00000396158 C633C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:39796070 C>G maps to ENST00000396158 S564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr14:39771433 G>A maps to ENST00000396158 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:132029994 G>A maps to NM_001145659.1 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:126681774 G>A maps to NM_022802.2 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:126715458 G>T maps to NM_022802.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr10:126716162 G>T maps to NM_022802.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:126682485 T>C maps to NM_022802.2 Q823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr10:126682530 C>A maps to NM_022802.2 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:126715137 G>A maps to NM_022802.2 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:126715548 G>A maps to NM_022802.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:126715968 T>C maps to NM_022802.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:85036298 G>T maps to NM_004388.2 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr16:67645172 C>A maps to NM_006565.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:67650750 G>A maps to NM_006565.3 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:67655478 C>T maps to NM_006565.3 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr16:67670699 A>T maps to NM_006565.3 K649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:67670669 C>T maps to NM_006565.3 Q639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr20:56099081 G>A maps to ENST00000423479 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr20:56094386 A>G maps to ENST00000423479 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr20:56073692 G>A maps to ENST00000423479 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr20:56098319 C>T maps to ENST00000423479 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr20:56098195 C>A maps to ENST00000423479 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr18:77513777 C>T maps to NM_004715.3 N958N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr18:77477673 G>A maps to NM_004715.3 Q736Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:77464882 C>T maps to NM_004715.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:58220808 G>A maps to NM_005730.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr15:44776529 C>T maps to NM_016396.2 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:132271471 G>A maps to NM_001901.2 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:132270616 G>A maps to NM_001901.2 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr1:70887339 A>G maps to NM_001902.5 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr8:104394751 C>G maps to NM_138455.2 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:204732683 C>T maps to NM_005214.3 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:138260996 G>A maps to ENST00000355078 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr2:80620358 T>C maps to ENST00000402739 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:80085145 G>A maps to ENST00000402739 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:80801321 C>A maps to ENST00000402739 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr2:80085217 G>A maps to ENST00000402739 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:80620388 T>C maps to ENST00000402739 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:80085226 T>G maps to ENST00000402739 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:80097015 G>T maps to ENST00000402739 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:80816526 C>G maps to ENST00000402739 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:80646672 G>T maps to ENST00000402739 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:80801426 G>T maps to ENST00000402739 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:80646681 G>T maps to ENST00000402739 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr2:80620361 T>C maps to ENST00000402739 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr2:80620406 A>C maps to ENST00000402739 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr10:68040263 T>C maps to NM_013266.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:67726464 G>A maps to NM_013266.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:68280483 C>A maps to NM_013266.2 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr10:67829213 C>A maps to NM_013266.2 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:67862932 G>A maps to NM_013266.2 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr10:68280453 A>G maps to NM_013266.2 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr9:111745496 C>T maps to NM_003798.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:111735077 T>C maps to NM_003798.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr3:41275253 C>T maps to NM_001904.3 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr3:41275707 C>T maps to NM_001904.3 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr3:41266589 A>G maps to NM_001904.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:41267195 C>T maps to NM_001904.3 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr3:41266470 C>T maps to NM_001904.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:57578935 C>G maps to NM_001085458.1 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr11:57563201 G>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:57559054 C>G maps to NM_001085458.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr11:57582973 T>C did not map to a codon.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr5:11384810 G>C maps to NM_001332.2 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:11346592 G>A maps to NM_001332.2 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr5:11022897 G>T maps to NM_001332.2 S994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:11236805 G>T maps to NM_001332.2 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:11023076 G>A maps to NM_001332.2 R935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:11346703 G>A maps to NM_001332.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr5:11082865 G>A maps to NM_001332.2 C910C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr5:10992675 G>T maps to NM_001332.2 P1066P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:11159791 C>T maps to NM_001332.2 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:11236907 C>A maps to NM_001332.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr5:11082913 C>A maps to NM_001332.2 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:11023089 G>T maps to NM_001332.2 G930G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr5:10981947 A>C maps to NM_001332.2 T1118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr5:11082942 G>A maps to NM_001332.2 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr5:11346496 G>A maps to NM_001332.2 Q539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr5:11022969 C>G maps to NM_001332.2 V970V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:3550807 C>T maps to NM_001031681.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:41471750 G>C maps to NM_001905.2 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr23:16635318 T>C did not map to a codon.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr23:16717104 A>G did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr8:11706667 G>A maps to NM_147783.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr11:88045587 G>A maps to NM_001814.4 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:1774843 C>T maps to NM_001909.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:1774753 G>A maps to NM_001909.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:1775231 G>A maps to NM_001909.3 Q322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr11:66332089 G>A maps to NM_003793.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr11:66335130 G>C maps to NM_003793.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:25043922 T>C maps to NM_001911.2 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr14:25043672 C>T maps to NM_001911.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr15:79231499 G>A maps to NM_004390.3 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr9:90343232 C>T maps to NM_145918.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr9:90343214 C>A maps to NM_145918.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr4:156860669 G>A maps to NM_001334.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:156858587 T>C maps to NM_001334.2 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr4:156850843 C>A maps to NM_001334.2 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:150724307 G>A maps to NM_004079.4 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:150724457 G>A maps to NM_004079.4 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:65649790 C>T maps to NM_001335.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr11:70267603 C>T maps to NM_005231.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:70260655 C>T maps to NM_001184740.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr11:70282396 C>T maps to NM_001184740.1 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr11:70282396 C>T maps to NM_001184740.1 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr11:70265885 C>T maps to NM_001184740.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:70271436 G>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:117432537 G>T maps to NM_033427.2 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:117407110 A>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:117375350 G>A maps to NM_033427.2 S1220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr7:117351771 A>T maps to NM_033427.2 L1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:117450884 G>A maps to NM_033427.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:117375086 G>A maps to NM_033427.2 A1252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr7:117450911 G>C maps to NM_033427.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr7:117407214 A>G maps to NM_033427.2 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:117431593 G>A maps to NM_033427.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr16:88780173 C>T maps to ENST00000378384 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:88778041 G>T did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr16:88780993 G>A did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:16957876 G>A maps to NM_001081.3 Q2385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:17142003 C>A maps to NM_001081.3 E589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:16955851 C>A maps to NM_001081.3 L2497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr10:16882890 G>A maps to NM_001081.3 I3273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:17142172 A>C maps to NM_001081.3 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:16918965 C>T maps to NM_001081.3 P3012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr10:17165685 A>T maps to NM_001081.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:17147563 A>T maps to NM_001081.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr10:16918893 A>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr10:16911692 G>A maps to NM_001081.3 F3132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr10:16949519 G>T maps to NM_001081.3 S2564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:16882499 G>A maps to NM_001081.3 T3287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:16955869 G>A maps to NM_001081.3 T2491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr10:16911674 C>T maps to NM_001081.3 Q3138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr10:16941114 G>T maps to NM_001081.3 P2826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:16948289 C>T maps to NM_001081.3 Q2608Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr10:17152948 A>T maps to NM_001081.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:17145222 G>A maps to NM_001081.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:16982124 G>A maps to NM_001081.3 L1818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr10:17032491 C>T maps to NM_001081.3 G1397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr10:16982079 G>T maps to NM_001081.3 I1833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7393-01A-11D-2012-08 chr17:55957075 A>G maps to NM_017949.1 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:104184419 G>A maps to NM_024040.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:148495715 G>T maps to NM_003592.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:148487476 C>T maps to NM_003592.2 Q584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:148427270 G>A maps to NM_003592.2 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr7:148496404 G>A maps to NM_003592.2 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:225365128 T>A maps to NM_003590.3 K521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:225376089 C>T maps to NM_003590.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:225365204 C>A did not map to a codon.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:225400285 G>A maps to NM_003590.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr2:225379490 T>C did not map to a codon.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr2:225379380 G>A maps to NM_003590.3 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr13:113887571 G>A maps to NM_001008895.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr13:113893750 C>T maps to NM_001008895.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr23:119672602 G>T did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:119660659 C>T did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:119666335 C>G did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:119677599 T>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:119694441 G>A did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:119672527 G>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:119670818 G>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:43015984 C>T maps to NM_001168370.1 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:43006427 C>T maps to NM_001168370.1 A1565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:43013125 C>G maps to NM_001168370.1 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr6:43014264 G>C maps to NM_001168370.1 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr6:43006376 G>C maps to NM_001168370.1 L1582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr6:43155035 C>T maps to ENST00000354495 Y480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr6:43188999 C>T maps to ENST00000354495 L2231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:43154057 T>C maps to ENST00000354495 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:101837128 A>T maps to ENST00000360264 K373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:101839912 G>A did not map to a codon.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr7:101844778 C>T maps to ENST00000360264 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:101813748 G>A maps to ENST00000360264 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr7:101845471 C>A maps to ENST00000360264 I976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr7:101559502 G>T maps to ENST00000360264 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:101845342 C>T maps to ENST00000360264 P933P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:101840037 C>T maps to ENST00000360264 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr12:111744813 C>T maps to NM_015267.3 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:111758443 G>A maps to NM_015267.3 K877K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr12:111746109 G>T maps to NM_015267.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:111776183 G>A maps to NM_015267.3 L1097L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:111655723 A>T maps to NM_015267.3 K69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:111746269 G>T maps to NM_015267.3 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr12:111745028 G>A maps to NM_015267.3 Q359Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:36977260 C>T maps to NM_017748.3 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr17:36963198 G>A maps to NM_017748.3 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:64267528 G>C did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:64079698 G>T maps to NM_005869.2 G97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:107197636 C>T maps to NM_152434.2 *895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr11:107219717 A>T maps to NM_152434.2 L716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr4:49034612 G>T maps to NM_025087.2 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr4:49030674 C>A maps to NM_025087.2 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:39307505 G>A maps to NM_001171174.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:39307931 A>T maps to NM_001171174.1 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr3:39306962 C>G maps to NM_001171174.1 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:74735495 C>T maps to NM_001511.2 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:4638417 C>T maps to NM_001100812.1 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:4638450 G>A maps to NM_001100812.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:4638731 G>A maps to NM_001100812.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:42933036 T>C maps to NM_198477.1 *120W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:74964367 G>C maps to NM_002089.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr4:74702556 G>A maps to NM_002993.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr4:76928537 C>T did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:219000051 G>A maps to NM_001168298.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:219000409 C>T maps to NM_001168298.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr2:219000420 C>T maps to NM_001168298.1 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr2:219000423 G>A maps to NM_001168298.1 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr23:70836724 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:70837231 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:118765005 C>T maps to NM_001716.3 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:237489773 C>T maps to NM_020311.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr18:47813189 C>T maps to NM_001101654.1 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr18:47812520 C>T maps to NM_001101654.1 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr18:47812184 C>T maps to NM_001101654.1 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr5:139060914 C>T maps to NM_016463.7 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr5:139061004 C>G maps to NM_016463.7 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr5:139060659 C>T maps to NM_016463.7 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr5:139060866 C>T maps to NM_016463.7 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr5:139061004 C>G maps to NM_016463.7 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr23:144909490 C>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:30578275 G>C did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr23:30578441 C>G did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr23:30578056 G>T did not map to a codon.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr23:30577997 A>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:30577867 T>C did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:30577958 G>T did not map to a codon.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr23:30577887 C>T did not map to a codon.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr23:36007602 G>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:35974207 C>G did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:35989849 G>T did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr23:35969426 C>A did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr23:35985813 T>A did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:35989885 A>C did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:35974237 G>C did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr23:35974177 C>T did not map to a codon.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr23:35974174 T>G did not map to a codon.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr23:35993983 C>A did not map to a codon.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr23:35938045 C>T did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr23:35966560 A>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:35990012 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:35994001 G>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:35974157 C>T did not map to a codon.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr23:35966479 A>T did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr23:35969931 C>T did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:35993267 T>G did not map to a codon.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr23:35989809 C>T did not map to a codon.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr23:19984741 C>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:19983782 G>C did not map to a codon.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr23:75395435 A>G did not map to a codon.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr23:75397551 G>A did not map to a codon.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr23:75393428 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:37850394 T>A did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:37850190 C>A did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr23:40496290 C>G did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:40498349 G>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:148628499 G>C did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:148627326 G>A did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr23:148627336 G>A did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:148627223 C>G did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:149100769 C>G did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr23:149101931 C>T did not map to a codon.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr23:149100950 G>C did not map to a codon.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr23:134292162 T>C did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:134305096 G>A did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:134305034 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr23:134305033 C>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:118675340 C>G did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:118675308 C>G did not map to a codon.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr23:118673706 C>G did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:118678341 T>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:105855462 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr23:105882882 C>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr23:105882843 G>T did not map to a codon.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr23:105882773 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:105879861 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr23:105875858 C>T did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr23:23928432 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:23933834 G>A did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:23934384 T>C did not map to a codon.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr23:23956698 C>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:23945484 C>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:36162887 A>T did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:36091372 A>G did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:36122646 G>T did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:36162676 G>C did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:36103428 A>T did not map to a codon.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr23:36091265 A>C did not map to a codon.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr23:36156477 T>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:36162702 A>G did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:36162700 G>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:36103496 C>A did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:36162721 T>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:115593059 G>T did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr23:139038790 T>A did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr23:139038791 C>A did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr23:139038573 T>C did not map to a codon.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr23:139038214 G>T did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr23:139038257 G>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:139040245 G>A did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:61512583 G>A maps to NM_001915.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr17:4053284 C>T maps to NM_144611.3 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr11:7689763 C>A maps to NM_016229.3 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr11:7693999 C>A maps to NM_016229.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:43015835 G>C maps to NM_001171660.1 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:84644344 C>T maps to NM_016230.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr6:84665106 G>A maps to NM_016230.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:37655261 T>C did not map to a codon.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr23:37641385 C>T did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr23:37651298 T>C did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:37660571 C>T did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr8:145150851 G>C maps to NM_001916.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:145151331 T>C maps to NM_001916.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr7:25163648 C>T maps to NM_018947.5 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:22993079 G>A maps to NM_014608.2 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr15:22956373 G>A maps to NM_001033028.1 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr15:22990178 G>C maps to NM_014608.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr15:22999448 C>G maps to NM_014608.2 P1107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr15:22933782 C>T maps to NM_014608.2 Y234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:22933612 C>T maps to NM_014608.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr15:22947043 G>A maps to NM_014608.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr15:22926025 C>T maps to NM_014608.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:156723751 C>A maps to ENST00000442283 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr5:156753239 A>T maps to ENST00000442283 K707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:156751059 C>T maps to ENST00000442283 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr5:156741392 G>A maps to ENST00000442283 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr5:156786086 C>A maps to ENST00000442283 I941I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr5:156760405 G>A maps to ENST00000442283 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr5:156741410 C>T maps to ENST00000442283 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:74527687 G>A maps to NM_134268.3 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr8:145689746 C>G maps to NM_001129888.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:83128481 G>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:83128537 G>A did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr23:83128621 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr23:83127917 G>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:83128941 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:83129260 G>A did not map to a codon.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr23:83128669 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr23:83128512 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr23:83129516 C>T did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr23:83129132 A>C did not map to a codon.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr23:83129426 G>A did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:83128053 C>A did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:83128054 A>C did not map to a codon.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr23:83128915 A>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:105765546 T>C did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr9:105767307 C>G maps to NM_001340.3 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr16:50820853 A>T maps to ENST00000311559 K680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr16:50811825 C>A maps to ENST00000311559 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr16:50811744 C>G maps to ENST00000311559 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr16:50811807 C>G maps to ENST00000311559 S365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr15:74659878 G>T maps to NM_000781.2 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr15:74630345 G>A maps to NM_000781.2 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:74631109 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:74636149 C>T maps to NM_000781.2 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr15:74637400 G>A maps to NM_000781.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:143957719 C>T maps to ENST00000377675 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:143961151 C>G maps to ENST00000377675 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr8:143994786 C>G maps to NM_000498.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:143999223 C>T maps to NM_000498.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:143994780 G>T maps to NM_000498.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:143994843 C>A maps to NM_000498.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr8:143993503 C>G maps to NM_000498.3 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr10:104591346 G>A maps to NM_000102.3 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:51534992 C>T maps to NM_031226.2 W39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr15:75013357 G>A maps to NM_000499.3 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:75047130 G>C did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr15:75042738 G>A maps to NM_000761.3 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:38301664 G>A maps to NM_000104.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr2:38302532 C>T did not map to a codon.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:38301496 G>A maps to NM_000104.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr2:38302189 G>A maps to NM_000104.3 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:32007954 C>T maps to NM_000500.5 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:31975462 T>C maps to NM_000500.5 *316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr10:94824175 G>A maps to NM_183374.2 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr10:94828252 G>A maps to NM_183374.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:219677073 G>T maps to NM_000784.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:58160809 G>C maps to NM_000785.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr12:58160729 G>C maps to NM_000785.3 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr12:58160779 G>A maps to NM_000785.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:127957113 G>A maps to NM_001001665.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:41594862 C>T maps to NM_000766.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr19:41594865 T>A maps to NM_000766.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:41594901 A>G maps to NM_000766.3 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:41597686 A>G maps to NM_000766.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr19:41354624 G>A maps to NM_000762.5 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr19:41382567 G>A maps to NM_000764.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:41386405 G>A maps to NM_000764.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr19:41510325 G>A maps to NM_000767.4 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:41516002 C>T maps to NM_000767.4 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:41509944 G>T maps to NM_000767.4 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr19:41497218 C>A maps to NM_000767.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:96454786 G>T maps to NM_000772.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:96454827 G>A maps to NM_000772.2 W212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr10:96484145 G>C maps to NM_000772.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:96612542 C>T maps to NM_000769.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr10:96698525 C>T maps to NM_000771.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr10:96748782 T>A maps to NM_000771.3 *491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr10:96745812 G>C maps to NM_000771.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr22:42522958 C>G maps to NM_000106.4 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr10:135346243 A>T maps to NM_000773.3 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr10:135350630 G>A maps to NM_000773.3 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr19:41622400 A>G maps to NM_000774.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr1:60381633 G>A maps to NM_000775.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:60381703 G>A maps to NM_000775.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr11:14899668 C>A maps to NM_024514.4 *502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:41704508 C>G maps to ENST00000301173 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr7:1027133 C>G maps to NM_017781.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr6:46518113 G>A maps to NM_016593.3 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr6:46620226 G>A maps to NM_016593.3 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr7:99447258 G>A maps to NM_022820.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr7:99258196 A>G maps to NM_000777.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:99270238 T>G maps to NM_000777.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:99305455 G>A maps to ENST00000292414 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr7:99308495 G>C maps to ENST00000292414 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr14:100172988 T>A maps to NM_006668.1 L150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:100157457 G>T maps to NM_006668.1 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:100192928 G>A maps to NM_006668.1 Q456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:47399864 A>G maps to ENST00000371904 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:47398444 G>C maps to ENST00000371904 S452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:47609431 A>C did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:47606534 C>G maps to NM_001010969.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr1:47607907 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr1:47607876 G>A maps to NM_001010969.2 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:47614435 C>G maps to NM_001010969.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:47282726 C>T maps to NM_001099772.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:47282749 C>G maps to NM_001099772.1 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:47264770 C>T maps to NM_001099772.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr1:47279206 T>C maps to NM_001099772.1 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:47283804 C>G maps to NM_001099772.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:16025590 G>A maps to NM_021187.3 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr19:16038132 C>A maps to NM_021187.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:16025611 C>T maps to NM_021187.3 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:16034705 G>A maps to NM_021187.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:16034645 G>A maps to NM_021187.3 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:15807870 G>A maps to NM_023944.2 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:15807025 G>A maps to NM_023944.2 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr19:15791301 C>A maps to NM_023944.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr19:15789114 G>A maps to NM_023944.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:15807253 C>T maps to NM_023944.2 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:16001225 C>T maps to NM_001082.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr19:15989613 G>T maps to NM_001082.3 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:16006352 G>A maps to NM_001082.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:15989673 G>A maps to NM_001082.3 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr19:15997109 G>A maps to NM_001082.3 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:15769191 C>A maps to NM_000896.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr19:15769112 T>C maps to NM_000896.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:15760803 A>T maps to NM_000896.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr19:15769313 C>T maps to NM_000896.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:15739138 G>T maps to NM_007253.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr4:187120146 C>T maps to NM_207352.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:47548130 C>T maps to NM_178134.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:47571829 G>A maps to NM_178134.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr7:91756927 C>T maps to NM_000786.3 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr7:91758199 A>G maps to NM_000786.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr8:59409509 G>A maps to NM_000780.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr8:59410988 T>C maps to NM_000780.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:59410843 A>G maps to NM_000780.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:65528304 G>A maps to NM_004820.3 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr8:65528524 G>T maps to NM_004820.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr8:65537089 G>A maps to NM_004820.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr3:42916885 C>T maps to NM_004391.2 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr23:77529008 G>A did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr13:49281381 C>T maps to NM_020377.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr13:49281444 C>A maps to NM_020377.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:49281696 C>T maps to NM_020377.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr7:6204941 C>T maps to ENST00000396741 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr22:37708146 C>A maps to NM_013385.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr22:37695299 C>T maps to NM_013385.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:158283871 C>T maps to NM_004288.4 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:158272442 G>T maps to NM_004288.4 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr2:158272256 G>A maps to NM_004288.4 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr22:24718348 C>T maps to NM_015330.2 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr17:20130898 G>A maps to NM_001033553.1 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr17:20109065 C>T maps to NM_001033553.1 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr21:27840861 C>T maps to ENST00000435845 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr2:242707143 C>G maps to NM_152783.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr14:59791159 C>G maps to NM_014992.1 S326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:39855275 C>T maps to ENST00000398904 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:39869181 G>T maps to ENST00000398904 R972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:39846339 G>C maps to ENST00000398904 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr6:39869652 C>A maps to ENST00000398904 S1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr6:39843214 G>A maps to ENST00000398904 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr6:39864720 C>G maps to ENST00000398904 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr6:39859409 G>A maps to ENST00000398904 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr1:57535056 G>T maps to ENST00000371231 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:57480775 C>T maps to ENST00000371231 Q441Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr1:57480883 A>G maps to ENST00000371231 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr1:57480847 G>A maps to ENST00000371231 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr5:39381568 G>T maps to NM_001343.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr9:124526080 C>T maps to ENST00000408936 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr9:124522453 C>T maps to ENST00000408936 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr9:124544671 G>T maps to ENST00000408936 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr9:124535129 C>T maps to ENST00000408936 Q775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr9:124528889 C>T maps to ENST00000408936 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr9:124329481 C>T maps to NM_032552.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr13:72440351 G>A maps to ENST00000359684 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr13:72053409 T>C maps to ENST00000359684 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:72440246 G>A maps to ENST00000359684 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr13:72134000 G>A maps to ENST00000359684 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:85994838 T>A did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:86068179 G>T did not map to a codon.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr23:86068140 G>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:85404038 C>G did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:85994869 C>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:86067961 T>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr23:85969651 A>G did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:85950136 G>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:85969659 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:85403796 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:85906076 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr14:59113332 G>T maps to NM_016651.5 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr14:59112453 G>A maps to NM_016651.5 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:59112861 A>G maps to NM_016651.5 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:59105249 G>T maps to NM_016651.5 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr14:59112195 T>C maps to NM_016651.5 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr14:59112624 C>A maps to NM_016651.5 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:59113413 G>A maps to NM_016651.5 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:59113677 C>T maps to NM_016651.5 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:59113461 G>A maps to NM_016651.5 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr14:59113479 C>T maps to NM_016651.5 Y713Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:47151759 G>C maps to NM_145056.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:47151924 G>A maps to NM_145056.2 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:49569251 G>A maps to NM_004393.4 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr11:61502368 C>T maps to NM_006133.2 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr11:61505661 C>T maps to NM_006133.2 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:61502440 G>A maps to NM_006133.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:61502470 T>C maps to NM_006133.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr11:61511762 C>G maps to NM_006133.2 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr7:6452470 G>A maps to NM_139179.3 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:6476141 C>T maps to NM_139179.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr7:6474644 G>A maps to NM_139179.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr11:61106813 G>A maps to NM_015533.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:49054726 C>T maps to NM_001009996.1 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:49055217 G>A maps to NM_001009996.1 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:109290807 C>T maps to NM_001917.4 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr13:106124953 C>T maps to NM_172370.3 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:155695219 A>G maps to NM_004632.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:155686885 G>A maps to NM_004632.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr9:90313649 G>T maps to NM_004938.2 P897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr9:90317990 G>T maps to NM_004938.2 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr9:90264867 G>A maps to NM_004938.2 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr9:90321942 G>A maps to NM_004938.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr9:90296351 C>T maps to NM_004938.2 R679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:90272958 C>T maps to NM_004938.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr9:90321663 G>A maps to NM_004938.2 T1226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr15:64231509 C>T maps to NM_014326.3 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr15:64204145 C>T maps to NM_014326.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr19:3964799 C>T maps to NM_001348.1 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:3964691 G>C maps to NM_001348.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:3964739 G>A maps to NM_001348.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:159175964 C>T maps to NM_001122951.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr1:159176122 G>C maps to NM_001122951.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:159176032 C>T maps to NM_001122951.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr2:136743007 G>A maps to NM_001349.2 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:136736888 C>A maps to NM_001349.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr1:173795823 G>A did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr6:33288741 G>A maps to NM_001350.4 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:33287563 G>C maps to NM_001350.4 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr6:33287305 G>A maps to NM_001350.4 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr6:33288804 G>A maps to NM_001350.4 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr19:1428914 G>A maps to NM_018959.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:51636286 C>T maps to ENST00000332845 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr12:51634128 C>T maps to NM_014764.3 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr9:121930237 C>T maps to NM_014618.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr9:121930222 G>A maps to NM_014618.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:122004442 G>T maps to NM_014618.2 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr9:122004327 G>T maps to NM_014618.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr9:121929787 A>T maps to NM_014618.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:121976296 C>G maps to NM_014618.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:122075567 G>A maps to NM_014618.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr9:122011376 C>T maps to NM_014618.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr9:121929388 C>T maps to NM_014618.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr9:121971049 G>A maps to NM_014618.2 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:121930285 G>T maps to NM_014618.2 Y454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:42786684 C>T maps to NM_145663.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:42824478 C>T maps to NM_145663.2 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr17:42827995 G>A maps to NM_145663.2 W408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr9:136508638 C>T maps to NM_000787.3 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr9:136501744 C>T maps to NM_000787.3 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:136501546 A>T maps to NM_000787.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr2:120128363 G>A maps to NM_001178017.1 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:120125494 G>A did not map to a codon.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr7:44098508 C>T maps to NM_001122956.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr7:44091507 C>T maps to NM_001122956.1 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:49140148 G>A maps to NM_001352.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr1:100684181 A>G maps to NM_001918.2 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:20180737 T>G maps to ENST00000227256 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr11:20178645 C>T maps to ENST00000227256 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr11:20178008 C>T maps to ENST00000227256 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr9:37860054 A>G maps to NM_024345.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr14:24592243 C>T maps to NM_025230.4 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr9:34107380 C>A maps to NM_015397.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr23:125685718 G>A did not map to a codon.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr23:125685919 C>T did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr23:125686311 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr23:125685628 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr23:125685552 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:125685233 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:125686093 G>T did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr23:125686263 G>T did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr23:125686190 G>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:125685765 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:125685407 G>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:125686072 G>C did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:125685744 C>T did not map to a codon.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr23:125686181 C>T did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr23:125298828 T>A did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr23:125298829 G>T did not map to a codon.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr23:125298804 C>T did not map to a codon.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr23:125298718 G>T did not map to a codon.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr23:125298867 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:125299011 A>T did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:125299535 G>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:125299775 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:125299101 G>T did not map to a codon.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr23:125298774 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr23:125298688 C>T did not map to a codon.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr23:125299868 C>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:125298904 G>C did not map to a codon.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr23:125298762 A>G did not map to a codon.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr8:104427337 G>A maps to NM_015420.6 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr19:14070878 C>T maps to NM_138353.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr19:14069866 T>C maps to NM_138353.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:14069908 G>A maps to NM_138353.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:14070283 G>A maps to NM_138353.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:14070848 C>T maps to NM_138353.2 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:17805712 C>A maps to NM_017741.3 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr2:172309701 G>T maps to NM_025000.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr2:172309701 G>T maps to NM_025000.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr14:73404778 G>A did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr14:73408451 G>C did not map to a codon.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr14:73412677 G>T maps to NM_015604.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr4:41984018 G>T maps to NM_001029955.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr4:41984279 G>A maps to NM_001029955.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:41984114 C>T maps to NM_001029955.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr4:41984153 C>T maps to NM_001029955.3 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:88885611 C>T maps to NM_152418.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr8:88885716 C>T maps to NM_152418.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:88885722 G>T maps to NM_152418.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:88885083 G>A maps to NM_152418.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr8:88885017 G>A maps to NM_152418.3 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:168007625 C>T maps to ENST00000367840 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:168037615 C>T maps to ENST00000367840 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr1:167944228 G>A maps to ENST00000367840 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:27998580 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:27999219 C>G did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:27998654 C>T did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:27998100 C>T did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr23:27999310 C>G did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:27998026 G>A did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:27998997 G>C did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:27998266 G>C did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:27998282 G>T did not map to a codon.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr23:27997957 G>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:27766843 C>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:27766737 G>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:27766813 C>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:27765881 G>T did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr23:27766112 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:27766218 G>A did not map to a codon.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr23:27766661 T>C did not map to a codon.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr6:117866740 C>T maps to ENST00000338728 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:117825023 A>G maps to ENST00000338728 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr6:117846585 G>T maps to ENST00000338728 G192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:98518386 G>A maps to ENST00000326857 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr3:98538220 C>T maps to ENST00000326857 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr3:98538044 C>T did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr18:50451654 G>C maps to NM_005215.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr18:50278743 G>T maps to NM_005215.3 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr18:50923745 G>A maps to NM_005215.3 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr18:50450074 A>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:51013296 G>T maps to NM_005215.3 V1289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr18:50432615 G>T maps to NM_005215.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:50589705 C>T maps to NM_005215.3 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr18:50278719 C>A maps to NM_005215.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr18:50683729 C>T maps to NM_005215.3 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr18:51025690 C>T maps to NM_005215.3 Q1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:50866164 G>A maps to NM_005215.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:50918136 C>A maps to NM_005215.3 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:31312292 C>T maps to NM_181807.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr11:31312207 C>A maps to NM_181807.2 E316*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-6224-01A-11D-1912-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CR-7395-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:24357945 C>T maps to NM_181337.3 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr6:24357840 G>C maps to NM_016356.3 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:32678153 T>C maps to NM_001099434.1 Y197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:32678089 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:32674855 T>C maps to NM_001099434.1 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:6643192 G>A maps to NM_003737.2 P3238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:6661269 G>T maps to NM_003737.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr11:6648869 T>C maps to NM_003737.2 L1800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr11:6648365 A>G maps to NM_003737.2 R1968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:6662064 G>A maps to NM_003737.2 Y260Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:6662628 C>G maps to NM_003737.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:6661320 G>A maps to NM_003737.2 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:6655465 G>A maps to NM_003737.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr11:6648161 G>C maps to NM_003737.2 L2036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:6645100 A>G maps to NM_003737.2 F2602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr4:155256200 C>T maps to NM_017639.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:155256094 T>A maps to NM_017639.3 K381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:155156537 G>C maps to NM_017639.3 S2634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr4:155278468 A>C maps to NM_017639.3 Y234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr4:155158174 G>A maps to NM_017639.3 N2088N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:155161883 A>G maps to NM_017639.3 N1933N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr4:155158156 G>A maps to NM_017639.3 F2094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:155249331 G>A maps to NM_017639.3 Q856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:155176798 A>G maps to NM_017639.3 S1816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:155157871 T>A maps to NM_017639.3 P2189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:155253698 C>A maps to NM_017639.3 G722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:155249305 A>G maps to NM_017639.3 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr4:155254035 C>T maps to NM_017639.3 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr4:155157457 C>A maps to NM_017639.3 L2327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:2290113 G>A maps to NM_001919.3 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:71888146 C>T maps to ENST00000504952 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr13:36402441 G>T maps to NM_004734.4 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr13:36700075 G>T maps to NM_004734.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr13:36700049 G>A maps to NM_004734.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr4:151168814 G>A maps to NM_001040261.4 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr10:115601163 C>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:115595054 T>C maps to NM_014881.3 E993E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr10:115603954 G>C maps to NM_014881.3 V809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr10:14961767 C>A maps to NM_001033855.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr12:91558411 A>G maps to NM_133503.2 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr3:53322223 C>T maps to ENST00000480258 Q511Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:112343709 C>T maps to NM_152624.4 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:155023289 G>A maps to NM_152494.3 E689E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:155023187 C>T maps to NM_152494.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:155004225 C>T maps to NM_144622.2 W188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:155002951 C>G maps to NM_144622.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:155001820 G>A maps to NM_144622.2 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr1:154991184 G>C maps to NM_144622.2 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr13:95098002 C>T maps to NM_001129889.1 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:74598188 G>A maps to NM_004082.4 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr2:74598255 T>C maps to NM_004082.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr2:74597183 G>A maps to NM_004082.4 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:57924486 C>T maps to ENST00000434715 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:57929538 C>T maps to ENST00000434715 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr16:23678399 C>T maps to NM_032486.3 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr16:30440484 G>T maps to NM_024096.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr3:182665101 T>G maps to NM_020640.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr16:20871315 G>C maps to NM_173475.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr16:20873494 G>T maps to NM_173475.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr16:20871624 G>A maps to NM_173475.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr4:52779749 G>A maps to ENST00000451288 *337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:110653580 T>C did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:110653582 G>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:110644423 T>C did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:110654065 A>G did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:110644216 C>A did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr23:110653365 C>G did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:110644289 G>C did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr23:110576306 A>T did not map to a codon.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr23:110653984 C>G did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr23:110653293 C>A did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr23:110644381 G>C did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:110644280 G>C did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr17:79994504 G>A maps to NM_016286.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:61097014 G>T maps to NM_001923.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:61094320 T>A maps to NM_001923.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr11:61084031 C>T maps to NM_001923.3 W411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr11:61069778 C>T maps to NM_001923.3 Q1055Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr11:61067676 G>A maps to NM_001923.3 S1118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:47256376 C>T maps to NM_000107.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr7:50611615 G>A maps to NM_000790.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr7:50611623 C>A maps to NM_000790.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr7:50534958 C>A maps to NM_000790.3 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr7:50611651 G>A maps to NM_000790.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:53513590 C>T maps to NM_001160148.1 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:15956838 C>T maps to NM_032341.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr1:15959964 G>A maps to NM_032341.4 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:15983118 G>A maps to NM_032341.4 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr12:57911135 C>T maps to NM_001195056.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr12:49391989 C>T maps to NM_015086.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr12:49391305 G>A maps to NM_015086.1 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:110714169 C>T maps to NM_003649.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr6:110714070 G>T maps to NM_003649.2 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr6:110714265 C>A maps to NM_003649.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr6:30866961 G>A maps to NM_013994.2 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:30861115 C>G maps to NM_013994.2 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr6:30865888 C>T maps to NM_013994.2 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:30859859 C>G maps to NM_013994.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:30860255 C>T maps to NM_013994.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:30862323 C>G maps to NM_013994.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr6:30856981 G>A maps to NM_013994.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:30863277 C>T maps to NM_013994.2 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:30862380 C>T maps to NM_013994.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:30863239 C>T maps to NM_013994.2 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:162724443 G>A maps to NM_006182.2 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:162748506 C>T maps to NM_006182.2 D807D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:162725085 C>T maps to NM_006182.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:15737537 C>T maps to NM_004939.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr12:31242844 G>A maps to NM_030653.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr12:31256664 G>A maps to NM_030653.3 K897K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:31253967 G>C maps to NM_030653.3 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr2:118579835 A>G maps to NM_006773.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr16:70404239 C>T maps to NM_018332.3 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:70367482 T>G maps to NM_007242.4 *480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:112304935 A>T maps to NM_007204.4 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:112309283 G>A maps to NM_007204.4 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:112309064 C>T maps to NM_007204.4 Y673Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr1:112303129 G>A maps to NM_007204.4 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr10:70741336 G>A maps to NM_004728.2 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr10:70728813 A>G maps to NM_004728.2 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:49225033 G>C maps to NM_004818.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr12:49225033 G>C maps to NM_004818.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr14:94526559 G>A maps to NM_020414.3 C599C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr11:125791158 T>C maps to NM_013264.3 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:134680704 G>T did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr23:134706907 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:134681180 A>G did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:134690126 T>G did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:134713947 C>T did not map to a codon.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr23:134679458 C>G did not map to a codon.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr23:134711239 G>A did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr20:47858648 C>G maps to NM_017895.7 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:68056394 C>A maps to NM_018380.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr19:14521048 C>A maps to ENST00000451994 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:14521828 G>A maps to ENST00000451994 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr23:41205841 C>T did not map to a codon.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr23:41206678 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:41206167 G>C did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:41206209 G>C did not map to a codon.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr23:41203624 G>C did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:41205604 G>C did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:41205820 G>C did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr24:15029412 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr24:15028312 C>A did not map to a codon.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr24:15025641 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr24:15016852 T>C did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr5:176943152 C>A maps to NM_016222.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr5:176940688 G>A maps to NM_016222.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr17:61892948 C>T maps to NM_203499.1 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr6:74104705 G>T maps to NM_018665.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr6:74104732 G>A maps to NM_018665.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr5:134153310 G>A maps to ENST00000452510 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:134131841 T>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:134130684 C>G maps to ENST00000452510 S591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr12:12966312 C>T maps to NM_016355.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr17:62499305 T>C maps to NM_004396.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr12:132624978 C>T maps to NM_175066.3 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:35992313 C>A maps to NM_007010.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:23019336 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:23019110 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:23019810 G>A did not map to a codon.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr23:23018797 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:113614712 C>A maps to NM_001111322.1 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr12:124104213 G>A maps to NM_020936.1 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:44609414 G>A maps to NM_019082.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr9:32493812 G>A maps to NM_014314.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr9:32488811 C>T maps to NM_014314.3 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:200635067 G>A maps to NM_001031725.4 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr1:200619731 G>A maps to NM_001031725.4 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr11:118630663 G>A maps to NM_004397.4 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:118638970 G>A maps to NM_004397.4 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:118656870 G>A maps to NM_004397.4 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:169215015 G>A maps to NM_017631.5 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr4:169227709 G>A maps to NM_017631.5 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:169305795 G>T maps to NM_001012967.1 S1361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:169348296 A>G maps to NM_001012967.1 N618N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:169317110 G>C maps to NM_001012967.1 S1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr4:169315636 G>A maps to NM_001012967.1 L1263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr4:169383026 C>T maps to NM_001012967.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:691545 G>A maps to NM_021008.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr11:687912 G>C maps to NM_021008.2 S221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr8:91057168 C>T maps to NM_001359.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr8:91033150 T>C maps to NM_001359.1 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:42720874 G>A maps to NM_133328.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:35280428 G>A maps to NM_022047.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr6:35287468 T>A did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr6:35280092 G>A maps to NM_022047.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr16:90016034 G>A maps to NM_207514.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:90015942 T>C maps to NM_207514.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr16:90028151 G>A maps to NM_207514.1 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr16:90020770 C>T maps to NM_207514.1 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:6794388 G>T maps to NM_001925.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr8:6913048 G>A maps to NM_021010.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr6:50011491 G>A maps to NM_001037498.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:29960870 G>A maps to NM_054112.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr20:29965129 C>T maps to NM_153289.2 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:30028509 C>T maps to NM_153324.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr20:139649 G>A maps to NM_139074.2 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr20:210097 C>T maps to NM_080831.3 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr8:11842020 A>G maps to NM_001033017.2 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:40980311 A>G maps to NM_022774.1 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr9:126414315 G>A maps to NM_020946.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr9:126214553 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:6476962 G>A maps to NM_024898.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:115153709 G>C maps to ENST00000393274 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:111738608 G>A maps to NM_024901.3 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:111731344 G>A maps to NM_024901.3 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr8:142146791 G>A maps to NM_014957.2 W16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:65994822 T>G maps to ENST00000443035 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr15:65959831 T>C maps to ENST00000443035 L1732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr15:65995209 C>T did not map to a codon.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:153906273 C>G maps to NM_014856.2 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:153905171 G>A maps to NM_014856.2 D1235D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:153914418 G>A maps to NM_014856.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:153903540 C>A did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:19316772 C>G maps to NM_017925.4 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr9:19335102 G>A maps to NM_017925.4 K627K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr9:19316462 G>T maps to NM_017925.4 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr9:19346743 C>G maps to NM_017925.4 S1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7593-01A-11D-2229-08 chr9:19296091 G>A maps to NM_017925.4 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:19332076 T>C maps to NM_017925.4 C549C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:9182328 C>T maps to NM_015213.2 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:9225276 G>A maps to NM_015213.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr12:31586166 C>G maps to NM_144973.3 R676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr12:31555437 G>T maps to NM_144973.3 T981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:31605305 A>T maps to NM_144973.3 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr12:31540539 C>A maps to NM_144973.3 V1274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:31545219 G>C maps to NM_144973.3 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:68948053 G>A maps to NM_001114120.1 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:68948182 C>T maps to NM_001114120.1 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:68947900 A>C maps to NM_001114120.1 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:68943582 C>A maps to NM_001114120.1 E729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr5:59943360 C>T did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:100657383 C>A maps to ENST00000422147 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr22:32198786 A>T maps to NM_001136029.1 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr22:32161046 G>A did not map to a codon.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr8:121015324 C>T maps to NM_022783.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr11:33053025 A>G maps to NM_001077242.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr8:124042887 G>C maps to NM_024295.4 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr2:220286274 G>T maps to NM_001927.3 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:10523545 G>A maps to NM_004401.2 L191L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-H7-7774-01A-21D-2078-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-BA-4075-01A-01D-1434-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr9:117266865 G>A maps to NM_015404.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:117266937 C>T maps to NM_015404.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr8:145542403 G>C maps to NM_012079.4 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:69424863 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:69420190 C>A did not map to a codon.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr23:69420162 A>C did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:69424815 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:69424804 G>A did not map to a codon.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr23:69424195 T>C did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr22:19127504 G>A maps to NM_022719.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:19121855 G>T maps to NM_022719.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr22:19127409 T>C maps to NM_022719.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr22:19028790 G>A maps to NM_005137.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr22:19036127 G>A maps to NM_005137.2 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr22:20307264 G>C maps to NM_033257.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr22:20094893 C>T maps to NM_022720.6 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr12:56334130 G>T maps to NM_201554.1 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr12:56334183 G>T maps to NM_201554.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:56334469 C>T maps to NM_201554.1 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr7:14378223 G>A maps to NM_004080.2 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:14613863 G>A maps to NM_004080.2 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr7:14758227 C>T maps to NM_004080.2 L135L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-A45Z-01A-21D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr7:14378223 G>A maps to NM_004080.2 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr2:234296983 C>T maps to NM_152879.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr2:234343482 G>A maps to NM_152879.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr2:234354352 C>T maps to NM_152879.2 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:234355439 G>T maps to NM_152879.2 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr2:234346040 G>T maps to NM_152879.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:54940146 G>T maps to NM_003647.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr3:185882751 C>G maps to NM_001346.2 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:185882739 G>A maps to NM_001346.2 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr3:185975670 C>T maps to NM_001346.2 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr3:185986616 C>T maps to NM_001346.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr3:185978225 A>T did not map to a codon.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr13:42701666 C>T maps to NM_178009.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr13:42729852 C>A maps to NM_178009.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:137271854 G>T maps to NM_004717.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:137363311 G>C maps to NM_004717.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:137255998 T>A maps to NM_004717.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:137271842 C>A maps to NM_004717.2 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr23:50121609 C>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr23:50127733 C>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:50163497 G>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:50167294 C>G did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr23:50135407 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr23:50121102 T>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:50131608 G>A did not map to a codon.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr23:50119799 G>A did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:50119164 C>A did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr23:50134544 G>A did not map to a codon.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr23:50119143 A>T did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr23:50213156 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:50213564 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:50147113 C>T did not map to a codon.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr23:50129579 T>C did not map to a codon.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr23:50213141 G>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:50122667 T>C did not map to a codon.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr23:50213405 G>C did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:50213566 C>T did not map to a codon.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr23:50167322 A>G did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:50165506 C>T did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:957072 C>T maps to NM_001347.2 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr4:959303 G>A maps to NM_001347.2 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:954458 G>A maps to NM_001347.2 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:46397932 G>A maps to NM_001105540.1 W904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr11:46393101 C>T maps to NM_001105540.1 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr11:46400011 G>T maps to NM_001105540.1 E982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:46396314 G>C did not map to a codon.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr11:46394043 G>T maps to NM_001105540.1 G520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:55317917 G>A maps to NM_014762.3 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr11:71148917 G>A maps to NM_001360.2 H301H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr11:71146831 G>A maps to NM_001360.2 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:49439397 G>A maps to NM_014475.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:93780280 C>T maps to NM_001195643.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr12:49488007 G>A maps to NM_021044.2 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:49484968 G>A maps to NM_021044.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:12790280 C>T maps to NM_001930.2 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:34955436 G>C maps to NM_024308.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr17:34951447 C>T maps to NM_024308.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:52348131 C>T maps to NM_001031719.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:27228112 C>A maps to NM_144683.3 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:24108189 C>A maps to NM_182908.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr14:24113649 G>A maps to NM_182908.4 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr14:24114423 G>A maps to NM_182908.4 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr14:24459414 T>C maps to NM_198083.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr14:24470636 C>A maps to NM_198083.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:60619716 G>A maps to NM_016029.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr14:60622826 C>T maps to NM_016029.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr14:60616103 C>T maps to NM_016029.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr17:9680513 C>T maps to ENST00000330255 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr17:9674888 G>A maps to ENST00000330255 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr2:169952066 G>A maps to NM_001142271.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr2:169952186 C>T maps to NM_001142271.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:12162208 G>A maps to NM_018706.5 Q867Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr10:12160759 C>T maps to NM_018706.5 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:12155014 C>T maps to NM_018706.5 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr4:24529591 G>A maps to NM_001358.2 D781D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr4:24578254 G>A maps to NM_001358.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:30624383 G>C maps to NM_003587.4 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr6:30622987 G>C maps to NM_003587.4 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr6:30622518 G>A maps to NM_003587.4 H987H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:30627338 G>A maps to NM_003587.4 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr6:30638811 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:30624425 A>G maps to NM_003587.4 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:30633511 T>A did not map to a codon.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr6:30632610 C>T maps to NM_003587.4 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:54569132 T>A maps to NM_019030.2 P921P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr5:54565330 C>T maps to NM_019030.2 P1068P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:47889746 C>T maps to NM_138615.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr17:5357157 G>A maps to ENST00000457531 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr17:5353645 G>T maps to ENST00000457531 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr17:5357144 G>A maps to ENST00000457531 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:47884110 C>G maps to NM_014681.5 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:47865832 G>C maps to NM_014681.5 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:37639040 C>T maps to NM_021931.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:154018466 T>C maps to NM_020865.2 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:154013096 C>T maps to NM_020865.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr3:154027539 G>A maps to NM_020865.2 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr12:125470689 C>T maps to NM_032656.3 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:125467154 T>C maps to NM_032656.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr12:125438654 G>A maps to NM_032656.3 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr16:72143369 C>T maps to NM_014003.3 P1146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:72137933 C>T maps to NM_014003.3 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr16:72139498 C>A maps to NM_014003.3 I821I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:57679959 C>T maps to NM_024612.4 F628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr17:57643052 C>G maps to NM_024612.4 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr2:39025461 C>T maps to NM_198963.1 V1380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr2:39088438 G>A maps to NM_198963.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:39070333 C>G maps to NM_198963.1 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr17:40263443 C>G maps to NM_024119.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:41599573 C>T maps to NM_004941.1 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr17:41597586 A>T maps to NM_004941.1 T963T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:182836127 C>T maps to NM_001357.4 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:182856370 C>A maps to NM_001357.4 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:182852454 T>C maps to NM_001357.4 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr5:140960399 G>C maps to ENST00000398557 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr5:140903713 A>G maps to ENST00000398557 R1219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr5:140908744 G>A maps to ENST00000398557 G924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr5:140905923 G>A maps to ENST00000398557 P1126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr5:140957874 C>T maps to ENST00000398557 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr23:96213114 G>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:96220177 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr23:95993659 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr23:96136645 G>C did not map to a codon.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr23:96136679 G>C did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:96204002 G>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:96396709 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:96136646 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr23:96171500 C>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:96369955 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:96136710 C>T did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr13:60590251 C>T maps to NM_001042517.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr13:60544171 A>T maps to NM_001042517.1 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr13:60485886 A>T maps to NM_001042517.1 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr14:95570036 G>A maps to NM_177438.2 S1232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr14:95571505 T>A maps to NM_177438.2 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr14:95596529 C>T did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr14:95574698 T>G maps to NM_177438.2 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:95590837 T>C maps to NM_177438.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr20:61512618 C>T maps to NM_033081.2 A1563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr20:61511733 G>A maps to NM_033081.2 A1858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr20:61527744 C>G did not map to a codon.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr20:61512689 G>A maps to NM_033081.2 Q1540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:61512068 G>A maps to NM_033081.2 Q1747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr20:61526188 C>T maps to NM_033081.2 E803E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr20:61513652 G>A maps to NM_033081.2 Q1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:54370405 G>A maps to NM_000792.5 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr14:80669403 G>A maps to NM_001007023.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr14:102028294 C>T maps to NM_001362.3 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:102028009 C>G maps to NM_001362.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr21:47969741 C>T maps to ENST00000318711 Q862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr21:47965128 C>T maps to ENST00000318711 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:51116997 C>T maps to NM_173602.2 I1060I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr12:51072581 G>A maps to NM_173602.2 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:51138606 G>A maps to NM_173602.2 V1572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr12:51080374 G>A maps to NM_173602.2 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr10:412283 C>G maps to NM_014974.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr10:518436 G>A maps to NM_014974.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:2717765 G>A maps to NM_145173.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:2717399 C>G maps to NM_145173.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:93375923 C>T maps to NM_017594.3 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr9:93375944 G>A maps to NM_017594.3 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:93375902 C>T maps to NM_017594.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7593-01A-11D-2229-08 chr9:93375575 G>A maps to NM_017594.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr9:93375707 G>A maps to NM_017594.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:93375518 C>A maps to NM_017594.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:68512776 C>T maps to NM_004675.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:68512914 G>A maps to NM_004675.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:68512578 G>A maps to NM_004675.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr1:68512803 G>A maps to NM_004675.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:122545832 C>T maps to NM_032839.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr13:73334726 G>T maps to NM_014953.3 I911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:73346902 A>G maps to NM_014953.3 D438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr15:66618576 C>T maps to NM_001143688.1 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:233198641 G>A maps to NM_152383.4 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:233128056 C>T maps to NM_152383.4 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr2:233198569 G>C maps to NM_152383.4 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr1:223177008 C>A maps to NM_032890.2 S757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:223177960 C>T maps to NM_032890.2 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:223116609 C>T maps to NM_032890.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr1:223178941 G>C maps to NM_032890.2 S1401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:223179193 A>G maps to NM_032890.2 R1485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:40657437 G>A maps to NM_033510.1 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:40660843 G>A maps to NM_033510.1 W844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr15:40661396 C>G maps to NM_033510.1 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:40659296 G>A maps to NM_033510.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr15:40661540 C>T maps to NM_033510.1 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr11:111839270 C>T maps to NM_001037954.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:111844774 C>T maps to NM_001037954.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr11:111864233 G>A maps to NM_001037954.2 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:153994588 G>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:153997471 G>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:65546370 C>G maps to NM_138368.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr11:65547194 G>A maps to NM_138368.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr10:54074845 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:107845852 G>A maps to NM_014421.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:107845355 C>A maps to NM_014421.2 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr11:11986064 C>T maps to ENST00000450094 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:42234518 G>A maps to NM_014420.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr19:49867983 C>G maps to NM_014419.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:111916645 C>T maps to NM_001931.4 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:13357322 G>A maps to NM_182643.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr8:12952313 T>A maps to NM_182643.2 P1160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:13356614 C>T maps to NM_182643.2 K322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr8:12957133 G>A maps to NM_182643.2 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:12957370 G>A maps to NM_182643.2 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr8:12950233 G>A maps to NM_182643.2 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr8:12956983 C>A maps to NM_182643.2 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:38101287 G>A maps to NM_007335.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr3:38138179 C>T maps to NM_007335.2 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:38087116 G>A maps to NM_007335.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr3:38135259 T>A did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr3:38158094 C>G maps to NM_007335.2 L1336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:84996410 T>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr11:83770408 G>A maps to NM_001142699.1 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr11:83984276 G>T maps to NM_001142700.1 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:83770502 C>A maps to NM_001142699.1 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:69670068 G>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:69699024 A>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:69719859 T>C did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr23:69673591 A>G did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:69672597 G>C did not map to a codon.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr17:7099546 G>A maps to NM_001365.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:7096289 G>A maps to NM_001365.3 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr10:79556323 G>A maps to NM_004747.3 V1731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:79581718 G>A maps to NM_004747.3 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr10:79581667 T>A maps to NM_004747.3 P858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr18:3879504 G>A maps to NM_004746.2 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr18:3880017 G>A maps to NM_004746.2 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr18:3879987 G>A maps to NM_004746.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:3534552 G>A maps to NM_004746.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr18:3879246 C>T maps to NM_004746.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:1513940 C>T maps to ENST00000357934 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr8:1496891 G>A maps to ENST00000357934 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:1497719 G>A maps to ENST00000357934 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:1497608 G>A maps to ENST00000357934 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:1626529 C>T maps to ENST00000357934 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:35350637 G>C maps to NM_001080418.1 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:35333226 G>T maps to NM_001080418.1 I829I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:35365841 G>A maps to NM_001080418.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:35370702 A>G maps to NM_001080418.1 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr20:35154396 C>A maps to ENST00000339266 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:35155432 G>C maps to ENST00000339266 *993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:35060383 C>T maps to ENST00000339266 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:35128967 C>T maps to ENST00000339266 C822C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr20:35060692 G>C maps to ENST00000339266 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr20:35154313 C>T maps to ENST00000339266 Q889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr20:35075161 G>A maps to ENST00000339266 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:55625315 C>G maps to NM_014750.4 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:101200716 C>T maps to NM_003836.5 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:101200977 C>T maps to NM_003836.5 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:170592410 G>A maps to NM_005618.3 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:170597814 A>G did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:39998559 G>A maps to NM_016941.3 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:39989649 G>A maps to NM_016941.3 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr19:39994819 C>T maps to NM_016941.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:39990097 C>T maps to NM_016941.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:75359640 C>T maps to NM_001933.4 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr14:75369020 C>G maps to NM_001933.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:75348709 C>T maps to NM_001933.4 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr14:75361059 G>T maps to NM_001933.4 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr2:172951394 G>A maps to NM_178120.4 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr2:172950419 C>T maps to NM_178120.4 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr17:48070808 G>A maps to NM_005220.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:48050614 C>T maps to NM_138281.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:96650323 G>A maps to NM_005221.5 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr7:96651679 C>T maps to NM_005221.5 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr7:96639322 A>G maps to NM_005222.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr7:96637142 G>A maps to NM_005222.3 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:44685698 G>A maps to NM_019100.4 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:44685130 C>G maps to NM_019100.4 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:124399935 G>C maps to ENST00000368915 T2441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr10:124345705 G>T maps to ENST00000368915 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr10:124339304 C>A maps to ENST00000368915 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr10:124351998 T>A maps to ENST00000368915 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr10:124348655 C>T maps to ENST00000368915 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr10:124339337 C>T maps to ENST00000368915 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr10:124336112 C>A maps to ENST00000368915 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:124345744 C>T maps to ENST00000368915 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:46977889 G>C maps to NM_147192.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:31893374 C>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:32459327 C>G did not map to a codon.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr23:31854841 G>T did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:31676188 G>A did not map to a codon.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr23:32305784 G>T did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr23:32482776 C>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:31164449 T>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:32663244 A>G did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr23:32613910 C>G did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:31165576 G>T did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr23:31497124 T>C did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:32536237 C>G did not map to a codon.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr23:32591888 G>C did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:32519945 T>C did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:32429884 A>C did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:32536237 C>A did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr23:32716088 A>T did not map to a codon.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr23:31947846 A>G did not map to a codon.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr23:31986457 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr23:31792156 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr23:33038268 G>T did not map to a codon.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr23:32509575 C>T did not map to a codon.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr23:31838156 C>T did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr23:31950340 T>C did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:33146265 G>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:31496267 G>C did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:31496479 C>G did not map to a codon.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr23:31200899 T>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:31792248 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:32361264 C>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:32366522 C>T did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:32716005 C>T did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr23:32328319 G>A did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr23:32404496 G>T did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:32366609 G>T did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:32398770 C>A did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr23:31986548 G>C did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:31947739 G>C did not map to a codon.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr23:32380922 G>T did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr23:32305681 C>T did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:31986603 G>T did not map to a codon.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr23:32380944 T>C did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:32398773 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:32305751 C>A did not map to a codon.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr23:32834616 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr23:31950312 A>G did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:31496419 C>G did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:32519916 C>A did not map to a codon.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr23:31697646 G>T did not map to a codon.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr23:32486770 A>T did not map to a codon.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr23:32235083 C>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:32235179 C>T did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:32662421 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:32404564 C>G did not map to a codon.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr23:32328383 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr23:31227741 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:33146273 C>T did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:31279122 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr23:32632459 G>A did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr23:32382753 G>T did not map to a codon.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr23:32613896 C>G did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:32305700 A>T did not map to a codon.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr23:32328383 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:78322354 C>A maps to NM_013391.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr5:78359573 C>T maps to NM_013391.2 W46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr5:78338268 G>A maps to NM_013391.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:78338146 G>A maps to NM_013391.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr4:88580598 C>A maps to NM_004407.3 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr4:88584471 G>C maps to NM_004407.3 *514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr19:46281005 G>A maps to NM_004409.3 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr9:1057242 T>C maps to NM_181872.4 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:990053 A>G maps to NM_021240.2 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr9:22451197 C>G maps to NM_022160.2 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr9:22447588 C>G maps to NM_022160.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:50885278 C>T maps to NM_032110.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:53930413 G>A maps to NM_033067.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr1:53927257 C>T maps to NM_033067.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:42352589 C>A maps to ENST00000427618 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr19:42353198 C>A maps to ENST00000427618 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:86817561 C>T maps to NM_021145.3 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr7:86817522 T>C maps to NM_021145.3 H439H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr19:46289910 C>T maps to NM_004943.1 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:46290015 G>A maps to NM_004943.1 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr19:46289613 G>A maps to NM_004943.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr5:118469799 G>A maps to NM_005509.4 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr5:118485778 T>A maps to NM_005509.4 C1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:51809331 G>A maps to NM_001174116.1 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr15:51741320 G>A maps to NM_001174116.1 R2992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr15:51773095 G>A maps to NM_001174116.1 L2069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr15:51914709 G>A maps to NM_001174116.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr15:51828990 G>A maps to NM_001174116.1 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr10:70225524 G>A maps to NM_001080449.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:70190225 G>A maps to NM_001080449.1 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:52404530 C>T maps to ENST00000273600 I2099I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr3:52394092 G>A maps to ENST00000273600 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:52428567 C>A maps to ENST00000273600 R3636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:52417478 C>T maps to ENST00000273600 D2673D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:52422519 C>T maps to ENST00000273600 D3086D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr3:52394095 G>C did not map to a codon.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr3:52406959 C>T maps to ENST00000273600 F2292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr3:52380762 C>T maps to ENST00000273600 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr3:52394002 C>T maps to ENST00000273600 I1493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:124293436 C>T maps to NM_207437.3 P909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:124268603 C>T maps to NM_207437.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:124285881 G>A maps to NM_207437.3 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:124257475 C>T maps to NM_207437.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:124383261 G>T maps to NM_207437.3 E3063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr12:124330338 C>T maps to NM_207437.3 N1733N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr12:124268651 C>T maps to NM_207437.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:124298072 C>G maps to NM_207437.3 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr12:124401152 G>A maps to NM_207437.3 R3506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:124285852 T>C maps to NM_207437.3 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr12:124335580 C>T maps to NM_207437.3 I1965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:21654859 G>A maps to NM_003777.3 K1327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:21747447 T>C maps to NM_003777.3 D2233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr7:21639712 A>C maps to NM_003777.3 T992T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr7:21904160 G>A maps to NM_003777.3 L3801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr7:21750197 C>G maps to NM_003777.3 L2244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:21781777 C>T maps to NM_003777.3 V2723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:21779239 C>T maps to NM_003777.3 V2628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:21639715 C>T maps to NM_003777.3 H993H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:21628906 T>A maps to NM_003777.3 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr7:21784486 G>T did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:21639529 G>A maps to NM_003777.3 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:21678665 G>T maps to NM_003777.3 G1648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:21737691 G>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:21627719 T>G maps to NM_003777.3 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:21639523 C>T maps to NM_003777.3 F929F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:21744164 G>A maps to NM_003777.3 R2136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr7:21818700 C>T maps to NM_003777.3 I3161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr7:21639562 G>T maps to NM_003777.3 P942P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr7:21744170 G>A maps to NM_003777.3 K2138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:76487581 G>A maps to ENST00000389840 D2190D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-6020-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr17:76464797 G>A maps to ENST00000389840 I2879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr17:76506501 G>A maps to ENST00000389840 I1396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:76455097 G>A maps to ENST00000389840 I3268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:76455951 G>A maps to ENST00000389840 I3175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:76420118 C>T maps to ENST00000389840 K4442K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:76568946 C>T maps to ENST00000389840 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:76447631 G>A maps to ENST00000389840 F3537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr17:76476819 G>A maps to ENST00000389840 Y2552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr17:76422536 C>A did not map to a codon.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:7623113 G>A maps to NM_020877.2 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:7734484 C>T maps to NM_020877.2 G4104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr17:7663188 C>T maps to NM_020877.2 V906V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr17:7668742 G>A maps to NM_020877.2 W1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:7695574 G>A maps to NM_020877.2 T2353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:7689566 C>T maps to NM_020877.2 C2085C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:7667310 C>G maps to NM_020877.2 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:7734556 C>A maps to NM_020877.2 T4128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr17:7673915 C>T maps to NM_020877.2 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:7736072 C>T maps to NM_020877.2 N4301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:7696465 C>T maps to NM_020877.2 L2504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:7735023 C>G maps to NM_020877.2 V4219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr17:7734766 G>C maps to NM_020877.2 G4173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:7702036 G>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:7702464 T>C maps to NM_020877.2 P2868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:7726881 G>A maps to NM_020877.2 E3755E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr17:7736221 C>T maps to NM_020877.2 D4318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr17:7699804 C>T maps to NM_020877.2 F2566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr16:21014469 G>A maps to NM_017539.1 Q2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr16:20996902 C>A maps to NM_017539.1 V2387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr16:21136513 G>A maps to NM_017539.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:21038392 G>A maps to NM_017539.1 F1832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr16:20975194 C>T maps to NM_017539.1 T3337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr16:21147729 C>T maps to NM_017539.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:21011750 G>A maps to NM_017539.1 F2072F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr16:20999080 G>C maps to NM_017539.1 V2272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr16:20994155 C>T maps to NM_017539.1 S2582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:20948069 C>T maps to NM_017539.1 V3920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:20990732 C>G maps to NM_017539.1 L2665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:21011789 G>A maps to NM_017539.1 F2059F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr16:21073916 G>T maps to NM_017539.1 C1202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr16:21060916 C>T maps to NM_017539.1 A1478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr16:21038386 G>A maps to NM_017539.1 P1834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr16:21136516 A>C maps to NM_017539.1 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr16:20981270 G>A maps to NM_017539.1 L2767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr16:21078641 C>T maps to NM_017539.1 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr16:21151925 G>A maps to NM_017539.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:13735960 G>A maps to NM_001369.2 Q3846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:13864528 G>A maps to NM_001369.2 L1525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:13894842 C>A maps to NM_001369.2 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:13752340 C>A maps to NM_001369.2 G3644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:13794110 C>T maps to NM_001369.2 A2648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:13830149 C>A maps to NM_001369.2 G2078G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:13792156 A>G maps to NM_001369.2 S2798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:13692193 G>T maps to NM_001369.2 R4592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:13716598 G>T maps to NM_001369.2 I4302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:13841179 A>G maps to NM_001369.2 N1848N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr5:13883147 G>A maps to NM_001369.2 S1013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:13721171 A>T maps to NM_001369.2 Y4072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:13845070 G>T maps to NM_001369.2 R1716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr5:13751204 G>T maps to NM_001369.2 V3731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr5:13864592 G>A maps to NM_001369.2 T1503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr5:13792167 G>A maps to NM_001369.2 R2795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr5:13871016 G>A maps to NM_001369.2 N1231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:13871061 G>A maps to NM_001369.2 V1216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:13786379 G>A maps to NM_001369.2 L2910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr5:13919308 C>T maps to NM_001369.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:13841091 G>A maps to NM_001369.2 L1878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:13859685 G>A maps to NM_001369.2 Q1609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr5:13788882 C>T maps to NM_001369.2 V2863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr5:13885170 A>C maps to NM_001369.2 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr5:13719183 G>T maps to NM_001369.2 C4102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr5:13708444 C>T did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:13762884 C>T maps to NM_001369.2 W3409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:13928287 C>A did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:13719087 A>G maps to NM_001369.2 A4134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:13737359 C>A did not map to a codon.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:13830754 G>A maps to NM_001369.2 F2004F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:13735279 C>T maps to NM_001369.2 R3907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:13865991 C>T maps to NM_001369.2 R1380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:13883177 C>T maps to NM_001369.2 K1003K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr5:13717546 A>G maps to NM_001369.2 T4194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:13717483 C>T maps to NM_001369.2 A4215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:13900482 C>T maps to NM_001369.2 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr5:13814731 A>G maps to NM_001369.2 D2404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr5:13719059 G>A maps to NM_001369.2 Q4144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr5:13841232 A>G maps to NM_001369.2 L1831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr5:13714729 C>A did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr5:13900338 G>C maps to NM_001369.2 Y745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr5:13751221 G>A maps to NM_001369.2 Q3726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:196723251 A>T maps to NM_018897.2 G2671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr2:196825056 A>G maps to NM_018897.2 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:196737028 G>C maps to NM_018897.2 S2193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:196661352 G>A maps to NM_018897.2 Q3488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:196729232 C>G maps to NM_018897.2 V2382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr2:196602679 G>A maps to NM_018897.2 R4014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:196749472 A>G maps to NM_018897.2 L1867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:196750876 G>A maps to NM_018897.2 Y1842Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:196726484 G>C maps to NM_018897.2 L2564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr2:196837115 G>A maps to NM_018897.2 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:196729520 G>T maps to NM_018897.2 I2286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr2:196726633 G>T maps to NM_018897.2 R2515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr2:196825354 G>T maps to NM_018897.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:196788387 T>C maps to NM_018897.2 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr2:196722213 G>A maps to NM_018897.2 I2767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr2:196786825 C>A maps to NM_018897.2 T1307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:38840415 C>T maps to ENST00000327475 C2353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:38791363 G>C maps to ENST00000327475 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr6:38893983 C>T maps to ENST00000327475 Q3694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:38950168 C>T maps to ENST00000327475 F4282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:38863889 G>A maps to ENST00000327475 A2931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:38754682 G>A maps to ENST00000327475 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:38830054 G>A did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr6:38831661 G>T maps to ENST00000327475 S2096S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:38759380 C>T maps to ENST00000327475 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:38885915 G>A maps to ENST00000327475 K3496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr6:38891904 G>A maps to ENST00000327475 L3631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:38885711 A>G maps to ENST00000327475 A3428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr6:38704880 C>G maps to ENST00000327475 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr6:38889168 C>A maps to ENST00000327475 R3505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr6:38819386 C>T maps to ENST00000327475 F1789F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr6:38906572 G>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:38816450 C>T maps to ENST00000327475 I1679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr6:38825333 C>G maps to ENST00000327475 S1913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr6:38840790 C>T maps to ENST00000327475 R2437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:11607760 T>C did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr17:11738199 C>G maps to NM_001372.3 L3164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:11631205 C>T maps to NM_001372.3 I1927I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:11835354 G>T maps to NM_001372.3 E4044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:11597643 C>T maps to NM_001372.3 C1584C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr17:11684443 G>A maps to NM_001372.3 T2557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:11648368 A>T maps to NM_001372.3 K2123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:11543608 C>T maps to NM_001372.3 N603N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr17:11778324 C>T maps to NM_001372.3 D3434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:11607548 G>A maps to NM_001372.3 W1727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:11520909 C>T maps to NM_001372.3 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr17:11672473 G>T maps to NM_001372.3 V2460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:11522983 G>A maps to NM_001372.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:11872630 A>G maps to NM_001372.3 T4416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr17:11592933 C>A maps to NM_001372.3 I1265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:34490413 C>A maps to NM_012144.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr17:72278069 C>A maps to NM_023036.4 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr17:72285735 C>T maps to NM_023036.4 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr9:33030453 A>G maps to NM_001539.2 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr9:33034295 G>T maps to NM_001539.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr9:33036572 C>T maps to NM_001539.2 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:14627499 T>C maps to NM_006145.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr3:186302283 C>T maps to NM_016306.4 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:73679415 C>T maps to NM_153614.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr4:100830006 T>C maps to NM_001031723.2 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr2:220144590 A>T maps to NM_006736.5 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr9:34996640 C>G maps to NM_001135005.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr7:157160130 C>T maps to NM_058246.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr7:157208713 G>A maps to NM_058246.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr22:41257197 C>T maps to NM_145174.1 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr3:128181437 C>T maps to NM_153330.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr3:128181845 C>T maps to NM_153330.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr3:128181533 G>A maps to NM_153330.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:22208790 G>C maps to NM_022365.3 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:22209806 C>A maps to NM_022365.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr10:22209837 G>A maps to NM_022365.3 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr10:22048518 C>T maps to NM_022365.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:183594598 A>C maps to NM_018981.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr2:183627483 A>C maps to NM_018981.1 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr2:183616458 C>T maps to NM_018981.1 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr1:6699996 C>G maps to NM_018198.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:6698378 C>T maps to NM_018198.3 Q433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:6738498 G>A maps to NM_018198.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:6697513 G>A maps to NM_018198.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr1:6711663 T>A did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:6697275 G>A maps to NM_018198.3 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:69571400 G>A maps to NM_021800.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr3:132185173 C>G maps to NM_015268.3 S667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr3:132166223 C>T maps to NM_015268.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:132207164 C>T maps to NM_015268.3 I1097I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr3:132180003 G>A maps to NM_015268.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr12:56221561 C>T maps to NM_032364.5 W294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56216452 A>G maps to NM_032364.5 H566H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr12:56221369 C>T maps to NM_032364.5 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr13:43597851 C>T maps to NM_013238.2 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:102982243 G>A maps to NM_014377.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr5:34936259 G>C maps to NM_194283.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:96416175 G>A maps to NM_006260.4 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr11:64001428 C>A maps to NM_005528.3 Y197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:62562254 C>T maps to NM_025219.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:66992625 C>T maps to NM_033105.4 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr2:27500789 C>T maps to NM_173650.1 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr2:27499676 C>A maps to NM_173650.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:65858190 G>T maps to ENST00000371069 E516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr1:65867546 C>A maps to ENST00000371069 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr17:40134297 C>T maps to NM_003315.3 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:74125576 G>T maps to NM_031427.2 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr14:74125656 C>T maps to NM_031427.2 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr22:39176932 C>A maps to NM_005740.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr1:38023217 A>G maps to NM_003462.3 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:153631468 G>T did not map to a codon.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr23:153631067 G>C did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr16:2288403 C>T maps to NM_001374.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr16:2287937 C>T maps to NM_001374.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:2287440 G>T maps to NM_001374.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr19:12991694 C>G did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:84864282 A>T maps to NM_021233.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:6588903 C>T maps to NM_144666.2 A4055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr11:6524003 T>C maps to NM_144666.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:6587844 G>C maps to NM_144666.2 L3745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr9:139256511 C>T maps to NM_001080849.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr9:131010932 G>C maps to ENST00000372923 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr9:131001791 C>T maps to ENST00000372923 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr9:130982550 C>T maps to ENST00000372923 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr12:32895603 A>G maps to ENST00000381000 K705K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr12:32886734 T>C maps to ENST00000381000 N524N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:10893765 C>T maps to NM_001005361.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr19:10887830 G>C maps to NM_001005361.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:10923010 T>C maps to NM_001005361.2 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:172357711 G>T did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:172011155 C>T maps to ENST00000359070 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:172356475 C>T maps to ENST00000359070 D764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:172376928 C>A maps to ENST00000359070 S857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:172013589 C>T maps to ENST00000359070 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:101658518 T>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr10:101715776 G>C maps to ENST00000342239 S485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr10:101716098 C>A maps to ENST00000342239 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr10:101715079 G>C maps to ENST00000342239 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:101716888 G>A maps to ENST00000342239 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr10:101648653 C>T maps to ENST00000342239 E1095E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:10257200 C>G did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:10265724 G>A maps to NM_001130823.1 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr19:10254620 G>A maps to NM_001130823.1 P979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:10247830 A>G maps to NM_001130823.1 Y1473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr19:10250384 G>A maps to NM_001130823.1 R1305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr2:25467434 G>A maps to NM_175629.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:25463263 G>A maps to NM_175629.1 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr2:25469958 C>T maps to NM_175629.1 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:25468196 G>A maps to NM_175629.1 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:25470968 G>A maps to NM_175629.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:25457168 C>T maps to NM_175629.1 K906K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr2:25467059 G>A maps to NM_175629.1 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr2:25469606 G>A maps to NM_175629.1 C387C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr2:25469930 C>A maps to NM_175629.1 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr20:31379432 G>A maps to NM_006892.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr20:31386316 C>T maps to NM_006892.3 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr21:45680689 G>A maps to NM_013369.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:220247867 G>C maps to NM_012100.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr10:98078207 C>A maps to NM_004088.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr10:98095646 G>A did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr10:98064367 C>T maps to NM_004088.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr20:44439537 C>T maps to NM_052951.2 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr20:44422616 C>T maps to NM_052951.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr20:44439737 C>T maps to NM_052951.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:94342344 G>A maps to NM_014597.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:94337702 C>T maps to NM_014597.4 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:129207595 G>A maps to ENST00000398025 V1473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr10:128795023 G>A maps to ENST00000398025 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr10:129209188 G>A did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr10:129046279 C>T maps to ENST00000398025 F997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:225651807 T>C maps to NM_014689.2 K1862K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr2:225670157 C>T maps to NM_014689.2 E1301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr2:225751177 C>A maps to NM_014689.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr2:225652093 T>C maps to NM_014689.2 L1813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:225740755 C>A maps to NM_014689.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:117773417 C>G did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:117758579 C>G did not map to a codon.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr23:117699985 C>T did not map to a codon.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr23:117775256 C>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:117788709 C>G did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:117700004 T>C did not map to a codon.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr23:117700103 G>A did not map to a codon.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr23:117676916 C>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr23:117783068 C>G did not map to a codon.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr23:117773474 C>T did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr23:117775196 G>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:117817177 C>T did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:117815168 G>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:117712610 G>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:117727279 A>C did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr23:117815130 G>C did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr23:117707859 C>T did not map to a codon.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:169506011 G>A maps to NM_004946.2 P1676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:169509799 C>T maps to NM_004946.2 L1811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr5:169135204 C>A maps to NM_004946.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr5:169111348 C>T maps to NM_004946.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr5:169503007 C>T maps to NM_004946.2 R1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr5:169474560 C>A maps to NM_004946.2 P1338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr5:169508957 G>A maps to NM_004946.2 R1800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:169461489 G>A maps to NM_004946.2 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:169468121 G>C maps to NM_004946.2 T1243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:169454880 C>T maps to NM_004946.2 I1132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:169127105 G>A maps to NM_004946.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:169125438 C>T maps to NM_004946.2 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr3:51198104 G>T maps to NM_004947.4 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr3:51400016 G>A maps to NM_004947.4 S1735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:51197995 C>T maps to NM_004947.4 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:51394394 G>A maps to NM_004947.4 V1502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:51394559 A>G maps to NM_004947.4 A1557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:111395597 G>T maps to ENST00000428084 R1463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:111400291 G>A maps to ENST00000428084 I1369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr7:111368575 C>T maps to ENST00000428084 P1894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:111379255 G>A maps to ENST00000428084 N1722N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr7:111368446 C>T maps to ENST00000428084 P1937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr7:111368415 G>A maps to ENST00000428084 R1948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr7:111462467 G>A maps to ENST00000428084 R960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr8:25159857 C>T maps to NM_024940.6 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr8:25156590 C>A maps to NM_024940.6 Y246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr8:25174610 G>T maps to NM_024940.6 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr8:25203030 C>A maps to NM_024940.6 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr8:25154151 C>T maps to NM_024940.6 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:25198425 T>C maps to NM_024940.6 F787F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:25258485 A>G maps to NM_024940.6 K1610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:11354275 C>T maps to ENST00000319867 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr19:11363490 G>A maps to ENST00000319867 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:11333758 G>C maps to ENST00000319867 L993L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-7390-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:11332855 G>A maps to ENST00000319867 F1103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:11327706 C>T maps to ENST00000319867 W1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr19:11353807 G>A maps to ENST00000319867 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:62954603 C>A did not map to a codon.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr1:63018485 G>A maps to ENST00000371140 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:62960062 T>C maps to ENST00000371140 E1700E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:62962078 A>G maps to ENST00000371140 R1618R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr1:62921090 A>G maps to ENST00000371140 D2139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:368026 C>G maps to NM_203447.3 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr9:289551 C>T maps to NM_203447.3 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:406991 C>T maps to NM_203447.3 S1151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:396930 G>A maps to NM_203447.3 Q1039Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr9:390520 G>A maps to NM_203447.3 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr13:99554562 G>A maps to ENST00000428223 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr13:99476723 G>C maps to ENST00000428223 V1686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr13:99449734 A>G maps to ENST00000428223 A1989A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr13:99476708 G>T maps to ENST00000428223 I1691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr13:99483676 G>C maps to ENST00000428223 S1497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr13:99532803 C>T maps to ENST00000428223 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:3494055 C>T maps to NM_001145165.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:74784054 C>A maps to NM_001381.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:74783946 G>A maps to NM_001381.3 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr5:176935516 C>A maps to NM_024872.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr16:57509779 G>T maps to NM_018110.3 C52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr20:53208153 G>C did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr20:53260097 A>G maps to NM_018431.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr20:53208299 G>T maps to NM_018431.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr18:67406318 G>T maps to NM_152721.5 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr9:131843486 G>C did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:34957050 G>A maps to NM_017613.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:83847360 C>T maps to NM_015018.2 S1200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:83850047 C>T maps to NM_015018.2 Q1781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:83841950 G>A maps to NM_015018.2 Q891Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:83863896 A>T did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr6:83834482 T>A maps to NM_015018.2 L467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:83829545 C>T maps to NM_015018.2 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:83863922 G>C maps to NM_015018.2 L2138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr21:37609639 G>T maps to NM_005128.2 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr21:37603424 G>A maps to NM_005128.2 Q781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr21:37626125 C>G maps to NM_005128.2 L1726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr21:37650302 C>T maps to NM_005128.2 R1915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:2213554 C>T maps to ENST00000221482 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:2226521 T>C maps to ENST00000221482 G1334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:2216356 C>T maps to ENST00000221482 D667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:2210790 C>T maps to ENST00000221482 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:2210645 G>A maps to ENST00000221482 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr19:2220105 G>C did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr16:89702703 G>A maps to NM_004413.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr16:68021882 G>A maps to NM_022355.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr16:68026030 C>T maps to NM_022355.2 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr16:68011732 C>G did not map to a codon.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr11:65116373 C>T maps to NM_006268.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr14:73159871 A>T maps to NM_012074.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr1:101490908 G>A maps to NM_015958.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:116510866 T>C maps to NM_020868.3 C356C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:115200369 C>A maps to NM_020868.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:116257181 T>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:116497459 G>T maps to NM_020868.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:116510842 C>T maps to NM_020868.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:116593792 G>T maps to NM_020868.3 G671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr2:116257181 T>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:66276598 C>T maps to NM_005700.3 I697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr11:66260376 C>T maps to NM_005700.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr2:162865770 G>A maps to NM_001935.3 R623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr2:162865096 C>T maps to NM_001935.3 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:154679392 G>A maps to NM_130797.2 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:154681007 C>T maps to NM_130797.2 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr7:154664385 C>A maps to NM_130797.2 Y622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:154595623 C>T maps to NM_130797.2 D486D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:154561125 G>C did not map to a codon.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr7:154681010 G>A maps to NM_130797.2 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:154263979 T>G maps to NM_130797.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:154598805 C>T maps to NM_130797.2 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr15:65793045 G>A maps to NM_197960.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:4714207 G>A maps to ENST00000357909 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr19:4679885 G>A maps to ENST00000357909 V928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr19:4694748 G>A maps to ENST00000357909 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:4697573 C>T maps to ENST00000357909 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr19:4689614 C>G maps to ENST00000357909 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:109023500 C>A maps to NM_138815.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr3:109031509 C>T maps to NM_138815.3 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:7864204 G>T maps to NM_199286.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:109047836 T>A maps to NM_018189.3 K260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr3:109050770 G>T maps to NM_018189.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr3:109049599 C>T maps to NM_018189.3 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:109047777 C>T maps to NM_018189.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr3:109049490 C>A maps to NM_018189.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:74063747 G>A maps to NM_001025290.2 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:34981466 T>C maps to NM_015283.1 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr7:35009098 G>T maps to NM_015283.1 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr7:35009116 C>T maps to NM_015283.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:63964554 G>T maps to NM_173812.4 Y661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:97658798 G>A maps to NM_000110.3 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:98164953 G>A maps to NM_000110.3 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:97564047 G>T maps to NM_000110.3 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:97915725 G>C maps to NM_000110.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:98157299 A>T maps to NM_000110.3 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr1:98164959 C>T maps to NM_000110.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr8:105456578 C>T maps to NM_001385.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr8:26492303 C>T maps to NM_001197293.1 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr5:146778659 G>T maps to NM_001197294.1 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr10:134004264 G>A maps to NM_006426.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:134008355 C>T maps to NM_006426.2 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr10:134014378 C>T maps to NM_006426.2 C334C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr10:134016256 G>T maps to NM_006426.2 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:134008361 C>T maps to NM_006426.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:27169817 T>C maps to NM_020134.3 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:27169818 C>A maps to NM_020134.3 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr2:27121555 C>T maps to NM_020134.3 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:27121504 C>T maps to NM_020134.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:27167531 G>A maps to NM_020134.3 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:27157444 G>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:74750493 G>A maps to NM_133637.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr2:74746712 C>T maps to NM_133637.2 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr12:102295156 T>C maps to NM_018370.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr11:65687306 G>A maps to ENST00000376991 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr5:174869349 G>A maps to NM_000794.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:113281595 C>T maps to ENST00000355319 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:113283502 G>A maps to ENST00000355319 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:113858409 C>T maps to NM_000796.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr11:639779 G>A maps to NM_000797.3 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:9784234 A>G maps to NM_000798.4 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr4:9783961 G>T maps to NM_000798.4 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:9783682 G>A maps to NM_000798.4 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr4:9783961 G>T maps to NM_000798.4 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr23:100511135 C>G did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:100496665 C>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:100486664 C>T did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr23:100494000 C>T did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr23:100497389 C>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:100510188 A>T did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr23:100497332 C>A did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:100505952 C>T did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:100492622 C>A did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:100503250 C>A did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr18:28728467 G>A maps to NM_024421.2 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr18:28663005 C>T maps to ENST00000438199 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:28586927 A>G maps to NM_001941.3 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:28602352 C>T maps to NM_001941.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr21:41684116 C>G maps to NM_001389.3 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr21:41559088 T>A maps to NM_001389.3 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr21:41447098 C>A maps to NM_001389.3 E1585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr21:41725413 C>T maps to NM_001389.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr21:41719756 A>G maps to NM_001389.3 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr21:41416161 C>T maps to NM_001389.3 A1742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr21:41684251 T>C maps to NM_001389.3 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr21:41385128 C>T maps to NM_001389.3 T1957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr21:41741076 G>A maps to NM_001389.3 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr21:41741068 G>A maps to NM_001389.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr21:41457577 G>T maps to NM_001389.3 A1361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:117387377 G>A maps to NM_020693.2 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:117403129 C>A maps to NM_020693.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:117302400 C>T maps to NM_020693.2 R1801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr11:117303095 G>A maps to NM_020693.2 I1777I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:117395754 G>A maps to NM_020693.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:117301447 C>T maps to NM_020693.2 R1952R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr11:117391932 C>T maps to NM_020693.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr8:120847201 G>A maps to NM_024094.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr6:116758058 C>T maps to NM_013352.2 R810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr18:65180849 G>T maps to NM_032160.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr18:65180984 G>A maps to NM_032160.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr18:65179742 T>C maps to NM_032160.2 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:65180744 G>A maps to NM_032160.2 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr18:65180624 T>C maps to NM_032160.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr18:28923431 C>T maps to NM_001942.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr18:28914134 A>G maps to NM_001942.2 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr18:29110981 C>T maps to NM_001943.3 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr18:29104494 C>T maps to NM_001943.3 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr18:29104785 G>T maps to NM_001943.3 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr18:29116339 C>G maps to NM_001943.3 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr18:29052737 C>T maps to NM_001944.2 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr18:29055985 C>T maps to NM_001944.2 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr18:29055667 C>A maps to NM_001944.2 I815I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr18:28993242 C>A maps to NM_001134453.1 T955T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr20:35399489 G>A maps to NM_001145315.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:7572177 G>A maps to NM_004415.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:7569463 G>T maps to NM_004415.2 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr6:7581189 C>T maps to NM_004415.2 C1589C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:7566621 C>T maps to NM_004415.2 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:7570714 C>T maps to NM_004415.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr6:7571656 C>T maps to NM_004415.2 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:7586032 G>A maps to NM_004415.2 R2846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:7569531 C>T maps to NM_004415.2 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:7581447 C>T maps to NM_004415.2 V1675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:7571786 C>T maps to NM_004415.2 Q625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr6:7580248 C>T maps to NM_004415.2 Q1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:7574982 C>G maps to NM_004415.2 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H8-01A-21D-A34J-08 chr4:88535049 C>T maps to NM_014208.3 G412G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-UF-A71D-01A-12D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:56458613 C>T maps to ENST00000361203 L3980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr6:56489976 G>T maps to ENST00000361203 S1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:56357811 G>A maps to ENST00000361203 Q6613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr6:56505115 G>C maps to ENST00000361203 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr6:56394428 C>T maps to ENST00000361203 E5593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr6:56443678 C>T maps to ENST00000361203 T4109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr6:56496809 G>C maps to ENST00000361203 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr6:56495120 G>T maps to ENST00000361203 L1190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:56484145 C>T maps to ENST00000281662 L2126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr6:56374647 G>A maps to ENST00000361203 I6057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:56484117 G>A maps to ENST00000281662 L2136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr6:56495046 A>C maps to ENST00000361203 L1215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr6:56418441 G>A maps to ENST00000361203 Q4839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:56457057 C>T maps to ENST00000361203 E4064E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:56357098 G>A maps to ENST00000361203 R6684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:56484763 A>G maps to ENST00000281662 H1920H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr6:56482917 C>A maps to ENST00000281662 E2536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr6:56420404 G>A maps to ENST00000361203 S4747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr6:56437562 T>C maps to ENST00000361203 E4301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr6:56505362 C>A maps to ENST00000361203 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr6:56482993 G>C maps to ENST00000281662 L2510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr20:17581472 A>C maps to NM_006870.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr20:17585238 T>A maps to NM_006870.3 Y117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:205116741 G>T maps to NM_015375.2 R912R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:18724747 C>G maps to NM_080820.4 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr18:32345947 C>T maps to NM_001390.4 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr18:32443989 A>G maps to NM_001390.4 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr18:32400876 C>T maps to NM_001390.4 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:118176650 G>C maps to NM_173666.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr12:113515367 C>T maps to NM_004416.2 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:113534539 G>T maps to NM_004416.2 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:113496125 C>T maps to NM_004416.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:113534671 C>T maps to NM_004416.2 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:76112068 C>T maps to NM_020892.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:58002907 G>A maps to NM_178502.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr3:122287598 T>A maps to NM_138287.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:122288165 T>C maps to NM_138287.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr11:58956680 C>T maps to NM_015177.1 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:58949290 C>T maps to NM_015177.1 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:58949497 G>A maps to NM_015177.1 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr2:242617875 C>T maps to NM_012145.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:7149393 G>A maps to NM_015343.4 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr15:45434284 C>T maps to NM_175940.1 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr15:45426425 C>T maps to NM_175940.1 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr15:45428811 C>T maps to NM_175940.1 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr15:45439713 G>A maps to NM_175940.1 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr15:45444586 C>G maps to NM_175940.1 Y1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr15:45401150 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr15:45402884 C>A maps to NM_014080.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr15:45391946 G>A maps to NM_014080.4 R1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr15:45387289 C>A did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:45415128 G>A maps to NM_144565.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr15:45411393 G>T maps to NM_144565.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:45408912 C>T maps to NM_207581.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr15:45410061 G>A maps to NM_207581.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr15:45406916 C>T maps to NM_207581.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr10:76803729 C>T maps to NM_001003892.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:76803759 G>A maps to NM_001003892.1 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:80019149 G>A maps to NM_022156.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr19:5786533 T>G maps to NM_020175.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr7:107211588 G>A did not map to a codon.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:221913035 G>A maps to NM_007207.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr2:73993699 G>C maps to NM_003584.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:161719653 C>T maps to NM_007240.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:161722870 A>T maps to NM_007240.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr10:76868870 G>T maps to NM_001007272.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:12630840 C>T maps to NM_030640.2 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr22:31059930 G>C maps to NM_152511.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr22:31059927 C>T maps to NM_152511.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr2:183960310 C>T maps to NM_080876.3 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr2:96811087 C>A maps to NM_004418.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr23:44703873 G>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr23:44703890 G>C did not map to a codon.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr23:44703846 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr23:44703763 T>C did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:348267 C>G maps to ENST00000457386 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr6:348126 G>A maps to ENST00000457386 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:348138 C>T maps to ENST00000457386 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr1:159752121 G>A maps to NM_017823.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr1:167095193 G>T maps to NM_001080426.1 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr1:167097228 G>A maps to NM_001080426.1 W954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:167095718 C>T maps to NM_001080426.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr1:167095879 G>A maps to NM_001080426.1 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:167097472 G>A maps to NM_001080426.1 E1035E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr1:167096485 C>A maps to NM_001080426.1 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr8:29207651 C>T maps to NM_001394.5 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:29195913 G>C maps to NM_001394.5 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:52089868 G>A maps to NM_001947.3 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr11:1579115 G>A maps to NM_004420.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr11:1586849 G>A maps to NM_004420.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:152915659 A>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:57666724 G>T maps to NM_001012729.1 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:1277123 G>A maps to ENST00000378888 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr1:1273763 C>A maps to ENST00000378888 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:1277864 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr1:1271767 G>A maps to ENST00000378888 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr17:7132325 G>A maps to NM_004422.2 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr18:46905006 G>A maps to NM_017653.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:46906125 C>A maps to NM_017653.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr18:46889583 A>T maps to NM_017653.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:102453803 G>T maps to NM_001376.4 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr14:102509075 G>A maps to NM_001376.4 R4168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr14:102516785 C>G maps to NM_001376.4 V4609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr14:102453024 G>A maps to NM_001376.4 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr14:102506066 G>T maps to NM_001376.4 V3896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr14:102509066 C>T maps to NM_001376.4 P4165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr14:102504834 G>C maps to NM_001376.4 L3649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr14:102476267 C>T maps to NM_001376.4 Y2022Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr14:102502846 C>A maps to NM_001376.4 P3592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr14:102510383 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr14:102482714 C>T maps to NM_001376.4 S2501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr14:102449516 C>T maps to NM_001376.4 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr14:102516441 C>T maps to NM_001376.4 N4573N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:102505825 G>A maps to NM_001376.4 L3846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr14:102508994 G>A maps to NM_001376.4 A4141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr7:95457425 T>C maps to NM_004411.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:95668587 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:95606908 G>A maps to NM_004411.4 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:95664995 G>A maps to NM_004411.4 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr7:95614202 G>T maps to NM_004411.4 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr3:32612232 G>A maps to NM_016141.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:66766352 G>C maps to NM_006141.2 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:66759797 C>T maps to NM_006141.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:103047051 G>C maps to NM_001080463.1 L1921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr11:102987415 C>T maps to NM_001080463.1 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr11:102988493 C>T maps to NM_001080463.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr11:102988372 A>T maps to NM_001080463.1 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:103022984 G>T maps to NM_001080463.1 E1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:102991187 A>T maps to NM_001080463.1 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:103060454 T>C maps to NM_001080463.1 V2449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr11:103070181 C>T maps to NM_001080463.1 Q2689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr11:103058261 C>T maps to NM_001080463.1 L2363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:103027224 C>T maps to NM_001080463.1 Q1285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr17:56166588 C>T maps to NM_080677.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr16:80583379 G>C did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr21:38862526 G>T maps to NM_001396.3 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr21:38858908 C>T maps to NM_001396.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:40317963 C>A maps to NM_004714.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:68052289 C>T maps to NM_006482.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:206821331 G>A maps to NM_003582.2 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:71797012 C>A maps to NM_001130987.1 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:71886124 C>T maps to NM_001130987.1 R1625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr2:71762411 C>T maps to NM_001130987.1 C488C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:71780157 C>G maps to NM_001130987.1 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr2:71901426 G>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:71797808 C>T maps to NM_001130987.1 R1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:71838716 G>A maps to NM_001130987.1 K1394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr2:71762191 G>A maps to NM_001130987.1 W474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:71709053 G>T maps to NM_001130987.1 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:71892331 C>T maps to NM_001130987.1 Q1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:71747931 C>A maps to NM_001130987.1 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr2:71755437 C>T maps to NM_001130987.1 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:207530692 C>T maps to NM_001093730.1 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:96293611 T>C maps to NM_198968.2 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:137822453 G>A maps to NM_173543.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:137803005 G>C maps to NM_173543.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:137802999 G>A maps to NM_173543.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:137816635 G>T maps to NM_173543.2 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:108403091 G>C maps to NM_014648.3 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr3:108344784 G>T maps to NM_014648.3 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:108380810 C>T maps to NM_014648.3 Q763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr3:108396444 G>A maps to NM_014648.3 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:108363275 C>T maps to NM_014648.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:108335437 G>A maps to NM_014648.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:32266050 A>G maps to NM_005225.2 C227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr6:20490659 G>C maps to NM_001949.3 *466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:86114379 A>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:2283181 G>T maps to NM_004424.3 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:2273688 G>A maps to NM_004424.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr16:2273706 G>A maps to NM_004424.3 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr3:15478026 C>T maps to NM_033083.6 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr16:23541091 G>A maps to NM_001083614.1 Y398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr5:158139993 T>C maps to NM_024007.3 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:158140038 C>T maps to NM_024007.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr5:158139243 G>A maps to NM_024007.3 N489N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr5:158522675 C>T maps to NM_024007.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:25715904 G>T maps to NM_022659.2 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:25715940 G>T maps to NM_022659.2 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr10:131640455 C>T maps to ENST00000355311 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr10:131761668 C>A maps to ENST00000355311 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr10:131641454 C>T maps to ENST00000355311 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:131639252 G>T maps to ENST00000355311 Y472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:131666136 C>T maps to ENST00000355311 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr10:131755565 A>G maps to ENST00000355311 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:43636429 C>T maps to NM_001159936.1 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:43630161 C>T maps to NM_001159936.1 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr1:43636550 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:48382450 T>A did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr10:74914174 G>A maps to NM_001135752.1 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:21560051 G>A maps to NM_001397.2 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:21585218 G>C maps to NM_001397.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr1:21564650 G>A maps to NM_001397.2 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:21616666 G>A maps to NM_001113349.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr1:21585218 G>C maps to NM_001397.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:184008347 G>A maps to NM_014693.3 W671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr3:184002872 C>A maps to NM_014693.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr3:183975423 C>G maps to NM_014693.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:183996309 C>A maps to NM_014693.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:184005698 C>T maps to NM_014693.3 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr3:184008410 C>T maps to NM_014693.3 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr3:184008620 G>T maps to NM_014693.3 E721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr2:233344943 G>C maps to NM_004826.2 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:53373582 C>G maps to ENST00000371522 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:53370494 C>T maps to ENST00000371522 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr1:53377415 C>T maps to ENST00000371522 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr1:53362206 T>C maps to ENST00000371522 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr1:150482212 C>T maps to ENST00000369049 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr5:138842246 G>A maps to NM_001077693.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:11624044 T>C maps to NM_016581.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:11618647 G>A maps to NM_016581.3 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr3:172501695 C>T maps to ENST00000392692 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr3:172474891 C>G maps to ENST00000392692 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr3:172486830 C>T maps to ENST00000392692 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:139159494 C>A maps to NM_001195037.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr6:139167807 G>A maps to NM_001195037.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr6:139164330 G>C maps to NM_001195037.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:139206876 C>G maps to NM_001195037.2 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr6:139202176 G>A maps to NM_001195037.2 Q583Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:68836325 G>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:69255291 G>A did not map to a codon.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr23:69255283 G>T did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:69253319 G>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:65824894 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr23:65819586 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:65835805 T>G did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:109547446 C>A maps to ENST00000376651 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr2:109539884 C>G maps to ENST00000376651 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr2:109513506 G>A maps to ENST00000376651 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:74967309 G>A maps to NM_025083.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:74963874 T>C maps to NM_025083.3 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr16:67913011 C>T maps to NM_014329.3 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:67912723 C>T maps to NM_014329.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:67913614 G>T maps to NM_014329.3 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:67917556 G>A maps to NM_014329.3 P1312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:67911498 G>A maps to NM_014329.3 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:67915423 C>T maps to NM_014329.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr16:67910784 C>T maps to NM_014329.3 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr14:21216173 C>T maps to NM_006683.4 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr3:5246815 G>A maps to NM_014674.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr20:33730262 C>A maps to NM_018217.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:184723708 C>T maps to NM_025191.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr6:12294601 C>A maps to NM_001955.4 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:78477473 C>T maps to ENST00000377211 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr13:78492393 C>T maps to ENST00000377211 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr12:93175724 C>T did not map to a codon.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr12:93251230 G>T maps to NM_003566.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:85979510 C>T maps to ENST00000351625 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:85977216 A>T maps to ENST00000351625 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:74229716 G>A maps to NM_001402.5 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr11:62327591 G>A maps to ENST00000378019 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr11:62340159 G>A maps to ENST00000378019 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr19:3977870 G>A maps to NM_001961.3 Y671Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr19:3983150 G>C maps to NM_001961.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:3983258 C>T maps to NM_001961.3 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:3977900 G>A maps to NM_001961.3 I661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:3980974 A>G maps to NM_001961.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr19:3979392 G>A maps to NM_001961.3 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:22271781 G>C did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr16:22268647 C>G maps to NM_013302.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr16:22268674 G>A maps to NM_013302.3 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:128060188 C>T maps to NM_021937.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr3:127983608 G>A maps to NM_021937.3 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:128060073 A>T did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr17:60493470 T>C maps to NM_001144933.1 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:3757679 C>T maps to NM_032680.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr12:3757779 C>A did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:28361325 G>T maps to NM_198529.3 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr17:28296202 G>A maps to NM_198529.3 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr22:43924775 G>C maps to NM_022785.3 S1488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr22:44079706 C>A maps to NM_022785.3 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:44022346 T>C maps to NM_022785.3 E815E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr22:44083442 G>A maps to NM_022785.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:56149557 G>A maps to NM_001039349.1 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:65635367 G>T maps to NM_016938.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:65638807 C>A maps to NM_016938.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:65634508 C>A maps to NM_016938.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:22113513 G>A maps to NM_152726.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr13:22088518 T>G maps to NM_152726.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr8:16948071 A>T maps to NM_181723.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:52318994 C>T maps to NM_018100.3 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:52303382 C>T maps to NM_018100.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr6:52343896 C>T maps to NM_018100.3 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr6:52355017 C>G maps to NM_018100.3 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr23:44171824 A>T did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:155106044 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:1299892 C>T maps to NM_001405.2 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:155057800 G>A maps to ENST00000505139 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr1:155058670 C>T maps to ENST00000505139 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:155039241 C>G maps to NM_182689.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:68058465 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:68060231 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr23:68058610 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr23:68058575 G>C did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr13:107145597 C>T maps to NM_004093.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr13:107145690 T>C maps to NM_004093.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:132982750 C>T maps to NM_015137.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:132999914 G>A maps to NM_015137.3 E677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:132952767 T>G maps to NM_015137.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr8:133015480 A>T did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr14:23829050 C>T maps to NM_005864.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr15:82443854 C>G maps to NM_024580.5 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr15:82444534 G>A maps to NM_024580.5 R754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:42931929 G>A maps to NM_004247.3 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr4:110890204 G>T maps to NM_001963.4 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:110902033 G>A maps to NM_001963.4 K758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:110866312 A>G maps to NM_001963.4 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:110884391 G>A maps to NM_001963.4 W459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:110884392 G>A maps to NM_001963.4 W459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr4:110914520 C>T maps to NM_001963.4 C951C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:13612976 G>T did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr23:13645319 G>A did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:139563026 C>T maps to NM_201446.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr9:139563122 C>T maps to NM_201446.1 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr6:32134034 C>T maps to NM_030652.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:38448427 G>A maps to ENST00000354891 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:38427201 C>T maps to ENST00000354891 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:38451421 C>G maps to ENST00000354891 S858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:38427225 G>T maps to ENST00000354891 R642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:38427333 C>T maps to ENST00000354891 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:38438423 C>T maps to ENST00000354891 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:38350679 G>A maps to ENST00000354891 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr5:38427144 T>C maps to ENST00000354891 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:55240702 G>A maps to NM_005228.3 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:55221792 G>A maps to NM_005228.3 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr7:55242488 G>A maps to NM_005228.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:55233025 C>T maps to NM_005228.3 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr7:55240687 G>C maps to NM_005228.3 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr7:55259560 A>C maps to NM_005228.3 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr7:55260486 C>G maps to NM_005228.3 S885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr1:231557040 G>A maps to NM_022051.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr5:137802444 G>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:137802773 G>T maps to NM_001964.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:137802792 G>T maps to NM_001964.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr10:64573803 G>A maps to NM_001136178.1 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr10:64573020 G>A maps to NM_001136178.1 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr10:64572999 G>A maps to NM_001136178.1 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr2:73518917 G>A maps to NM_001965.3 H479H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr2:63086363 C>G maps to NM_015252.3 S267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr11:65347885 G>A maps to NM_001099409.1 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr11:65349859 G>T maps to NM_001099409.1 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr11:65350464 G>A maps to NM_001099409.1 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr11:65350804 G>T maps to NM_001099409.1 E888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:65350671 G>A maps to NM_001099409.1 E843E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:48229327 C>T maps to NM_014601.3 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:48220234 C>T maps to NM_014601.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr2:31483526 G>C maps to NM_014600.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:31489392 C>T maps to NM_014600.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:31483476 G>T maps to NM_014600.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr2:31484542 C>T maps to NM_014600.2 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:42192956 G>A maps to NM_139265.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr11:34668199 C>G maps to NM_012153.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr3:184922273 C>T maps to NM_001966.3 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr9:140708935 C>T maps to NM_024757.4 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:140728823 C>T maps to NM_024757.4 D1188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr9:140611324 C>T maps to NM_024757.4 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr9:140611504 G>A maps to NM_024757.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr9:140657181 C>G maps to NM_024757.4 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:140729233 T>C maps to NM_024757.4 Y1242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr9:140637883 C>T maps to NM_024757.4 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr9:140652377 A>G maps to NM_024757.4 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr6:31864766 C>T maps to ENST00000395728 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr6:31847880 G>A maps to ENST00000395728 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr6:31864039 C>T maps to ENST00000395728 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr6:31855969 G>C maps to ENST00000395728 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr11:125453531 C>A maps to ENST00000278903 S342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:40030623 C>T maps to NM_153232.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:40023355 G>A maps to NM_152361.1 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:39847032 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:20153882 A>G did not map to a codon.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr23:20156730 C>T did not map to a codon.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr3:150285972 G>A maps to NM_032025.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr3:150289838 C>T maps to NM_032025.3 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr3:150301644 C>T maps to NM_032025.3 Q569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:6066484 C>A maps to NM_014413.3 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr7:6077065 G>A maps to NM_014413.3 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr2:37347200 G>A maps to NM_001135651.1 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:88885505 G>A maps to NM_004836.5 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:88874651 G>A maps to NM_004836.5 H783H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:88870487 G>A maps to NM_004836.5 D963D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr2:88858449 C>T maps to NM_004836.5 Q1045Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr15:40241350 C>G maps to NM_001013703.2 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr15:40313218 C>T maps to NM_001013703.2 D1431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr15:40268784 G>A maps to NM_001013703.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr15:40295428 C>T maps to NM_001013703.2 R1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:40265841 A>G maps to NM_001013703.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr15:40259876 C>T maps to NM_001013703.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr12:124107221 G>A maps to NM_001414.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:75475785 C>T maps to NM_014239.3 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr3:183858376 C>A maps to NM_003907.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:183855539 G>A maps to NM_003907.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:36367908 C>A maps to NM_012199.2 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr1:36372604 C>T maps to NM_012199.2 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr8:141572715 C>T maps to NM_012154.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:141561466 G>A maps to NM_012154.3 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr8:141542696 C>T maps to NM_012154.3 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr1:36282502 C>T maps to NM_017629.2 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:36291378 G>T maps to NM_017629.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr1:36291345 C>A maps to NM_017629.2 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr14:67850069 G>A maps to NM_004094.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:67843301 A>C maps to NM_004094.4 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr20:32685310 C>A maps to NM_003908.3 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr20:32677564 G>A maps to NM_003908.3 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr20:32685275 A>G maps to NM_003908.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr23:24091372 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:120809437 G>A maps to NM_003750.2 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr10:120829136 G>A maps to NM_003750.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr7:2409151 G>T maps to ENST00000314800 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:36912641 C>T maps to NM_003753.3 W363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:109215286 G>T maps to NM_001568.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:10227614 C>T maps to NM_003755.3 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr19:10226177 G>C maps to NM_003755.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:117658758 G>C maps to ENST00000411422 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr8:117668120 T>C maps to ENST00000411422 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr8:117671058 G>A maps to ENST00000411422 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:117658785 C>A maps to ENST00000411422 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:39114837 G>A did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:38254698 G>C maps to ENST00000262832 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr22:38247440 C>G maps to ENST00000262832 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr17:7479954 C>T maps to NM_001416.2 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:186504983 C>G maps to ENST00000440191 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr17:78113870 G>A maps to NM_014740.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:176072439 C>G maps to NM_001099408.1 V179V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-6441-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:37914653 G>T maps to NM_004095.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr22:31864188 G>A maps to NM_019843.3 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr22:31837895 G>C maps to NM_019843.3 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr22:31838039 G>A maps to NM_019843.3 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr22:31859947 G>A maps to NM_019843.3 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:184043112 G>A maps to NM_001194947.1 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr3:184049827 G>T maps to NM_001194947.1 A1531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:184033994 C>T maps to NM_001194947.1 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:184043059 C>T maps to NM_001194947.1 R961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:184039823 C>T maps to NM_001194947.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr3:184041345 C>T maps to NM_001194947.1 R754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr3:184043327 G>T maps to NM_001194947.1 E1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr3:184043142 C>T maps to NM_001194947.1 D988D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr11:10825923 C>A maps to ENST00000429377 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:10825037 C>A maps to ENST00000429377 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr11:10821736 G>A maps to ENST00000429377 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr11:10823637 T>C maps to ENST00000429377 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:10823242 G>T maps to ENST00000429377 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:21268029 C>T maps to NM_001198801.1 E482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr1:21205842 G>A maps to NM_001198801.1 Y845Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr7:73609191 C>T maps to NM_022170.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:73604021 C>T maps to NM_022170.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr14:103802211 C>G maps to NM_183004.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr17:7214722 C>T maps to NM_001143760.1 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr20:33867550 C>T did not map to a codon.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr20:33872143 C>G maps to NM_181466.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:33872097 G>A maps to NM_181466.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:48510847 C>G maps to NM_018696.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr18:48513076 C>G maps to NM_018696.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:12905652 C>A maps to NM_018127.6 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:12916587 C>A maps to NM_018127.6 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:12905676 C>T did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:852882 G>A maps to NM_001972.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr19:8028516 G>A maps to ENST00000351593 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr9:23701495 G>A maps to ENST00000359598 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:50666795 G>T maps to NM_021952.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:50642773 G>T maps to NM_021952.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr13:41517196 G>A maps to NM_172373.3 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:139981704 A>G maps to ENST00000379550 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:139980634 C>T maps to ENST00000379550 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr23:129201146 G>A did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr23:129201443 G>A did not map to a codon.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr23:129201443 G>A did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:129203539 C>T did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:129205092 G>C did not map to a codon.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr23:129201240 G>A did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:34502383 T>A maps to NM_198381.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr22:37770533 C>T maps to NM_052906.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr22:37769204 G>A maps to NM_052906.3 H790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr22:37770764 G>A maps to NM_052906.3 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr22:37769435 G>A maps to NM_052906.3 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr22:37770212 G>A maps to NM_052906.3 H454H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr22:37770944 G>A maps to NM_052906.3 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:47497247 C>A did not map to a codon.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr23:47498683 G>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:96641259 A>C maps to NM_005230.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr19:18555653 T>A maps to NM_006532.3 K592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:44067751 T>C maps to NM_025165.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr7:37355564 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:36917672 G>T maps to NM_014800.9 Y588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:37172812 G>A maps to NM_014800.9 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr7:37264523 G>A maps to NM_014800.9 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:37262252 C>G maps to NM_014800.9 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:36934499 G>A maps to NM_014800.9 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr7:36895203 C>T maps to NM_014800.9 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr16:67237407 T>C maps to NM_024712.3 Y677Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr16:67234108 G>A maps to NM_024712.3 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr16:67236794 G>T maps to NM_024712.3 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:85598301 G>T maps to NM_001135023.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:73455549 C>T maps to ENST00000358929 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr7:73480042 C>T maps to ENST00000358929 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:73474264 T>A maps to ENST00000358929 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:73474270 T>C maps to ENST00000358929 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:73477972 C>T maps to ENST00000358929 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr19:11665078 G>A maps to NM_032377.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:43830979 G>A maps to NM_022821.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:43830432 G>A maps to NM_022821.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr6:10984105 G>A maps to NM_017770.3 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:103988897 A>G maps to NM_152310.1 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:53138059 A>G maps to ENST00000370918 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr4:110980840 T>G maps to NM_024090.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:60067894 G>A maps to NM_024930.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr8:27964291 T>C maps to NM_018091.5 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr8:27995258 C>T maps to NM_018091.5 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr8:28017756 A>T maps to NM_018091.5 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr8:27995294 T>C maps to NM_018091.5 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr11:31671744 A>G maps to ENST00000395934 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr11:31541611 T>A maps to ENST00000395934 L78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:31531418 C>T maps to ENST00000395934 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr11:31616336 T>A maps to ENST00000395934 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr1:79387449 G>A maps to NM_022159.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:79387471 C>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:79403498 C>A maps to NM_022159.3 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:79357298 G>A maps to NM_022159.3 H640H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:79385873 A>T maps to NM_022159.3 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr1:79383342 T>A maps to NM_022159.3 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr1:79357358 G>A maps to NM_022159.3 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr5:49706780 G>A maps to NM_198449.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr4:101337094 G>A maps to NM_016242.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:153608305 G>C did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr23:153608359 T>A did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr23:153609535 T>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:48457819 T>C maps to NM_001166131.1 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr16:1825246 C>G maps to NM_001010865.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr22:29629428 T>G maps to NM_133455.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr22:29627076 G>T maps to NM_133455.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:29621205 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr22:29627088 C>A maps to NM_133455.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:101063332 C>T maps to ENST00000397927 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr7:101187375 T>A maps to ENST00000397927 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:27306172 G>A maps to NM_007046.3 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:27306409 C>G maps to NM_007046.3 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr18:2913161 C>T maps to NM_032048.2 N974N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr18:2891729 C>A maps to NM_032048.2 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr20:39990015 C>T maps to NM_052846.1 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr20:39993775 C>T maps to NM_052846.1 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr14:100387173 A>T maps to NM_001008707.1 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr14:100376628 T>G maps to NM_001008707.1 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr14:100363568 G>A maps to NM_001008707.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:100331944 C>T maps to NM_001008707.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr19:46117911 C>T maps to NM_001193268.1 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:46137674 C>A maps to NM_001193268.1 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:46137674 C>T maps to NM_001193268.1 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr11:62374472 C>T maps to ENST00000278845 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr11:62373365 C>G maps to ENST00000278845 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr11:62373657 G>A maps to ENST00000278845 H512H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr2:42557334 G>A maps to NM_019063.3 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:42472705 A>G maps to NM_019063.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr14:89091393 C>T maps to ENST00000380664 A1606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr14:89088974 A>G maps to ENST00000380664 D1662D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:89087642 G>A maps to ENST00000380664 G1672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:89202826 C>T maps to ENST00000380664 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:48832732 C>G maps to NM_001425.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr19:6897558 G>T did not map to a codon.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:6919743 C>T maps to ENST00000381407 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:6924813 G>T maps to ENST00000381407 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr19:14877868 G>A maps to NM_013447.2 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:14875329 C>T maps to NM_013447.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:14741006 G>A maps to NM_032571.3 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr19:14748917 G>T maps to NM_032571.3 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr10:119307741 A>G maps to NM_004098.3 *253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr2:119600537 G>T maps to NM_001426.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:119603945 C>T maps to NM_001426.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:155255139 G>T maps to NM_001427.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:225702366 T>C maps to ENST00000284563 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:71507742 T>C maps to NM_031889.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr4:71509350 T>C maps to NM_031889.2 T736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr4:71509482 G>A maps to NM_031889.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr4:71508561 G>A maps to NM_031889.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:71509144 C>T maps to NM_031889.2 Q668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr4:71510265 G>A maps to NM_031889.2 E1041E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr5:73931268 G>T maps to NM_003633.2 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr11:94861542 C>T maps to NM_015036.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr11:94862700 G>T maps to NM_015036.2 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:130581105 C>T maps to NM_001114753.1 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr17:77073808 C>G maps to NM_001042573.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:25284721 C>T maps to NM_145010.2 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr1:8928110 C>G maps to NM_001428.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr12:7025013 C>T maps to NM_001975.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr12:7028877 T>A maps to NM_001975.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr17:4858479 C>T maps to NM_053013.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr17:4858563 C>T maps to NM_053013.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr17:4859306 C>T maps to NM_053013.3 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:83375979 G>A maps to NM_021204.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr4:83378132 T>C maps to NM_021204.3 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr13:43986995 G>A maps to NM_001127615.1 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr13:43839570 A>T maps to NM_001127615.1 L525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:129822944 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:129759342 G>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:129799650 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:129813717 G>A did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:129771374 G>C did not map to a codon.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr23:129771268 T>G did not map to a codon.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr23:129761944 C>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:111431454 G>T maps to NM_001977.3 G417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr4:111430848 G>A maps to NM_001977.3 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:111397695 G>A maps to NM_001977.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr4:111397713 C>T maps to NM_001977.3 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr4:111397843 C>T maps to NM_001977.3 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr6:132201069 C>T maps to NM_006208.2 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr6:132195425 A>G maps to NM_006208.2 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr6:132206201 C>T maps to NM_006208.2 Q815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr6:132198249 C>T maps to NM_006208.2 C614C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7596-01A-11D-2229-08 chr6:132181555 C>T maps to NM_006208.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:120602743 C>A did not map to a codon.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:120596203 G>A maps to NM_006209.3 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:120569895 G>C maps to NM_006209.3 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr6:132068002 C>T maps to NM_005021.3 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr6:132061453 C>T maps to NM_005021.3 C797C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:132059243 T>C maps to NM_005021.3 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr6:132006585 G>A maps to NM_005021.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:46108937 C>T maps to NM_014936.4 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:46108042 C>T maps to NM_014936.4 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr6:46129473 G>A maps to NM_021572.4 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr17:77709257 C>T maps to NM_178543.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr22:40283602 G>C maps to NM_152512.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr22:40283600 G>C maps to NM_152512.3 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:97583063 G>A maps to NM_001098175.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr10:97607264 C>T maps to NM_001098175.1 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:139944948 G>A maps to NM_203468.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:40457534 G>T maps to NM_001248.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:40433580 A>T maps to NM_001248.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr14:74454624 G>T maps to NM_001249.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr20:25205949 G>T maps to NM_001247.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr20:25205868 G>A maps to NM_001247.2 Q424Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr20:25199203 G>A maps to NM_001247.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr20:25197284 C>A maps to NM_001247.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr20:25203552 G>A maps to NM_001247.2 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr9:140332686 C>T maps to NM_001033113.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr9:140330689 G>A maps to NM_001033113.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:140330689 G>A maps to NM_001033113.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr9:140329380 G>A maps to NM_001033113.1 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr22:41556726 G>T did not map to a codon.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr22:41556726 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr22:41547911 C>T maps to NM_001429.3 Q965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr22:41531854 C>T maps to NM_001429.3 Q523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr22:41574518 G>A maps to NM_001429.3 Q2268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr22:41572249 G>A did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr22:41573027 C>A maps to NM_001429.3 C1771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr22:41489078 C>A maps to NM_001429.3 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr22:41574913 C>G maps to NM_001429.3 S2400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr22:41525913 C>T maps to NM_001429.3 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr12:132529946 C>T maps to ENST00000333577 L2326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr12:132546771 C>T maps to ENST00000333577 R2704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr12:132445397 C>T maps to ENST00000333577 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:132554095 G>A maps to ENST00000333577 A3013A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:132498088 C>T maps to ENST00000333577 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:132510275 G>T maps to ENST00000333577 A1683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:132471078 C>T maps to ENST00000333577 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:132549424 C>T maps to ENST00000333577 A2885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr12:132547185 A>G maps to ENST00000333577 P2794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr12:132527955 G>C maps to ENST00000333577 P2141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr12:132446057 C>T maps to ENST00000333577 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr2:46587817 C>A maps to NM_001430.4 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr2:46605174 C>T maps to NM_001430.4 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:34778666 C>T maps to NM_012156.2 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:34797519 C>T maps to NM_012156.2 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr20:34806808 C>T maps to NM_012156.2 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr6:131190863 C>A maps to NM_001431.3 E816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr18:5394710 C>A maps to NM_012307.2 E1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr18:5410588 G>A maps to NM_012307.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr18:5397158 G>T maps to NM_012307.2 V913V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr18:5415858 G>A maps to NM_012307.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr18:5397374 C>A maps to NM_012307.2 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr18:5489137 C>T maps to NM_012307.2 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr18:5397175 C>A maps to NM_012307.2 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr18:5394793 T>A did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr18:5438038 G>A maps to NM_012307.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr18:5416371 A>T maps to NM_012307.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr18:5416178 G>A maps to NM_012307.2 Q569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:111976075 G>T maps to NM_019114.3 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:111979250 G>A maps to NM_019114.3 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:111976098 C>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:112018729 G>A maps to NM_019114.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr9:111970305 C>T maps to NM_019114.3 E592E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr9:111956583 G>A maps to NM_019114.3 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:120885270 C>T maps to NM_020909.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:120844791 G>A maps to NM_020909.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:43502556 G>A maps to NM_000119.2 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:21925102 C>T maps to ENST00000265800 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr10:32582603 C>T maps to NM_025209.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:149526742 G>A maps to NM_015630.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr2:149541325 G>A did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:47596656 C>T maps to NM_002354.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:47600695 C>T maps to ENST00000426238 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr7:37960495 C>A maps to NM_017549.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:37989862 C>A maps to NM_017549.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr7:37988619 G>T maps to NM_017549.3 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr7:143088774 G>T maps to NM_005232.4 Y930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr7:143088617 G>A maps to NM_005232.4 Q955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:38227326 C>T maps to NM_001099439.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr1:38197200 G>A maps to NM_001099439.1 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:38227605 G>A maps to NM_001099439.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:38227470 G>A maps to NM_001099439.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr1:38227317 C>T maps to NM_001099439.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:38188812 G>A maps to NM_001099439.1 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:38227229 G>A maps to NM_001099439.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr1:38185712 C>T maps to NM_001099439.1 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:16464403 G>C maps to NM_004431.3 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:16462184 G>A maps to NM_004431.3 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr1:16456779 G>A maps to NM_004431.3 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr1:16456788 G>A maps to NM_004431.3 I867I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:16464403 G>C maps to NM_004431.3 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:16464346 C>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:16456828 C>T maps to NM_004431.3 W854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:16477389 C>G did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:16475421 C>A maps to NM_004431.3 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:16464403 G>C maps to NM_004431.3 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr1:16464403 G>C maps to NM_004431.3 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:89521721 G>T maps to NM_005233.5 T933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr3:89499367 C>T maps to NM_005233.5 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:89259516 C>T maps to NM_005233.5 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr3:89478307 T>C maps to NM_005233.5 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:89156986 G>C did not map to a codon.
Alternatively spliced codon TCGA-CV-6953-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr3:89456491 C>G maps to NM_005233.5 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr3:89480487 A>T maps to NM_005233.5 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:89390207 C>A maps to NM_005233.5 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr3:89259050 C>T maps to NM_005233.5 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:89456440 T>C maps to NM_005233.5 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:222428964 G>A maps to NM_004438.3 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:222298866 G>A maps to NM_004438.3 Q831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:222322666 T>C maps to NM_004438.3 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr2:222294820 G>A maps to NM_004438.3 C849C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:66509101 C>T maps to NM_004439.5 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:66270138 C>T maps to NM_004439.5 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr4:66230768 A>G maps to NM_004439.5 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr4:66270111 G>T maps to NM_004439.5 I590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr4:66467878 G>C maps to NM_004439.5 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:66197746 C>T maps to NM_004439.5 E984E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr4:66213888 T>A maps to NM_004439.5 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr4:66356239 G>A maps to NM_004439.5 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:66201717 T>A maps to NM_004439.5 I928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr4:66467890 G>A maps to NM_004439.5 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:96706793 C>T maps to NM_001080448.2 C357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:96962793 A>T did not map to a codon.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr3:96706229 A>G maps to NM_001080448.2 V169V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-7402-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr6:93967233 T>A maps to NM_004440.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr6:94120845 G>A maps to NM_004440.3 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:94066615 G>T maps to NM_004440.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr6:94120309 C>T maps to NM_004440.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr6:93955065 G>A maps to NM_004440.3 F944F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:22923820 C>T maps to NM_020526.3 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:22919855 G>A maps to NM_020526.3 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr1:22927548 T>C maps to NM_020526.3 P899P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:22927810 C>T maps to NM_020526.3 F916F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:22921774 G>A maps to NM_020526.3 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:22920125 C>G maps to NM_020526.3 S517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:22927161 G>A maps to NM_020526.3 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr3:134880876 C>T maps to NM_004441.4 N480N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr3:134851754 G>A maps to NM_004441.4 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:134670218 G>T maps to NM_004441.4 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr3:134884900 C>T maps to NM_004441.4 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr3:134920368 C>A maps to NM_004441.4 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr3:134911541 G>A maps to NM_004441.4 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr1:23191379 C>T maps to ENST00000400191 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:23234657 C>A maps to ENST00000400191 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:23234651 C>T maps to ENST00000400191 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:23235658 C>T maps to ENST00000400191 Q833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:184298533 C>T maps to NM_004443.3 I802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:184298945 C>T maps to NM_004443.3 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr7:100421280 C>T maps to NM_004444.4 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr7:100410410 G>A maps to NM_004444.4 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:142564287 C>T maps to NM_004445.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:226032237 C>G maps to NM_001136018.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:226027610 C>T maps to NM_001136018.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:27348770 C>T maps to ENST00000458037 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:92495680 C>T maps to NM_173567.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr1:92495737 C>T maps to NM_173567.4 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr1:92528794 C>T maps to NM_173567.4 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:92495662 C>G maps to NM_173567.4 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:92515904 G>A maps to NM_173567.4 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr1:92518078 C>T maps to NM_173567.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:37033929 G>A maps to NM_014805.3 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:37034471 C>A maps to NM_014805.3 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr19:56203253 C>T maps to NM_001130071.1 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr19:56206140 G>A maps to NM_001130071.1 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:19235286 C>T maps to NM_014964.4 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr17:19232090 C>T maps to NM_014964.4 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr17:48618683 C>T maps to NM_017957.2 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr17:48619235 C>T maps to NM_017957.2 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:144941430 G>A maps to NM_031308.1 L1997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr8:144947142 G>A maps to NM_031308.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr8:144940257 G>A maps to NM_031308.1 D2388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr8:144944661 G>A maps to NM_031308.1 D920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:144941997 G>A maps to NM_031308.1 D1808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr8:144940689 G>A maps to NM_031308.1 S2244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7391-01A-11D-2012-08 chr8:144946713 G>A maps to NM_031308.1 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:144940191 C>G maps to NM_031308.1 T2410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr8:144944532 C>T maps to NM_031308.1 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr8:144940653 G>A maps to NM_031308.1 P2256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:144946382 G>A maps to NM_031308.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:144941346 G>A maps to NM_031308.1 L2025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr8:144942423 G>T maps to NM_031308.1 A1666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:144940344 C>T maps to NM_031308.1 V2359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr8:144943114 G>C maps to NM_031308.1 S1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:144940347 G>A maps to NM_031308.1 P2358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:144940740 C>T maps to NM_031308.1 A2227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:144943050 G>A maps to NM_031308.1 V1457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr8:144940785 C>T maps to NM_031308.1 E2212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr8:144940410 G>A maps to NM_031308.1 R2337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:220206925 G>C maps to NM_004446.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:220170408 A>G maps to NM_004446.2 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:51930971 G>A maps to NM_001981.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:51926823 T>A did not map to a codon.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr1:51829610 G>A maps to NM_001981.2 V762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr1:51829571 G>A maps to NM_001981.2 I775I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:16528863 C>A maps to ENST00000455140 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:16504766 G>C maps to ENST00000455140 S654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:16515512 G>A maps to ENST00000455140 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr19:16514681 G>A maps to ENST00000455140 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr12:15811036 G>A maps to NM_004447.5 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:721617 G>A maps to NM_022772.3 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr11:720676 G>A maps to NM_022772.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:110294643 C>T maps to NM_139053.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:110294290 G>A maps to NM_139053.1 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:110294747 G>A maps to NM_139053.1 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr17:56274610 C>T maps to NM_000502.4 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:56276416 G>A maps to NM_000502.4 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr17:56271374 C>T maps to NM_000502.4 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:91358090 G>A maps to NM_004950.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr17:27185505 T>C did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:96130757 G>A maps to NM_016442.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr5:96121616 G>A maps to NM_016442.3 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:96112180 A>G maps to NM_016442.3 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr5:96222494 T>A did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr5:96245439 C>T maps to NM_001130140.1 Q776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:96248383 C>T maps to NM_001130140.1 Q800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr5:96235856 A>G maps to NM_001130140.1 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr5:96238048 C>G maps to NM_001130140.1 S607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr5:96244817 C>G maps to NM_001130140.1 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:48687837 A>T did not map to a codon.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr23:48687627 G>A did not map to a codon.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr17:37868214 C>G maps to NM_004448.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:37879628 G>T maps to NM_004448.2 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:37866345 C>T maps to NM_004448.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:37883981 G>A maps to NM_004448.2 S1151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:65342329 C>T maps to ENST00000506030 N584N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr5:65349482 G>A maps to ENST00000506030 E779E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:56495415 G>C maps to NM_001982.2 R1202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:56477580 G>A maps to NM_001982.2 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr12:56492687 G>A maps to NM_001982.2 K946K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:56477586 A>G maps to NM_001982.2 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr12:56494867 T>C maps to NM_001982.2 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:56480408 T>C maps to NM_001982.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr12:56481627 C>G maps to NM_001982.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:212530142 T>C maps to NM_005235.2 K592K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:212488769 C>A did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:212589878 G>A maps to NM_005235.2 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:212251599 A>C maps to NM_005235.2 P1153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:212543813 C>A maps to NM_005235.2 G529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr2:212568851 G>A maps to NM_005235.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:212495210 G>A maps to NM_005235.2 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr2:212426725 G>A maps to NM_005235.2 Q797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr2:212286829 C>A did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr12:1250923 G>T maps to NM_178040.2 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:55984541 G>A maps to ENST00000460849 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:56173587 G>C maps to ENST00000460849 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:55984514 G>A maps to ENST00000460849 Q781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr3:56468820 G>T maps to ENST00000460849 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr19:45920134 G>C maps to NM_202001.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:45860922 T>C maps to NM_000400.3 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:45872212 G>T maps to NM_000400.3 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr2:128029026 T>A maps to NM_000122.1 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:128044294 T>C maps to NM_000122.1 E442E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:128036884 A>G maps to NM_000122.1 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:14015907 G>A maps to NM_005236.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr13:103520607 G>C did not map to a codon.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr13:103504603 G>T maps to NM_000123.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr13:103524679 C>G maps to NM_000123.2 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr13:103515433 G>A maps to NM_000123.2 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:50690804 C>A maps to NM_000124.2 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr10:50690870 C>G maps to NM_000124.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr23:71427610 T>C did not map to a codon.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr23:71425944 C>T did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:71425659 G>C did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr23:71426164 A>C did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr4:75231039 G>A maps to NM_001432.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr19:42754039 G>A maps to NM_006494.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:42753747 G>A maps to NM_006494.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr19:42754668 G>C maps to NM_006494.2 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr19:42754071 G>A maps to NM_006494.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr21:39755447 G>A maps to NM_001136154.1 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr12:29514591 C>T maps to NM_016570.2 Q120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:29509319 C>A maps to NM_016570.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr12:29523087 T>A maps to NM_016570.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:44820584 C>G maps to NM_024066.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr8:642490 C>G maps to NM_207332.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr8:37607143 C>T maps to NM_007175.6 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr1:43308788 C>T maps to NM_018538.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:158177884 G>A maps to NM_001009959.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr2:158177959 G>T maps to NM_001009959.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr9:5823979 G>A maps to NM_024896.2 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:62122728 G>A maps to NM_001433.3 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr17:62126508 A>T maps to NM_001433.3 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr17:62121348 C>T maps to NM_001433.3 *978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr17:62122833 G>A maps to NM_001433.3 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr16:23702253 C>T maps to NM_033266.3 T941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:23706159 G>A maps to NM_033266.3 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:23713532 C>T maps to NM_033266.3 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr1:236389815 C>G did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr12:112460444 G>T maps to NM_006817.3 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr1:8074115 G>A maps to NM_018948.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:11104999 G>A maps to NM_207582.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr8:27634269 C>T maps to NM_001017420.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr20:13756719 C>T maps to NM_016649.3 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr20:13753255 A>T maps to NM_016649.3 Y385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr20:13747567 C>A maps to NM_016649.3 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr5:54275231 A>G maps to NM_007036.4 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:53680437 G>A maps to NM_012291.4 E1306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr12:53663739 G>A maps to NM_012291.4 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr12:53664559 G>A maps to NM_012291.4 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:53684656 G>T maps to NM_012291.4 L1799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:53663847 G>A maps to NM_012291.4 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:53675380 C>T maps to NM_012291.4 R864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr12:53662896 C>A maps to NM_012291.4 C57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:53681817 G>A maps to NM_012291.4 E1413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:152129445 G>A maps to NM_001122741.1 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:152382207 C>T maps to NM_001122741.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr6:152163815 C>A maps to NM_001122741.1 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr14:64746774 G>A maps to NM_001437.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:64746789 G>A maps to NM_001437.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:64727452 C>T maps to NM_001437.2 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr14:64716326 G>A maps to NM_001437.2 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:95653587 C>T maps to NM_017697.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr8:95677422 T>A maps to NM_017697.3 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K0-01B-21D-A31L-08 chr8:95690545 G>A maps to NM_017697.3 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr8:95658448 C>T maps to NM_017697.3 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr14:76905770 G>A maps to NM_004452.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:216850601 A>T maps to NM_001438.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:216850745 G>A maps to NM_001438.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:216850475 G>C maps to NM_001438.2 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:216680463 C>A maps to NM_001438.2 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:216850529 G>A maps to NM_001438.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:216680457 C>T maps to NM_001438.2 Q400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:216680337 T>C maps to NM_001438.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr1:216850524 G>T maps to NM_001438.2 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:103499186 C>G did not map to a codon.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr23:103498949 C>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:103495024 C>A did not map to a codon.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr23:103495253 C>T did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:103498856 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr23:103499134 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr23:103495338 C>T did not map to a codon.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr12:56527376 C>T maps to NM_001184796.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:56522297 G>C maps to NM_001184796.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr12:56525334 C>T maps to NM_001184796.1 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr7:158529771 G>C maps to NM_020728.2 S816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:158557394 G>A maps to NM_020728.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr7:158552832 G>A maps to NM_020728.2 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:138178863 C>T maps to NM_031913.3 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr3:138178049 C>T maps to NM_031913.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:76588078 C>A did not map to a codon.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr19:51856529 G>A maps to NM_001014763.1 T168T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-T2-A6X2-01A-12D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:128360448 T>A maps to NM_001143820.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr11:128354826 C>G maps to NM_001143820.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr21:40194811 G>T maps to NM_005239.4 *470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:40186266 T>C maps to NM_005239.4 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr7:13950932 C>G did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr7:13975370 C>T maps to NM_004956.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr7:13935628 T>C maps to NM_004956.4 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:14027741 G>A maps to NM_004956.4 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr7:13935562 A>G maps to NM_004956.4 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr19:36134281 C>T maps to ENST00000222279 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr1:157105333 C>T maps to NM_001145312.1 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr1:157068946 C>T maps to NM_001004341.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:41622707 C>A maps to NM_001079675.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:41605895 G>A maps to NM_001079675.1 Y482Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:185783683 C>T maps to NM_004454.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:12022502 C>T maps to NM_001987.4 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7593-01A-11D-2229-08 chr4:5809990 C>T maps to NM_153717.2 H875H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:5627481 T>C maps to NM_147127.4 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr17:29632279 G>T maps to NM_006495.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:93167772 C>A did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:92979213 C>G maps to NM_005665.4 *811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr19:7916348 C>T maps to NM_001159944.1 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr19:7914194 C>T maps to NM_001159944.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr17:74005784 C>T maps to NM_001988.2 A1167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr17:74006564 A>G maps to NM_001988.2 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:74006417 C>T maps to NM_001988.2 E956E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:74018541 C>T maps to NM_001988.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr17:74019474 C>T maps to NM_001988.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:74019696 G>A maps to NM_001988.2 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K0-01B-21D-A31L-08 chr17:74005010 G>A maps to NM_001988.2 F1425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr17:18286167 G>A maps to NM_001145127.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:176946953 G>A maps to NM_001080458.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr22:29695244 C>T maps to NM_013986.3 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr22:29682944 G>A maps to NM_013986.3 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr15:41488236 T>A did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr14:69701562 C>T maps to NM_001193363.1 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr14:69704567 G>T maps to NM_001193363.1 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr14:69704289 A>G did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr9:140245540 A>G maps to NM_017820.3 H481H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:242020735 A>G maps to NM_006027.4 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:242045250 C>T maps to NM_006027.4 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:56744195 G>A maps to NM_018261.3 K396K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr4:56762880 A>C did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr6:562845 C>T did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:556004 T>C maps to NM_018303.4 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr5:453740 C>T maps to ENST00000315013 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr16:67218810 G>A maps to NM_178516.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:133041327 G>A did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:133689721 G>T maps to NM_021807.3 V802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr7:133682383 G>C maps to NM_021807.3 V782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr14:57699410 G>C maps to ENST00000340918 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr14:57675356 T>C maps to ENST00000340918 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:94773978 A>G maps to NM_019053.4 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:94679785 T>C maps to NM_019053.4 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr2:72968447 T>C maps to NM_015189.1 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:72562090 G>A maps to NM_015189.1 F727F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:72406523 C>T maps to NM_015189.1 Q792Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr2:72968462 C>T maps to NM_015189.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr17:74085375 C>T maps to NM_001145297.2 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr17:74097809 G>T maps to NM_001145297.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:231473419 C>T maps to NM_175876.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:38537875 C>T maps to NM_005107.3 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:99205727 C>T maps to NM_016046.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr1:11141273 G>T maps to NM_001001998.1 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr9:133573565 G>A maps to NM_014285.5 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr9:133569282 G>A maps to NM_014285.5 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr19:41895668 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr19:41898787 C>T maps to NM_020158.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr3:45049057 G>A maps to NM_015004.3 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:45052821 C>T maps to NM_015004.3 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:108380449 G>A maps to NM_015065.2 N1928N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr11:108380961 G>A maps to NM_015065.2 L1758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:108381349 G>A maps to NM_015065.2 G1628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:108383614 C>A maps to NM_015065.2 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr11:108380743 C>G maps to NM_015065.2 L1830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr8:118847730 A>T maps to NM_000127.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr8:119123159 A>T maps to NM_000127.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:26349619 C>T maps to NM_004455.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:26349592 A>G maps to NM_004455.2 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:26349151 G>A maps to NM_004455.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr1:26360197 C>T maps to NM_004455.2 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr1:26349535 C>T maps to NM_004455.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:101342388 G>A maps to NM_001439.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr8:28573797 C>T maps to NM_001440.2 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr8:28573737 G>T maps to NM_001440.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr8:72184107 G>T maps to NM_000503.4 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr8:72234071 A>C maps to NM_000503.4 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr20:45725800 C>T maps to ENST00000360649 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:133783786 G>A maps to ENST00000452339 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr6:133802715 G>T maps to ENST00000452339 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr6:133783831 C>A maps to ENST00000452339 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:133836543 A>T maps to ENST00000452339 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr6:133783511 A>G maps to ENST00000452339 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:133846195 T>C maps to NM_172105.3 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:133785941 T>G maps to ENST00000452339 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:133846192 C>G maps to NM_172105.3 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr6:133769264 T>C maps to ENST00000452339 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:66204796 C>T maps to ENST00000370616 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr6:66094289 C>A maps to ENST00000370616 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr6:66205190 G>C maps to ENST00000370616 S38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:66204658 A>G maps to ENST00000370616 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr17:40870630 G>A maps to ENST00000264646 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:40865278 T>C maps to ENST00000264646 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:40879702 G>A maps to ENST00000264646 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:159188023 G>A maps to NM_001111077.1 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr6:159188385 C>T maps to NM_001111077.1 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr13:113777198 C>T maps to NM_000504.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr4:187208887 G>T maps to NM_000128.3 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr4:187205255 C>T maps to NM_000128.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:160970526 G>A maps to NM_016946.4 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:160990821 G>C maps to NM_016946.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr6:6266818 C>T maps to NM_000129.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr6:6305590 G>T maps to NM_000129.3 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr6:6266931 G>T maps to NM_000129.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:6266847 G>A maps to NM_000129.3 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:197029574 A>G maps to NM_001994.2 H242H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:197026220 T>A maps to NM_001994.2 K365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:197026302 C>T maps to NM_001994.2 E337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:197008534 C>A maps to NM_001994.2 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:94997875 C>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:94997898 G>T maps to NM_001993.4 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr1:95007177 G>A maps to NM_001993.4 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:169510645 G>A maps to ENST00000367796 Q1233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:169529960 G>A maps to ENST00000367796 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:169510535 C>T maps to ENST00000367796 Q1269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:169511662 T>A maps to ENST00000367796 K894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:169525914 G>A maps to ENST00000367796 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr1:169509962 T>C maps to ENST00000367796 S1460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:169505919 T>C did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr13:113773174 G>A maps to NM_000131.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:154225260 C>G did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:154194877 T>C did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr23:154221233 C>G did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:154159319 T>G did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:154128149 A>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:154157818 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:154213058 T>G did not map to a codon.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr23:154250783 C>T did not map to a codon.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr23:154194411 A>G did not map to a codon.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr23:154158239 A>G did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:154185289 C>G did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:154194840 G>A did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:138643013 G>T did not map to a codon.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr23:138633413 C>A did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:138612943 C>G did not map to a codon.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr23:138643693 A>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:138642992 G>A did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:138619216 G>A did not map to a codon.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr23:138643975 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr23:138643736 G>A did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:138623272 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:57337060 A>T did not map to a codon.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr23:57337037 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr23:57474970 G>T did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:57313309 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:57358174 G>A did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:57367791 C>G did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:57367815 T>G did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:57337082 G>T did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:57337083 G>T did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:88424027 G>A maps to NM_001443.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr2:88425817 C>T maps to NM_001443.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:120240197 A>T maps to NM_000134.3 *133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr4:120243206 C>T maps to NM_000134.3 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:82395375 C>T maps to NM_001442.2 W9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr11:61596041 C>T maps to NM_004265.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr11:61605284 C>T maps to NM_004265.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr1:51049376 G>A maps to NM_007051.2 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:96072817 C>T maps to NM_016044.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr16:4664714 C>G maps to NM_145253.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr16:4659673 G>C maps to NM_145253.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr12:124798974 C>A maps to ENST00000389727 C185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr12:124799004 C>T maps to ENST00000389727 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr12:124796440 C>T maps to ENST00000389727 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr9:130712746 C>T maps to NM_001035254.2 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:109170787 G>C did not map to a codon.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr17:71223342 A>G maps to NM_001098832.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr23:55172658 A>G did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr5:14601328 G>T maps to NM_019018.2 G78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr5:14602299 G>A maps to NM_019018.2 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr3:58555542 C>G maps to ENST00000474531 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:14816384 G>C maps to NM_031453.2 S93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr15:81041862 G>T maps to NM_021214.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr15:80988171 G>T maps to NM_021214.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr8:59059283 C>A maps to NM_147189.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:46007 G>C maps to NM_001077710.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr2:45626 G>A maps to NM_001077710.2 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:58920181 G>T maps to NM_198847.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:58920370 G>A maps to NM_198847.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr11:58919995 G>A maps to NM_198847.2 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:58919320 C>T maps to NM_198847.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr11:58891900 C>T maps to NM_198947.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr20:2820549 G>A maps to NM_022760.3 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr20:2816811 C>T maps to NM_022760.3 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr20:2819569 A>C maps to NM_022760.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr20:2819521 C>T maps to NM_022760.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr12:47629133 C>T maps to NM_138371.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:153390821 G>A maps to ENST00000442256 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:143573296 T>C maps to NM_014719.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:143417114 C>T maps to ENST00000441159 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr3:57658126 T>C maps to NM_152678.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:57613941 C>G maps to NM_152678.2 *609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr3:57614607 A>C maps to NM_152678.2 L542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr22:50750770 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:47797211 G>A maps to NM_030802.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:47797714 C>T maps to NM_030802.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:203621982 G>A maps to NM_173511.3 Q384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr22:45728403 C>T maps to NM_017911.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr22:45723892 C>T maps to NM_017911.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr22:45732283 C>G maps to NM_017911.2 S349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr22:45719277 C>T maps to NM_017911.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:126110785 C>G maps to NM_024556.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:208486554 C>T maps to ENST00000272839 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr2:208486635 G>A maps to ENST00000272839 I51I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-6219-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:96209967 G>A maps to NM_198841.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:170626881 C>G maps to NM_032448.1 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr23:54209175 C>G did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:54112313 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:54099641 C>T did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:54099677 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr9:71395142 G>C maps to NM_138333.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:71395718 G>A maps to NM_138333.3 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:133979246 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr13:25744230 C>T maps to NM_152704.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr13:25744107 G>T maps to NM_152704.2 Y550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr13:25745571 C>T maps to NM_152704.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:63410292 C>A did not map to a codon.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr23:63411780 T>C did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:63412150 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr23:63412535 C>A did not map to a codon.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr23:63412438 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr23:63411089 G>A did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr23:63410936 C>G did not map to a codon.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr23:63412938 T>C did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:63413126 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:63412058 C>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:63410015 C>T did not map to a codon.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr23:63410342 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:63411018 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:63412635 G>A did not map to a codon.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr23:63412848 A>G did not map to a codon.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr23:63410189 T>A did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:131521972 G>A maps to NM_001105195.1 Q776Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:131521445 C>T maps to NM_001105195.1 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr2:131519911 G>A maps to NM_001105195.1 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr7:22985393 G>A maps to NM_032581.3 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:201846099 G>T maps to NM_173822.3 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:134166727 T>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:134185807 C>G did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:134185957 C>G did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr23:134156230 C>G did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:184868310 C>T did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:184764620 G>A maps to NM_052966.2 H759H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr9:130272454 G>A maps to NM_022833.2 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:17664288 C>T maps to ENST00000335393 Q671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr3:184060001 C>G maps to NM_144635.4 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:143053831 C>T maps to NM_001031690.2 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:16385162 C>T maps to NM_182623.2 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr23:92964762 C>G did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:92964592 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:92964536 C>T did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:92195341 G>A maps to NM_152789.2 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr2:220045436 G>T maps to NM_024293.4 G201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr5:16616783 G>A maps to NM_001034850.1 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr17:40761275 G>A maps to NM_178126.3 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr17:40734007 C>A maps to NM_178126.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr17:40733938 G>T maps to NM_178126.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr17:40733929 G>A maps to NM_178126.3 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr17:40761329 C>A maps to NM_178126.3 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:71185188 T>C maps to NM_001162529.1 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:71232223 A>G maps to NM_001162529.1 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr6:71247997 C>T maps to NM_001162529.1 L1374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr6:71235239 C>G maps to NM_001162529.1 S818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:139263090 A>G maps to NM_015912.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr8:139180195 G>T maps to NM_015912.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr8:139163783 A>C maps to NM_015912.3 A978A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr8:139144919 G>T maps to NM_015912.3 G1379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:139155261 G>T maps to NM_015912.3 R1211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:139165259 C>T maps to NM_015912.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:139323162 C>T maps to NM_015912.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:139151250 G>C maps to NM_015912.3 L1293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr8:139190885 C>A maps to NM_015912.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:139153564 G>T maps to NM_015912.3 I1222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:139158207 C>T maps to NM_015912.3 K1178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:139164562 G>A maps to NM_015912.3 R719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr8:139165052 G>A maps to NM_015912.3 D555D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr8:139163459 C>T maps to NM_015912.3 E1086E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr8:139209764 C>A maps to NM_015912.3 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:139165178 C>T maps to NM_015912.3 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:89668808 C>A maps to NM_014883.2 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:89652579 C>G did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr4:89827586 G>C maps to NM_014883.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr5:137354084 G>A maps to NM_016603.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr10:61112149 C>T maps to ENST00000442566 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:61022289 G>A maps to ENST00000442566 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr4:187088345 G>T maps to ENST00000356371 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr4:187074900 C>T maps to ENST00000356371 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:53451005 G>C maps to NM_207413.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:55089032 G>C maps to NM_176782.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:55089014 G>T maps to NM_176782.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:55081831 G>T maps to NM_176782.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr5:177163582 C>A maps to ENST00000425383 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr13:108518371 G>A maps to NM_001080396.2 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr13:108518104 T>C maps to NM_001080396.2 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr13:108518791 C>A maps to NM_001080396.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr13:107822852 C>A maps to NM_001080396.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr13:108518288 G>T maps to NM_001080396.2 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr13:108518152 G>A maps to NM_001080396.2 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr13:108518287 C>T maps to NM_001080396.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr23:68725655 C>A did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr23:68749787 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:53108621 C>T maps to NM_001042693.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr11:6244315 T>A maps to NM_032127.3 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr11:6238877 G>C maps to NM_032127.3 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr10:116595330 C>T maps to NM_020940.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:116593010 C>T maps to NM_020940.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr10:116605221 C>T maps to NM_020940.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:116620557 C>T maps to NM_020940.3 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:21957262 G>C maps to NM_022749.5 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr8:21960043 C>T maps to NM_022749.5 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:62067352 G>A maps to ENST00000404929 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:62066962 T>C maps to ENST00000404929 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:74411194 C>T maps to NM_152445.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr14:74409086 G>A maps to NM_152445.1 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:74411449 G>A maps to NM_152445.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr14:74409109 G>A maps to NM_152445.1 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr14:74404815 C>G did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr6:117086361 G>A maps to NM_001085480.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr8:79588091 A>T maps to NM_016010.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr9:140138196 C>G maps to NM_001001710.1 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr2:131812998 C>T maps to NM_001009993.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:74077285 C>G maps to NM_015566.1 *671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:15256455 C>G maps to NM_001010924.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:187626380 C>T maps to NM_177454.3 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:187627042 C>T maps to NM_177454.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr5:93120105 G>A maps to NM_032042.5 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr16:772478 C>T maps to NM_023933.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:10239376 C>T maps to NM_199133.2 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:99871503 G>T maps to NM_198507.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:99871266 C>T maps to NM_198507.1 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr4:84383770 G>T maps to NM_139076.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:84390288 T>C maps to NM_139076.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:102684053 G>A maps to NM_001136123.1 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:102684485 C>T maps to NM_001136123.1 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr2:97543731 C>T maps to ENST00000417561 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr2:29259408 C>T maps to NM_199280.2 V807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr2:29245048 G>A maps to NM_199280.2 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:29249762 C>G maps to NM_199280.2 S633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr2:29240093 G>A maps to NM_199280.2 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:29245102 G>A maps to NM_199280.2 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr2:29274947 C>T maps to NM_199280.2 Q1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr14:94394801 G>T maps to NM_138344.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr14:94394756 G>A maps to NM_138344.3 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr11:82444615 C>A maps to NM_175885.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr11:82444684 G>A maps to NM_175885.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr6:119297189 G>C maps to NM_024581.4 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr6:119341141 C>T did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr6:119341264 C>A maps to NM_024581.4 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:119337959 A>T maps to NM_024581.4 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr12:49992672 G>A maps to NM_032130.2 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:49982391 C>T maps to NM_032130.2 W793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:35715961 G>A maps to NM_152481.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr7:30890111 C>T maps to NM_032222.2 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr9:72006632 G>C maps to NM_001127608.1 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:71986446 T>C maps to NM_001127608.1 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:155223907 A>T maps to ENST00000368370 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr17:18708851 A>G did not map to a codon.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr17:15458636 C>T maps to NM_145301.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr4:91549259 G>T maps to NM_001145065.1 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:91230448 G>C maps to NM_001145065.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:91230658 A>G maps to NM_001145065.1 K408K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr4:91230514 G>A maps to NM_001145065.1 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr4:91229926 C>T maps to NM_001145065.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:86131077 T>C maps to ENST00000372088 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:86259713 G>A maps to NM_018999.2 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:2641514 C>T maps to ENST00000324666 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr4:2717748 G>C did not map to a codon.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr5:176951738 G>A maps to ENST00000442143 N661N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr3:150377924 C>T maps to NM_152394.3 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:128974407 G>T maps to NM_001039762.2 Y84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr10:128974487 C>A maps to NM_001039762.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr10:128974170 G>C maps to NM_001039762.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr10:128973750 A>T maps to NM_001039762.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:103432976 G>A did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:103411633 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:62147516 C>T maps to NM_178539.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr12:62104198 C>A did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr22:49042508 A>G maps to ENST00000336769 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:66548054 C>T maps to NM_017565.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr17:66551868 G>C maps to NM_017565.3 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:179013305 G>A maps to NM_014864.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr1:179041167 C>T maps to NM_014864.3 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:179033562 C>G maps to NM_014864.3 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:47915914 C>A maps to NM_018232.1 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr10:46250492 C>G maps to ENST00000399588 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr10:46250555 T>C maps to ENST00000399588 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr10:46222967 C>A maps to ENST00000399588 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr10:88988215 C>T maps to NM_001099338.1 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr10:88994222 C>T maps to NM_001099338.1 Q799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr10:89118156 T>C maps to ENST00000330762 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr9:97080989 A>T maps to NM_017561.1 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:99694505 G>A maps to NM_001170741.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:124672280 T>A maps to NM_001029888.1 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr10:124672389 C>T maps to NM_001029888.1 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:124608955 C>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:124608783 G>A maps to NM_152644.2 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr10:88930359 T>C maps to ENST00000298786 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr10:88946847 G>A maps to ENST00000298786 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr18:10672763 C>T maps to NM_022068.2 P2643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:10672751 G>C maps to NM_022068.2 A2647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:153741191 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr23:153735816 G>C did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr23:153735752 C>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:153736910 A>T did not map to a codon.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr23:153740199 T>A did not map to a codon.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr21:42720564 G>T maps to ENST00000398652 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:110590407 G>A maps to NM_033088.2 K526K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:110590434 A>T maps to NM_033088.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr7:129083913 C>T maps to ENST00000450266 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr7:129110494 C>A maps to ENST00000450266 S687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr10:120889084 G>A maps to NM_207009.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr10:120877148 C>T maps to NM_207009.2 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:82459575 A>G maps to ENST00000369756 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr6:82461309 G>C maps to ENST00000369756 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:27332875 G>A maps to NM_052943.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:118165573 C>A maps to NM_017709.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:118165681 C>T maps to NM_017709.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:79698889 C>T did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr23:79698218 G>C did not map to a codon.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr23:79698630 C>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:79698468 G>T did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr23:79698715 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:79698392 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr23:79698532 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:79698351 T>C did not map to a codon.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr23:79698544 T>A did not map to a codon.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr23:34149588 A>C did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:34148686 G>A did not map to a codon.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr23:34150164 T>G did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:34149419 G>A did not map to a codon.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr23:34148156 C>A did not map to a codon.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr23:34149743 T>G did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:34149228 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:34149281 C>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:34149263 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:34149175 C>G did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr23:34149649 G>T did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:34150047 C>A did not map to a codon.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr23:34149002 C>T did not map to a codon.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr23:34149632 G>A did not map to a codon.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr23:34148618 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:34148302 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:34148927 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:34149010 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:34149011 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:34149345 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:34148481 G>T did not map to a codon.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr23:34149965 C>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:34148157 C>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:34149138 A>C did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:34148910 A>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:34148022 A>G did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:34149641 G>C did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:34149052 C>T did not map to a codon.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr23:34149313 C>T did not map to a codon.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr23:34150180 C>T did not map to a codon.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr23:34150219 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:34149857 C>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:34150315 G>C did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:34149446 G>T did not map to a codon.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr23:34149865 G>T did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:34148916 C>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr23:34962247 C>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:34962222 G>T did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:34962574 C>A did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr23:34961478 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:34962223 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr23:34962351 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:34962277 C>T did not map to a codon.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr23:34961337 C>T did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:34961652 C>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:34960983 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:34962804 C>G did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr23:34962242 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:34961392 G>C did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:34961044 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr23:34961657 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:34961440 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr23:34961285 C>A did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:34962365 G>C did not map to a codon.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr23:34962045 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:34962125 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr23:34962545 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr23:34961675 G>A did not map to a codon.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr23:34962237 C>T did not map to a codon.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr23:34961122 C>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:37027497 G>T did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:37028612 G>C did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr23:37027441 C>T did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr23:37028586 C>T did not map to a codon.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr23:37029319 A>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:37028000 C>T did not map to a codon.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr23:37027834 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr23:37028770 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr23:37026575 G>A did not map to a codon.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr23:37029108 C>A did not map to a codon.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr23:37029109 C>T did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:37027149 C>A did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr23:37028481 C>T did not map to a codon.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr23:37026543 T>C did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr23:37027193 G>A did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:37027221 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:37026700 G>T did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:37026871 C>G did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:37026872 C>A did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr23:37028184 T>C did not map to a codon.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr23:37026591 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:37028491 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:37028492 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr23:37027330 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:37026586 A>C did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr23:37028872 C>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:37027419 T>C did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr13:37602361 A>T maps to NM_001014286.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr13:37614571 T>G maps to NM_001014286.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:153677637 G>C did not map to a codon.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr23:153678775 G>A did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:153674847 G>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:1643076 C>T maps to NM_001174070.1 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:126370313 C>A maps to NM_014661.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:114392968 G>A maps to ENST00000424269 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:114393790 T>C maps to ENST00000424269 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:101535733 C>T maps to NM_145037.2 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr17:644737 C>T maps to NM_024792.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr16:30038046 G>A maps to NM_031478.4 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr23:152860036 G>T did not map to a codon.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr18:29848298 G>A maps to ENST00000269209 C722C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr18:29867971 C>T maps to ENST00000269209 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:29848106 C>T maps to ENST00000269209 P786P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:177226507 G>T maps to NM_021165.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr1:177247849 G>A maps to NM_021165.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr1:177199062 C>G maps to NM_021165.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:177249838 G>A maps to NM_021165.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:190068140 G>C maps to NM_199051.1 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:190067942 C>T maps to NM_199051.1 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:190067932 T>A maps to NM_199051.1 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:190423906 C>T maps to NM_199051.1 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:190067660 C>T maps to NM_199051.1 W596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:190129882 G>A maps to NM_199051.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr1:190423782 A>G did not map to a codon.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr1:190067945 C>T maps to NM_199051.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr1:190067720 G>A maps to NM_199051.1 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr1:190423918 A>T maps to NM_199051.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr12:31435798 C>T maps to NM_001135812.1 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:150972983 G>C maps to NM_001163258.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr15:59064130 C>T maps to NM_001040450.1 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr16:67572622 G>A maps to NM_001193523.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr16:67574373 C>T maps to NM_001193523.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr16:67573996 C>T maps to NM_001193523.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:67578270 G>A maps to NM_001193523.1 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr6:24848285 C>T maps to NM_014722.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:24843780 G>C maps to NM_014722.2 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr20:49204342 C>A maps to NM_080829.2 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr9:139617955 C>T maps to NM_152421.3 Y342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr23:119410743 T>C did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr23:119421059 G>T did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr23:119427903 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:212799451 G>A maps to NM_153606.3 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr5:156590333 C>A maps to NM_130899.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr5:156592711 G>C maps to NM_130899.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr12:100042509 C>T maps to NM_153364.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr19:50979182 G>T maps to ENST00000391816 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr7:128359079 T>A maps to NM_032599.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:128356920 C>T maps to NM_032599.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:206145507 C>T maps to NM_001123168.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:78332058 A>T maps to NM_198549.2 K516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:78279428 G>A maps to NM_198549.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr9:131825525 G>A maps to NM_032809.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr9:40704231 C>A maps to NM_001083124.1 S630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr9:43624936 G>A maps to NM_001145196.1 F1250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:43628677 C>G maps to NM_001145196.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:43630656 C>T maps to NM_001145196.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr9:43627186 C>T maps to NM_001145196.1 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:90536022 C>T maps to NM_001145124.1 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr9:90535172 G>C maps to NM_001145124.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:166039588 C>T maps to NM_001017961.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:94764360 G>A maps to NM_152548.2 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr2:38178429 T>C maps to NM_144713.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr2:38231328 G>A maps to NM_144713.3 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr8:124219420 G>C maps to NM_032899.4 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr8:124204206 C>T maps to NM_032899.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:54792427 C>A maps to NM_001010872.1 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:54806054 G>A maps to NM_001010872.1 K762K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr6:54805669 C>G maps to NM_001010872.1 S634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr20:33876322 C>T maps to NM_178468.4 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr22:40417674 C>T maps to NM_138435.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:18881946 G>A maps to NM_001039999.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr17:18881188 G>C maps to NM_001039999.2 S597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:144810244 C>T maps to NM_198488.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:144808543 G>A maps to NM_198488.3 N1029N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:144808903 G>A maps to NM_198488.3 P909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:127569306 C>A maps to NM_174911.4 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:127569448 A>G maps to NM_174911.4 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:5143490 G>T maps to NM_201400.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:71507070 T>C maps to NM_018172.2 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:71510691 G>A maps to NM_018172.2 *166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:8375317 G>A maps to NM_018088.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:8374609 G>A maps to NM_018088.3 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr12:8375059 G>C maps to NM_018088.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:8375059 G>A maps to NM_018088.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:124810475 C>T maps to NM_144963.2 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr15:64380931 G>A maps to NM_032231.4 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:33813506 A>G maps to ENST00000395190 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr15:38773632 G>A maps to NM_173611.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr19:38897629 C>T maps to NM_174905.3 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:38893837 C>T maps to NM_174905.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr23:8759386 T>G did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:8764376 T>C did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:8997415 G>A did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr23:8995922 C>G did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:13061273 G>C did not map to a codon.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr16:89807209 A>T did not map to a codon.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr16:89811461 C>T maps to NM_000135.2 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr16:89869666 C>T maps to NM_000135.2 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr16:89837009 C>T maps to NM_000135.2 Q728Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr23:14883404 G>C did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:14883254 T>A did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:14861943 A>C did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:14882731 C>G did not map to a codon.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr23:14883284 A>G did not map to a codon.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr23:14877434 G>T did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr9:97897695 C>A maps to NM_000136.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr3:10084813 G>A maps to NM_033084.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr3:10089665 G>A maps to NM_033084.3 Q448Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr3:10088286 C>T maps to NM_033084.3 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:35425700 G>A maps to NM_021922.2 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:22646834 C>A maps to NM_022725.3 L174L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-F7-A622-01A-11D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr15:89843084 G>A maps to NM_001113378.1 K897K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr15:89844555 G>A did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr15:89802002 C>T maps to NM_001113378.1 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr2:58431262 A>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr14:45665673 C>T maps to NM_020937.2 F1880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:45669147 T>C maps to NM_020937.2 Y2028Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr14:45639846 A>G maps to NM_020937.2 K686K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:127677182 G>A maps to ENST00000368692 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:163076363 A>T maps to NM_004460.2 L162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr2:163059580 G>T maps to NM_004460.2 Y374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:163027569 G>A maps to NM_004460.2 H734H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:13733494 A>T maps to NM_032228.5 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr12:29486609 C>T maps to NM_018099.3 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr12:29469873 G>A maps to NM_018099.3 W352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr12:29464013 C>T maps to NM_018099.3 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr12:29485598 A>T maps to NM_018099.3 K442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:99042215 G>A maps to NM_005766.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr13:99047719 G>A maps to NM_005766.2 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr13:99092243 G>T maps to NM_005766.2 V821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr13:99042296 C>A maps to NM_005766.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr13:99087857 G>C maps to NM_005766.2 V724V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:99047623 T>C maps to NM_005766.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:99061620 G>T maps to NM_005766.2 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr13:99037975 G>T maps to NM_005766.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr13:99098960 G>A maps to NM_005766.2 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:242312557 G>A maps to NM_014808.2 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr2:242407682 C>T maps to NM_014808.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:242380774 C>G maps to NM_014808.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:242401975 G>A maps to NM_014808.2 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr2:242415336 C>T maps to NM_014808.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr6:5368980 C>T maps to NM_006567.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr19:13035606 C>T maps to NM_004461.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:223464698 G>T maps to NM_005687.3 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr2:223494890 T>G maps to NM_005687.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:223497945 G>A maps to NM_005687.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:90762892 T>A maps to NM_000043.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr10:90770294 G>C did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:172628385 G>C maps to NM_000639.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr17:80041947 G>A maps to NM_004104.4 P1667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr17:80045896 C>T maps to NM_004104.4 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr17:80045300 C>T maps to NM_004104.4 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:80046139 G>A maps to NM_004104.4 T879T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:80037283 C>T maps to NM_004104.4 K2449K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:80046904 G>A maps to NM_004104.4 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr17:80045998 G>C maps to NM_004104.4 P926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:150774981 G>A maps to NM_006712.3 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr7:150775681 G>A maps to NM_006712.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr2:170428348 G>C maps to NM_024622.3 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:170403041 G>A maps to NM_024622.3 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:7859653 T>C did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:7867641 C>G maps to NM_024091.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:7862999 A>G maps to NM_024091.3 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr20:3128840 A>C maps to NM_021826.4 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr4:187628172 G>A maps to ENST00000260147 R937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr4:187542356 G>A maps to ENST00000260147 R1798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr4:187539650 C>A maps to ENST00000260147 E2700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:187518255 G>A maps to ENST00000260147 H4149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:187541442 G>A maps to ENST00000260147 V2102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr4:187539226 G>T maps to ENST00000260147 S2841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr4:187630503 C>A maps to ENST00000260147 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr4:187557926 G>A maps to ENST00000260147 R1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr4:187630587 G>A maps to ENST00000260147 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr4:187530424 G>C maps to ENST00000260147 S3376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr4:187531170 T>A did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr4:187522448 G>A maps to ENST00000260147 R3875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr4:187560904 G>A maps to ENST00000260147 R1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr4:187584692 G>A maps to ENST00000260147 Q1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr4:187549313 C>A maps to ENST00000260147 E1602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr4:187549661 G>A maps to ENST00000260147 Q1527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr4:187540778 G>A maps to ENST00000260147 Q2324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr4:187530344 G>A maps to ENST00000260147 R3403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr4:187542659 G>A maps to ENST00000260147 Q1697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:187521276 C>A maps to ENST00000260147 G3963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:187532589 G>C maps to ENST00000260147 S3271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:187539226 G>C maps to ENST00000260147 S2841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:187629183 G>A maps to ENST00000260147 Q600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr4:187517873 C>A maps to ENST00000260147 E4277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:187535343 C>T did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr4:187628808 G>A maps to ENST00000260147 Q725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr4:187538163 C>A maps to ENST00000260147 E3027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr4:187524461 C>A maps to ENST00000260147 G3743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr4:187524462 C>A maps to ENST00000260147 A3742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr4:187524849 G>C maps to ENST00000260147 Y3613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr4:187627829 G>C maps to ENST00000260147 S1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr4:187524189 T>C did not map to a codon.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr4:187539416 G>A maps to ENST00000260147 Q2778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr4:187525002 G>C maps to ENST00000260147 Y3562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr4:187629099 G>A maps to ENST00000260147 R628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr4:187630410 G>A maps to ENST00000260147 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr4:187521087 G>A maps to ENST00000260147 Q4026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr4:187541759 C>A maps to ENST00000260147 E1997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr4:187627773 G>A maps to ENST00000260147 R1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr4:187539251 G>A maps to ENST00000260147 Q2833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr4:187525000 G>C maps to ENST00000260147 S3563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr4:187525109 G>A maps to ENST00000260147 Q3527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr4:187517825 C>A maps to ENST00000260147 E4293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr4:187629107 G>T maps to ENST00000260147 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr4:187557354 G>C maps to ENST00000260147 S1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr4:187540844 C>A maps to ENST00000260147 G2302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr4:187549811 G>A maps to ENST00000260147 Q1477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:187628328 G>A maps to ENST00000260147 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr4:187518090 G>C maps to ENST00000260147 L4204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr4:187554855 G>A maps to ENST00000260147 T1435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr4:187530424 G>C maps to ENST00000260147 S3376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr4:187628928 C>A maps to ENST00000260147 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr4:187542860 G>A maps to ENST00000260147 R1630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr4:187628109 G>A maps to ENST00000260147 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr4:187530424 G>C maps to ENST00000260147 S3376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr4:187628328 G>A maps to ENST00000260147 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr4:187538222 G>C maps to ENST00000260147 S3007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr4:187518159 C>G maps to ENST00000260147 G4181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr4:187542733 G>C maps to ENST00000260147 S1672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:187527362 G>C maps to ENST00000260147 S3407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:187549760 G>A maps to ENST00000260147 Q1494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:187560918 G>C maps to ENST00000260147 S1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr4:187630869 C>A maps to ENST00000260147 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr4:187554872 C>A maps to ENST00000260147 E1430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr4:187521450 G>A maps to ENST00000260147 Q3905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr4:187542860 G>A maps to ENST00000260147 R1630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr4:187538954 C>A maps to ENST00000260147 E2932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:187542753 G>A maps to ENST00000260147 N1665N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr4:187525007 C>A maps to ENST00000260147 E3561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr4:187530371 C>A maps to ENST00000260147 E3394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr4:187518852 C>T maps to ENST00000260147 S4120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr4:187560918 G>C maps to ENST00000260147 S1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr4:187542224 C>A maps to ENST00000260147 E1842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:187630532 G>C maps to ENST00000260147 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr4:187539162 G>C maps to ENST00000260147 S2862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr4:187542659 G>A maps to ENST00000260147 Q1697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr4:187530344 G>A maps to ENST00000260147 R3403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr4:187560920 C>T maps to ENST00000260147 T1199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr4:187509931 G>A maps to ENST00000260147 F4530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr4:187628172 G>A maps to ENST00000260147 R937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr4:187630899 C>A maps to ENST00000260147 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:150924597 C>T maps to NM_001447.2 R2030R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr5:150901064 G>A maps to NM_001447.2 Q3697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr5:150930201 C>T maps to NM_001447.2 V1509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:150925208 C>A maps to NM_001447.2 E1827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr5:150925422 A>G maps to NM_001447.2 A1755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr5:150924338 G>A maps to NM_001447.2 R2117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:150947316 G>A maps to NM_001447.2 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:150892005 G>A maps to NM_001447.2 S3875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr5:150928975 G>A maps to NM_001447.2 Q1557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr5:150947412 G>C maps to NM_001447.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr5:150922983 G>A maps to NM_001447.2 F2568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:92564959 T>A maps to ENST00000298047 S3218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr11:92577878 C>T maps to ENST00000298047 N3782N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr11:92532046 G>A maps to ENST00000298047 K1956K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr11:92531953 C>A maps to ENST00000298047 G1925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:92534059 C>T maps to ENST00000298047 P2627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:92534194 A>G maps to ENST00000298047 T2672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:92087365 A>G maps to ENST00000298047 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr11:92533681 C>T maps to ENST00000298047 Y2501Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr11:92620258 C>A maps to ENST00000298047 S4344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr11:92624270 C>T maps to ENST00000298047 Q4588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:92523336 G>T maps to ENST00000298047 E1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:92533402 C>G maps to ENST00000298047 P2408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr11:92615996 G>T maps to ENST00000298047 T4125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:92085507 G>A maps to ENST00000298047 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:92085508 G>A maps to ENST00000298047 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:92088499 G>A maps to ENST00000298047 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:92531549 T>C maps to ENST00000298047 L1791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:92577554 G>A maps to ENST00000298047 R3674R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr11:92498055 G>A maps to ENST00000298047 V1332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:92624017 G>A maps to ENST00000298047 T4503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr11:92600370 G>A maps to ENST00000298047 S4041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr11:92531573 C>T maps to ENST00000298047 R1799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:92532715 C>A maps to ENST00000298047 V2179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:92534473 T>C maps to ENST00000298047 I2765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:126241933 C>A maps to NM_024582.4 S1456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr4:126372964 A>G maps to NM_024582.4 G3598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:126237811 C>T maps to NM_024582.4 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr4:126411725 C>T maps to NM_024582.4 I4583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:126329824 C>T maps to NM_024582.4 F1932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr4:126241840 T>C maps to NM_024582.4 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr4:126239488 G>A maps to NM_024582.4 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr4:126336447 A>G maps to NM_024582.4 G2110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr4:126336741 A>T maps to NM_024582.4 T2208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:126408687 C>T maps to NM_024582.4 F4335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr4:126241669 C>T maps to NM_024582.4 N1368N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr4:126412580 C>A maps to NM_024582.4 P4868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr4:126371854 G>C maps to NM_024582.4 V3228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:126238051 G>T maps to NM_024582.4 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:126336531 A>T maps to NM_024582.4 T2138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:126336240 G>A maps to NM_024582.4 L2041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:126238057 C>T maps to NM_024582.4 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr4:126372349 C>T maps to NM_024582.4 V3393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:126241561 A>G maps to NM_024582.4 E1332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:126411359 C>T maps to NM_024582.4 T4461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr4:126398447 G>T maps to NM_024582.4 L4144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr4:126371056 C>A maps to NM_024582.4 S2962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr4:126373804 C>T maps to NM_024582.4 H3878H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr4:126238942 A>T maps to NM_024582.4 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr23:150889865 G>A did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr17:73915955 C>T did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr17:73929083 C>G maps to ENST00000389570 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr19:40327294 C>A maps to NM_001436.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:16093893 C>T maps to NM_017556.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:45959061 G>C maps to ENST00000402984 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr22:45931078 G>A did not map to a codon.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:13670671 G>T maps to NM_001165035.1 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr3:13670761 C>T maps to NM_001165035.1 Q938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr14:92403315 C>T maps to ENST00000267620 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:92347670 G>A maps to ENST00000267620 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:112933378 A>G maps to NM_153214.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr2:112942820 G>A maps to NM_153214.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:112944821 G>T maps to NM_153214.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:112942838 C>T maps to NM_153214.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr2:112922710 C>T maps to NM_153214.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr15:48752446 G>A maps to NM_000138.4 P1764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr15:48719885 G>T maps to NM_000138.4 S2361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr15:48755288 G>A maps to NM_000138.4 I1738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr15:48760183 C>G maps to NM_000138.4 L1566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr15:48818390 G>A maps to NM_000138.4 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr15:48826280 A>T maps to NM_000138.4 C286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr5:127670536 C>A did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:127645020 C>G maps to NM_001999.3 V1757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:127782270 C>A maps to NM_001999.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:127647622 G>C maps to NM_001999.3 P1634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:127686625 G>A maps to NM_001999.3 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr5:127595500 C>T maps to NM_001999.3 E2795E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr5:127654600 C>A maps to NM_001999.3 E1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:127728909 G>T maps to NM_001999.3 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:127681178 G>A maps to NM_001999.3 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr5:127614516 G>C maps to NM_001999.3 L2385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr5:127648347 C>T maps to NM_001999.3 E1619E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr5:127873056 C>T maps to NM_001999.3 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr19:8203163 G>A maps to NM_032447.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:8138158 C>A maps to NM_032447.3 S2575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:8181654 G>A maps to NM_032447.3 R1205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:8206822 C>A did not map to a codon.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr19:8191466 C>T maps to NM_032447.3 W813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:8131096 C>T maps to NM_032447.3 L2712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:8188396 G>A maps to NM_032447.3 C1011C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr19:8148206 G>T maps to NM_032447.3 C2379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr19:8174521 G>T maps to NM_032447.3 G1483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:8201185 G>A maps to NM_032447.3 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:8203088 T>A maps to NM_032447.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr9:97369180 A>G maps to NM_001127628.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr9:97333758 G>A maps to NM_003837.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:9921883 G>A maps to NM_017703.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr7:102453881 A>T maps to NM_145032.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr12:1702311 G>C maps to NM_152441.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:745765 G>T maps to NM_153350.3 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:107700444 G>C maps to NM_001163315.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr7:5521495 G>A maps to NM_024963.4 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr7:5540951 C>T maps to ENST00000312577 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr3:33427048 A>G maps to NM_012157.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:33425642 G>T maps to NM_012157.3 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:37421663 G>A maps to NM_032875.2 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr17:37499495 T>C did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:37431247 G>A maps to NM_032875.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr13:77581836 A>G maps to NM_012158.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr13:77589582 G>A maps to NM_012158.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:77581450 T>C maps to NM_012158.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr13:77581465 C>G maps to NM_012158.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:99347182 G>A maps to NM_012160.3 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr6:99353452 G>A maps to NM_012160.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr4:15627092 C>A maps to NM_012161.3 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr8:145580331 G>A maps to NM_012162.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr8:145582011 C>G maps to NM_012162.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr5:15936964 C>T maps to NM_012304.3 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr5:15937093 G>A maps to NM_012304.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr16:67197674 C>G maps to NM_018378.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr9:37512660 G>C maps to NM_012166.2 L918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr9:37512609 C>T maps to NM_012166.2 T935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr9:37521757 G>A maps to NM_012166.2 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:37537655 G>A maps to NM_012166.2 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:48040948 T>C maps to NM_001190274.1 G688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr18:71797838 C>T maps to NM_001142958.1 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr10:5948425 C>G maps to NM_032807.3 S246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr10:5958337 A>G maps to NM_032807.3 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr10:5956204 C>T maps to NM_032807.3 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:5958322 T>C maps to NM_032807.3 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:5953001 G>T maps to NM_032807.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:5966445 C>T maps to NM_032807.3 C908C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr1:11708855 C>T maps to NM_012168.4 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr12:117595802 C>A maps to NM_033624.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:117603391 C>T maps to NM_033624.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:100189356 C>T maps to NM_012172.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr7:100189425 G>A maps to NM_012172.4 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr8:381401 A>T maps to NM_183421.1 K66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:363093 T>C maps to NM_183421.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr19:39517587 G>A maps to NM_178820.3 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:39521761 C>T maps to NM_178820.3 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:33768825 G>A maps to NM_012175.3 Y363Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:33768855 T>C maps to NM_012175.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr11:33772197 G>A maps to NM_012175.3 H273H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr11:33768699 T>C maps to NM_012175.3 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:146127528 G>A maps to NM_032145.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr16:87365040 G>A maps to NM_024735.3 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr8:124515702 C>A did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr14:39871065 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:55818974 C>T maps to NM_152231.1 R623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr14:55817320 C>T maps to NM_152231.1 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr5:147796564 T>G maps to NM_205836.1 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:147781674 C>T maps to NM_205836.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:147803612 G>A maps to NM_205836.1 E557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr17:6683708 G>A maps to NM_153230.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr17:6683807 C>T maps to NM_153230.2 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr17:6684173 G>A maps to NM_153230.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr5:41929883 C>T maps to NM_012176.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:41939627 A>G maps to NM_012176.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:121340296 C>A maps to NM_016298.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr3:121340737 T>C maps to NM_016298.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr3:121341499 C>G maps to NM_016298.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:121342099 C>A maps to NM_016298.3 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr2:73492755 A>G maps to ENST00000295133 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr8:101153495 G>C maps to NM_001029860.3 S329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr8:101153459 A>T maps to NM_001029860.3 L341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr8:101149816 G>A maps to NM_001029860.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:11718435 C>T maps to NM_033182.5 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:11716068 G>A maps to ENST00000376768 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr1:11716048 C>T maps to ENST00000376768 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:46215858 G>A maps to NM_001080469.1 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr19:46215298 G>A maps to NM_001080469.1 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr2:68691490 C>T maps to NM_001024680.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr2:68691499 C>T maps to NM_001024680.1 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:11728955 C>T maps to NM_018438.5 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr22:32889194 G>C maps to NM_012179.3 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr22:32894168 G>A maps to NM_012179.3 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr22:32894342 T>A maps to NM_012179.3 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr22:32889110 A>G maps to NM_012179.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr22:32881149 C>T maps to NM_012179.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:175162339 G>T maps to NM_012180.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr4:175183943 G>A maps to NM_012180.2 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr17:18653344 G>C maps to ENST00000395665 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:18659467 G>A did not map to a codon.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr3:48415160 G>A maps to NM_207102.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:123550176 C>T maps to NM_012164.3 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr9:139837260 C>T maps to NM_018998.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr4:153250882 G>A maps to NM_033632.2 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr4:153332881 G>C maps to NM_033632.2 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr4:153249400 C>T maps to NM_033632.2 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:153247310 C>T maps to NM_033632.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:153249523 C>A maps to NM_033632.2 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr4:153245423 G>A maps to NM_033632.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr4:153244184 G>A maps to NM_033632.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr4:153271276 C>G did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr4:153247164 G>C maps to NM_033632.2 S546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:117465255 T>C maps to NM_153348.2 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:12800868 C>T maps to ENST00000380339 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:55401039 G>A maps to NM_002000.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:55396679 C>A maps to NM_002000.2 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:55401036 G>A maps to NM_002000.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr19:55396848 C>T maps to NM_002000.2 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr1:159276015 C>T maps to ENST00000368115 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:161188708 G>A maps to NM_004106.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:7754153 C>A maps to NM_002002.4 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:75181622 C>G maps to NM_015962.4 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr14:75200789 C>T maps to NM_015962.4 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr14:75199487 T>A maps to NM_015962.4 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:40357469 G>C maps to NM_003890.2 V5281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr19:40432972 G>A maps to NM_003890.2 C432C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:40430301 A>G maps to NM_003890.2 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:40367903 G>T maps to NM_003890.2 C4352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:40357439 C>A maps to NM_003890.2 V5291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:40368714 G>A maps to NM_003890.2 G4211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:40366445 G>A maps to NM_003890.2 F4596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:40366538 C>T maps to NM_003890.2 Q4565Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:40368525 G>A maps to NM_003890.2 Y4274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr19:40392568 G>A maps to NM_003890.2 S2645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:40354268 G>A maps to NM_003890.2 F5400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:40433611 G>A maps to NM_003890.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr19:40433525 C>T maps to NM_003890.2 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:40366394 G>A maps to NM_003890.2 C4613C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:40392045 G>A maps to NM_003890.2 C2780C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr19:40411940 G>A maps to NM_003890.2 C1229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr19:40433287 C>T maps to NM_003890.2 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr19:40368705 G>A maps to NM_003890.2 C4214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr1:149761631 G>A maps to NM_000566.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:161480735 G>A maps to NM_001136219.1 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:161479634 C>T maps to NM_001136219.1 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:161476259 C>G maps to NM_001136219.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:161487823 C>T maps to NM_001136219.1 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr1:161480678 G>A maps to NM_001136219.1 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr1:161642855 C>G maps to NM_004001.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr1:161596178 G>C maps to ENST00000367964 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:50017241 G>C maps to NM_004107.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:17875219 G>A maps to NM_015122.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:17877567 C>A maps to NM_015122.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr9:137801844 G>A maps to NM_002003.3 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:137809627 C>T maps to NM_002003.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr9:137806601 C>A maps to NM_002003.3 G91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr9:137779203 G>A maps to NM_004108.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr9:137777669 C>G maps to NM_004108.2 Y162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr1:27697412 G>A maps to NM_003665.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr1:27699997 G>A maps to NM_003665.2 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr1:27695885 C>G maps to NM_003665.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr1:27700853 A>C maps to NM_003665.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr1:157773647 C>T maps to NM_052938.4 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:157776892 G>A maps to NM_052938.4 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr1:157773848 G>A maps to NM_052938.4 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:157737156 C>T maps to NM_030764.3 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:157737022 G>C maps to NM_030764.3 S387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:157666928 C>G did not map to a codon.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:157666097 C>T maps to NM_052939.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:157665836 G>T maps to NM_052939.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:157666064 C>G maps to NM_052939.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr1:157666097 C>T maps to NM_052939.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr1:157667161 C>A maps to NM_052939.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:157659663 C>T maps to NM_052939.3 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr1:157667191 C>A maps to NM_052939.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr1:157557302 C>A maps to NM_031282.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:157545496 C>A maps to NM_031282.2 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr1:157557114 C>G maps to NM_031282.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr1:157559096 G>A maps to NM_031282.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:157557327 C>T maps to NM_031282.2 L195L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CN-A497-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:157497569 C>T maps to NM_031281.2 W599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:157514693 A>C maps to NM_031281.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:161677050 C>T maps to NM_001184866.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:11667352 C>T maps to NM_004462.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr11:110333128 T>C maps to NM_004109.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:72860033 C>A maps to ENST00000442102 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr17:72859025 G>C maps to ENST00000442102 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr18:55218579 A>G maps to NM_001012515.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:4793182 G>A maps to NM_018708.2 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:4792849 G>A maps to NM_018708.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:114860316 C>T maps to NM_020177.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr2:97370098 G>A maps to NM_001113382.1 P2019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:97368983 C>T maps to NM_001113382.1 P1900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:124975614 C>T maps to NM_001039112.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:124978245 G>A did not map to a codon.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr8:125076787 G>T maps to NM_001039112.2 E1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr8:125131952 C>T maps to NM_001039112.2 I1832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr8:125094565 C>T maps to NM_001039112.2 L1420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr8:125078775 G>A maps to NM_001039112.2 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr8:125113502 G>A maps to NM_001039112.2 K1683K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr8:125033800 C>T maps to NM_001039112.2 C675C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr7:19184631 G>A maps to NM_152898.2 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr14:53345311 A>G maps to NM_001134999.1 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr11:63990912 G>A maps to NM_178443.2 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:63986796 C>T maps to NM_178443.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr15:91433124 C>T maps to NM_002005.3 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:186358266 C>T maps to NM_014375.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:186358275 C>A maps to NM_014375.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr11:125359381 C>A maps to NM_005103.4 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr11:125359604 C>T maps to NM_005103.4 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:121942247 T>G maps to NM_001024613.2 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:121944098 C>G maps to NM_001024613.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr7:121942263 G>A maps to NM_001024613.2 C405C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:121942224 A>G maps to NM_001024613.2 H418H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr7:121942916 G>A maps to NM_001024613.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr7:121944203 C>T maps to NM_001024613.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr7:121943894 G>A maps to NM_001024613.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr7:121943747 G>A maps to NM_001024613.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr3:62355883 C>T maps to NM_018008.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr3:62356913 G>A maps to NM_018008.3 C366C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr3:62355880 G>A maps to NM_018008.3 C419C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr3:62358351 G>A maps to NM_018008.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr19:35842960 C>T maps to NM_005303.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:35941407 C>G maps to NM_005306.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:35940897 C>A maps to NM_005306.2 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:35849959 C>T maps to NM_005304.3 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr4:155510017 C>T maps to NM_000508.3 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr4:155506936 G>T maps to NM_000508.3 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr4:155506783 C>T maps to NM_000508.3 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr4:155507722 G>T maps to NM_000508.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr4:155507842 T>A maps to NM_000508.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr4:155489612 A>T maps to NM_005141.4 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr4:155487769 C>T maps to NM_005141.4 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:54476729 C>G did not map to a codon.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr23:54496603 C>A did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:54475345 G>A did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:54492270 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:54472807 C>G did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr23:54492196 C>T did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:54472831 G>C did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:54482959 A>T did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:54476095 G>A did not map to a codon.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr23:54497838 G>A did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:54492143 G>T did not map to a codon.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr23:54475630 T>A did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:54472621 C>T did not map to a codon.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr23:54475671 C>T did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr6:36989313 C>T maps to NM_173558.3 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr6:36981414 C>A maps to NM_173558.3 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:36989322 G>A maps to NM_173558.3 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:36982747 C>T maps to NM_173558.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr6:36978762 G>A maps to NM_173558.3 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:32793298 G>T maps to NM_139241.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr12:32793361 G>A maps to NM_139241.2 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr3:14960292 C>A maps to NM_152536.3 Y1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:14939484 G>A maps to NM_152536.3 R983R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr3:14965560 G>A maps to NM_152536.3 S1328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:14963955 C>T maps to NM_152536.3 P1236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr3:14862605 T>C maps to NM_152536.3 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr3:14939125 C>T maps to NM_152536.3 H953H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:95603901 C>T maps to NM_018351.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:95603435 G>A maps to NM_018351.3 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr12:95603799 T>C maps to NM_018351.3 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:141974898 G>A maps to NM_001144935.1 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr17:7345998 T>C maps to NM_004112.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr17:7346395 G>A maps to NM_004112.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr3:191861798 T>A maps to NM_021032.4 *244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:192125892 C>T maps to NM_021032.4 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:137717803 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr23:137791005 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr23:137715117 C>T did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:137715118 G>A did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr13:102375270 G>C maps to NM_175929.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr4:123797545 G>A maps to NM_002006.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:123813549 G>A maps to NM_002006.4 *289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:16850802 G>T maps to NM_019851.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr19:49261275 G>A maps to NM_019113.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr12:4479715 G>A maps to NM_020638.2 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:81188025 C>T maps to NM_004464.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr4:81188292 G>T maps to NM_004464.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr4:81196108 A>G maps to NM_004464.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr15:49776610 T>G maps to NM_002009.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr15:49776610 T>G maps to NM_002009.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:93668074 C>A maps to NM_152429.4 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:38287449 G>A maps to NM_001174067.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr12:27116342 C>T maps to NM_015633.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr12:27116351 G>A maps to NM_015633.2 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr5:176519744 C>T maps to NM_213647.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr5:176519732 A>G maps to NM_213647.1 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:176523643 C>T maps to NM_213647.1 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:176520153 G>A maps to NM_213647.1 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:176520154 G>A maps to NM_213647.1 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr5:176520483 C>T maps to NM_213647.1 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr4:155530880 C>T maps to ENST00000407946 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr4:155529727 A>G maps to ENST00000407946 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr1:60139744 C>A maps to NM_001113411.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:59812063 G>C maps to NM_001113411.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:17731929 G>A maps to NM_201552.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr7:76825862 G>A maps to NM_006682.2 H351H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:27942092 C>T maps to NM_005248.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:27941034 T>C maps to NM_005248.2 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr4:153896098 G>C maps to NM_033393.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr23:135289239 C>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:135291443 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:135288650 G>C did not map to a codon.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr23:135288732 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr2:105979871 G>A maps to ENST00000344213 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr2:105984179 C>T maps to ENST00000344213 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:97053871 C>A maps to NM_020482.4 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr16:67265093 G>A maps to NM_013241.2 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr16:67272350 C>T did not map to a codon.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr16:67264613 C>T maps to NM_013241.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:67272171 C>T maps to NM_013241.2 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr16:67267887 G>T maps to NM_013241.2 S573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr18:33935605 C>T maps to NM_025135.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr18:34081901 A>G maps to NM_025135.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr18:34081963 T>A did not map to a codon.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr9:133805082 G>A maps to NM_001145106.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr9:133799268 T>A did not map to a codon.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr9:133779572 G>A maps to NM_001145106.1 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr11:27016516 G>A maps to NM_203371.1 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:27016447 G>A maps to NM_203371.1 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:65651445 C>T maps to NM_198897.1 *365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr6:110113839 C>A maps to NM_014845.5 S811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr23:15381433 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:164466132 G>A maps to NM_018086.2 Q737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr2:164467455 G>A maps to NM_018086.2 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr2:164467771 G>A maps to NM_018086.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:164468077 G>T maps to NM_018086.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:164466529 C>T maps to NM_018086.2 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr2:164466820 C>T maps to NM_018086.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr7:50513221 G>A maps to NM_022116.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:50513305 C>T maps to NM_022116.3 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:50514816 T>A maps to NM_022116.3 K57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:76024584 C>T maps to NM_015687.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:76022358 C>T maps to NM_015687.2 E1063E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr3:99567228 G>A maps to NM_001042459.1 N1097N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr14:24600963 C>T maps to NM_203402.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr20:42935536 G>A maps to NM_001080472.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr19:56104199 C>T maps to NM_032836.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:56103956 G>A maps to NM_032836.2 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr11:35641068 C>T maps to NM_014344.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:39975507 G>C maps to NM_021939.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr17:39977975 C>A maps to NM_021939.3 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:49319148 C>A maps to NM_016594.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr7:30058664 C>A maps to NM_017946.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:30066079 A>T maps to NM_017946.2 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr9:115932872 G>T maps to ENST00000446284 R924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr9:115941030 C>A maps to ENST00000446284 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:64009963 C>G maps to NM_057092.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr6:35544860 G>C maps to NM_001145775.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr19:18649032 G>A maps to NM_012181.3 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr19:18649083 G>A maps to NM_012181.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:18652489 C>A maps to NM_012181.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:33044784 A>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:33039804 G>A maps to NM_007270.3 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr6:32097031 G>A maps to NM_022110.3 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:47259843 G>C maps to NM_024301.4 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IH-01A-11D-A25Y-08 chr9:108397457 G>A maps to NM_006731.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr9:108366710 T>A maps to NM_006731.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr9:108370141 C>G maps to NM_006731.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr9:108377581 G>A maps to NM_006731.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:154962991 C>T maps to NM_025207.4 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr17:17120451 G>A maps to NM_144997.5 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:17120409 G>A maps to NM_144997.5 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:17116980 C>T maps to NM_144997.5 E576E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:152280765 G>T maps to NM_002016.1 S2199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr1:152281223 G>A maps to NM_002016.1 D2046D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:152281431 G>C maps to NM_002016.1 S1977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:152286299 T>C maps to NM_002016.1 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:152278059 G>C maps to NM_002016.1 S3101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr1:152277106 G>A maps to NM_002016.1 R3419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:152283663 G>C maps to NM_002016.1 S1233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr1:152277136 G>A maps to NM_002016.1 R3409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:152275981 G>A maps to NM_002016.1 Q3794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:152278664 T>C maps to NM_002016.1 G2899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:152284281 G>C maps to NM_002016.1 S1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:152283934 C>A maps to NM_002016.1 G1143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:152277200 G>A maps to NM_002016.1 L3387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:152276849 C>T maps to NM_002016.1 S3504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr1:152279920 A>G maps to NM_002016.1 L2481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:152282918 T>C maps to NM_002016.1 A1481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr1:152285837 C>T maps to NM_002016.1 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:152283284 G>A maps to NM_002016.1 S1359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:152285009 C>T maps to NM_002016.1 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr1:152276429 G>A maps to NM_002016.1 H3644H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr1:152286681 C>T maps to NM_002016.1 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:152276144 G>A maps to NM_002016.1 H3739H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:152283116 T>C maps to NM_002016.1 Q1415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr1:152282184 G>T maps to NM_002016.1 S1726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:152280014 G>A maps to NM_002016.1 S2449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr1:152283695 C>T maps to NM_002016.1 K1222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr1:152275877 C>T maps to NM_002016.1 S3828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr1:152282444 A>G maps to NM_002016.1 D1639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr1:152277200 G>C maps to NM_002016.1 L3387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IF-01A-11D-A31L-08 chr1:152282738 G>A maps to NM_002016.1 S1541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:152284922 G>A maps to NM_002016.1 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr1:152276465 C>T maps to NM_002016.1 Q3632Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr1:152280353 C>T maps to NM_002016.1 Q2336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr1:152275778 G>A maps to NM_002016.1 S3861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr1:152276070 G>C maps to NM_002016.1 S3764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:152327319 G>C maps to NM_001014342.2 S981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:152326394 T>C maps to NM_001014342.2 S1289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:152327244 G>C maps to NM_001014342.2 S1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr1:152325210 G>T maps to NM_001014342.2 S1684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:152327480 A>G maps to NM_001014342.2 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr1:152328284 T>A maps to NM_001014342.2 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr17:18156742 C>T maps to NM_002018.2 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:18151260 C>T maps to NM_002018.2 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr17:18155349 C>A maps to NM_002018.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr14:21542698 G>T maps to NM_018071.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr14:21541241 C>T maps to NM_018071.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr17:78389500 G>A maps to NM_173627.3 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:142481270 C>T maps to NM_207414.2 R630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:142506528 C>T maps to NM_207414.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:142500262 G>A maps to NM_207414.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:84606905 C>G maps to NM_001001670.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr9:84607716 G>T maps to NM_001001670.2 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:84607176 C>T maps to NM_001001670.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr9:84609740 G>A maps to NM_001001670.2 E1452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr9:84605870 G>A maps to NM_001001670.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:84606512 C>T maps to NM_001001670.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr9:84607187 C>A maps to NM_001001670.2 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr9:84607775 G>C maps to NM_001001670.2 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr23:153595856 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:153588585 G>C did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:153594928 C>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:153577806 A>G did not map to a codon.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr23:153580771 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:153587739 C>G did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr23:153580936 G>A did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr23:153580055 C>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:153594776 T>A did not map to a codon.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr23:153591105 C>A did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr23:153596025 A>T did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr23:153588902 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153580035 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153586661 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153590891 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153596372 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr23:153590633 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr23:153588702 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr23:153583375 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:153589714 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:153590082 G>A did not map to a codon.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr23:153591106 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:153587511 G>C did not map to a codon.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr23:153594746 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr23:153592634 G>A did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr3:58104675 G>T maps to NM_001164317.1 P941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:58090939 C>T maps to NM_001164317.1 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:58089728 G>A maps to NM_001164317.1 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr3:58062870 G>T maps to NM_001164317.1 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr3:58064474 G>C maps to NM_001164317.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr7:128490527 G>T maps to NM_001458.4 E1797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr7:128492756 G>A maps to NM_001458.4 S1985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr7:128489487 G>A maps to NM_001458.4 P1685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr7:128485309 G>A did not map to a codon.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:30698342 C>G did not map to a codon.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr6:30698342 C>G did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:30709055 G>A maps to NM_005803.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr17:27209177 G>A maps to ENST00000394906 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr11:63884782 C>T maps to NM_013280.4 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr14:86088850 T>C maps to NM_013231.4 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr14:86089033 C>T maps to NM_013231.4 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr14:86088199 C>T maps to NM_013231.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:86087867 C>T maps to NM_013231.4 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:86088277 G>C maps to NM_013231.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:14306910 A>C maps to NM_198391.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr20:14307764 G>A maps to NM_198391.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr20:14306846 A>G maps to NM_198391.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:29001375 C>A maps to NM_002019.4 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr13:28931820 T>A maps to NM_002019.4 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:28599055 C>T maps to NM_004119.2 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr13:28636191 C>T maps to NM_004119.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr13:28589747 G>A maps to NM_004119.2 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr13:28636116 T>A maps to NM_004119.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr13:28601324 G>A maps to NM_004119.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:180057696 G>A maps to NM_182925.4 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:180043407 G>T maps to NM_182925.4 R1060R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:180047254 C>A maps to NM_182925.4 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr5:180048647 C>G maps to NM_182925.4 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:213062504 C>T maps to NM_014053.2 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr14:76088432 G>A maps to NM_017791.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr16:2983756 C>T maps to ENST00000399667 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:2979733 C>T maps to ENST00000399667 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:2946539 G>A maps to NM_138439.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2946650 C>T maps to NM_138439.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr15:33359986 G>A maps to NM_001103184.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr15:33218462 C>A did not map to a codon.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr15:33358885 T>A maps to NM_001103184.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:33359905 G>A maps to NM_001103184.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:240370400 G>C maps to ENST00000406993 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:240492373 A>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:240370892 C>T maps to ENST00000406993 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:240256602 C>A maps to ENST00000406993 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:240492683 C>G maps to ENST00000406993 V1594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:240256065 A>G maps to ENST00000406993 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:240492662 C>A maps to ENST00000406993 I1587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:240492665 C>A maps to ENST00000406993 P1588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:240371519 C>T maps to ENST00000406993 P1279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:240371744 C>T maps to ENST00000406993 P1354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:240370352 C>A maps to ENST00000406993 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:240256803 G>T maps to ENST00000406993 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr1:240371420 C>T maps to ENST00000406993 P1246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:240351555 C>G maps to ENST00000406993 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:240370979 G>A maps to ENST00000406993 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr1:240256017 C>T maps to ENST00000406993 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr1:240371579 A>C maps to ENST00000406993 P1299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr1:240256744 C>A maps to ENST00000406993 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr1:240256707 G>A maps to ENST00000406993 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:240370925 C>A maps to ENST00000406993 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr1:240370280 C>T maps to ENST00000406993 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr1:240371618 C>T maps to ENST00000406993 P1312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:43322407 T>C maps to NM_005892.3 I887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr17:43314942 G>A maps to NM_005892.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:153415271 G>C maps to NM_052905.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr2:153504403 C>T maps to NM_052905.3 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:153471450 A>G maps to NM_052905.3 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:153475612 C>A maps to NM_052905.3 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr12:50059691 C>G did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:171249963 C>T maps to NM_002021.1 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:171178064 C>G maps to NM_001460.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr1:171086407 C>T maps to NM_006894.5 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:171303577 G>T maps to NM_002022.1 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:203311479 G>A maps to NM_002023.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:203316798 C>T maps to NM_002023.3 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:203317163 C>A maps to NM_002023.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr1:203316864 C>G maps to NM_002023.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr23:147026444 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr23:147014271 G>T did not map to a codon.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr23:147084785 T>A did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:147084798 A>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:147063087 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:147106429 G>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:147063164 C>T did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr23:147106391 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:216269247 G>C maps to NM_212482.1 P1039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:216274732 G>A maps to NM_212482.1 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:216269262 G>A maps to NM_212482.1 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr2:216248066 A>C maps to NM_212482.1 T1678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr2:216288915 G>T maps to NM_212482.1 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr17:80680698 G>A maps to NM_024619.3 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:80674689 C>A maps to NM_024619.3 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr17:80684370 G>T maps to NM_024619.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr9:132691880 C>A maps to NM_015033.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:132658198 C>T maps to NM_015033.2 W588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr9:132740854 G>A maps to NM_015033.2 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr9:132658258 C>T maps to NM_015033.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr11:47741493 G>A maps to NM_015308.2 Q984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr11:47739053 C>A maps to NM_015308.2 E992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr11:47786900 C>T maps to NM_015308.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:47786822 T>C maps to NM_015308.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr11:47753077 G>T maps to NM_015308.2 S619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:159654084 C>T maps to NM_032532.2 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr6:159653379 G>A maps to NM_032532.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:159677660 G>T maps to NM_032532.2 T1724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:159636043 G>A maps to NM_032532.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr6:159655422 C>A maps to NM_032532.2 T1293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr13:49752753 G>A maps to NM_001079673.1 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr13:49720031 C>G maps to NM_001079673.1 S313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:172070741 G>A maps to NM_022763.3 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:172046815 G>T maps to NM_022763.3 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr3:172003755 G>A maps to NM_022763.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:172059018 C>T maps to NM_022763.3 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr2:27715570 C>A maps to NM_022823.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr2:27717516 G>T maps to NM_022823.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr1:33333956 C>T maps to ENST00000291421 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:109271296 C>T maps to NM_001144937.1 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr17:33454291 G>A maps to NM_017559.2 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:131080313 C>T maps to ENST00000514667 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:131007219 C>A maps to NM_133372.2 E973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:159791527 C>T maps to ENST00000379346 C975C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr4:159753080 C>T maps to ENST00000379346 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:159791563 C>T maps to ENST00000379346 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:65453805 C>T maps to NM_002028.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:49186310 C>T maps to NM_004476.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr11:49214403 C>A maps to NM_004476.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr11:49227671 A>G maps to NM_004476.1 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:89405124 A>T maps to NM_153696.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr11:89420576 T>C maps to NM_153696.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr11:71906661 C>T maps to NM_016729.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:71932329 G>A maps to NM_001113536.1 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:71850460 G>A maps to ENST00000442948 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr11:94038882 C>T maps to NM_001080486.1 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:94040452 G>A maps to NM_001080486.1 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:28627143 C>T maps to NM_005253.3 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr2:28631663 G>C maps to NM_005253.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr14:38061916 C>G did not map to a codon.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr14:38060647 C>T maps to NM_004496.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:22563618 G>C maps to NM_021784.4 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr20:22563765 G>A maps to NM_021784.4 N38N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr20:22563594 G>A maps to NM_021784.4 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr19:46375994 G>A maps to NM_004497.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:79635322 G>T maps to NM_001013735.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr9:79635499 C>T maps to NM_001013735.1 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr9:79634635 C>T maps to NM_001013735.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr9:79634743 G>A maps to NM_001013735.1 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr16:86601396 C>A maps to NM_005251.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr16:86601489 C>G maps to NM_005251.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr5:72743650 G>A maps to NM_004472.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:63789385 G>A maps to NM_012183.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr9:117663 G>A maps to NM_207305.3 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr9:117483 G>T maps to NM_207305.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:117888 G>A maps to NM_207305.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:117880 G>C maps to NM_207305.3 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:114257405 C>T maps to NM_012184.4 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr2:114257666 C>A maps to NM_012184.4 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr9:70177821 T>C maps to NM_001126334.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:100616543 C>G maps to NM_004473.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:47882289 C>T maps to NM_012186.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr6:1391350 C>G maps to NM_001452.1 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr6:1395021 C>T maps to NM_001452.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr14:29237741 C>T maps to NM_005249.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:29237756 G>A maps to NM_005249.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr14:29237168 C>A maps to NM_005249.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr14:29237513 C>T maps to NM_005249.3 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr14:29237006 G>A maps to NM_005249.3 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr14:29237438 C>T maps to NM_005249.3 H318H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr5:169535530 T>A maps to NM_012188.4 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr17:74136182 C>G maps to NM_001454.3 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr17:74136149 G>A maps to NM_001454.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:8201970 T>C maps to NM_018416.2 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:42660588 T>G maps to NM_001198850.1 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr1:42657218 G>C maps to NM_001198850.1 S369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:4722412 C>T maps to NM_001037165.1 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:4796622 A>G did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr7:4796635 G>A maps to ENST00000450194 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:80559212 C>T maps to NM_004514.3 H607H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr17:80477931 C>A maps to NM_004514.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr16:86612493 C>T maps to NM_005250.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr16:86612541 G>A maps to NM_005250.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr3:138665390 C>T maps to NM_023067.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr12:2968076 C>T maps to NM_202002.1 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr12:2983383 G>A maps to NM_202002.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:2968214 C>T maps to NM_202002.1 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:26851657 C>T maps to NM_003593.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:26862067 G>T maps to NM_003593.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:26861461 C>T maps to NM_003593.2 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:48573478 G>A maps to NM_002158.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:89628853 G>A maps to NM_001085471.1 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:89878382 T>C maps to NM_001085471.1 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr6:108985067 G>A maps to NM_001455.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:70321490 G>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:70316715 C>T did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr3:71019956 C>T did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr3:71247174 C>T maps to NM_001012505.1 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr7:114284742 G>C maps to NM_148898.3 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:49107876 A>C did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr6:41557786 G>A maps to NM_001012426.1 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr6:1313526 C>G maps to NM_033260.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:1313289 G>A maps to NM_033260.3 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:1313538 C>T maps to NM_033260.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:118850288 C>G maps to NM_181721.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:55650162 G>T did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:55650594 G>A did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr23:55650823 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:55650778 G>A did not map to a codon.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr23:55650296 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr23:55650773 C>T did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr22:36889785 G>A maps to NM_001102371.1 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr9:130566688 G>T maps to NM_004957.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:130569915 C>T maps to NM_004957.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr19:52249311 C>A maps to NM_002029.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr19:52249947 G>A maps to NM_002029.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:52272135 G>C maps to NM_001005738.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr4:79285131 C>T maps to NM_025074.6 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:79321967 C>T maps to NM_025074.6 I1352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:79285131 C>G maps to NM_025074.6 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:79455675 C>T maps to NM_025074.6 Q3667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr4:79403006 C>T maps to NM_025074.6 F2831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:79360166 C>T maps to NM_025074.6 I1826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr4:79328995 G>C did not map to a codon.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr4:79284754 G>T maps to NM_025074.6 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr4:79359800 A>C maps to NM_025074.6 S1765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:79360053 A>G did not map to a codon.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr4:79400834 C>T maps to NM_025074.6 S2802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr4:79362386 G>A maps to NM_025074.6 Q1867Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:79351552 C>T maps to NM_025074.6 R1651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr4:79434692 G>C maps to NM_025074.6 L3387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr9:14842545 G>A maps to ENST00000380880 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:14776176 C>T maps to ENST00000380880 R1492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:14797545 G>A maps to ENST00000380880 T1266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr13:39265020 C>T maps to NM_207361.4 P1180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr13:39264177 A>G maps to NM_207361.4 R899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr13:39266019 T>C maps to NM_207361.4 D1513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr13:39266020 G>T maps to NM_207361.4 G1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr13:39446955 G>T maps to NM_207361.4 G2687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr13:39262437 G>A maps to NM_207361.4 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr13:39435694 A>T maps to NM_207361.4 I2549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:39263622 G>A maps to NM_207361.4 Q714Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr13:39358892 C>T maps to NM_207361.4 I1989I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:39422640 A>G maps to NM_207361.4 A2071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr4:190876257 T>C maps to NM_004477.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:190878614 A>T maps to NM_004477.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:135438989 C>T maps to ENST00000443774 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr6:116288717 T>C maps to NM_002031.2 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:168464321 G>T maps to NM_024919.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr6:168467433 C>G did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr6:168475979 C>T maps to NM_024919.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr9:86153020 C>A maps to NM_174938.4 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr9:85987840 G>A maps to NM_174938.4 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:85862841 A>G maps to NM_174938.4 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr3:69242853 G>A maps to NM_015123.1 N553N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr15:44166083 C>T maps to NM_032892.3 *571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr15:44211673 C>T maps to NM_032892.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:52182161 C>G maps to ENST00000344768 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr14:52194512 C>T maps to ENST00000344768 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr23:131212867 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:131228104 T>C did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:131212240 G>A did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:131212466 A>G did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:131212467 G>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:37740291 G>T maps to NM_014907.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr9:37740132 C>A maps to NM_014907.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:37744408 G>T maps to NM_014907.2 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr10:49393656 T>A maps to NM_001018071.3 I766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr10:49446165 G>A maps to NM_001018071.3 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr10:49393602 A>G maps to NM_001018071.3 R784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr10:49381057 C>A maps to NM_001018071.3 E1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr10:49440329 G>C maps to NM_001018071.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr23:12736645 C>T did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:12701660 C>A did not map to a codon.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr23:12701690 C>T did not map to a codon.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr23:12736855 T>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:12736224 T>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:12734552 G>A did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr23:12736658 G>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:12632925 G>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:12736347 G>A did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr23:12735806 G>A did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:12734833 C>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:12734345 A>G did not map to a codon.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr23:12734912 G>A did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr23:12734431 T>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:12728535 G>A did not map to a codon.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr23:12712509 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr23:12735635 G>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:100212951 G>A maps to NM_001013660.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr6:41738929 C>G maps to NM_006653.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:32776557 C>G maps to NM_023037.2 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr13:32729800 T>A did not map to a codon.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr13:32798393 G>A maps to NM_023037.2 T1596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr13:32752453 C>G maps to NM_023037.2 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr13:32869542 C>A maps to NM_023037.2 Y2996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr13:32731435 C>T maps to NM_023037.2 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr13:32786435 C>T maps to NM_023037.2 T1533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr13:32812052 G>T maps to NM_023037.2 L2116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr13:32808874 G>T maps to NM_023037.2 G1898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr13:32849049 C>T maps to NM_023037.2 I2736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr4:48529996 C>T maps to NM_015030.1 K2377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr4:48546827 C>A maps to NM_015030.1 V1791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr4:48584665 C>A maps to NM_015030.1 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:48578165 G>A maps to NM_015030.1 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr4:48523207 C>A maps to NM_015030.1 E2516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:48542844 G>A maps to NM_015030.1 N1940N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr4:48622738 G>A maps to NM_015030.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:48542475 G>A maps to NM_015030.1 F2063F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr4:48559547 G>A maps to NM_015030.1 R1349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:183731214 G>A maps to NM_001463.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr14:44975347 C>T maps to NM_032135.3 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr14:44974981 G>A maps to NM_032135.3 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr14:44975152 A>T maps to NM_032135.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr14:44974105 G>T maps to NM_032135.3 T695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr14:44976016 A>T maps to NM_032135.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr14:44974861 T>C maps to NM_032135.3 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr14:44973940 C>T maps to NM_032135.3 E750E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr7:5644942 G>A maps to ENST00000340250 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:127236416 C>T maps to NM_020369.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:127238523 C>G maps to NM_020369.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr15:83451771 A>G maps to NM_001007122.2 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:30253577 C>T maps to NM_001018080.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:49190546 G>T maps to NM_000145.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:49381543 G>A maps to NM_000145.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr2:49190660 G>A maps to NM_000145.3 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr15:40005665 C>T maps to NM_152597.4 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:40068690 G>C maps to NM_152597.4 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:186672488 G>A maps to NM_173651.2 K6241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:186678740 C>G maps to NM_173651.2 S6855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr2:186672431 T>C maps to NM_173651.2 Y6222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr2:186672164 G>T maps to NM_173651.2 L6133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr2:186678684 A>G maps to NM_173651.2 R6836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr3:120128486 A>G maps to NM_007085.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr5:132652309 C>T maps to NM_015082.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr5:132556520 G>A maps to NM_015082.1 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr4:162307360 C>T maps to NM_020116.3 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr4:162306901 G>A maps to NM_020116.3 A847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr4:162841697 A>T maps to NM_020116.3 C89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr4:162307171 G>A maps to NM_020116.3 Y757Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr4:162841664 C>A maps to NM_020116.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr4:163032464 A>G maps to NM_020116.3 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr4:162680599 G>A maps to NM_020116.3 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:162307345 G>A maps to NM_020116.3 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H8-01A-21D-A34J-08 chr4:163032512 T>A maps to NM_020116.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr4:162577616 G>A maps to NM_020116.3 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr21:47557203 G>A maps to ENST00000397748 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:31089992 C>G did not map to a codon.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr19:49468782 C>T maps to NM_000146.3 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:121187729 C>T maps to NM_177478.1 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:121188056 G>A maps to NM_177478.1 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr16:53913759 C>G maps to NM_001080432.2 S327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr17:61901557 G>C maps to NM_017647.3 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr17:61902697 G>A maps to NM_017647.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:61901284 C>T maps to NM_017647.3 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:61902703 G>A maps to NM_017647.3 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr16:71318559 T>A maps to NM_018348.5 K422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr16:71318956 G>T maps to NM_018348.5 Y289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr6:37429755 C>T maps to NM_015050.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:37411844 C>T maps to NM_015050.2 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr1:78433857 G>A maps to ENST00000436586 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:78429829 C>A maps to ENST00000436586 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr9:133506174 C>T maps to NM_003934.1 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr6:143825111 G>A maps to NM_032020.4 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr6:143816917 C>A maps to NM_032020.4 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr6:143823692 C>A maps to NM_032020.4 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:70513581 G>A maps to NM_145059.2 *1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr23:44383461 C>T did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:154261753 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr23:154261753 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr15:91420199 C>G maps to NM_002569.2 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr16:31193978 C>T maps to NM_004960.3 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr8:33310866 G>A maps to ENST00000380081 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr10:75535418 C>T maps to NM_173540.2 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr11:94278549 G>A maps to NM_002033.3 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:5866612 C>T maps to NM_002034.2 *375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr14:66136077 C>T maps to NM_178155.1 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr6:96651726 T>C maps to NM_006581.3 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:96651162 C>A maps to NM_006581.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr11:6503306 G>C maps to NM_012192.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:180630487 G>T maps to NM_005087.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr3:180688141 G>T maps to NM_005087.3 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr3:180669129 G>A maps to NM_005087.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr17:7495897 T>C maps to NM_004860.3 Q583Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr17:7497596 G>A maps to NM_004860.3 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:117695378 C>T maps to NM_001127489.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr19:35613735 C>T maps to NM_021910.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:39153578 G>C maps to ENST00000263405 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:39135035 C>T maps to ENST00000263405 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr5:39110491 C>G did not map to a codon.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr3:46009274 G>A maps to NM_024513.2 F517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr3:46008281 G>A maps to NM_024513.2 C848C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:46008173 G>A maps to NM_024513.2 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr3:46000053 G>A maps to NM_024513.2 H1215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr6:112029201 G>A maps to NM_153047.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr7:90895604 C>T maps to NM_003505.1 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr7:90895580 C>T maps to NM_003505.1 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:130647820 C>T maps to NM_007197.3 Q112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:130648983 C>T maps to NM_007197.3 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:130648350 C>A maps to NM_007197.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr12:130648599 C>T maps to NM_007197.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr17:42636024 G>A maps to NM_001466.3 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr11:86662819 A>G maps to NM_012193.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:86662996 A>G maps to NM_012193.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr2:208633088 G>A maps to NM_003468.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr2:208632053 G>A maps to NM_003468.3 Y470Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr8:104343655 C>G maps to NM_003506.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr8:104337638 C>G maps to NM_003506.3 Y435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:104341954 A>G maps to NM_003506.3 K538K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:202900650 G>A maps to NM_003507.1 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr2:202900191 C>G maps to NM_003507.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr2:202899736 C>T maps to NM_003507.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:202900719 C>T maps to NM_003507.1 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr10:35929679 A>G maps to NM_031866.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:35929112 C>T maps to NM_031866.2 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr10:35929478 G>A maps to NM_031866.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:72849296 C>G maps to NM_003508.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:72849452 C>T maps to NM_003508.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:72849812 A>G maps to NM_003508.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr7:72849830 G>A maps to NM_003508.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr19:3526991 C>T maps to NM_001136198.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr1:209849178 C>T maps to NM_015714.3 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:31071099 G>T maps to NM_017769.3 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:151169927 C>G maps to NM_198395.1 S47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr2:169764144 G>A maps to NM_021176.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:153762677 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr23:153763389 T>G did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:153760232 C>A did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr23:153760876 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:153760788 C>G did not map to a codon.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr23:153762676 C>T did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr17:78086705 T>A maps to NM_001079804.1 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr11:77937652 G>A maps to NM_080491.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:77937682 C>T maps to NM_080491.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr23:153924264 C>A did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr23:153944336 G>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:153944559 G>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr22:17451083 C>G did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr22:17472946 G>A maps to NM_001037814.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:17472910 G>A maps to NM_001037814.1 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr22:17446135 C>G maps to NM_001037814.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr22:17469019 G>C maps to NM_001037814.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:7144690 G>A maps to NM_007278.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr9:101470779 G>A maps to NM_005458.7 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr9:101068555 G>A maps to NM_005458.7 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:101340228 C>T maps to NM_005458.7 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:101340228 C>T maps to NM_005458.7 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr21:27136925 C>T maps to NM_002040.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr15:50592996 G>T maps to NM_005254.5 S241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr5:161324317 C>T maps to NM_001127648.1 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:161324370 C>T maps to NM_001127648.1 Y438Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr5:161300262 G>A maps to NM_001127648.1 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr5:161309609 A>G maps to NM_001127648.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr4:46252333 G>A maps to ENST00000507069 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr4:46307678 A>G maps to ENST00000507069 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr4:46312205 A>T maps to ENST00000507069 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr4:46305522 A>C maps to ENST00000507069 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr4:46305630 T>G did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:151514090 A>G did not map to a codon.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr23:151393235 G>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:151366157 G>C did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr23:151336734 C>T did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:151336736 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:151358324 C>G did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:151336901 G>C did not map to a codon.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr4:46930430 G>A maps to NM_000809.2 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr4:46979497 G>C maps to NM_000809.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:46930547 A>C maps to NM_000809.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr4:46979461 T>C maps to NM_000809.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr15:27185170 C>G maps to NM_000810.3 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:27128608 C>T maps to NM_000810.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:27185147 C>G maps to NM_000810.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr15:27128605 G>C maps to NM_000810.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:27159965 G>T maps to NM_000810.3 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr15:27193199 C>G maps to NM_000810.3 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr5:161116007 G>A maps to NM_000811.2 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:161119064 C>T maps to NM_000811.2 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:161128535 G>A maps to NM_000811.2 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr5:161118947 G>A maps to NM_000811.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr4:47034443 C>T maps to NM_000812.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr4:47427767 C>T maps to NM_000812.3 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr5:160973364 C>T maps to NM_021911.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr5:160757943 T>A maps to NM_021911.2 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr5:160973364 C>G maps to NM_021911.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr5:160758096 G>A maps to NM_021911.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr5:160761786 G>A maps to NM_021911.2 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr15:26792996 C>A maps to NM_021912.4 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr15:26825562 G>A maps to NM_021912.4 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr15:26806093 C>T maps to NM_021912.4 K355K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr15:26806249 G>C maps to NM_021912.4 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:1961582 C>A maps to NM_000815.4 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:1957084 C>T maps to NM_000815.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:151123390 C>G did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr23:151123916 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:151128334 T>C did not map to a codon.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr23:151129819 C>G did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr23:151123411 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr23:151123412 C>G did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:151131097 G>A did not map to a codon.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr23:151131016 C>G did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:151128414 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr4:46043202 A>G maps to NM_173536.3 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:46053584 A>T maps to NM_173536.3 Y329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr4:46099275 T>A maps to NM_173536.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr5:161524780 C>T maps to NM_198903.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr5:161524717 C>T maps to NM_198903.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr5:161569194 C>G maps to NM_198903.2 Y305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr5:161531031 G>T maps to NM_198903.2 G297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:161580115 C>T maps to NM_198903.2 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr5:161524858 C>A maps to NM_198903.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr15:27772732 T>A maps to NM_033223.4 Y340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr15:27572156 A>T maps to NM_033223.4 K158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr15:27772657 C>A maps to NM_033223.4 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:170222387 C>A maps to NM_014211.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr23:151818952 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:151821292 G>T did not map to a codon.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr23:151815525 G>C did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr23:151806745 G>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:151820061 C>G did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr23:151821395 G>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:151821028 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:151821297 C>T did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:151821658 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:151808894 G>C did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:151821300 G>T did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:89974232 G>C maps to NM_002043.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:97711818 G>C maps to NM_001105580.1 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:26512887 C>A maps to NM_001134366.1 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr10:26581497 G>A maps to NM_001134366.1 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:26518693 C>T maps to NM_001134366.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:26581416 T>C maps to NM_001134366.1 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:68153399 C>T maps to NM_001924.3 C147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr19:2477209 C>T maps to NM_015675.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:30875410 G>T maps to NM_207359.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:49369620 G>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:49173662 G>C did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:49355892 C>G did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:49236840 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr4:853490 T>A maps to NM_005255.2 G1062G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr4:906583 T>A did not map to a codon.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr4:906520 A>G did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr22:30953271 C>T maps to NM_004861.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr22:30951884 A>G maps to NM_004861.1 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:30951149 G>A maps to NM_004861.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:242741243 C>T maps to NM_022134.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:65810580 C>T maps to NM_033036.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:65810463 G>A maps to NM_033036.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr11:65810592 G>T maps to NM_033036.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr7:99757676 G>A maps to NM_024637.4 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr14:88434806 T>C maps to NM_000153.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr14:88411944 C>T maps to NM_000153.2 W541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr14:88429748 G>A maps to NM_000153.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:88452836 G>A maps to NM_000153.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr14:88429778 G>A maps to NM_000153.2 Y370Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr15:49531555 C>T maps to NM_002044.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:38893362 G>A maps to NM_138801.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:38908570 C>T maps to NM_138801.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:88908344 G>A maps to NM_000512.4 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:33269222 G>A maps to NM_020474.3 W316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr18:33283588 C>G maps to NM_020474.3 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:153755895 C>T maps to NM_198321.3 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:153760020 G>A maps to NM_198321.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr7:151798007 T>C did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr9:101608272 G>A maps to NM_024642.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:155157933 G>T maps to NM_052917.2 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr2:155252509 C>T maps to NM_052917.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr2:155102336 C>T maps to NM_052917.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr2:31181272 G>A maps to NM_024572.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr2:31360928 C>A maps to NM_024572.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr1:230391091 T>C did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:230338961 C>G maps to NM_004481.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:166615259 G>A maps to NM_004482.3 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr12:89918284 C>T maps to NM_003774.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr12:89917405 A>T maps to NM_003774.4 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:158162304 T>C maps to NM_014568.1 T828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:158115562 G>C maps to NM_014568.1 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:51773259 G>A maps to NM_007210.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr12:51758104 C>A maps to NM_007210.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:4835950 C>T maps to NM_017417.1 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr12:4855414 T>C maps to NM_017417.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr12:4830001 C>T maps to NM_017417.1 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr12:132681768 G>T maps to NM_001122636.1 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr14:69805440 C>T maps to NM_020692.2 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:69808450 G>A maps to NM_020692.2 W414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr14:69799832 G>A maps to NM_020692.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr3:16264171 C>T maps to NM_054110.4 H560H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr3:16260956 G>T maps to NM_054110.4 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr3:16268943 G>T maps to NM_054110.4 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:151684343 G>C maps to NM_145292.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr7:151664375 A>G maps to NM_145292.3 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:173150915 G>T did not map to a codon.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr19:56693616 C>T maps to NM_033106.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:74071152 C>T maps to NM_003857.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:74071275 C>T maps to NM_003857.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr17:74073205 C>A maps to NM_003857.2 C286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:74073172 C>T maps to NM_003857.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr16:81348777 C>T maps to NM_022041.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:62398538 G>A maps to NM_198335.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr15:42635315 C>T maps to NM_198141.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr3:115395167 G>A maps to NM_001130064.1 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr3:115395101 C>T maps to NM_001130064.1 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr12:6646376 C>A maps to NM_002046.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:6646519 C>T maps to NM_002046.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:6646844 C>A maps to NM_002046.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr12:6646507 C>T maps to NM_002046.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:36035830 C>G maps to NM_014364.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr5:57790545 C>T maps to NM_152687.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:128124961 C>T maps to NM_015635.2 S1467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr9:130027239 G>A maps to NM_032293.4 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:130151297 C>A maps to NM_032293.4 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:30639565 C>T maps to NM_002047.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr21:34878304 C>T maps to NM_001136006.1 A853A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr21:34903797 C>T maps to NM_001136006.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr21:34878378 G>T maps to NM_001136006.1 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr21:34889434 G>A maps to NM_001136006.1 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:29706632 G>C maps to NM_152236.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:29708405 C>T maps to NM_152236.1 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr22:29708003 G>A maps to NM_152236.1 W521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:34074282 G>A maps to NM_139285.2 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr17:34079821 C>A maps to NM_139285.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr17:34077221 T>A maps to NM_139285.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr17:34077218 G>A maps to NM_139285.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:101017767 G>C maps to NM_174942.1 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr12:101017503 G>A maps to NM_174942.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr13:114549557 G>A maps to ENST00000357389 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr16:90103731 C>G maps to NM_001481.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:48650431 G>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:128200697 G>A maps to NM_032638.4 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:128202702 C>T maps to NM_032638.4 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:8100733 C>A maps to NM_001002295.1 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:8100436 G>A maps to NM_001002295.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr10:8115925 G>C maps to NM_001002295.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr10:8106040 C>T maps to NM_001002295.1 C288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:61039978 A>G maps to NM_080473.4 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr18:19780728 G>A maps to NM_005257.3 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr18:19762951 C>G maps to NM_005257.3 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr18:19761484 C>T maps to NM_005257.3 N458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:19761412 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr18:19780632 G>A maps to NM_005257.3 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:19606651 G>C maps to ENST00000404158 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:19612149 G>C maps to ENST00000404158 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:35738808 A>T maps to NM_020944.2 Y629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr9:35737882 G>A maps to NM_020944.2 N789N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr4:22749648 T>A maps to NM_020973.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr4:22749477 A>G maps to NM_020973.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr4:22820362 C>G maps to NM_020973.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr3:81695604 G>A maps to ENST00000264326 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:104125204 C>T maps to NM_004193.2 Q719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr9:136030584 G>A maps to NM_021996.4 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:136031309 G>A maps to NM_021996.4 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:136029194 C>T maps to NM_021996.4 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:89521737 C>T maps to NM_002053.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:89523673 C>A did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:89523837 G>C maps to NM_002053.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:89579770 C>T maps to NM_004120.3 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:89582906 C>T maps to NM_004120.3 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:89657031 G>A maps to NM_052941.4 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:89657043 C>T maps to NM_052941.4 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr1:89727992 C>T maps to NM_052942.3 E519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr1:89729474 G>A maps to NM_052942.3 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr1:89834113 G>T maps to NM_198460.2 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr1:89616097 C>T maps to NM_207398.2 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:89616256 G>A maps to NM_207398.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:89616154 T>C maps to NM_207398.2 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr1:89618014 C>T maps to NM_207398.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:237075003 C>A maps to NM_001485.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:72629168 G>C maps to ENST00000504199 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr4:72635072 G>A maps to ENST00000504199 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr4:72620733 G>A maps to ENST00000504199 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr4:72631246 A>T maps to ENST00000504199 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr4:72634064 C>A maps to ENST00000504199 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:72629138 C>T maps to ENST00000504199 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr4:72629178 G>T maps to ENST00000504199 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:38212607 C>T maps to NM_001171690.1 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:127222319 G>A maps to NM_024523.5 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:127223057 C>T maps to NM_024523.5 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr7:127222067 T>C maps to NM_024523.5 *776W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:109103016 G>A maps to NM_181453.3 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr2:109098190 G>A maps to NM_181453.3 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr2:109088521 C>T maps to NM_181453.3 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr21:34132254 G>T maps to NM_016631.3 Y342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr21:34127588 G>A maps to NM_016631.3 R487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:44185250 G>A maps to NM_000162.3 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr7:44187277 G>A maps to NM_000162.3 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:27730567 C>T maps to NM_001486.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr2:27730603 C>T maps to NM_001486.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr6:53373485 G>T maps to NM_001498.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr6:53374045 C>T maps to NM_001498.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:52998972 G>T maps to NM_003643.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:10874806 G>A maps to NM_004752.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr12:120600728 C>T maps to NM_006836.1 K695K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr12:120588997 C>A maps to NM_006836.1 A1420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:120585973 G>A maps to NM_006836.1 L1575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:120585974 G>A maps to NM_006836.1 I1574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr12:120597713 C>T maps to NM_006836.1 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:120572482 G>A maps to NM_006836.1 F2352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:120582207 G>A maps to NM_006836.1 R1799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:120585044 C>T maps to NM_006836.1 T1586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr12:120615319 T>C maps to NM_006836.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr12:120611883 G>A maps to NM_006836.1 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr12:120599311 G>A maps to NM_006836.1 I806I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr9:79117749 C>T maps to NM_001097636.1 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:79117758 G>A maps to NM_001097636.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:79117925 G>A maps to NM_001097636.1 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:79117926 G>A maps to NM_001097636.1 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:10556811 C>T maps to NM_001491.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:10529179 G>A maps to NM_145649.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:10556694 C>G maps to NM_001491.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:10557454 C>T maps to NM_001491.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr6:10529617 G>A maps to NM_145649.4 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr6:10586755 C>T maps to NM_145655.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:10529935 G>A maps to NM_145649.4 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr15:59911579 C>G maps to NM_004751.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr15:57925870 G>T maps to NM_001018090.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:57953655 A>G maps to NM_001018090.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr15:57913835 C>T maps to NM_001018090.3 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:58004191 C>T maps to NM_001018090.3 R439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr9:74842872 C>T maps to ENST00000238018 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr8:75276508 G>A maps to NM_018972.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:48438503 G>A maps to NM_004962.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr10:48428781 C>T maps to NM_004962.2 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:48438542 G>A maps to NM_004962.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr10:48429291 G>A maps to NM_004962.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:48428898 C>T maps to NM_004962.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:48429033 C>T maps to NM_004962.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr10:48438680 C>T maps to NM_004962.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:56143302 T>C maps to NM_005811.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:18499465 C>T maps to NM_004864.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr10:48414495 C>T maps to NM_016204.1 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr12:7842782 G>A maps to NM_020634.1 N262N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-6024-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:34021967 G>A maps to ENST00000374375 S4S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-6224-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr20:34022564 C>T maps to ENST00000374375 T203T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-A4CG-01A-11D-A25Y-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr20:34022216 G>A maps to ENST00000374375 A87A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-7388-01A-11D-2012-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CV-6940-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr20:34021892 G>A maps to NM_000557.2 H440H. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-H7-8501-01A-11D-2394-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr2:20871118 C>T maps to NM_182828.2 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr23:153670045 G>A did not map to a codon.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr23:153667401 T>G did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr23:153665645 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr23:153670498 G>T did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr23:69649353 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr23:69645275 G>C did not map to a codon.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr23:69649406 C>T did not map to a codon.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr16:30122797 C>T maps to NM_024307.2 W206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr16:30124098 G>A maps to NM_024307.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr11:76969568 G>A maps to ENST00000376217 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr11:75152210 G>A maps to NM_030792.6 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr12:58008470 G>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:95262786 G>A maps to NM_181702.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr5:154311745 G>A maps to NM_015465.3 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:154305442 G>T maps to NM_015465.3 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr5:154296702 C>T maps to NM_015465.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr5:154278773 G>A maps to NM_015465.3 G1037G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr2:39008727 G>A maps to NM_024775.9 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:14038648 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:14027045 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr2:17962284 A>G maps to NM_001130009.1 Q602Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr17:42992692 C>T maps to NM_002055.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:158399881 T>A maps to ENST00000264263 L586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr3:158363474 C>T maps to ENST00000264263 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr3:158363533 C>T maps to ENST00000264263 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:74017518 A>G maps to NM_032380.3 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:74034157 A>T maps to NM_032380.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:13487001 C>A maps to NM_018988.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr6:13365013 G>A maps to NM_018988.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:69565125 C>T maps to ENST00000357308 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:179731939 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr5:179743799 C>G maps to NM_005110.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr5:179765550 G>T maps to NM_005110.2 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr5:179762900 G>C maps to NM_005110.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr5:179763529 G>A maps to NM_005110.2 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr10:117885027 C>T maps to NM_005264.4 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr10:117823943 G>A maps to NM_005264.4 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:117884973 G>A maps to NM_005264.4 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr10:117884985 C>T maps to NM_005264.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr10:118030415 G>C maps to NM_005264.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr5:137599971 G>A maps to NM_001496.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:137593401 G>T maps to NM_001496.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:137593488 G>A maps to NM_001496.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr5:137593488 G>A maps to NM_001496.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr5:137593485 C>T maps to NM_001496.3 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr20:3644018 G>A maps to NM_145762.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr6:55223937 T>C did not map to a codon.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr6:55223757 C>A maps to NM_207410.2 C258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr6:55216135 T>G maps to NM_207410.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr22:38028117 G>A maps to ENST00000381756 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr22:38016246 T>C maps to ENST00000381756 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr16:23491206 G>C maps to NM_015044.4 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:73235979 G>A maps to NM_138619.2 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:85782638 A>T maps to NM_000821.4 Y231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:63938855 C>G did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr8:63951270 C>T maps to NM_003878.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr17:34935801 C>T maps to NM_024835.3 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr22:25023939 C>T maps to NM_005265.2 Q444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr22:24622661 C>G maps to NM_001099781.1 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr22:24627430 G>T maps to NM_001099781.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr20:33444645 G>A maps to NM_178026.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr20:33451190 G>A maps to NM_178026.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr20:33440232 C>A maps to NM_178026.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:33451196 C>T maps to NM_178026.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr20:33444657 G>A maps to NM_178026.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr20:23966369 C>T maps to NM_178311.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr20:23966390 G>A maps to NM_178311.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr20:23966522 C>T maps to NM_178311.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr22:22989483 G>C maps to ENST00000215938 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr22:22989340 C>T maps to ENST00000215938 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:61957806 C>T maps to NM_002059.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:61958158 T>C maps to NM_002059.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr17:61958487 C>T maps to NM_002059.3 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr17:61958451 G>A maps to NM_002059.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:85901367 C>T maps to ENST00000436406 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45T-01A-11D-A24D-08 chr5:42689049 A>G maps to NM_000163.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr20:35885220 A>T maps to NM_021081.4 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr3:172166086 G>A maps to NM_198407.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:172165498 G>A maps to NM_198407.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr3:172165819 G>A maps to NM_198407.2 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr3:172166086 G>A maps to NM_198407.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:59604755 G>C maps to NM_005142.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:59610012 C>T maps to NM_005142.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:59612890 G>A maps to NM_005142.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr11:59612918 C>T maps to NM_005142.2 W3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr11:59599163 T>C maps to NM_005142.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr7:100284281 G>A maps to NM_022574.4 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:100280796 C>G maps to NM_022574.4 V750V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:100281722 C>G maps to NM_022574.4 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:100280032 C>T maps to NM_022574.4 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:100279805 G>A maps to NM_022574.4 H938H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr2:233651922 C>G maps to ENST00000373566 S221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr2:233710511 C>T maps to ENST00000373566 Q1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr2:233651882 G>T maps to ENST00000373566 G208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr2:233651922 C>G maps to ENST00000373566 S221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:150417538 C>T maps to NM_130759.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr7:150389490 G>A maps to NM_015660.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr7:150389760 G>A maps to NM_015660.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr7:150325304 G>T maps to ENST00000438845 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr7:150325562 C>A maps to ENST00000438845 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:150325294 G>A maps to ENST00000438845 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr7:150217649 C>T maps to NM_153236.3 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr7:150217160 C>A maps to NM_153236.3 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:150164340 C>T maps to NM_175571.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:150164298 G>A maps to NM_175571.2 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:150174741 G>T maps to NM_175571.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:150171145 G>A maps to NM_175571.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr5:102442587 T>C maps to NM_017676.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr8:41394781 C>A maps to NM_032336.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:14591258 G>A maps to NM_202470.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr19:14591279 G>A maps to NM_202470.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr1:78546487 G>T maps to NM_017655.4 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:3586840 G>A maps to NM_133261.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:46181249 G>A maps to NM_000164.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr17:27908804 C>A maps to NM_001085454.1 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:27903554 C>G maps to NM_001085454.1 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:90604607 C>T maps to NM_032602.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:90604420 G>A maps to NM_032602.1 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr13:20717310 G>A maps to NM_021954.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr1:35260554 C>T maps to NM_002060.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr1:39341346 T>G maps to NM_030772.4 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr13:20763384 C>T maps to NM_004004.5 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr1:35250779 C>T maps to NM_001005752.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:35227130 C>T maps to NM_153212.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:35227412 C>T maps to NM_153212.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:35223200 C>T maps to NM_005268.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:20797247 C>T maps to NM_001110221.2 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:228346340 G>C maps to NM_020435.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr7:99527090 G>A maps to NM_181538.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:35045149 C>T maps to NM_020660.1 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:35896722 C>G maps to NM_153368.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr23:30739057 G>T did not map to a codon.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr23:30686181 A>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:30738842 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr23:30745635 A>T did not map to a codon.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr23:30714163 G>T did not map to a codon.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr4:80327776 G>A maps to NM_033214.2 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr9:86357453 G>A maps to NM_025211.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr9:86421372 T>C maps to NM_025211.3 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:69206026 C>T maps to NM_019617.3 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:69207907 C>T maps to NM_019617.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:69173531 G>A maps to NM_182536.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:69172544 G>A maps to NM_182536.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:100656685 C>T did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:100662805 G>A did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:33099620 C>A maps to NM_000404.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:33058317 G>A maps to NM_000404.2 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:33109731 G>A maps to NM_000404.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr2:220102440 C>T maps to NM_024506.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:134240999 C>A maps to NM_138342.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:134217281 G>T maps to NM_138342.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:134244921 C>T maps to NM_138342.3 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:134239779 G>A did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:134163102 G>A maps to NM_001080407.2 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:134182364 C>T maps to NM_001080407.2 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr7:8110642 C>T maps to NM_138426.2 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr9:6620305 G>A maps to NM_000170.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr9:6587231 G>A maps to NM_000170.2 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:6533115 C>T maps to NM_000170.2 R988R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr9:6606659 C>T maps to NM_000170.2 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr15:51696665 C>T maps to NM_181789.2 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:51696749 A>G maps to NM_181789.2 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr9:131285594 A>G maps to NM_001003722.1 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:131287587 C>T maps to NM_001003722.1 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:74519692 C>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr16:74527005 C>G maps to NM_012201.5 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr16:74537550 G>A maps to NM_012201.5 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr16:74499651 T>C maps to NM_012201.5 V863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr16:74511428 G>C maps to NM_012201.5 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr12:57858618 C>T maps to NM_005269.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr12:57865744 C>A maps to NM_005269.2 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:57865021 C>G maps to NM_005269.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr12:57857854 G>A maps to NM_005269.2 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:121740371 T>C maps to NM_005270.4 Y533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr2:121748214 C>T maps to NM_005270.4 L1575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:121742132 C>T maps to NM_005270.4 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr7:42005625 G>A maps to NM_000168.5 G1015G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr7:42262780 G>A maps to NM_000168.5 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr7:42079707 C>T maps to NM_000168.5 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr8:144358772 C>T maps to NM_138465.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:144358698 C>T maps to NM_138465.3 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:53972292 C>T maps to NM_147193.2 *621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:54060497 G>A maps to NM_147193.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr16:4382386 C>T maps to NM_032575.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr9:3856102 C>T maps to NM_001042413.1 Q793Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:38649809 T>C maps to NM_006708.2 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:685476 G>A maps to ENST00000397393 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr17:679060 C>T maps to ENST00000397393 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:679027 A>G maps to ENST00000397393 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr17:679147 G>A maps to ENST00000397393 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr23:48629491 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:39047474 C>T maps to NM_002062.3 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr17:9774113 C>G maps to NM_004246.1 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr17:9792817 C>T maps to NM_004246.1 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr17:9774113 C>T maps to NM_004246.1 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr17:9792805 G>A maps to NM_004246.1 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:151202404 G>A maps to NM_001146040.1 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:151271932 G>A maps to NM_001146040.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:151231079 G>A maps to NM_001146040.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:14627214 G>C did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr23:14708938 G>A did not map to a codon.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr23:14748490 G>A did not map to a codon.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr23:14550467 A>G did not map to a codon.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr23:14748409 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr23:14627287 G>A did not map to a codon.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr4:175710092 A>G maps to NM_006529.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:175565065 G>T maps to NM_006529.2 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:102979152 G>T did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr23:102979134 G>T did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:102979898 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr23:102978843 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr23:102979120 T>A did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:158073942 G>T maps to NM_001166060.1 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:158065103 G>T maps to NM_001166060.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr4:158060001 G>T maps to NM_001166060.1 G218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:193065759 G>A maps to NM_016066.3 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr12:56866514 C>G maps to NM_013267.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr12:56868435 G>T maps to NM_013267.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:129360458 G>A maps to ENST00000442111 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:129360581 C>G maps to ENST00000442111 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr19:17671237 G>T maps to NM_024656.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:183908158 C>T maps to NM_015101.2 K539K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:183944272 T>C maps to NM_015101.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:183907895 C>T maps to NM_015101.2 *627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr1:183944296 G>C maps to NM_015101.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr9:138516491 C>T maps to NM_182974.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr12:104397073 G>A maps to NM_031302.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:4692355 C>G maps to NM_001014985.2 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:48202268 C>T maps to NM_015711.3 Q1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:48185360 C>T maps to NM_015711.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr19:48253510 C>G maps to NM_015710.4 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:48255848 C>T maps to NM_015710.4 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr10:88836357 C>T maps to NM_005271.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr23:120182677 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:120181993 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr23:120182404 C>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:120183060 C>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr23:120181944 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:120183196 T>C did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr23:120182628 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:120182994 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:120181904 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:120182039 A>T did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:120181975 C>A did not map to a codon.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr23:120181741 G>C did not map to a codon.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr23:120181724 G>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:182354692 T>C did not map to a codon.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr11:58723305 C>T maps to NM_080661.2 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:4855257 C>A maps to NM_032569.3 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:4861227 G>T maps to NM_032569.3 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr16:4873863 G>A maps to NM_032569.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:150646296 T>C maps to NM_000405.4 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:29029012 C>G maps to NM_006582.2 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:62234365 G>T maps to NM_012384.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:62224424 A>T maps to NM_012384.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr14:54950434 C>G maps to NM_004124.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr14:54950443 C>T maps to NM_004124.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:19740867 C>T maps to NM_016573.2 E939E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr6:24784758 C>T maps to NM_015895.3 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:220369976 G>A maps to ENST00000373917 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr3:155615827 C>T maps to NM_003875.2 Q108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr3:155628610 G>A maps to NM_003875.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr3:155633845 A>T maps to NM_003875.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:155632271 A>G maps to NM_003875.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:155654226 T>C maps to NM_003875.2 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr17:63010656 G>A maps to NM_006572.4 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr9:80046235 C>A did not map to a codon.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr9:80262667 C>T maps to NM_004297.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:3148634 C>T maps to NM_002068.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr7:79840283 G>C did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr7:79828563 G>T maps to NM_002069.5 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr3:50289828 G>A maps to NM_002070.2 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr18:11872269 G>A maps to NM_182978.2 W345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr18:11868554 C>T maps to NM_182978.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:80537223 C>T maps to NM_002072.3 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr20:57429102 G>T maps to NM_080425.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr20:57430096 C>T maps to NM_080425.2 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:57415853 G>A maps to NM_016592.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr1:110152748 G>A maps to NM_005272.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr7:80091817 C>T maps to NM_001102386.1 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr22:23465616 G>A maps to NM_002073.2 *356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr22:23438556 T>C maps to NM_002073.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr22:19808241 G>A maps to NM_053004.2 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:100276154 C>T maps to NM_005273.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:180666084 G>A maps to NM_006098.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:6952354 C>A maps to NM_002075.2 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr12:6952859 G>A maps to NM_002075.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr9:36236907 T>A maps to NM_001128227.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:68171193 C>G maps to NM_018841.5 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr16:848820 C>T maps to NM_016541.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr14:52433375 G>T maps to NM_053064.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr19:47137456 G>T maps to NM_033258.1 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr6:30520891 C>G maps to NM_005275.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr6:30521325 A>G maps to NM_005275.3 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr1:38032592 G>A maps to NM_013285.2 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr1:38033323 C>A maps to NM_013285.2 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:52720818 T>C maps to NM_014366.4 H16H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:52723169 G>A maps to NM_014366.4 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:54574763 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:54577457 G>T did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr23:54569429 G>A did not map to a codon.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr1:231386813 A>T maps to NM_014236.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr5:141385882 G>A maps to NM_005471.4 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr12:102153833 G>A maps to NM_024312.4 Q1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:102142890 A>G maps to NM_024312.4 F1227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr16:1412217 G>A maps to NM_032520.4 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr4:68610289 G>A maps to NM_000406.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr4:68619924 G>A maps to NM_000406.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:65130828 T>C maps to ENST00000418919 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr9:127650554 G>A maps to NM_002077.3 Q628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr9:127652666 C>A did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr9:131019927 C>T maps to NM_004486.4 E863E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr9:131019938 G>T maps to NM_004486.4 R860R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr9:131022970 G>A maps to NM_004486.4 Q484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr9:131021582 G>A maps to NM_004486.4 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr9:131022866 C>T maps to NM_004486.4 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr12:100551500 G>C maps to ENST00000266746 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr12:133350894 C>T maps to NM_005895.3 P1385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:133358995 C>T maps to NM_005895.3 E1117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:133393321 C>G maps to NM_005895.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr3:37368467 A>T maps to NM_001172713.1 S1719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:93282744 T>C maps to NM_005113.2 H490H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:93273115 C>T maps to NM_005113.2 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr15:74368257 C>T maps to NM_001038640.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr15:74368271 C>A maps to NM_001038640.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:72953675 C>T maps to NM_018652.4 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr15:72953658 G>T maps to NM_018652.4 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr10:99619294 C>T maps to NM_001010917.1 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:99623700 C>G maps to NM_001010917.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr10:99623700 C>G maps to NM_001010917.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr10:99623814 C>G maps to NM_001010917.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr3:121396296 C>T maps to ENST00000393667 R2958R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr3:121411411 G>A maps to ENST00000393667 Q2267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr3:121435641 A>T maps to ENST00000393667 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr3:121383838 G>A maps to ENST00000393667 I3203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:121414935 T>C maps to ENST00000393667 E1478E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr3:121417476 T>G maps to ENST00000393667 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:167742807 G>A maps to NM_014498.3 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr9:88650316 G>A maps to ENST00000376023 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr5:32126602 G>A maps to NM_022130.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:150634350 C>T maps to ENST00000369003 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:204170840 C>T maps to NM_198447.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:204170909 G>A maps to NM_198447.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:21668637 A>G maps to NM_016072.4 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:155747429 G>A maps to ENST00000368331 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:155735585 G>A maps to ENST00000368331 H1226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:155744856 C>A maps to ENST00000368331 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:155744942 G>A maps to ENST00000368331 Q734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:155783568 G>A maps to ENST00000368331 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:155796640 G>A maps to ENST00000368331 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:155727075 G>A maps to ENST00000368331 D1764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr6:117896461 T>C maps to NM_020399.3 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr3:39142260 G>A maps to NM_031899.2 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:101190304 G>A maps to NM_002079.2 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:101163323 C>T maps to NM_002079.2 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr16:20331706 C>T maps to NM_001007240.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr16:20327362 C>A did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr3:194118030 C>G maps to NM_004488.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:194118336 G>A maps to NM_004488.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:194118044 G>A maps to NM_004488.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:167024301 A>T maps to NM_005814.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:167032957 T>C maps to NM_005814.1 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr8:145139717 C>T maps to NM_003801.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:145139720 C>T maps to NM_003801.3 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr8:145139220 G>A maps to NM_003801.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr10:113932771 G>A maps to NM_020918.4 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr2:96688756 C>A maps to NM_207328.2 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:96690535 G>T maps to NM_207328.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:96690175 G>A maps to NM_207328.2 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:96689185 G>A maps to NM_207328.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr2:96690047 C>T maps to NM_207328.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr2:96690235 G>A maps to NM_207328.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr19:33617573 C>T maps to NM_018025.2 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:33604788 C>G maps to NM_018025.2 S670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:217783736 G>A maps to NM_018040.2 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:217793360 C>T maps to NM_018040.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:217793351 G>A maps to NM_018040.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:27220787 C>T maps to NM_022078.2 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:27224199 G>A maps to NM_022078.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr1:27224088 C>T maps to NM_022078.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:42476284 T>A maps to NM_001002909.2 R1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:42475960 C>A maps to NM_001002909.2 E1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:42483419 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:42477275 G>A maps to NM_001002909.2 A723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:42475679 G>A maps to NM_001002909.2 S1255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr17:42476498 C>T maps to NM_001002909.2 W982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr17:42477203 C>T maps to NM_001002909.2 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:56531815 G>A maps to NM_001127236.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr2:241404609 C>T maps to NM_002081.2 N417N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr7:99773974 C>T maps to NM_152742.1 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:99773452 G>A maps to NM_152742.1 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:99773203 G>T maps to NM_152742.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:132887677 C>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:133087116 C>A did not map to a codon.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr23:132826429 G>A did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:132795856 C>T did not map to a codon.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr23:132888181 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr23:133087226 G>C did not map to a codon.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr23:133087077 T>C did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:132436979 C>A did not map to a codon.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr23:132438873 C>G did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:132548981 G>A did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr23:132438793 G>A did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:132440098 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr13:92380901 G>A maps to NM_004466.4 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr13:92797180 T>C maps to NM_004466.4 D500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr13:92408603 C>T maps to NM_004466.4 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr13:92345949 C>T maps to NM_004466.4 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr13:92346020 C>T maps to NM_004466.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr13:92797192 C>T maps to NM_004466.4 C504C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr13:92380811 A>T maps to NM_004466.4 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr13:92797234 C>T maps to NM_004466.4 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr13:95055461 G>T maps to NM_005708.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:94938601 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:5528363 A>G maps to NM_019593.3 C654C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr20:5528492 T>G maps to NM_019593.3 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr12:50500209 G>C did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:50500129 C>T maps to NM_005276.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:157406153 T>C maps to NM_000408.4 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:1132335 C>T maps to NM_001505.2 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr7:1132134 G>A maps to NM_001505.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:34887237 C>T maps to NM_000175.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr8:144295189 G>T maps to NM_178172.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:48972602 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr23:48979985 C>G did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:48979049 G>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:48979050 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:48974027 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr6:24467489 G>C maps to NM_001503.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:176573009 A>G maps to NM_005277.3 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:176573000 C>T maps to NM_005277.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr23:13794419 G>C did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:27861750 G>C did not map to a codon.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr1:27216254 G>A maps to NM_018066.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr7:23306161 C>T maps to ENST00000435486 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:136112904 C>T did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr23:136113429 T>C did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:136113045 C>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:136112421 T>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:136112566 C>T did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:136113290 G>C did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr23:136113300 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr23:136113732 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:132891022 C>T maps to NM_001136557.1 D563D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr9:132862906 G>A did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:6734256 C>A maps to NM_001080452.1 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:6733589 G>A maps to NM_001080452.1 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:123187371 G>A maps to NM_177551.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr12:123200126 G>A maps to NM_006018.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:123200717 G>A maps to NM_006018.2 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:46977115 C>T maps to ENST00000283297 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:46977148 C>T maps to ENST00000283297 W675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:46977337 C>T maps to ENST00000283297 W612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:46977655 C>G maps to ENST00000283297 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:47646750 C>T maps to NM_153839.6 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr6:47649189 G>T maps to NM_153839.6 G231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:135439902 A>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:135427078 C>G did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:135453551 G>C did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:135429437 C>T did not map to a codon.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr23:135404983 G>C did not map to a codon.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr23:135429019 C>G did not map to a codon.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr23:135432496 C>T did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr23:135430992 G>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:135429617 C>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:135431249 T>G did not map to a codon.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr23:135430045 T>C did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr23:135439889 G>C did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:135429168 G>T did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr23:135431706 A>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:135431894 C>G did not map to a codon.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr23:135487936 G>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:135426793 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:135482270 T>A did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr23:135431430 C>G did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr23:135428692 C>T did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:135431832 T>A did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr23:135496376 C>G did not map to a codon.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr23:135429655 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr23:135429649 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:135455199 T>G did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:135455214 G>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:135405142 G>T did not map to a codon.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr23:135431790 G>T did not map to a codon.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr23:135405363 T>A did not map to a codon.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr23:135496330 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr23:135431038 C>T did not map to a codon.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr23:135405237 G>C did not map to a codon.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr23:135405025 C>T did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:135429619 C>G did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:26533859 C>T maps to NM_001145168.1 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:26533571 G>C maps to NM_001145168.1 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:26533787 G>A maps to NM_001145168.1 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:26534141 G>A maps to NM_001145168.1 C818C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr16:57597827 C>T maps to ENST00000349457 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:57597803 C>A maps to ENST00000349457 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:47681655 C>A maps to NM_153838.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:47678615 C>G maps to NM_153838.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr6:46849210 G>T maps to NM_015234.4 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr6:46847684 C>T maps to NM_015234.4 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:46826147 G>C maps to NM_015234.4 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr6:46846092 C>T maps to NM_015234.4 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr6:46826147 G>C maps to NM_015234.4 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:46849829 G>A maps to NM_015234.4 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr6:46826414 C>T maps to NM_015234.4 Q1075Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:129518601 G>C did not map to a codon.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr23:129518775 G>T did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr23:129518926 G>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:129519166 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:129519307 A>G did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:129518518 G>C did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:129518495 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr13:27333649 G>C maps to NM_005288.3 Y105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr13:27333514 C>G maps to NM_005288.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr13:27333244 C>T maps to NM_005288.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr10:95347155 C>T maps to NM_181745.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:95347059 C>T maps to NM_181745.3 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr10:134941871 C>G maps to ENST00000368577 Y720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr8:37691310 C>T maps to NM_032777.9 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr8:37699032 C>T maps to NM_032777.9 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:37696478 G>C maps to NM_032777.9 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:37687367 G>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr4:22414905 C>A maps to NM_145290.2 G711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr4:22389444 G>C maps to NM_145290.2 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H8-01A-21D-A34J-08 chr4:22390103 C>A maps to NM_145290.2 G1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr6:142688949 A>G maps to NM_198569.2 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:100362379 T>C maps to NM_032787.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:105518368 G>A maps to NM_013345.2 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr12:131484962 G>T maps to NM_198827.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr12:131593381 G>A maps to NM_198827.3 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr12:131476849 C>T maps to NM_198827.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:131466552 G>A maps to NM_198827.3 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr12:131476933 C>A maps to NM_198827.3 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr14:59931023 C>T maps to NM_022571.5 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:64054130 C>G maps to NM_001170726.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:236306299 T>C maps to NM_003272.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr1:236341830 A>T maps to NM_003272.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr14:53020233 C>A maps to NM_001099652.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr16:20043131 C>T maps to NM_001002911.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr16:20043920 G>C maps to NM_001002911.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr16:20043512 C>T maps to NM_001002911.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr7:37780084 C>T maps to NM_181791.1 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr17:72368687 G>A maps to ENST00000440684 A1409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr17:72367968 C>T maps to ENST00000440684 Q1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr23:9728792 C>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:9707604 G>T did not map to a codon.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr2:131487509 C>A maps to NM_207364.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:154138917 T>C maps to NM_001038705.1 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:154146444 G>T maps to NM_001038705.1 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr3:154055682 C>T maps to NM_001038705.1 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:154055727 T>A maps to NM_001038705.1 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:154146951 G>A maps to NM_001038705.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr3:154146789 G>A maps to NM_001038705.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr3:98251011 G>T maps to NM_005290.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr5:145895391 T>C maps to NM_194251.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:67220093 G>A maps to NM_206997.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:6314149 G>A maps to NM_207370.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:175326174 G>A maps to NM_152529.5 H505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr3:119886326 G>C maps to NM_153002.2 S666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr3:119886625 G>A maps to NM_153002.2 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr3:119887189 G>A maps to NM_153002.2 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:9188804 G>A maps to NM_024980.4 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:25701182 G>A maps to NM_020752.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr10:25464375 C>T maps to NM_020752.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr10:25861685 C>A maps to NM_020752.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr10:25464906 G>T maps to NM_020752.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:25464375 C>T maps to NM_020752.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:25887023 C>T maps to NM_020752.2 H823H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:169802026 C>T maps to NM_014373.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:169801876 T>C maps to NM_014373.2 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr3:169802119 T>C maps to NM_014373.2 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr1:168054804 G>A maps to NM_153832.1 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:128408389 G>A maps to NM_005291.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:128409253 A>G maps to NM_005291.2 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr3:150916864 G>T maps to NM_013308.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr8:145584282 G>A maps to NM_024531.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr8:145583548 C>T maps to NM_024531.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr8:145583286 G>A maps to NM_024531.3 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr17:4936856 C>T maps to NM_017986.3 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr17:4937012 C>A maps to NM_017986.3 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr23:53105970 T>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:53106004 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:53105859 C>T did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:78427028 G>C did not map to a codon.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr23:78426985 C>A did not map to a codon.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr23:78427417 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:78426810 T>C did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr15:40093483 G>T maps to NM_007223.1 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:36491541 G>A maps to ENST00000398597 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:36485439 G>A maps to ENST00000398597 Q1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:36483634 T>A maps to ENST00000398597 T1940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr17:36483160 G>A maps to ENST00000398597 S2098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:36484371 C>A maps to ENST00000398597 E1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:36485275 C>A maps to ENST00000398597 G1393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr17:36482451 C>A maps to ENST00000398597 E2335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr17:36489265 C>T maps to ENST00000398597 G636G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr17:36485311 C>A maps to ENST00000398597 P1381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr8:142367228 C>T maps to NM_005293.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr9:125797358 G>T maps to NM_005294.1 G172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:107115362 T>A maps to NM_005295.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:200842299 C>G maps to NM_005298.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:200842780 C>T maps to NM_005298.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr10:125426258 G>A maps to NM_153442.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:167571175 C>A maps to NM_005299.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:51274483 C>A maps to NM_001506.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:51274591 G>T maps to NM_001506.1 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:51274297 C>G maps to NM_001506.1 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr19:51274036 C>A maps to NM_001506.1 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:41555477 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr2:241569680 C>T maps to NM_001195381.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:124386638 C>T maps to NM_005302.2 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IH-01A-11D-A25Y-08 chr1:202092406 C>T maps to NM_004767.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr2:133402926 C>T maps to NM_001508.2 H370H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:133175181 C>A maps to NM_001508.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr2:133402870 C>A maps to NM_001508.2 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:133174855 T>C maps to NM_001508.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:133174974 C>A maps to NM_001508.2 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr2:133403121 A>T maps to NM_001508.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:133402677 G>A maps to NM_001508.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr2:133403120 C>G maps to NM_001508.2 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr19:46094974 G>A maps to NM_005282.2 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:46094692 C>T maps to NM_005282.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:60620856 G>C maps to NM_004778.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:105858866 G>T maps to NM_007227.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:105859166 C>T maps to NM_007227.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:105858977 G>A maps to NM_007227.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr2:105858932 G>A maps to NM_007227.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:105859280 C>T maps to NM_007227.3 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:150348693 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:150349069 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr23:150348703 G>A did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr23:150348723 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr23:150349839 C>G did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:150348249 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:150345220 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:150345221 C>T did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:150348594 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:150349598 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr1:174417580 C>G maps to NM_005684.4 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr2:231774924 C>T maps to NM_005683.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr16:57689387 G>A maps to NM_005682.5 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr6:110301052 G>A maps to ENST00000414000 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr6:110300830 C>T maps to ENST00000414000 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:110086822 G>A maps to NM_031936.4 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:110086036 C>G maps to NM_031936.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:110086441 C>T maps to NM_031936.4 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:97246863 G>C maps to NM_030784.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr6:97247015 G>A maps to NM_030784.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr23:19022961 C>A did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr23:19022896 A>G did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:19039219 A>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:19032135 G>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:19009029 G>C did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr23:19014209 C>T did not map to a codon.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr23:19022939 A>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr14:88477766 T>C maps to NM_003608.3 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr14:88477469 C>T maps to NM_003608.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:54081572 G>A maps to NM_006794.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:47844439 C>G maps to NM_018485.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr19:47844466 C>T maps to NM_018485.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:8588801 C>T maps to NM_080819.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:94113677 G>C maps to NM_016540.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr11:94113653 G>A maps to NM_016540.3 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:94134044 G>C maps to NM_016540.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:94129657 C>T maps to NM_016540.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:94134086 G>A maps to NM_016540.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr12:54756500 G>A maps to NM_020370.2 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr7:112724578 A>G maps to NM_018970.6 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:101004650 C>A maps to NM_022049.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr1:145765383 T>C maps to NM_001097612.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr16:57719692 G>A maps to NM_170776.4 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:89986665 G>A maps to NM_032119.3 K2253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr5:89981639 G>A maps to NM_032119.3 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:90149124 C>A maps to NM_032119.3 C5743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr5:90106532 T>C maps to NM_032119.3 P5152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:90106676 T>A maps to NM_032119.3 A5200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:89930998 C>T maps to NM_032119.3 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:89954096 T>A did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:90040950 T>A maps to NM_032119.3 P3546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:90106736 C>T maps to NM_032119.3 F5220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:90074288 C>T maps to NM_032119.3 Q4238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:89943366 C>T maps to NM_032119.3 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr5:89970028 C>A maps to NM_032119.3 I1696I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:89949314 C>T maps to NM_032119.3 F1308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:90106721 C>T maps to NM_032119.3 S5215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:90445959 C>T maps to NM_032119.3 F6182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr5:89953815 G>A maps to NM_032119.3 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:90107096 G>A maps to NM_032119.3 Q5340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr5:90051001 G>T maps to NM_032119.3 P3860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:89979644 T>C maps to NM_032119.3 V1969V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr5:89953720 G>T did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:101911991 C>T did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:101909692 G>T did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr23:101912581 T>C did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:101911282 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:101910569 G>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:101912156 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:101911581 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr23:101912649 A>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:101910957 C>T did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:101909129 C>T did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr23:101910479 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:101909467 C>G did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr23:101970807 G>A did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr23:101969804 G>C did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:101969963 C>T did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:101971266 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:101970136 G>C did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:101971014 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:101969892 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:101971498 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr23:101971736 T>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:101970657 G>A did not map to a codon.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr23:101971751 C>A did not map to a codon.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr23:101969905 A>C did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:101970215 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr12:13061573 C>T maps to NM_003979.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:13061986 C>T maps to NM_003979.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:19883696 G>T maps to NM_016235.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr6:117128261 C>G maps to NM_148963.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:117128035 G>A maps to NM_148963.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr10:46999983 G>T maps to NM_014696.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr4:90170586 T>C maps to NM_198281.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr4:90168948 C>A maps to NM_198281.2 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:80014846 C>T maps to NM_212492.1 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:7216602 G>C maps to NM_004489.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:109446789 C>G maps to NM_013296.4 S369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:109461320 G>A maps to NM_013296.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr6:32159205 C>T maps to NM_022107.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr16:46960922 G>A maps to NM_133443.2 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:1105706 C>G maps to NM_002085.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr6:28499612 C>A maps to NM_001509.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:28473518 C>A maps to NM_182701.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr6:28473479 C>T maps to NM_182701.1 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:53074033 G>A maps to NM_015696.4 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:35502415 C>T maps to NM_020895.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:35512501 C>T maps to NM_020895.3 H524H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:35517043 G>C maps to NM_020895.3 *725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:35516978 C>T maps to NM_020895.3 H703H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr11:123481026 C>A maps to ENST00000456860 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:123480965 C>T maps to ENST00000456860 H477H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:123484352 C>T maps to ENST00000456860 I602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:113659106 C>G maps to NM_017577.4 S608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:72460094 G>T maps to NM_001012642.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:47033857 G>T did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr22:47033813 C>T maps to NM_015124.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr22:47071406 G>A maps to NM_015124.2 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr7:50742256 G>A maps to NM_005311.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:165349693 T>A did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:165365021 G>A maps to NM_004490.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr2:165383571 T>C maps to NM_004490.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:37899469 G>T maps to ENST00000445327 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:11728899 G>C maps to NM_014668.3 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:11737976 G>T maps to NM_014668.3 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:11741111 C>T maps to NM_014668.3 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:11718541 G>T maps to NM_014668.3 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr2:11780420 G>A maps to NM_014668.3 A1897A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr2:11725891 C>T maps to NM_014668.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:11774277 G>A maps to NM_014668.3 R1671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:11729025 C>A maps to NM_014668.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:11750975 C>T maps to NM_014668.3 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr2:11770225 G>C maps to NM_014668.3 V1534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr2:11725951 A>T maps to NM_014668.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:240656400 G>T maps to NM_022469.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:240656337 G>T maps to NM_022469.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:102656367 C>G maps to NM_024915.3 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr8:102585905 C>T maps to NM_024915.3 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr8:102589742 C>T maps to NM_024915.3 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:24680894 C>T maps to NM_021180.3 Q581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr1:24663184 G>A maps to NM_021180.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr9:37428507 C>G maps to ENST00000377824 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr9:37429759 C>T maps to ENST00000377824 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:153077674 A>T maps to NM_001114183.1 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr5:153056595 G>T maps to NM_001114183.1 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr5:153026581 C>T maps to NM_001114183.1 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:153175080 C>G maps to NM_001114183.1 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr5:152873563 G>A maps to NM_001114183.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:153077647 C>A maps to NM_001114183.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:153078485 C>T maps to NM_001114183.1 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr5:153077602 G>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr4:158262466 C>T maps to NM_000826.3 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr4:158284165 C>T maps to NM_000826.3 N874N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr4:158262421 C>T maps to NM_000826.3 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr4:158255199 C>A maps to NM_000826.3 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:122598929 A>T did not map to a codon.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr23:122561965 C>T did not map to a codon.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr23:122532518 G>A did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:122537304 G>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:122318399 A>G did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:122459925 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:122551586 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr23:122599620 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:122387311 C>A did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr23:122551329 G>C did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr23:122387298 C>A did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:122599614 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:122538683 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:122528857 G>A did not map to a codon.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr11:105769023 T>C maps to NM_000829.3 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:105795454 C>T maps to NM_000829.3 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:105758285 C>A maps to NM_000829.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:105804579 G>T maps to NM_000829.3 E727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:87362281 C>G maps to NM_017551.2 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:87482887 A>G maps to NM_017551.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr10:87487644 G>A maps to NM_017551.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr10:87614372 C>A did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr10:87966142 G>T maps to NM_017551.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr10:87614309 G>C maps to NM_017551.2 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:87379724 A>G maps to NM_017551.2 D753D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:94031950 T>C maps to NM_001510.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr4:94031920 C>T maps to NM_001510.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:94376931 A>T maps to NM_001510.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr4:94145811 T>A maps to NM_001510.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr4:94690471 C>T maps to NM_001510.2 G824G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr21:31311809 G>A maps to ENST00000327783 H3H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr21:30934005 G>T maps to ENST00000327783 C765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr21:30934038 G>T maps to ENST00000327783 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr21:31015181 C>T maps to ENST00000327783 W354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr21:31015182 C>T maps to ENST00000327783 W354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr21:30927504 T>C maps to ENST00000327783 K825K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr6:102074477 G>A maps to NM_021956.4 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:102130435 T>A maps to NM_021956.4 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr6:102134191 G>A maps to NM_021956.4 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:102074489 G>A maps to NM_021956.4 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr6:102134197 C>T maps to NM_021956.4 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr6:102247606 C>T maps to NM_021956.4 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr1:37285382 A>G maps to NM_000831.3 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:37291331 G>T maps to NM_000831.3 I542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:37271717 G>A maps to NM_000831.3 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:37271711 C>T maps to NM_000831.3 T769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:42569483 G>A maps to NM_002088.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:42557774 G>A maps to NM_002088.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:42510940 G>A maps to NM_002088.3 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr19:42509941 G>C maps to NM_002088.3 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr19:42566781 G>A maps to NM_002088.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr9:140058118 C>G maps to ENST00000371546 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:140056968 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr9:140058286 C>T maps to ENST00000371546 H861H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr9:140057650 G>A maps to ENST00000371546 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:9857425 G>A maps to NM_000833.3 Y1325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr16:9923429 G>T maps to NM_000833.3 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr16:9857767 G>A maps to NM_000833.3 S1211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr16:10273896 G>A maps to NM_000833.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr16:10032165 C>T maps to NM_000833.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr16:9858457 C>T maps to NM_000833.3 Q981Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr16:10032120 G>A maps to NM_000833.3 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:9892209 A>C maps to NM_000833.3 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr16:9858382 C>T maps to NM_000833.3 A1006A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr12:13717096 G>A maps to NM_000834.3 I1025I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:13716469 C>A maps to NM_000834.3 S1234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr12:13716226 G>A maps to NM_000834.3 A1315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:14019073 G>C maps to NM_000834.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr12:13722779 C>A maps to NM_000834.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:13828793 C>T did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr12:14018731 C>T maps to NM_000834.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr12:13906827 G>A maps to NM_000834.3 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:13906600 G>T maps to NM_000834.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr12:13828684 C>T maps to NM_000834.3 W373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr12:13715992 G>A maps to NM_000834.3 D1393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr12:13768123 A>G maps to NM_000834.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr12:13768576 C>T maps to NM_000834.3 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr12:13716094 G>A maps to NM_000834.3 A1359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr17:72842376 G>A maps to NM_000835.3 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:72848615 G>A maps to NM_000835.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr17:72850831 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:48946543 C>T maps to NM_000836.2 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:48908442 A>C maps to NM_000836.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr19:48917262 C>T maps to NM_000836.2 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr19:48917265 G>T maps to NM_000836.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:48922548 C>T maps to NM_000836.2 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr9:104375798 A>T maps to NM_133445.2 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:104449191 G>A maps to NM_133445.2 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr9:104448990 T>G maps to NM_133445.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr9:104432437 G>A maps to NM_133445.2 F752F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr9:104499571 C>T maps to NM_133445.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:1005350 C>A maps to NM_138690.1 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr19:1005278 C>T maps to NM_138690.1 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:1004693 G>A maps to NM_138690.1 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:66770983 G>A maps to ENST00000359742 C901C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:66814549 T>A maps to ENST00000359742 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:66773094 C>G maps to ENST00000359742 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:66990675 C>T maps to ENST00000359742 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:66765602 C>G maps to ENST00000359742 R961R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr12:66932902 C>A maps to ENST00000359742 G125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr12:66935716 G>A maps to ENST00000359742 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:48846086 G>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:48841724 C>T did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:48846042 C>T did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:48846090 C>T did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:3021417 C>T maps to NM_182982.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr4:3037153 C>T maps to NM_182982.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr10:121212265 C>T maps to NM_005308.2 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr10:121196338 G>A maps to NM_005308.2 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr10:121086085 T>A maps to NM_005308.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr10:121196182 C>T maps to NM_005308.2 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:176859792 C>T maps to NM_002082.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:176863227 C>T maps to NM_002082.3 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:141497260 C>T maps to NM_139209.2 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr3:141499574 G>T maps to NM_139209.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr3:141497566 G>A maps to NM_139209.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:141499322 G>A maps to NM_139209.2 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:47422367 G>T maps to NM_004491.4 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr19:47423336 G>T maps to NM_004491.4 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:47423171 C>T maps to NM_004491.4 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr19:47503646 G>A maps to NM_004491.4 W1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:47503785 C>T maps to NM_004491.4 A1447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:47503695 C>A maps to NM_004491.4 A1417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:47503752 C>T maps to NM_004491.4 F1436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr19:47425030 G>A maps to NM_004491.4 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr6:146480577 T>C maps to NM_000838.3 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr6:146678784 G>A maps to NM_000838.3 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:146673563 C>T maps to NM_000838.3 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:146720538 G>C maps to NM_000838.3 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:146720757 C>T maps to NM_000838.3 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr6:146755793 G>A maps to NM_000838.3 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr6:146480532 G>A maps to NM_000838.3 Q250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr6:146720162 T>A maps to NM_000838.3 L663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:146350787 C>T maps to NM_000838.3 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr6:146351240 T>C maps to NM_000838.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr6:146755544 C>T maps to NM_000838.3 Y1066Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr3:51746778 C>T maps to NM_000839.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr3:51743448 G>A maps to NM_000839.3 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr7:86415677 C>T maps to NM_000840.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:86468290 A>T maps to NM_000840.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:86416015 G>A maps to NM_000840.2 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:86468528 G>T maps to NM_000840.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr7:86394697 C>T maps to NM_000840.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:86479717 C>T maps to NM_000840.2 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:86415995 C>A maps to NM_000840.2 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr7:86493652 C>A maps to NM_000840.2 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr7:86468446 C>T maps to NM_000840.2 Y539Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr7:86493655 C>G maps to NM_000840.2 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:33995957 C>T maps to NM_000841.1 K876K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr6:34029791 G>T maps to NM_000841.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:34004191 C>G maps to NM_000841.1 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:88781021 G>A maps to NM_001143831.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr11:88338040 G>A maps to NM_001143831.2 N413N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:88300969 C>A maps to NM_001143831.2 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:88780521 T>A maps to NM_001143831.2 S173S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BB-7871-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:178410114 G>A maps to NM_000843.3 C744C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr5:178416068 C>T maps to NM_000843.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:178413883 G>A maps to NM_000843.3 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr5:178413415 C>T maps to NM_000843.3 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:6903212 G>A maps to NM_181874.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr3:6903380 C>T maps to NM_181874.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr3:7456771 G>T maps to NM_181874.2 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr3:7728107 A>C maps to NM_181874.2 T921T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr3:6903386 G>T maps to NM_181874.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr3:7188348 G>T maps to NM_181874.2 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr3:7620567 C>T maps to NM_181874.2 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:126173020 G>T maps to NM_001127323.1 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:126173227 G>T maps to NM_001127323.1 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr7:126410116 G>A maps to NM_001127323.1 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr7:126883114 C>T maps to NM_001127323.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr7:126883062 C>A maps to NM_001127323.1 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr7:126544618 G>A maps to NM_001127323.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr7:126544681 T>C maps to NM_001127323.1 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:126173497 G>T maps to NM_001127323.1 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr7:126882898 C>A maps to NM_001127323.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr7:126542665 G>A maps to NM_001127323.1 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:42428418 C>T maps to NM_002087.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr17:42427093 C>T maps to NM_002087.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr17:42427097 C>T maps to NM_002087.2 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr18:56897645 C>G maps to NM_002091.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:16142342 C>T did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr23:16142364 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr23:16168685 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr4:71691067 G>A maps to NM_002092.3 H446H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr4:71702028 C>T maps to NM_002092.3 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr4:71698925 C>T maps to NM_002092.3 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr13:114009695 G>C maps to NM_024719.2 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr19:48953935 C>T maps to NM_031485.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:48954340 G>T maps to NM_031485.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr4:43022368 A>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:43032385 G>A maps to NM_001080476.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr5:145252447 G>A maps to NM_001080516.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:95235375 G>A maps to NM_173849.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:95234859 C>A maps to NM_173849.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr17:38133088 G>A maps to NM_178171.4 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr17:38073422 G>A maps to NM_001165958.1 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr8:130765052 G>A maps to NM_031415.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:130760898 C>A maps to NM_031415.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr8:144644482 C>T maps to NM_024736.6 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr8:144643206 G>A maps to NM_024736.6 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:13243617 G>A maps to NM_001080555.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr17:3628633 C>T maps to NM_031965.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr17:3627402 G>A maps to NM_031965.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:3627783 T>C maps to NM_031965.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:42737443 G>A maps to NM_019884.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr19:42740861 C>A maps to NM_019884.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:51488353 C>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:51488051 A>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:51488375 G>T did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:51486869 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:51487556 G>A did not map to a codon.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr23:51487157 C>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr8:30546803 C>T maps to NM_000637.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr8:30557644 G>A maps to NM_000637.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr20:33524590 G>A maps to NM_000178.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr20:33519178 G>A maps to NM_000178.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr6:52619847 C>A maps to NM_000846.4 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:52619862 C>T maps to NM_000846.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:52767199 G>A maps to NM_000847.4 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr6:52847395 G>A maps to NM_001512.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:52701146 C>T maps to NM_153699.1 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr6:52701089 A>G maps to NM_153699.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:106763286 C>T maps to NM_001031720.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr7:142964717 G>A maps to NM_001143679.1 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr1:110211612 T>A did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:110199341 C>T maps to NM_000850.4 H15H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:110201530 G>A maps to NM_000850.4 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:106014945 G>A maps to NM_004832.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr11:67353606 G>T maps to NM_000852.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:28368039 G>A maps to NM_145657.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr2:144966261 G>A maps to NM_001164629.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr2:48897096 C>T maps to NM_172311.2 D1109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:48873733 A>G maps to NM_172311.2 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:48874000 T>C maps to NM_172311.2 G970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:48906535 G>A maps to NM_172311.2 G1168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:48869596 G>C did not map to a codon.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr3:120469671 C>G maps to NM_005513.2 Y91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr3:120495327 G>T maps to NM_005513.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr3:120469576 C>T maps to NM_005513.2 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr8:30472201 G>A maps to NM_002095.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr8:30511010 C>A maps to NM_002095.4 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:6389540 C>G maps to NM_002096.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:6380414 G>A maps to NM_002096.2 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr13:45725937 A>G maps to NM_004128.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:18361121 G>A maps to NM_005316.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:30878469 C>T maps to NM_001517.4 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr7:74114629 C>T maps to NM_032999.2 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr7:73960125 C>T maps to NM_016328.2 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:73969807 G>A maps to NM_016328.2 K684K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:73933912 G>T maps to NM_016328.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr7:73933771 C>T maps to NM_016328.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:27539952 G>A maps to NM_001520.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr16:27561046 C>T maps to NM_001520.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:27480792 C>G maps to NM_001520.3 R1631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr16:27476144 G>A maps to NM_001520.3 Q1790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr16:27504018 C>T maps to NM_001520.3 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:27566300 C>A maps to NM_001521.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr2:197641345 T>C maps to NM_012086.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr2:197636550 C>T maps to NM_012086.2 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr9:135546191 G>A maps to NM_012204.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr9:135553692 G>A maps to NM_012204.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr9:135553527 C>T maps to NM_012204.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr9:135554901 G>A maps to NM_012204.2 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr9:135917544 C>T maps to NM_001122823.1 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr9:135933277 G>T maps to NM_001122823.1 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr9:135919235 G>A maps to NM_001122823.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr6:111283709 T>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:39123306 C>T maps to NM_004286.4 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:89982158 C>G maps to NM_033107.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:43590531 G>A maps to NM_019096.3 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr10:1061733 T>C maps to NM_012341.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr10:1056447 A>T maps to NM_012341.2 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr10:1046660 G>A maps to NM_012341.2 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr20:60768649 G>A maps to NM_015666.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr20:60774194 G>A maps to NM_015666.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:60774251 G>A maps to NM_015666.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr20:60776030 G>A maps to NM_015666.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr22:46725346 C>T maps to NM_016426.6 C673C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr22:46719096 G>A maps to NM_016426.6 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr22:46704347 G>A maps to NM_016426.6 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:54857042 G>A maps to NM_144594.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr6:42146619 C>T maps to NM_000409.3 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:42153508 G>A maps to NM_002098.5 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:108635028 C>G maps to NM_005459.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:42628641 C>G did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:106681088 G>C maps to ENST00000282249 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr11:106680814 G>T maps to ENST00000282249 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr11:106810419 A>G maps to ENST00000282249 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr4:156632327 G>T maps to NM_001130684.1 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr4:156643192 C>T maps to NM_001130684.1 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr4:156618129 A>G maps to NM_001130684.1 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:156632129 C>A maps to NM_001130684.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:156717622 T>A maps to ENST00000502959 L335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:14796619 G>T maps to NM_004963.3 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:14796619 G>T maps to NM_004963.3 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:14772148 G>T maps to NM_004963.3 G957G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr12:14794055 C>T maps to NM_004963.3 R676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr17:7918082 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr17:7910381 G>A maps to NM_000180.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr17:7917289 C>T maps to NM_000180.3 Q786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr17:7915472 C>G maps to NM_000180.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr17:7907215 G>A maps to NM_000180.3 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:108625365 C>G did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:108696909 G>A did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr23:108708520 G>A did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr23:108691318 G>C did not map to a codon.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr23:108718933 A>G did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:108708625 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:108718438 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:108652356 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr23:108641865 A>C did not map to a codon.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr23:108708492 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:108636204 A>G did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:44688652 A>G maps to NM_021927.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr4:44682766 C>T maps to NM_021927.2 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:228336070 G>T did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr2:189387545 A>T maps to NM_016315.2 K52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:189434753 G>T did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:189458683 A>T maps to NM_016315.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:65439418 G>A maps to NM_000181.3 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:65441106 G>A maps to NM_000181.3 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:65444431 G>T maps to NM_000181.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:73016866 G>T maps to NM_001080393.1 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr3:148714190 C>A maps to NM_004130.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:2793881 C>T did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:2773148 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr23:2793873 G>C did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:45950272 C>G maps to NM_152312.3 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:145039885 G>T maps to NM_002099.6 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr2:127453588 G>A maps to NM_002101.3 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr2:127451473 C>A maps to NM_002101.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr2:127447861 C>A maps to NM_002101.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:49477909 G>T maps to NM_002103.4 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:49477903 G>A maps to NM_002103.4 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:49485571 G>A maps to NM_002103.4 F334F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-7568-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:49494738 C>T maps to NM_002103.4 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr19:49481246 G>T maps to NM_002103.4 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr12:21757450 C>A maps to NM_021957.3 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr12:21692266 G>A maps to NM_021957.3 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr20:23345440 C>T maps to NM_022482.3 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr20:23346090 C>T maps to NM_022482.3 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr22:38202087 G>A maps to NM_005318.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:48723520 C>T maps to NM_181788.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:129267878 G>A maps to NM_153833.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr3:129034139 C>T maps to NM_006026.3 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr12:14927721 C>T maps to NM_177925.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:44880521 C>A maps to ENST00000421098 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr5:134724630 G>A maps to NM_138610.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:71851565 C>T maps to NM_018649.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr4:100870879 T>A maps to NM_002106.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:103267304 G>A did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr23:103268088 T>C did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:103267901 G>C did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:103267976 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr23:103267971 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr23:103267792 G>A did not map to a codon.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr9:99252295 G>A maps to NM_014282.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr6:105224985 C>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:105198278 A>G maps to NM_020771.3 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:105224669 G>A maps to NM_020771.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:15609958 C>T maps to NM_012260.2 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:108954330 G>A did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr4:108935702 G>A maps to ENST00000351726 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:26438044 C>T did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr2:26427037 C>G maps to NM_000182.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:26502172 C>T maps to NM_000183.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr12:96384169 C>G did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr5:153855398 C>T maps to NM_004821.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr5:153855461 G>A maps to NM_004821.2 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:174449900 C>T maps to NM_021973.2 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:174449905 C>A maps to NM_021973.2 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr4:174449918 G>A maps to NM_021973.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr20:7866451 G>A maps to NM_017545.2 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr20:7875860 G>T maps to NM_017545.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr20:7866456 G>A maps to NM_017545.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr20:7886942 A>G maps to NM_017545.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:119927520 C>T maps to ENST00000361035 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:119925633 A>T maps to ENST00000361035 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr17:39881314 C>A maps to ENST00000310778 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr17:39881039 C>T maps to ENST00000310778 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr5:82969303 G>A maps to NM_001884.3 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr5:82948497 G>T maps to NM_001884.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr15:89422471 G>A maps to NM_178232.2 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:89424726 G>A maps to NM_178232.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:19372351 G>A maps to NM_023002.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr11:46637145 C>A maps to NM_173811.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr11:46637289 C>T maps to NM_173811.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr11:46625091 A>G maps to NM_173811.3 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:52217096 G>A maps to NM_001523.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:122626423 C>T maps to NM_005328.2 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr8:122641507 C>A maps to NM_005328.2 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:69148600 G>A maps to NM_005329.2 W365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr16:69148736 C>T maps to NM_005329.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr4:2240602 C>T maps to NM_024511.5 Q359Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:36113849 G>A maps to NM_015302.1 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:36113524 C>T maps to NM_015302.1 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:36113525 C>T maps to NM_015302.1 Q559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr23:152730471 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:152722629 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:156482380 G>C maps to NM_001173393.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr5:156522383 G>A maps to NM_032782.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr5:156533767 G>A maps to NM_032782.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr5:156533908 G>A maps to NM_032782.3 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:156533647 G>A maps to NM_032782.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:154246315 C>G maps to NM_006118.3 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr16:223473 C>T maps to NM_000517.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr11:5248167 G>A maps to NM_000518.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr11:5255268 C>G maps to NM_000519.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr11:5254313 G>T maps to NM_000519.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr11:5254301 C>A maps to NM_000519.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:5290722 C>A maps to NM_005330.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr11:5275520 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:5274589 T>A maps to ENST00000399563 K126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr16:216646 A>G maps to NM_001003938.3 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr16:216067 C>T maps to NM_001003938.3 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:106822944 A>G maps to NM_012257.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:106826263 C>T maps to NM_012257.3 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:202961 C>T maps to NM_005332.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:11139817 G>T did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:11135449 G>C did not map to a codon.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr23:153223610 A>T did not map to a codon.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr23:153218116 G>A did not map to a codon.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr23:153215721 G>C did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:153227685 T>C did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:153218075 C>A did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:153215716 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153220648 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153224145 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153228797 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153228798 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr23:153216399 A>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:153225814 G>A did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:104461750 G>C maps to NM_013320.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr12:104492253 C>G maps to NM_013320.2 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr20:30659560 G>A maps to NM_002110.3 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:121352000 C>A maps to NM_005335.4 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:45396680 G>T maps to NM_021072.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr5:45262155 G>T maps to NM_021072.2 S847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:45262355 G>C maps to NM_021072.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:45396680 G>T maps to NM_021072.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:45396680 G>C maps to NM_021072.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr5:45396671 G>C maps to NM_021072.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:45262556 G>C maps to NM_021072.2 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:45695880 C>A maps to NM_021072.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:45353207 C>T maps to NM_021072.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr5:45262439 G>C maps to NM_021072.2 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr5:45262556 G>T maps to NM_021072.2 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:45462019 A>G maps to NM_021072.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr5:45303854 C>T maps to NM_021072.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:608034 C>T maps to NM_001194.3 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:615972 C>T maps to NM_001194.3 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr1:155258184 C>A maps to NM_020897.1 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:155257695 C>T maps to NM_020897.1 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:155254457 C>T maps to NM_020897.1 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:73659939 G>A maps to NM_005477.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:73616078 G>A maps to NM_005477.2 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr15:73616246 G>C maps to NM_005477.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:32089282 C>T maps to NM_001525.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:32085226 C>T maps to NM_001525.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr22:50687865 C>T maps to NM_032019.5 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr22:50686180 C>T maps to NM_032019.5 E454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:13538258 C>T maps to NM_024827.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr3:13544480 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:114267235 G>A maps to ENST00000398283 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:114270367 A>T maps to ENST00000398283 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr2:240061463 G>A maps to NM_006037.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:239990185 T>C maps to NM_006037.3 R951R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:240029766 C>T maps to NM_006037.3 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr2:239988449 C>A maps to NM_006037.3 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:42169797 A>G maps to NM_001015053.1 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H8-01A-21D-A34J-08 chr17:42156001 G>A maps to NM_001015053.1 A1066A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr17:42168665 C>T maps to NM_001015053.1 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr17:42170771 G>A maps to NM_001015053.1 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr23:48683002 A>T did not map to a codon.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr23:48672856 T>G did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:48661585 G>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:48678560 G>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:48681695 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:48672939 C>A did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:48665099 A>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:48681333 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:48674001 G>T did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr23:48682631 A>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:71681888 C>G did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:71792515 G>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:18624935 G>T maps to NM_178425.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr7:18633555 C>T maps to NM_178425.2 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:18806739 C>T maps to NM_178425.2 Q726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr7:18788640 C>T maps to NM_178425.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr7:18705909 G>T maps to NM_178425.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:18767276 A>G maps to NM_178425.2 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:18833005 C>A maps to NM_178425.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:18669024 G>A maps to NM_178425.2 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr7:18684344 C>T maps to NM_178425.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr15:50544695 C>A maps to NM_002112.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr15:50550635 G>A maps to NM_002112.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr15:50555448 G>A maps to NM_002112.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:125614025 T>A maps to NM_016063.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr6:22570199 G>T maps to NM_138574.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr6:22570124 G>A maps to NM_138574.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:22570037 G>T maps to NM_138574.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr19:4499510 G>A maps to ENST00000301284 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr15:83820107 G>A maps to NM_016073.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr23:7023725 T>C did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr9:116136273 G>A maps to NM_031219.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:116136604 C>T maps to NM_031219.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr2:242196113 G>A maps to NM_005336.3 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:242194962 C>G maps to NM_005336.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:242169036 G>A maps to NM_005336.3 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:242174625 G>A maps to NM_005336.3 I1018I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:242170209 G>A maps to NM_005336.3 R1146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:83616509 C>G did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr23:83723927 A>G did not map to a codon.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr23:83599377 G>C did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:83724400 T>C did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:83723802 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr23:83616597 C>G did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:83723603 C>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:83588801 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:83724251 G>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:83724154 G>A did not map to a codon.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:236766583 G>A maps to NM_018072.5 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:236718635 A>G maps to NM_018072.5 P1961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:236724550 A>G maps to NM_018072.5 P1540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:236729216 A>T did not map to a codon.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:236760192 T>C maps to NM_018072.5 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:236714246 C>T maps to NM_018072.5 Q2130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:236718728 C>T maps to NM_018072.5 K1930K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr1:236749197 G>T maps to NM_018072.5 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:794331 G>A maps to NM_017802.3 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr16:50102744 T>C maps to NM_182922.2 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr14:73973233 A>T maps to ENST00000334988 C594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr14:73989499 G>A maps to ENST00000334988 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr2:37310506 G>A maps to NM_019024.1 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:37217853 G>C maps to NM_019024.1 V1878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:37232866 C>A maps to NM_019024.1 E1605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:37235841 T>C maps to NM_019024.1 P1478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:37267571 A>G maps to NM_019024.1 L982L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr2:37287852 G>A maps to NM_019024.1 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr8:145235409 C>T maps to NM_032450.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr5:41018009 G>A maps to ENST00000296803 T943T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:41000407 G>A maps to ENST00000296803 Q1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr5:41033141 C>T did not map to a codon.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr5:41047839 C>A maps to ENST00000296803 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr5:41008748 C>T maps to ENST00000296803 V1190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr5:41008748 C>T maps to ENST00000296803 V1190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:41052599 G>T maps to ENST00000296803 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr5:41065469 G>A maps to ENST00000296803 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr5:40999782 G>A maps to ENST00000296803 L1528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr5:41004498 C>G maps to ENST00000296803 V1382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr5:41052689 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr5:41065520 C>T maps to ENST00000296803 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr5:41004594 G>A maps to ENST00000296803 I1350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr5:41039603 T>C maps to ENST00000296803 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr6:139495642 C>T maps to NM_016217.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr6:139487784 G>T maps to NM_016217.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr14:31581698 T>C maps to NM_015382.2 L2067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr14:31572141 C>T maps to NM_015382.2 K2510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr14:31602802 C>T maps to NM_015382.2 G1219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr14:31598316 A>C maps to NM_015382.2 A1420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:31574595 G>A maps to NM_015382.2 A2464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr14:31602772 G>A maps to NM_015382.2 L1229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr10:93221955 A>T maps to NM_173497.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:45472641 T>A maps to NM_024602.5 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:45474373 C>A did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr7:43581557 A>G maps to NM_015052.3 L1403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr7:43519315 G>A maps to NM_015052.3 Q1069Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:43400527 G>T maps to NM_015052.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:43503398 G>A did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:43590144 C>T maps to NM_015052.3 R1450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:43484378 C>T maps to NM_015052.3 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:43484408 C>T maps to NM_015052.3 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr2:197183645 C>T maps to NM_020760.1 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:197105284 A>G maps to NM_020760.1 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr2:197183282 A>G maps to NM_020760.1 A777A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr12:66703542 C>T maps to NM_033647.2 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr12:66696406 G>T maps to NM_033647.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:66712488 C>G maps to NM_033647.2 S691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:96342813 C>T maps to NM_018063.3 Q442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr4:84370110 C>T maps to NM_133636.2 W339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr4:84352816 C>T maps to NM_133636.2 K765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr4:185940786 C>T maps to NM_001029887.1 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:65156471 G>A maps to NM_014877.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr17:65104672 C>T maps to NM_014877.3 P1553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:65119121 G>C maps to NM_014877.3 V1198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:65186377 T>G maps to NM_014877.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr17:65116532 G>A maps to NM_014877.3 Q1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr17:65105670 G>A maps to NM_014877.3 H1350H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:124794744 A>G maps to NM_152722.4 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:92826822 T>A maps to ENST00000453812 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:92848477 C>T maps to ENST00000453812 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr23:65411984 A>C did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:65474967 A>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:65417621 T>A did not map to a codon.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr23:65413404 C>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:65413476 C>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:65486345 G>C did not map to a codon.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr23:65427084 A>G did not map to a codon.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr23:65413377 C>T did not map to a codon.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr23:65393538 C>T did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:65392279 A>T did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:65393632 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:65486458 G>T did not map to a codon.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr23:65476115 A>G did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr23:65480092 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:65409594 A>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:65413358 T>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:65417575 G>C did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:65390433 T>C did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr23:65480036 G>A did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr23:65486457 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr23:65420533 G>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr23:65476076 G>T did not map to a codon.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr23:65390539 G>A did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr23:65474919 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:65413475 C>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:93797617 C>A maps to NM_001098672.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:93821973 C>T maps to NM_001098672.1 Q712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr11:93778849 T>G maps to NM_001098672.1 L61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr11:93803696 C>T maps to NM_001098672.1 N407N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr15:64067316 A>C maps to ENST00000261887 L169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:64017533 C>T maps to ENST00000261887 T1175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr15:63904478 G>A maps to ENST00000261887 Q4792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr15:28386661 A>C maps to NM_004667.4 T3977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr15:28408272 C>A maps to NM_004667.4 A3571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr15:28389947 G>A maps to NM_004667.4 R3671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr15:28458988 C>A maps to NM_004667.4 G2229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:28413736 C>G did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:28459834 G>A maps to NM_004667.4 L2108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr15:28538127 C>T maps to NM_004667.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr15:28517375 G>A maps to NM_004667.4 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr15:28375380 G>A maps to NM_004667.4 Q4244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:28358820 G>A maps to NM_004667.4 L4639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr15:28380750 G>A maps to NM_004667.4 Q4035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr15:28377281 G>A maps to NM_004667.4 G4178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr15:28375740 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:28502275 G>A maps to NM_004667.4 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr15:28502311 G>C maps to NM_004667.4 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr15:28473445 G>A maps to NM_004667.4 T1794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr15:28357064 G>A maps to NM_004667.4 Y4783Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr4:89583678 C>G maps to NM_014606.1 S415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr4:89583676 C>T maps to NM_014606.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:89589131 T>C maps to NM_014606.1 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:89599158 C>T maps to NM_014606.1 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:69695986 T>A maps to NM_022079.2 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr10:69699407 G>A maps to NM_022079.2 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr10:69684938 T>C maps to NM_022079.2 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:89407375 T>C maps to NM_016323.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr4:89414185 G>A maps to NM_016323.2 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr4:89407342 A>G maps to NM_016323.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:89345805 G>T maps to NM_017912.3 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr7:35674849 C>T maps to NM_022373.4 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:35673919 A>G did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr3:193855478 G>A maps to NM_005524.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr1:934935 G>A maps to NM_001142467.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr15:72668094 G>A maps to ENST00000457859 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr15:72638652 C>T maps to ENST00000457859 Q459Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr15:72647898 C>A did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr17:80377698 G>A maps to NM_173620.2 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr17:43227433 G>T maps to NM_006460.2 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:43227081 G>A maps to NM_006460.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr17:43246701 A>G maps to NM_144608.1 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:126080455 C>T maps to NM_012259.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr6:126080845 C>T maps to NM_012259.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr6:126080848 G>T maps to NM_012259.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:126080821 A>G maps to NM_012259.2 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr6:26093371 C>T maps to NM_000410.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr1:145415834 G>A maps to NM_213653.3 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:91731617 G>A maps to NM_001017975.3 P1310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:91728094 G>A maps to NM_001017975.3 P1343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:91851391 C>G did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr3:120365174 G>A maps to NM_000187.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr3:120365156 C>T maps to NM_000187.3 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr7:81392159 A>T maps to NM_000601.4 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr7:81355325 G>A maps to NM_000601.4 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:81381475 C>T maps to NM_000601.4 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:81381562 G>A maps to NM_000601.4 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr4:3446392 G>C maps to ENST00000511533 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr17:79658577 G>A maps to NM_004712.4 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr17:79663006 C>T maps to NM_004712.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:79667587 C>T maps to NM_004712.4 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:79655762 G>A maps to NM_004712.4 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:79661855 G>A maps to NM_004712.4 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr17:79652674 G>A maps to NM_004712.4 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr8:43002089 G>T did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr8:43053069 G>A maps to ENST00000458501 W595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:43048964 G>A maps to ENST00000458501 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr8:43054708 C>T maps to ENST00000458501 I663I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:94452164 G>A maps to NM_002729.4 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:145580833 G>C maps to NM_022475.1 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:145580834 C>T maps to NM_022475.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr14:100119153 C>T maps to NM_001127258.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:100125953 C>T maps to NM_001127258.1 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:222721185 G>A maps to NM_024746.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:222721185 G>A maps to NM_024746.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:222717465 G>A maps to NM_024746.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr1:70832203 C>T maps to ENST00000432224 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:100546112 C>A maps to NM_033055.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:100527483 A>G maps to NM_033055.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr1:100533615 G>C maps to NM_033055.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:191116989 G>A maps to NM_014362.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:21799709 C>T maps to NM_015094.2 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr22:21799897 C>T maps to NM_015094.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:21799756 C>T maps to NM_015094.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr22:21799303 G>A maps to NM_015094.2 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr14:62204928 G>A maps to ENST00000394997 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:102304786 C>T maps to ENST00000442724 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:46832528 C>G maps to NM_152795.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:46811509 C>T maps to NM_152795.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:75174441 C>T maps to NM_005338.4 W868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:75189090 G>A maps to NM_005338.4 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr7:75192563 C>T maps to NM_005338.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:75172194 G>A maps to NM_005338.4 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:75172175 C>A maps to NM_005338.4 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr7:75171236 C>T did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:114499829 C>T maps to ENST00000426820 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:114499368 C>T maps to ENST00000426820 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:114484036 T>C maps to ENST00000426820 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:139258059 C>T maps to NM_022740.4 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:139288948 G>T maps to NM_022740.4 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:139285287 T>C maps to NM_022740.4 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:33358704 G>T maps to NM_005734.3 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr11:33373366 C>T maps to NM_005734.3 A1007A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr11:33308478 G>A maps to NM_005734.3 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:40886622 G>T maps to NM_144685.3 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:40886276 G>A maps to NM_144685.3 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:40887042 G>C maps to NM_144685.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr19:40889932 G>A maps to NM_144685.3 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr22:19340888 G>A maps to NM_003325.3 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr22:19384357 C>T maps to NM_003325.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr22:19344525 G>T maps to NM_003325.3 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:19363263 G>A maps to NM_003325.3 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr22:19343783 C>T maps to NM_003325.3 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr22:19343811 C>G did not map to a codon.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr22:19384465 A>T maps to NM_003325.3 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:30005772 G>A maps to NM_003609.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:26017459 C>T maps to NM_005325.3 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:26017360 C>A maps to NM_005325.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr6:26017378 C>T maps to NM_005325.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:27834626 C>T maps to NM_005322.2 *227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:27835169 C>T maps to NM_005322.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:27835241 C>T maps to NM_005322.2 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr6:26056368 C>G maps to NM_005319.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr6:26056551 C>T maps to NM_005319.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr6:26056368 C>G maps to NM_005319.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr6:26056116 C>T maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr6:26157169 G>T maps to NM_005321.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr6:26156773 G>A maps to NM_005321.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:26108147 T>A maps to NM_005323.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:26124696 C>T maps to NM_003512.3 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr6:26199447 G>A maps to NM_021065.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr6:26217593 G>A maps to NM_021052.2 *131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr6:26217504 G>C maps to NM_021052.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr6:27101003 C>T maps to NM_021064.4 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr6:27101059 G>A maps to NM_021064.4 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr6:27100993 G>T maps to NM_021064.4 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:27101035 G>A maps to NM_021064.4 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr6:27100930 C>G maps to NM_021064.4 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr6:27806003 G>A maps to NM_003510.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr6:27833179 G>A maps to NM_003511.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr6:27833209 C>T maps to NM_003511.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr6:27860842 C>A maps to NM_003514.2 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr6:27860846 A>G maps to NM_003514.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr6:27860653 C>A maps to NM_003514.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:26043801 C>T maps to NM_021062.2 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr6:26043603 C>T maps to NM_021062.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr6:26158594 C>T maps to NM_138720.1 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr6:26251970 A>G maps to NM_003524.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr6:26251910 G>A maps to NM_003524.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr6:26273431 G>T maps to NM_003525.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr6:27100328 C>T maps to NM_021058.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr6:27114532 C>T maps to NM_080593.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr6:27114364 G>A maps to NM_080593.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr6:27114532 C>A maps to NM_080593.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr6:27806705 C>T maps to NM_003520.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr6:27861563 C>T maps to NM_003527.4 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr6:26021037 C>T maps to NM_003529.2 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr6:26032186 G>T maps to NM_003537.3 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr6:26032096 C>T maps to NM_003537.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:26046018 G>T maps to NM_003531.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr6:26045673 C>G maps to NM_003531.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:26197202 C>A maps to NM_003530.3 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:26197325 C>T maps to NM_003530.3 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr6:26197304 C>T maps to NM_003530.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr6:26250637 G>A maps to NM_021018.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr6:26271402 G>A maps to NM_003534.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:26271336 G>T maps to NM_003534.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:27778003 G>A maps to NM_003536.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr6:27839967 G>A maps to NM_003533.2 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:27839888 G>A maps to NM_003533.2 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr6:27839919 C>T maps to NM_003533.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:27839925 C>T maps to NM_003533.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:26027336 G>A maps to NM_003544.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr6:26027282 C>T maps to NM_003544.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr6:26205024 C>A maps to NM_003545.3 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr6:26205144 G>A maps to NM_003545.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr6:26205069 G>A maps to NM_003545.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr6:26240712 C>T maps to NM_003540.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:26240865 A>G maps to NM_003540.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr6:26246947 G>T maps to NM_003547.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr6:26247099 G>T maps to NM_003547.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7593-01A-11D-2229-08 chr6:26285430 G>A maps to NM_003543.3 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr6:27107284 G>A maps to NM_003495.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:149859410 G>T maps to NM_175065.2 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr1:149859277 A>G maps to NM_175065.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:149859286 G>T maps to NM_175065.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:149859142 G>C maps to NM_175065.2 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr1:149858607 A>G maps to NM_003517.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:149858568 C>G maps to NM_003517.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr1:149858589 T>A maps to NM_003517.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr1:149858145 G>C maps to NM_003528.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr1:149783656 G>A maps to ENST00000427880 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:149783711 G>T maps to ENST00000427880 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:149784912 C>G maps to NM_001123375.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:149785050 C>G maps to NM_001123375.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:228612627 C>A maps to NM_003493.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:228612918 C>A maps to NM_003493.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:12120395 C>G maps to NM_002114.2 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr6:12122535 C>T maps to NM_002114.2 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr6:143092671 C>T maps to NM_006734.3 T1068T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr1:42046334 G>A maps to NM_024503.3 P1378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:41976646 C>G maps to NM_024503.3 L2232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:41990556 T>C maps to NM_024503.3 V1744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:42045957 G>C maps to NM_024503.3 S1504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr1:42049847 G>A maps to NM_024503.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr1:42041237 C>T maps to NM_024503.3 A1728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:234749403 C>T maps to NM_018410.3 R674R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:75100415 C>G maps to NM_000189.4 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:176310831 C>T maps to NM_002115.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:176308466 G>A maps to NM_002115.2 D821D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:176314713 G>C maps to NM_002115.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr5:176308808 G>A maps to NM_002115.2 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:37853872 T>A maps to NM_181786.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr6:29912275 G>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:29912175 T>C did not map to a codon.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:29910348 C>T maps to ENST00000376806 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:29910404 T>G did not map to a codon.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:29910348 C>T maps to ENST00000376806 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr6:29911171 G>A maps to ENST00000376806 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr6:29912174 G>T did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:29910683 G>A maps to ENST00000376806 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:29912343 G>A maps to ENST00000376806 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:29910586 G>T maps to ENST00000376806 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr6:29910586 G>T maps to ENST00000376806 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr6:29910356 C>G maps to ENST00000376806 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr6:29910348 C>T maps to ENST00000376806 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:29911303 G>A maps to ENST00000376806 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr6:29911087 G>C maps to ENST00000376806 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr6:31323369 C>T did not map to a codon.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr6:31323246 G>A maps to ENST00000428231 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:31324861 C>G did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:31324664 G>T maps to ENST00000428231 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr6:31324612 C>T maps to ENST00000428231 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr6:31324916 G>A maps to ENST00000428231 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr6:31323942 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:31324147 G>A maps to ENST00000428231 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr6:31324916 G>A maps to ENST00000428231 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr6:31323240 G>A maps to ENST00000428231 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr6:31238164 C>A maps to ENST00000383329 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:31238115 C>A maps to ENST00000383329 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr6:31239381 C>A maps to ENST00000383329 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr6:31238975 G>A maps to ENST00000383329 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr6:32917063 C>T maps to NM_006120.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr6:32906578 C>T maps to NM_002118.4 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr6:32974912 G>A maps to NM_002119.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr6:32975991 G>A maps to NM_002119.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr6:32714065 C>T maps to NM_020056.4 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr6:32629759 G>T maps to ENST00000374943 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr6:32629837 G>A maps to ENST00000374943 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr6:30457629 G>T maps to NM_005516.5 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:29796371 C>T maps to ENST00000376828 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:29796425 G>T maps to ENST00000376828 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr6:29797591 G>T did not map to a codon.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr21:38308958 T>C maps to NM_000411.5 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:38308877 G>A maps to NM_000411.5 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr3:148791053 A>G maps to NM_003071.3 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr20:30154065 G>A maps to NM_178581.1 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr20:30155979 G>A maps to NM_178581.1 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr8:28906498 A>T maps to ENST00000444075 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:28904908 C>T maps to ENST00000444075 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:186050342 G>A maps to NM_031935.2 P2868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:186039756 C>T maps to NM_031935.2 I2669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:185953401 C>T maps to NM_031935.2 N964N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr1:186106020 C>T maps to NM_031935.2 R4512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr1:186072799 G>A maps to NM_031935.2 Q3590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:185833651 G>A maps to NM_031935.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:186026438 G>A maps to NM_031935.2 L2406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:185946935 C>T maps to NM_031935.2 Q797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:186158871 G>A maps to NM_031935.2 V5590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:186072766 A>G maps to NM_031935.2 G3579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr1:186063419 T>C maps to NM_031935.2 A3403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:186084056 C>T maps to NM_031935.2 R3795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:185939516 G>T maps to NM_031935.2 G755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:185985315 C>T maps to NM_031935.2 C1712C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:186089236 G>A maps to NM_031935.2 P4063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr1:185891514 C>G maps to NM_031935.2 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:186088920 C>T maps to NM_031935.2 L4001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr1:185958708 T>C maps to NM_031935.2 S1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:34208573 C>A maps to NM_145899.2 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:66357046 C>G maps to NM_003483.4 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr13:31037727 C>T maps to NM_002128.4 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:174254785 G>A maps to NM_002129.3 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:150156301 C>T did not map to a codon.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:34329944 C>A maps to NM_145205.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K0-01B-21D-A31L-08 chr1:34330061 C>T maps to NM_145205.4 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:24129000 C>T maps to NM_000191.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:24137223 A>C did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:55441887 A>C maps to NM_019036.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr5:43298224 G>A maps to NM_002130.6 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr1:120293523 G>A maps to NM_005518.3 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr21:40720241 C>T maps to NM_004965.6 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:80374255 T>C did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr22:35661484 C>G maps to NM_001003681.2 Y368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:1080349 T>A maps to NM_012292.2 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:1080084 C>T maps to NM_012292.2 Y557Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr5:162891727 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr10:124909539 G>A maps to NM_005519.1 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr10:124896592 G>A maps to NM_001105574.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:1741946 C>T maps to ENST00000382711 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr16:1748968 G>T maps to ENST00000382711 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr12:121431329 C>T maps to NM_000545.5 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:121426776 G>A maps to NM_000545.5 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr12:121438952 C>A maps to NM_000545.5 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:121434486 T>A maps to NM_000545.5 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:121416882 G>A maps to NM_000545.5 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr12:121435466 C>T maps to NM_000545.5 H500H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:36104542 G>A maps to NM_000458.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr17:36091643 C>T maps to NM_000458.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:36104707 G>A maps to NM_000458.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:36070600 G>A maps to NM_000458.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr20:43030050 C>T maps to ENST00000338692 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:43047075 C>T maps to ENST00000338692 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr8:76471034 G>A did not map to a codon.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr8:76456181 C>T maps to NM_004133.4 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:138771666 T>C maps to NM_006895.2 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr12:54675201 C>G maps to NM_031157.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr13:53217476 A>T maps to NM_001011725.1 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:26236078 T>G maps to NM_031243.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr2:178080539 T>C maps to NM_194247.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:21679384 A>G maps to NM_031314.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:12907548 C>A maps to NM_001013631.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:83279809 A>G did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:43882405 G>A maps to NM_001098204.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr10:43882507 T>C maps to NM_001098204.1 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:179044052 G>A maps to NM_005520.2 Y372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:100668286 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:100667348 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:100668236 G>T did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr19:39329126 C>T maps to ENST00000221419 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:39330891 G>A maps to ENST00000221419 Y359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr19:39329239 T>C did not map to a codon.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr19:8551951 C>T maps to NM_005968.3 N674N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:8550505 C>T maps to NM_005968.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:8531137 G>A maps to NM_005968.3 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr19:8550637 C>T maps to NM_005968.3 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr1:23645002 T>C maps to ENST00000414299 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:245021345 T>C maps to NM_031844.2 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr19:41807559 C>T maps to NM_007040.3 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:41770635 G>A maps to NM_007040.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr19:41812380 C>T maps to NM_007040.3 Q828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:41811766 C>T maps to NM_007040.3 Q817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:62489735 G>A maps to NM_001079559.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr4:83348704 C>A maps to NM_031372.2 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr4:83350588 G>T maps to NM_031372.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:78752756 A>G maps to NM_004272.3 H30H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:83518565 C>T maps to NM_199330.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr19:19049611 C>T maps to NM_004838.3 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr19:19043824 G>A maps to NM_004838.3 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr14:23746103 A>G maps to NM_020834.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr14:23746121 G>A maps to NM_020834.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:60331553 C>T maps to NM_015888.4 I585I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr1:60309253 C>T maps to NM_015888.4 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:60309234 A>G maps to NM_015888.4 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:60314746 T>G maps to NM_015888.4 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr1:60314089 G>T maps to NM_015888.4 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:12874124 G>A maps to NM_013312.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:42821702 G>C maps to NM_032410.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:150679211 A>T maps to NM_032132.4 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr7:27134301 C>T maps to NM_005522.4 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:27149905 C>A maps to NM_153631.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:27185534 A>G maps to NM_024014.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr17:46607142 G>A maps to NM_002144.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr17:46805631 C>T maps to NM_006361.5 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr17:46620657 C>T maps to NM_002145.3 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr17:46622096 G>A maps to NM_002145.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr17:46627998 C>T maps to NM_002146.4 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr17:46628229 C>T maps to NM_002146.4 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:46669597 A>T maps to NM_002147.3 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:46673815 G>A maps to NM_018952.4 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:46673847 C>T maps to NM_018952.4 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:46685394 C>A maps to NM_004502.3 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr17:46700291 C>T maps to NM_024017.4 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:54379123 G>A maps to NM_017409.3 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:54367366 C>A maps to NM_014212.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr12:54367024 G>A did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:54367024 G>A did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:54448754 C>A maps to NM_153633.2 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:54396286 G>A maps to NM_006897.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr12:54396247 C>A maps to NM_006897.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:54394073 T>C maps to NM_006897.1 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr12:54396310 C>T maps to NM_006897.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr12:54396385 A>G maps to NM_006897.1 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:177054764 C>T maps to ENST00000331462 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:176981710 C>A maps to NM_002148.3 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:176964534 T>C maps to NM_021193.3 C2C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr2:176964811 G>T maps to NM_021193.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr2:176958145 C>T maps to NM_000523.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr2:176958040 G>A maps to NM_000523.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr2:177036311 C>T maps to NM_006898.4 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:177033898 G>A maps to NM_006898.4 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr2:177036314 G>A maps to NM_006898.4 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr2:177036641 C>A maps to NM_006898.4 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr16:72094423 C>A maps to NM_005143.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr16:72094647 C>T maps to NM_005143.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr16:72094608 A>G maps to NM_005143.3 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr16:72094488 C>T maps to NM_005143.3 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:21074116 G>A maps to NM_016287.3 C391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr2:10560020 C>T maps to NM_002149.2 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:122281717 T>C maps to NM_002150.2 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr1:45793530 G>A maps to NM_032756.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:45793380 C>T maps to NM_032756.2 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:175414435 C>T maps to NM_000860.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:95223374 C>T maps to NM_014485.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:35556163 G>A maps to NM_182983.2 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr16:72110553 C>T maps to ENST00000228226 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:72108243 C>G maps to ENST00000228226 Y88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr16:72108201 C>G maps to ENST00000228226 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr23:133620519 A>G did not map to a codon.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr23:133609218 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:100179846 C>T maps to NM_000195.2 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr3:148857965 G>A maps to NM_032383.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:148858877 G>T maps to NM_032383.3 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr3:148858921 G>A maps to NM_032383.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:148858055 G>A maps to NM_032383.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr22:26860539 G>A maps to NM_022081.4 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr11:18320446 G>A maps to NM_181507.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:18332377 G>A maps to NM_181507.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr11:18320455 G>C maps to NM_181507.1 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:103825449 C>T maps to NM_024747.4 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:100219420 A>T maps to NM_021828.4 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:100503693 G>A maps to NM_021828.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr10:100481442 C>A maps to NM_021828.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr10:100374775 C>G did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr11:6452482 C>T maps to NM_000613.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:6459601 G>A maps to NM_000613.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr8:21973239 G>A maps to NM_005144.4 A1181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:21973245 C>T maps to NM_005144.4 K1179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr8:21973914 G>A maps to NM_005144.4 S1135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr8:21986632 C>T maps to NM_005144.4 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:533829 C>A maps to NM_005343.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr19:49657228 G>C maps to NM_002152.2 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr3:186395210 G>T maps to NM_000412.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr3:186392969 C>T maps to NM_000412.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr3:186392951 C>G maps to NM_000412.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr3:11300944 G>A maps to NM_001098211.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr3:11300989 C>G maps to NM_001098211.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr5:175111012 G>T maps to NM_001131055.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr20:60791508 G>A maps to ENST00000317393 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr20:60794906 G>A maps to ENST00000317393 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr20:60791961 C>T maps to ENST00000317393 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr1:152187689 T>A maps to NM_001009931.1 R2139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr1:152188127 G>A maps to NM_001009931.1 R1993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr1:152192430 A>G maps to NM_001009931.1 Y558Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr1:152191917 G>A maps to NM_001009931.1 H729H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:152188506 A>T maps to NM_001009931.1 G1866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr1:152191392 G>T maps to NM_001009931.1 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:152188023 C>T maps to NM_001009931.1 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:152191467 G>T maps to NM_001009931.1 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:152192106 C>T maps to NM_001009931.1 G666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:152191926 G>A maps to NM_001009931.1 Y726Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:152187528 C>T maps to NM_001009931.1 S2192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:152188176 G>A maps to NM_001009931.1 S1976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:152188304 A>G maps to NM_001009931.1 L1934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:20818830 C>T maps to NM_022460.3 Q365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr2:20818935 G>T maps to NM_022460.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:11401038 G>A maps to NM_005114.2 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr4:11400945 G>A maps to NM_005114.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:22926537 C>G maps to NM_006043.1 Y253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr17:13399972 C>T maps to NM_006042.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:26147208 G>T maps to NM_006040.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr16:26147115 C>T maps to NM_006040.2 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr16:25704370 C>G maps to NM_006040.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr16:26147191 C>T maps to NM_006040.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:114378933 G>A maps to NM_153612.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr6:114379097 C>A maps to NM_153612.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:1961638 G>A maps to ENST00000454677 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:1962145 G>A maps to ENST00000454677 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr2:129026287 C>T maps to NM_004807.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:129025881 G>A maps to NM_004807.2 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr23:132091166 G>A did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr13:97485338 C>A maps to NM_153456.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:96743703 C>G maps to NM_153456.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr22:29139935 C>T maps to NM_172002.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr22:29153090 T>C maps to NM_172002.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:67469872 C>T maps to NM_000196.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr17:40705592 T>C maps to NM_000413.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:53458382 C>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr4:88231423 C>T maps to NM_178135.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:82131824 G>A maps to NM_002153.2 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:118832265 G>C maps to NM_000414.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr12:57175986 T>C maps to NM_003725.2 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:57167653 G>A maps to NM_003725.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr12:57167905 C>T maps to NM_003725.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:120057079 C>T maps to ENST00000235547 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:119964588 G>A maps to NM_000198.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:119965035 C>T maps to NM_000198.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:30998162 C>T maps to NM_025193.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:30999362 G>A maps to NM_025193.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:84163847 G>A maps to NM_031463.4 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:115171277 G>A maps to NM_032303.4 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr9:115216389 C>G maps to NM_032303.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:145533468 G>A maps to NM_005526.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:145535876 C>T maps to NM_005526.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr21:45076540 T>A maps to NM_007031.1 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:67203678 C>T maps to NM_001040667.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:67201121 G>A maps to NM_001040667.2 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:67200483 A>G maps to NM_001040667.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:56540555 G>A maps to NM_001080439.1 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr17:56536135 C>T maps to NM_001080439.1 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:16259619 C>T maps to NM_032855.2 H20H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr6:44217785 G>A maps to NM_007355.2 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr6:44217203 C>T maps to NM_007355.2 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:44219989 A>T maps to NM_007355.2 K573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr6:44220883 C>A maps to NM_007355.2 R612R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:104327924 C>T maps to NM_003299.1 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr12:104336573 G>A maps to NM_003299.1 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr10:118460579 C>A maps to NM_025015.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr20:3726198 G>A maps to NM_052970.4 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr20:3729033 T>G maps to NM_052970.4 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr20:3726234 C>T maps to NM_052970.4 H183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr10:14894528 A>T maps to NM_016299.2 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:14909101 T>C maps to NM_016299.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr10:14909271 C>G maps to NM_016299.2 S395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr10:14891736 T>C maps to NM_016299.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr6:31785353 C>T maps to NM_005345.5 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:31797592 C>T maps to NM_005346.4 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr6:31779659 G>A maps to NM_005527.3 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:31778360 C>G maps to NM_005527.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:31778483 G>A maps to NM_005527.3 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr6:31778360 C>T maps to NM_005527.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr14:65007845 C>T maps to NM_021979.3 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:65007833 A>G maps to NM_021979.3 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr14:65007731 C>T maps to NM_021979.3 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr5:132412461 C>T maps to NM_002154.3 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr5:132427045 C>T maps to NM_002154.3 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr5:132427044 T>C maps to NM_002154.3 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:132439955 C>G maps to NM_002154.3 S784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:128726264 A>T maps to ENST00000438626 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:128001049 C>T maps to NM_005347.4 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr9:128003179 G>C maps to NM_005347.4 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:127999356 C>T maps to NM_005347.4 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:161495704 C>T maps to NM_002155.3 N419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:122930646 C>T maps to NM_006597.3 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:122930364 G>C maps to NM_006597.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:137906698 G>A maps to NM_004134.6 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:53751685 C>T maps to NM_006308.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:122474118 C>G maps to NM_024610.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr3:122459416 C>G maps to NM_024610.4 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr19:55776656 C>A maps to NM_012267.4 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr19:55776690 G>C maps to NM_012267.4 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:22168730 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr1:22204944 G>A maps to NM_005529.5 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:22157583 C>G did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:22163404 G>C maps to NM_005529.5 A3415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:22169403 C>T maps to NM_005529.5 L2923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:22179292 C>T maps to NM_005529.5 V2208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:22201440 G>A maps to NM_005529.5 P1119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:22206875 G>A maps to NM_005529.5 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:22182343 G>A maps to NM_005529.5 P1879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:22178185 G>A maps to NM_005529.5 A2337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr1:22181342 G>C maps to NM_005529.5 S2044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr1:22216608 C>A maps to NM_005529.5 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:22175512 C>G maps to NM_005529.5 S2486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:22191362 C>T maps to NM_005529.5 P1533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr1:22213789 G>A maps to NM_005529.5 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr1:22170646 C>T maps to NM_005529.5 R2870R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr13:31728850 C>T maps to NM_006644.2 Q116Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr13:31711646 T>C maps to NM_006644.2 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr13:31722147 T>C maps to NM_006644.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr13:31722150 C>T maps to NM_006644.2 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr11:20403773 A>G maps to NM_001098520.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr11:20404741 C>G maps to NM_001098520.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr23:135581840 G>C did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:70898909 T>C maps to NM_000200.2 Y43Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:63256427 G>A maps to NM_000524.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr5:63257048 G>A maps to NM_000524.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr5:63257090 G>A maps to NM_000524.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:63256364 C>A maps to NM_000524.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:63256922 C>A maps to NM_000524.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:63256466 G>A maps to NM_000524.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:63256580 C>T maps to NM_000524.2 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:63256535 C>A maps to NM_000524.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr5:63257480 G>A maps to NM_000524.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr5:63257048 G>A maps to NM_000524.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:78172871 C>A maps to NM_000863.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr6:78172529 C>T maps to NM_000863.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:78172127 G>A maps to NM_000863.1 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr6:78172112 C>T maps to NM_000863.1 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr1:23520574 G>A maps to NM_000864.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr1:23520601 G>C maps to NM_000864.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:23520169 G>A maps to NM_000864.4 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr1:23519917 C>T maps to NM_000864.4 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr6:87725711 G>A maps to NM_000865.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr6:87726086 G>A maps to NM_000865.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr3:88040985 C>T maps to NM_000866.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:47466710 G>A maps to NM_000621.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr2:231973476 C>A maps to NM_000867.4 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:114141459 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:113965751 C>A did not map to a codon.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr23:114141283 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:113856809 G>A maps to NM_213621.3 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr11:113860272 C>A maps to NM_213621.3 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:113816675 C>T maps to NM_006028.3 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr11:113803664 C>T maps to NM_006028.3 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:183777426 C>T maps to NM_130770.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr3:183778025 G>A maps to NM_130770.2 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr3:183778118 C>G maps to NM_130770.2 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr3:183777667 C>T maps to NM_130770.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:183756392 C>T maps to NM_001145143.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:183756392 C>T maps to NM_001145143.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:183824075 C>A maps to NM_182589.2 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr3:183824396 C>T maps to NM_182589.2 H444H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr5:147845448 G>T maps to NM_199453.3 C372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:154863244 G>T maps to NM_024012.2 P212P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BB-A5HY-01A-11D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr7:154863001 C>T maps to NM_024012.2 N131N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-6992-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:154862704 C>T maps to NM_024012.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:154875974 C>G maps to NM_024012.2 A284A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-6948-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:154862902 G>A maps to NM_024012.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:154875954 C>T maps to NM_024012.2 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr7:154863064 C>A maps to NM_024012.2 R152R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-UF-A719-01A-12D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr7:154862764 G>A maps to NM_024012.2 A52A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-UF-A71A-01A-22D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:19992530 G>A maps to NM_000871.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:19992251 C>A maps to NM_000871.1 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:19992626 C>G maps to NM_000871.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr10:92509029 G>A maps to NM_019859.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr10:92617224 G>T maps to NM_019859.3 S68S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-6441-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:92508597 C>A maps to NM_019859.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr10:124273754 C>A maps to NM_002775.4 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr10:124249009 C>A maps to NM_002775.4 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:74757144 G>A maps to NM_013247.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr4:8305955 C>G maps to NM_053044.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr4:8293146 G>A maps to NM_053044.3 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr8:38834101 C>T maps to NM_153692.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr4:3219627 C>T maps to NM_002111.6 I2397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr4:3101072 G>A maps to NM_002111.6 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr4:3134445 A>T maps to NM_002111.6 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:3117071 C>T maps to NM_002111.6 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:3234933 G>A maps to NM_002111.6 T2770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:3144491 G>C did not map to a codon.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr4:3189496 G>A maps to NM_002111.6 P1703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr4:3129099 A>T maps to NM_002111.6 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr4:3225278 C>T maps to NM_002111.6 L2539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr4:3105591 C>G maps to NM_002111.6 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:3240618 C>T maps to NM_002111.6 F3043F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr21:33346915 A>T maps to NM_014586.1 K354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:656503 C>T maps to NM_148959.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr23:53570869 C>T did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr23:53631657 G>A did not map to a codon.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr23:53560974 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr23:53560285 C>T did not map to a codon.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr23:53563109 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr23:53622347 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr23:53573399 T>C did not map to a codon.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr23:53563193 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:53572035 C>T did not map to a codon.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr23:53619410 C>G did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr23:53618006 C>T did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr23:53654386 C>T did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr23:53589796 C>T did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr23:53560307 C>A did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr23:53589154 C>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:53658552 G>C did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:53634557 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:53571656 G>C did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:53573554 T>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:53619396 G>A did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:53602641 C>G did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr23:53617985 G>A did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr23:53619383 G>C did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:53560989 G>A did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr23:53613474 G>C did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr23:53620463 C>T did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr23:53672317 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:53560983 G>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:53561066 A>C did not map to a codon.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr23:53620322 C>A did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr23:53570869 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:53588761 C>T did not map to a codon.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr23:53571697 T>G did not map to a codon.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr23:53581596 T>C did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr23:53674495 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7596-01A-11D-2229-08 chr23:53563553 C>T did not map to a codon.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr23:53600714 T>A did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:53577937 C>A did not map to a codon.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr23:53571555 C>T did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:53563109 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:53562350 T>C did not map to a codon.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr23:53563189 T>A did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:53588761 C>G did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr23:53560364 G>C did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:53612083 T>C did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:53641649 T>C did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:53575990 C>T did not map to a codon.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr12:111099132 C>A maps to NM_001040107.1 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:111093077 C>G maps to NM_001040107.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:111098970 G>A maps to NM_001040107.1 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:111098986 G>A maps to NM_001040107.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:111099154 G>A maps to NM_001040107.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr3:50339649 G>T maps to NM_153281.1 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr3:50339661 G>A maps to NM_153281.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:50355697 C>T maps to NM_033158.4 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:50332190 G>A maps to NM_003549.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:123516941 C>T maps to NM_012269.2 N393N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:123508734 A>G maps to NM_012269.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr7:123516944 G>A maps to NM_012269.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr7:123508441 C>T maps to NM_012269.2 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr7:123508422 C>T maps to NM_012269.2 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr16:70852358 C>T maps to NM_032821.2 A4847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr16:70894072 G>T maps to NM_032821.2 Y4008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr16:70841640 G>T maps to NM_032821.2 R5069R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:71054109 C>T maps to NM_032821.2 E1099E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr16:70841773 C>T maps to NM_032821.2 K5024K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr16:70863518 A>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr16:71212845 C>T maps to NM_032821.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:71015348 C>G maps to NM_032821.2 L1484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr16:71025262 T>C maps to NM_032821.2 E1274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr16:70866891 C>T maps to NM_032821.2 E4585E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:70843904 C>T maps to NM_032821.2 T4887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr16:70841728 G>A maps to NM_032821.2 I5039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr16:70841731 G>T maps to NM_032821.2 I5038I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr11:118925376 G>A maps to NM_001130991.1 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:118916307 T>C maps to NM_001130991.1 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr11:118917446 G>C maps to NM_001130991.1 S888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr2:9616150 G>A maps to NM_001039613.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:95018989 G>T maps to ENST00000375660 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:95050072 C>T maps to ENST00000375660 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr9:95027218 G>C maps to ENST00000375660 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:95013062 C>T maps to ENST00000375660 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:95043132 C>A maps to ENST00000375660 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:95030485 G>A maps to ENST00000375660 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr4:88732602 C>T maps to NM_004967.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr6:82923969 T>C maps to NM_015525.2 K726K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr6:82943950 G>A maps to NM_015525.2 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr7:8196805 A>T maps to ENST00000422063 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:8167668 G>A maps to ENST00000422063 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr7:8257988 G>A maps to ENST00000422063 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr2:203686197 G>C maps to NM_138468.4 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr2:203693717 C>T maps to NM_138468.4 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:10395131 G>T maps to NM_000201.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:10395702 C>T maps to NM_000201.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:10394871 C>T maps to NM_000201.2 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:10385696 C>A maps to NM_000201.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr17:62080238 C>T maps to NM_001099789.1 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr19:10444649 G>A maps to NM_002162.3 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:10403430 C>T maps to NM_003259.3 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr19:10405161 C>T maps to NM_003259.3 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr2:8822624 C>T maps to NM_002166.4 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr2:8822471 G>A maps to NM_002166.4 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr10:94294474 T>C maps to NM_004969.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr15:90634787 C>T maps to NM_002168.2 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr15:78454628 G>A maps to NM_005530.2 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr15:78454589 C>T maps to NM_005530.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:2640907 C>T did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr20:2640752 G>A maps to NM_006899.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr20:2640690 G>A maps to NM_006899.2 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr20:2639111 G>A maps to NM_174855.1 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr23:153059757 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153051681 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr23:153053582 G>C did not map to a codon.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr8:39782291 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:39785652 C>T maps to NM_002164.4 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:39872931 C>T maps to NM_194294.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:148577954 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:148586601 G>A did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr23:148585742 G>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:148564744 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:148568457 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:148568458 G>A did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:148586583 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr23:148582532 T>A did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:148571966 T>C did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:996876 G>T maps to NM_000203.3 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:981719 G>A maps to NM_000203.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:996896 G>A maps to NM_000203.3 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:13264164 C>G maps to NM_004907.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:181058478 G>C maps to NM_016545.4 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:181058847 C>T maps to NM_016545.4 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:131939287 C>A maps to NM_203434.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:6659914 C>T maps to NM_001193457.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr12:6657689 G>A maps to NM_001193457.1 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr12:6659914 C>T maps to NM_001193457.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr1:158990175 A>T maps to ENST00000295809 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr14:94578102 C>T maps to ENST00000448882 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr19:18286134 T>C maps to NM_006332.3 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:41165073 C>G maps to NM_005533.4 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:79119926 G>C did not map to a codon.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr1:79126275 C>T maps to NM_006417.4 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:79093944 T>C maps to NM_006820.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr1:79107492 G>C maps to NM_006820.2 *453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:163133238 C>G maps to NM_022168.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:163144764 G>A maps to NM_022168.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:163133417 C>A maps to NM_022168.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr10:91066450 A>T maps to NM_001547.4 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr10:91099030 C>T maps to NM_001549.4 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr10:91098945 T>C maps to NM_001549.4 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:91177810 G>A maps to NM_012420.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:91177399 C>T maps to NM_012420.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr12:25671776 A>G maps to NM_001145728.1 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:25702359 A>T maps to NM_001145728.1 Y70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:21367982 C>T maps to NM_006900.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr9:21227788 C>T maps to NM_021268.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr9:21384910 G>A maps to NM_000605.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:21166098 G>A maps to NM_002175.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr9:21166338 G>A maps to NM_002175.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr9:21350757 T>C maps to NM_021002.2 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:21409279 G>A maps to NM_002170.3 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr21:34635243 G>T maps to NM_207585.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:21481363 G>A maps to NM_176891.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:137527278 G>A maps to NM_000416.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr6:137527278 G>A maps to NM_000416.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr21:34809232 G>A maps to ENST00000381995 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr21:34799242 C>T maps to ENST00000381995 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:34787220 C>T maps to ENST00000381995 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr9:21141433 T>A maps to NM_002177.1 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr3:129183606 C>T maps to NM_052985.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr3:129183549 C>T maps to NM_052985.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr3:129182444 C>G maps to NM_052985.2 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr3:129180116 C>T maps to NM_052985.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:129236438 T>C did not map to a codon.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr3:129233285 G>A maps to NM_052985.2 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:1652540 G>A maps to NM_014714.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr16:1633321 C>T maps to NM_014714.3 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr16:1621493 C>T maps to NM_014714.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr16:1561082 C>T maps to NM_014714.3 P1417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr16:1642225 C>T maps to NM_014714.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr16:1608000 G>A maps to NM_014714.3 H778H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:27684339 C>T maps to NM_015662.1 W746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:27706460 C>T maps to NM_015662.1 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:27680752 C>T maps to NM_015662.1 K1022K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:27712511 C>T maps to NM_015662.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:27695134 G>A maps to NM_015662.1 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr20:42271215 C>T maps to NM_016004.2 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr20:42264607 C>A maps to NM_016004.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:107941067 G>T maps to ENST00000457963 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr9:27056420 A>G maps to NM_025103.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr3:159997001 C>G maps to ENST00000483754 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:160099509 G>A maps to ENST00000326448 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr3:160095272 G>A maps to ENST00000326448 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:160037640 A>G maps to ENST00000483754 C459C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr3:160099294 A>G maps to ENST00000326448 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr3:160025458 G>A maps to ENST00000483754 Y527Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr12:110574582 A>G maps to NM_014055.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:21205186 G>A maps to NM_175605.3 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:69385732 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr23:69354493 C>T did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:65667660 C>A maps to NM_004884.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr15:65623394 C>A maps to NM_004884.3 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr15:65621832 T>G maps to NM_004884.3 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:65624370 T>C maps to NM_004884.3 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:65676727 G>T maps to NM_020962.1 A1124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr15:65703568 C>T maps to NM_020962.1 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr15:65703520 G>A maps to NM_020962.1 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr15:65682658 C>A maps to NM_020962.1 G748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr15:99467896 C>T maps to NM_000875.3 F922F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:99459286 G>C maps to NM_000875.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:99251052 C>A maps to NM_000875.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:99456350 C>T maps to NM_000875.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr15:99251265 G>A maps to NM_000875.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr3:185363332 G>A maps to NM_006548.4 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:23383460 A>T maps to NM_006547.2 L318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:23391087 C>T maps to NM_006547.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr7:23391150 G>C maps to NM_006547.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr6:160505045 A>G maps to NM_000876.2 P1966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr6:160464219 G>A maps to NM_000876.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:160496886 C>T maps to NM_000876.2 G1725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:217528727 G>A maps to NM_000597.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr7:45956910 T>C maps to NM_001013398.1 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr2:217543683 C>T maps to NM_000599.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr2:217543629 C>T maps to NM_000599.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr12:53495920 C>T maps to NM_002178.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr9:38413281 G>C maps to NM_001007563.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:46664117 C>T maps to NM_001002915.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:46543471 C>T maps to NM_001002923.1 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:201195237 C>A maps to NM_001164586.1 I3591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:201193889 C>T maps to NM_001164586.1 L3458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr1:201185879 G>A maps to NM_001164586.1 E3198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:201196110 G>T maps to NM_001164586.1 E3630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr1:201195147 C>T maps to NM_001164586.1 I3561I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr11:68696780 G>A maps to NM_002180.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr11:68696741 C>T maps to NM_002180.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr4:71522210 T>A maps to NM_144646.3 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr22:23237591 G>T maps to ENST00000410090 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:130416469 C>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:130409660 C>T did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr23:130409170 G>C did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr23:130409177 C>G did not map to a codon.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr23:130410971 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr23:130419170 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr23:130416549 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:130410217 G>A did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr23:130412063 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:130416527 A>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:130417183 C>A did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr23:130409626 G>T did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:130415219 T>G did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr23:130408087 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:130411003 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:130413125 C>T did not map to a codon.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr23:130412549 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:130411897 C>T did not map to a codon.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr23:130409573 C>T did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:151155922 C>T maps to NM_178822.4 R2142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:151155346 C>G maps to NM_178822.4 L2334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:151155739 C>T maps to NM_178822.4 V2203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:151154851 A>G maps to NM_178822.4 Y2499Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr3:151166370 C>T maps to NM_178822.4 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:151166889 C>G maps to NM_178822.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:151155337 C>T maps to NM_178822.4 P2337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:151155069 C>A maps to NM_178822.4 E2427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:118621621 G>A maps to NM_152538.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:118621702 T>C maps to NM_152538.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr3:118621616 G>C maps to NM_152538.2 S348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:18741304 C>A maps to NM_173588.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:18743174 T>C maps to NM_173588.3 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr11:18735567 G>T maps to NM_173588.3 Y642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:117208930 C>G maps to NM_001542.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:117158882 G>A maps to NM_001542.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:117158812 G>A maps to NM_001542.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:117150894 C>T maps to NM_001542.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr21:41142993 T>C maps to NM_001080444.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr21:41142936 C>T maps to NM_001080444.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr21:41165459 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr21:41143077 C>A maps to NM_001080444.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:159898078 G>A maps to NM_001135050.1 F1033F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:159897612 G>A maps to NM_001135050.1 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr1:159904571 G>A maps to NM_001135050.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:133792106 G>C maps to NM_014987.1 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:133794769 G>T maps to NM_014987.1 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr11:133789938 G>A maps to NM_014987.1 G1227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:133801413 G>A maps to NM_014987.1 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr2:219925176 G>T maps to NM_002181.3 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr5:140031307 C>T maps to NM_006083.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:99020187 T>C maps to NM_153687.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr12:99007410 C>T maps to NM_201612.1 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr9:111631430 G>A maps to NM_003640.3 N1321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr9:111670655 C>T maps to NM_003640.3 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:111679847 G>T maps to NM_003640.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr9:111656253 A>T maps to NM_003640.3 Y943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:42178272 G>C maps to NM_001556.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:42171929 C>T maps to NM_001556.2 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr8:42176071 C>T maps to NM_001556.2 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:206651634 C>T maps to NM_014002.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:50450283 G>A maps to NM_006060.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr7:50468216 C>T maps to NM_006060.3 H484H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:50450283 G>A maps to NM_006060.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:50467664 G>A maps to NM_006060.3 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:213914593 G>A maps to ENST00000342002 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:213872490 G>A maps to ENST00000342002 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr2:213921698 G>A maps to ENST00000342002 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr2:213921664 G>A maps to ENST00000342002 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr17:37933963 G>A maps to NM_012481.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr17:37922444 G>A maps to NM_012481.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:56429105 G>A maps to NM_022465.3 K583K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:56428580 C>T maps to NM_022465.3 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:56428793 C>T maps to NM_022465.3 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr12:56427055 G>A maps to NM_022465.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:124753990 G>A maps to NM_022466.5 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:206942022 G>A maps to NM_000572.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:117869497 C>A maps to NM_001558.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr21:34640811 C>T maps to ENST00000433395 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr21:34668541 G>A maps to NM_000628.3 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr9:34655638 G>A maps to NM_001142784.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:34660856 G>A maps to NM_001142784.1 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:159711263 G>A maps to NM_000882.2 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:158750295 C>A maps to NM_002187.2 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:18191666 C>T maps to NM_005535.1 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:18179337 T>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:18182997 G>A maps to NM_005535.1 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:18188355 C>A maps to NM_005535.1 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45T-01A-11D-A24D-08 chr1:67787342 C>T maps to NM_001559.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr1:67792497 C>T maps to NM_001559.2 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr1:67855742 C>T maps to NM_001559.2 Q660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:131993988 G>T maps to NM_002188.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:117900504 A>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:117880976 C>A did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:114238662 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:114239800 T>C did not map to a codon.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr23:114239847 C>T did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:114239875 C>T did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:114251808 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr10:6008174 C>T maps to NM_002189.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr15:81585275 A>T maps to NM_172217.3 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr15:81592384 G>A maps to NM_172217.3 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr15:81578131 T>C maps to NM_172217.3 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr15:81592331 C>A maps to NM_172217.3 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr5:148756444 C>T maps to NM_014443.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr13:21295936 C>T maps to NM_138284.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr22:17589872 G>A maps to NM_014339.5 E588E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr22:17578690 C>T maps to NM_014339.5 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr22:17579698 T>A maps to NM_014339.5 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:9972628 T>C did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr22:50439547 C>T maps to NM_001001694.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr2:103003413 C>T maps to NM_003855.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr2:103012988 A>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:103068541 C>T maps to NM_003853.2 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:103067346 G>A maps to NM_003853.2 W417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr2:103053682 C>A maps to NM_003853.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:207013253 C>T maps to NM_153758.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:207010081 C>T maps to NM_153758.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr2:113590981 C>G maps to NM_000576.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr2:113591056 C>T maps to NM_000576.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:113780313 G>C maps to NM_014438.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:113788709 A>G maps to NM_173178.1 Y12Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:113780313 G>A maps to NM_014438.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr2:102636164 C>T maps to NM_004633.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr2:102642599 C>T maps to NM_004633.3 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr3:190362142 C>G maps to NM_002182.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr3:190338139 C>G maps to NM_002182.3 S205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:190362142 C>T maps to NM_002182.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:190326879 G>T maps to NM_002182.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:190363560 C>T maps to NM_002182.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr3:190326945 C>G maps to NM_002182.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr23:29972679 G>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:29414382 C>A did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:29973757 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:29938140 G>T did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr23:29972704 C>G did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:29414434 A>T did not map to a codon.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr23:29417341 G>T did not map to a codon.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr23:29417364 A>G did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:29301227 G>C did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:29686563 C>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:29973486 G>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:29973703 C>G did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr23:29938079 A>G did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr23:29973399 T>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:29417301 A>T did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:29973893 C>T did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:29973722 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:29301113 C>T did not map to a codon.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr23:29973843 G>A did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:28807463 A>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:29301190 T>C did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:29938092 G>A did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:29414439 G>A did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:29973739 G>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:104478564 G>A did not map to a codon.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr23:104728330 C>A did not map to a codon.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr23:104728331 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:105011319 G>T did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr23:104993009 T>C did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr23:104512215 A>C did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:104984566 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:105011307 C>G did not map to a codon.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr23:105011443 T>C did not map to a codon.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr23:105011500 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:104440199 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:104728345 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:104984616 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:105011205 G>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:105011448 G>C did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:104440331 C>A did not map to a codon.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr2:102968038 G>A maps to NM_016232.4 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:113885245 C>T maps to NM_173842.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr4:123373005 T>G maps to NM_000586.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr4:123377562 T>C maps to NM_000586.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr6:137325844 T>A maps to NM_014432.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr6:137323365 C>A maps to NM_014432.2 G331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr3:136714352 G>T maps to NM_144717.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:123542010 A>G maps to NM_021803.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr4:123542010 A>C maps to NM_021803.2 Y52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:123542072 G>A maps to NM_021803.2 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr16:27460060 G>T maps to NM_181079.4 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:68647177 G>T maps to NM_020525.4 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:67724678 A>G maps to NM_144701.2 E586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:207072724 C>A maps to NM_001185156.1 C36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr19:14161618 C>A maps to NM_004843.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:14163008 C>A maps to NM_004843.2 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:39760160 C>T maps to NM_172138.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr19:39735520 C>G maps to ENST00000392072 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr19:39734469 T>G maps to ENST00000392072 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr22:37539601 C>T maps to ENST00000406505 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:37524552 C>T maps to ENST00000406505 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr23:70331332 C>A did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr5:131396410 G>T maps to NM_000588.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:55192205 C>T maps to NM_139017.4 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr5:55192223 G>A maps to NM_139017.4 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:1464239 G>C did not map to a codon.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr23:1471025 C>T did not map to a codon.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr23:1484133 C>T did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr23:1471250 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr23:1471371 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:1467385 C>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:1484091 C>G did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr23:1464251 T>C did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr23:1464253 A>G did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:50394715 G>C maps to NM_172374.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr19:50399113 G>A maps to NM_172374.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr16:27374286 G>A maps to NM_000418.2 E538E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:27367195 C>T maps to NM_000418.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr16:27353503 G>T maps to NM_000418.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr3:3139680 G>A maps to NM_000564.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:35876314 C>T maps to NM_002185.2 C369C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:35876315 C>T maps to NM_002185.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr23:155232634 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:155233354 G>A did not map to a codon.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr23:155227435 C>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:155239823 A>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr23:155233506 G>T did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:155234998 T>A did not map to a codon.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr23:155233407 A>G did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:155235021 A>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:155233457 A>G did not map to a codon.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr23:155239600 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr3:121712218 G>A maps to ENST00000344209 H459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:166890012 G>A maps to NM_199351.2 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:166927158 G>T maps to NM_199351.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:166905900 C>T maps to NM_199351.2 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:166927306 G>A maps to NM_199351.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:166904661 A>T maps to NM_199351.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr1:153640103 G>C maps to NM_004515.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:153642699 G>A maps to NM_004515.2 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:10794208 T>C maps to NM_017620.2 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr19:10791115 G>A maps to NM_017620.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:10793295 G>A maps to NM_017620.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:10789316 C>T maps to NM_017620.2 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr11:6631165 G>A did not map to a codon.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr11:6630567 G>A maps to NM_001014795.1 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr2:239090739 G>T maps to NM_030768.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr19:15226687 G>A maps to NM_006844.3 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr19:15228701 C>T maps to NM_006844.3 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:15226871 C>T maps to NM_006844.3 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:31484807 G>A maps to NM_144981.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:110303747 G>A maps to NM_032549.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr2:86374881 A>G maps to NM_006839.2 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr2:131100504 G>A did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr17:43923105 C>T maps to NM_175882.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr17:43923891 C>T maps to NM_175882.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr8:82572901 C>G maps to NM_001144878.1 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:12028873 C>T maps to NM_014214.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr18:12012167 G>A did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr18:12028067 G>T maps to NM_014214.1 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr18:11999163 C>T maps to NM_014214.1 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:22020583 T>C did not map to a codon.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr7:128034604 C>T maps to NM_000883.3 Q533Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr3:49064206 C>T maps to NM_000884.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr6:76751727 G>A maps to NM_001563.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr6:76751765 C>A maps to NM_001563.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:76744039 G>A maps to NM_001563.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr6:76713617 C>A maps to NM_001563.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:100962534 C>A maps to NM_016247.2 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr3:100963027 G>C maps to NM_016247.2 S716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr3:100963245 C>T maps to NM_016247.2 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr3:100963143 T>C maps to NM_016247.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:100995506 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr3:100964679 C>T maps to NM_016247.2 E503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:62393501 G>T did not map to a codon.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:62321820 T>C maps to NM_176877.2 C744C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr1:62455838 G>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:62503684 C>A maps to NM_176877.2 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:62594529 C>T maps to NM_176877.2 V1728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7596-01A-11D-2229-08 chr1:62274163 C>T maps to NM_176877.2 Q549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr11:61897976 C>T maps to NM_001040694.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr14:105181074 C>A maps to ENST00000252520 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr14:105174313 G>A maps to ENST00000252520 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr14:105174902 G>A maps to ENST00000252520 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr14:105173356 C>G maps to ENST00000252520 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr13:111371618 C>T maps to NM_005537.3 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:111371615 T>C maps to NM_005537.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr7:120590961 A>G maps to NM_019071.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:242662622 A>T did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:242650883 C>T maps to NM_032329.4 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:242648715 G>T maps to NM_032329.4 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:242650890 C>T maps to NM_032329.4 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:220439821 T>C maps to NM_002191.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:220437167 G>A maps to NM_002191.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr7:30791837 C>T maps to NM_006774.4 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:41350927 G>A maps to NM_017553.1 Q632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr15:41276074 G>A maps to NM_017553.1 D1374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr15:41337137 G>C maps to NM_017553.1 L957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr2:74684885 C>T maps to ENST00000452361 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:74684870 G>C maps to ENST00000452361 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:206869166 A>G maps to NM_017759.4 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr2:206884550 C>T maps to NM_017759.4 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr2:99160453 C>T maps to NM_001134224.1 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:99155433 G>A maps to NM_001134224.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr2:99156096 C>A maps to NM_001134224.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:99149903 C>T maps to NM_001134224.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr2:99155442 G>A maps to NM_001134224.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:143081511 C>T maps to NM_003866.2 W521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:143130162 C>A maps to NM_003866.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:143235900 G>T maps to NM_003866.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr10:134464008 G>T maps to NM_005539.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr10:134563022 G>A maps to NM_005539.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:38345770 G>A maps to ENST00000373026 D589D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:233986854 G>A maps to ENST00000359570 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr2:234104108 C>T maps to ENST00000359570 H887H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr2:234112939 G>A maps to ENST00000359570 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr9:139333154 C>A maps to NM_019892.3 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr9:139326413 C>A maps to NM_019892.3 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:71942178 G>A maps to NM_001567.3 W481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr11:71939891 G>A did not map to a codon.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr11:71948272 G>A maps to NM_001567.3 Q995Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:71941166 G>A maps to NM_001567.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:15134051 G>T maps to NM_001031853.3 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr7:155090045 G>A maps to ENST00000344756 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr9:5233852 A>G maps to NM_002195.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr9:5185353 C>T maps to NM_007179.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr20:20350276 C>T maps to NM_002196.2 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr14:36003679 G>T maps to NM_032594.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr14:36004165 C>T maps to NM_032594.3 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr19:7184589 G>A maps to NM_000208.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr19:7117405 G>T maps to NM_000208.2 R1270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:7267737 G>A maps to NM_000208.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:156819089 A>G maps to NM_014215.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr7:1528987 C>T maps to ENST00000389470 V898V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:1526590 G>A maps to ENST00000389470 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:1515968 G>A maps to ENST00000389470 I1972I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr7:1538158 C>T maps to ENST00000389470 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr8:19683949 G>T maps to NM_018142.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr8:19681555 G>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:106604000 G>A maps to NM_020395.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:59968948 C>T maps to NM_020748.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr17:59946708 G>A maps to NM_020748.2 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:59999128 T>C maps to NM_020748.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:153745727 G>A maps to ENST00000428986 V1038V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:153744403 C>T maps to ENST00000428986 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:77602819 G>T maps to NM_033547.3 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:77669820 G>A maps to NM_033547.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:62415547 G>A maps to NM_030628.1 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr11:62414589 G>A maps to NM_030628.1 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr11:62416261 G>A maps to NM_030628.1 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr11:62416623 G>A maps to NM_030628.1 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr13:52026640 C>A maps to NM_012141.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:212120047 C>T did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:212115324 C>T maps to NM_015434.3 V910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr8:95863868 A>G maps to NM_017864.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr8:95866049 C>G maps to NM_017864.2 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr8:95837160 G>A maps to NM_017864.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr8:28625719 G>A maps to NM_018250.3 D640D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr8:28747392 G>A maps to NM_018250.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr8:28651376 G>A maps to NM_018250.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr8:28651412 G>A maps to NM_018250.3 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:128637584 C>T maps to NM_015693.3 T941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr9:103055251 A>T maps to NM_014425.2 R905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr6:33703226 G>A maps to NM_054111.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:33693271 C>T maps to NM_054111.4 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr10:59976031 G>A maps to NM_152230.4 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:59956301 C>T maps to NM_152230.4 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:61747670 C>T maps to NM_001134779.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:61923012 A>G maps to NM_001134779.1 S972S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:44422612 G>A maps to NM_014652.3 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:44415342 C>T maps to NM_014652.3 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:44422117 C>T maps to NM_014652.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:44424509 T>C maps to NM_014652.3 D659D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr14:24652821 G>A maps to ENST00000458132 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:24650799 G>T maps to ENST00000458132 A988A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr14:24649653 G>A maps to ENST00000458132 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr13:98642691 G>A maps to NM_002271.4 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr13:98655278 G>A maps to NM_002271.4 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr11:9456493 C>T maps to NM_006391.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr11:9466642 G>C did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:9466671 A>C maps to NM_006391.2 G1016G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:9462000 G>A did not map to a codon.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr11:9435862 C>T maps to NM_006391.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr11:9451225 G>T maps to NM_006391.2 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr11:9455311 C>T maps to NM_006391.2 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:30783891 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr12:30783829 G>T maps to NM_006390.3 S1026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:30802156 C>A maps to NM_006390.3 G728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr12:30792495 A>G maps to NM_006390.3 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr12:30822216 C>G did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:201839979 C>T maps to NM_018085.4 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:201821286 C>T maps to NM_018085.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr1:46211900 G>T maps to NM_005897.2 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:95405068 C>T maps to NM_022755.5 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr2:237374155 G>A maps to ENST00000457693 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:32673133 G>A maps to NM_001160042.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:2623916 G>A maps to NM_152558.3 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:2645611 C>T maps to NM_152558.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr7:2632712 C>T maps to NM_152558.3 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:197665492 C>T maps to NM_001134435.1 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr3:197665570 C>T maps to NM_001134435.1 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:197665629 C>A maps to NM_001134435.1 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr15:67757466 G>T maps to NM_001031715.2 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr15:67768122 C>A maps to NM_001031715.2 I922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr15:67571826 C>T maps to NM_001031715.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:67555492 C>T maps to NM_001031715.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr3:158980416 C>G maps to NM_001197113.1 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:19838427 C>T maps to NM_153208.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:19775177 A>G maps to NM_153208.1 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr15:91021067 G>T maps to NM_003870.3 V1092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr15:91019983 C>G maps to NM_003870.3 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr15:91030267 C>T maps to NM_003870.3 F1369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr15:91021016 C>A maps to NM_003870.3 V1075V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr15:91029359 G>A maps to NM_003870.3 L1340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr5:75991295 G>A maps to NM_006633.2 T1337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr5:75989260 G>T maps to NM_006633.2 A1329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr5:75906863 C>T maps to NM_006633.2 Y459Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:156500966 C>A maps to NM_178229.4 S1392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:156502887 G>A maps to NM_178229.4 I1329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr1:156510538 G>T maps to NM_178229.4 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr1:156518470 A>T maps to NM_178229.4 L632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:156504952 G>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:156513970 C>T maps to NM_178229.4 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr1:156509199 G>A maps to NM_178229.4 Q1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr1:156499964 G>A maps to NM_178229.4 R1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:12983122 G>C maps to ENST00000429247 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr3:12962068 C>A maps to ENST00000429247 G627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:53276217 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr23:53277967 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr23:53277993 G>C did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:53308796 T>A did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:53279947 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:53268427 G>A did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr12:247992 C>T maps to NM_001170738.1 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr12:247431 G>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr12:248430 C>T maps to NM_001170738.1 C634C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr12:247959 C>T maps to NM_001170738.1 H477H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr7:123143277 G>A maps to NM_178827.4 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:123152339 C>A maps to NM_178827.4 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr7:123152313 G>A maps to NM_178827.4 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr7:123101542 A>T maps to NM_178827.4 C625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr7:123142650 C>T maps to NM_178827.4 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:123097515 G>T maps to NM_178827.4 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:123092826 C>T maps to NM_178827.4 K782K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr23:153278544 C>T did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr23:153284100 C>A did not map to a codon.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr23:153278840 A>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153282472 G>A did not map to a codon.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr23:153283527 G>A did not map to a codon.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr23:153284055 C>T did not map to a codon.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr6:79607894 A>G maps to NM_001010844.1 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr12:66641853 C>G maps to NM_007199.2 S565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr12:44177512 G>T maps to NM_016123.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:44180496 G>A maps to NM_016123.3 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:78758819 A>G maps to NM_004136.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:78765605 A>G maps to NM_004136.2 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr15:78768538 C>T maps to NM_004136.2 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr5:131819735 G>A maps to NM_002198.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:131822062 G>A maps to NM_002198.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:131822537 T>C did not map to a codon.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr5:131822819 G>A maps to NM_002198.2 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr4:185311903 C>G did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr4:185340659 T>C maps to NM_002199.3 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:46387754 C>T maps to NM_015649.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr19:46388990 C>A maps to NM_015649.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr19:46388615 C>T maps to NM_015649.1 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:234745080 C>A maps to NM_182972.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr19:50165478 C>T maps to NM_001571.5 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr19:50165568 C>T maps to NM_001571.5 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr19:50165706 C>T maps to NM_001571.5 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr7:128588063 C>T maps to NM_001098629.1 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:209969691 C>G did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr1:209964160 G>A maps to NM_006147.2 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr1:209965671 G>A maps to NM_006147.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr11:613227 G>A maps to NM_004031.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr11:613569 C>G maps to NM_004031.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr11:613848 T>A maps to NM_004031.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:85953823 C>T maps to NM_002163.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr19:44223567 G>A maps to NM_019612.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr19:44223072 G>A maps to NM_019612.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:44222838 C>A maps to NM_019612.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:44223318 G>A maps to NM_019612.3 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr19:44096354 G>A maps to NM_001007561.2 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:110436744 A>G maps to NM_003749.2 C552C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr13:110435124 C>T maps to NM_003749.2 K1092K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr23:107977583 G>A did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr23:107978637 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:107977921 G>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:107978168 C>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:107977345 G>C did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr23:107979061 G>A did not map to a codon.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr23:107979140 C>T did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:107978578 A>G did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:107978531 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:107978561 G>T did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:107976959 G>A did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:107976980 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:107977791 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:107979237 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:107977074 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:107979423 G>A did not map to a codon.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr23:107976933 G>T did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:107977793 G>C did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:3599662 G>T maps to NM_024337.3 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:3599604 G>C maps to NM_024337.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:3600252 C>T maps to NM_024337.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr5:3600114 G>A maps to NM_024337.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr5:3599487 C>G maps to NM_024337.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr5:2748624 G>A maps to NM_033267.4 N399N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:54319186 C>T maps to NM_024336.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr16:54319354 G>C maps to NM_024336.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:1880912 C>G maps to NM_016358.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr5:1878822 C>A maps to NM_016358.2 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr16:54966558 C>T maps to NM_005853.5 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr16:54965244 C>T maps to NM_005853.5 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr16:55363083 C>T maps to NM_024335.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr16:55360336 C>T maps to NM_024335.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:55362876 C>T maps to NM_024335.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr9:88881056 T>C maps to ENST00000452279 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:108959131 T>C maps to NM_213595.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:949560 C>A maps to NM_005101.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:949533 C>T maps to NM_005101.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:156693182 G>C maps to NM_030980.1 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:156693939 C>T maps to NM_030980.1 Q316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr5:50685738 C>G maps to NM_002202.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:76630853 C>A maps to NM_145805.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr15:76634115 C>A maps to NM_145805.1 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr15:74467615 C>T maps to NM_201526.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:74467468 C>T maps to NM_201526.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr15:74427050 C>T maps to NM_001130137.1 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr20:13280033 C>T maps to NM_080826.1 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr20:13279971 C>T maps to NM_080826.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr20:13260525 C>G maps to NM_080826.1 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr20:13260438 G>A maps to NM_080826.1 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:77942411 G>A maps to NM_199296.2 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:77944600 C>A maps to NM_199296.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr14:77941988 G>A maps to NM_199296.2 N555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr5:128430635 C>T maps to NM_016048.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr19:55966721 C>T maps to NM_024710.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:18545773 G>A maps to NM_016368.4 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:18548555 G>A maps to NM_016368.4 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr20:33033214 T>C maps to ENST00000262650 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr20:33077106 A>G maps to ENST00000262650 E751E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:47488013 G>A maps to NM_030790.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr16:47196539 G>A maps to NM_030790.3 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:2929960 G>A maps to NM_018463.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:312519 C>G maps to NM_032039.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr16:304624 G>A maps to NM_032039.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr5:52201635 C>G maps to NM_181501.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:145538041 C>A maps to NM_003637.3 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr1:145533499 C>T maps to NM_003637.3 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr15:68623326 C>T maps to ENST00000423218 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:68624318 G>A maps to ENST00000423218 R550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:52344593 G>A maps to NM_002203.3 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:52347332 G>A maps to NM_002203.3 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr5:52366017 T>C maps to NM_002203.3 N721N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr5:52376452 T>C did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr5:52361765 C>T maps to NM_002203.3 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:52361759 C>T maps to NM_002203.3 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr5:52360896 A>G maps to NM_002203.3 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:42457387 G>A maps to NM_000419.3 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:42452041 G>A maps to NM_000419.3 P976P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr17:48166565 G>A maps to NM_005501.2 G1046G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:48148224 C>T maps to NM_002204.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:48154039 G>A maps to NM_002204.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:182392029 A>G maps to NM_000885.4 V782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:182387034 C>T maps to NM_000885.4 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:182363381 A>C maps to NM_000885.4 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:182347239 G>A did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr2:182346358 G>A maps to NM_000885.4 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:54797969 T>A maps to NM_002205.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr12:54797555 T>C maps to NM_002205.2 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:56094760 G>A maps to ENST00000347027 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:56089325 C>T maps to ENST00000347027 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr12:56091492 G>A maps to ENST00000347027 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:56078979 C>T maps to ENST00000347027 K1136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr12:56078993 G>A maps to ENST00000347027 R1132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr12:56086663 T>G maps to ENST00000347027 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:15617508 T>C maps to NM_003638.1 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr10:15590479 G>A maps to NM_003638.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr10:15559212 G>A maps to NM_003638.1 Q1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr10:15649677 G>A maps to NM_003638.1 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr10:15760876 C>T maps to NM_003638.1 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr10:15700996 C>T did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr10:15726023 C>A maps to NM_003638.1 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr3:37555267 C>T maps to NM_002207.2 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:37514890 C>G maps to NM_002207.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:37860478 G>A maps to NM_002207.2 *1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:37523000 C>T maps to NM_002207.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr16:31404707 G>A maps to ENST00000444228 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr16:31419084 A>T maps to ENST00000316569 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:31421726 C>T maps to ENST00000444228 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:3658513 G>T maps to NM_002208.4 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr16:30510406 G>A maps to NM_002209.2 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr16:30492808 C>G maps to NM_002209.2 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr16:30522384 C>G maps to NM_002209.2 S905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr16:30525151 C>T maps to NM_002209.2 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:30490650 G>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr16:30518131 G>C maps to NM_002209.2 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr16:30518143 G>A maps to NM_002209.2 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45T-01A-11D-A24D-08 chr16:30531236 C>T maps to NM_002209.2 S1096S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr16:30490667 C>T maps to NM_002209.2 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:30495264 C>T maps to NM_002209.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:31342509 G>T maps to NM_001145808.1 E1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:31332572 C>A maps to NM_001145808.1 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr16:31308839 C>T maps to NM_001145808.1 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr16:31308945 C>T maps to NM_001145808.1 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr16:31336819 G>C did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr16:31282332 C>T maps to NM_001145808.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:187455217 C>T maps to NM_002210.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr2:187506310 C>T maps to NM_002210.3 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr10:33200865 G>A maps to ENST00000374956 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:33199264 G>A maps to ENST00000374956 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr10:33199208 A>C maps to ENST00000374956 Y702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr10:33200430 G>A maps to ENST00000374956 Q626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr23:70524108 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:70523355 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr23:70523744 A>C did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:70523726 G>T did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:70524840 C>G did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:3938599 G>C did not map to a codon.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr19:3942081 C>T maps to NM_170678.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr21:46320372 G>A maps to NM_000211.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr21:46320234 G>A maps to NM_000211.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr21:46320381 G>A maps to NM_000211.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:45361914 C>T maps to NM_000212.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:73751848 A>C maps to NM_001005619.1 T1525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr17:73748647 C>T maps to NM_001005619.1 S1366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr17:73753344 C>T maps to NM_001005619.1 S1744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:73751884 G>A maps to NM_001005619.1 E1537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr17:73725496 C>T maps to NM_001005619.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr17:73729738 C>T maps to NM_001005619.1 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:73738819 C>T maps to NM_001005619.1 N980N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:73748587 C>T maps to NM_001005619.1 F1346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:124515328 G>A maps to NM_002213.3 C533C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr3:124540207 G>A maps to NM_002213.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr2:161029175 A>G maps to NM_000888.3 H275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr2:160983071 G>A maps to NM_000888.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:161052753 G>A maps to NM_000888.3 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr2:161030574 G>A maps to NM_000888.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:160994113 C>G maps to NM_000888.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr2:160994680 T>C maps to NM_000888.3 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:53589184 C>T maps to NM_000889.1 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr12:53589908 G>A maps to NM_000889.1 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:20421483 C>T maps to NM_002214.2 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:20403257 A>T did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:20371491 A>T maps to NM_002214.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:20441435 C>T maps to NM_002214.2 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:52825551 C>T maps to NM_002215.2 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr3:52819103 T>C maps to NM_002215.2 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:52823858 G>A maps to NM_002215.2 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:7773949 G>A maps to NM_002216.2 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr10:7765487 C>T maps to NM_002216.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr10:7765478 C>T maps to NM_002216.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr10:7763676 G>A maps to NM_002216.2 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr10:7786081 G>A maps to NM_002216.2 K749K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr3:52860946 G>A maps to ENST00000485816 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:52858009 G>A maps to ENST00000485816 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr3:52858521 G>C maps to ENST00000485816 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:7708843 C>A maps to ENST00000256861 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:7683945 C>T maps to ENST00000256861 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:7684024 G>C maps to ENST00000256861 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:54814943 A>T did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr23:54783976 T>C did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:54823473 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:54785153 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:54784244 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:54818414 C>T did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:54780192 G>T did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr23:54784136 C>T did not map to a codon.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr23:54784568 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr23:54784514 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr23:54784494 G>C did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr23:54784524 G>C did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:54785329 T>C did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:54814981 C>A did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:54817503 C>T did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr5:156668656 C>T maps to NM_005546.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:160853236 G>A maps to NM_017625.2 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr1:160920895 A>G maps to NM_080878.2 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr23:78616958 A>C did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:78616843 G>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:78616912 G>A did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:78616832 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:78622601 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr23:78616622 T>G did not map to a codon.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr23:78618172 G>C did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:231742260 G>A maps to NM_030926.4 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr2:231740462 C>T maps to NM_030926.4 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr20:3202540 C>T maps to NM_033453.2 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr14:93483110 G>A maps to NM_014216.4 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr14:93412778 G>A maps to NM_014216.4 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr14:93408121 G>A maps to NM_014216.4 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr15:41795315 G>A maps to NM_002220.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr1:226822563 G>A maps to NM_002221.3 F883F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:41235182 G>A maps to NM_025194.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr19:41223946 T>C maps to NM_025194.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr3:4687339 C>T maps to ENST00000356617 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr3:4774815 C>T maps to ENST00000356617 N1751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:4715982 A>C maps to ENST00000356617 R848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr3:4725401 G>T maps to ENST00000356617 E1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr12:26808651 G>A maps to NM_002223.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:26580956 C>A maps to NM_002223.2 L2278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr12:26818844 G>A maps to NM_002223.2 Q517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr12:26750064 C>T maps to NM_002223.2 L1335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:26985672 G>A maps to NM_002223.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr12:26493138 G>C maps to NM_002223.2 V2660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr12:26493170 G>A maps to NM_002223.2 Q2650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr12:26493216 G>A maps to NM_002223.2 L2634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:33662852 C>G maps to ENST00000374316 L2646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:33636357 C>G maps to ENST00000374316 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:33660554 C>T maps to ENST00000374316 I2503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:33660548 C>T maps to ENST00000374316 F2501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:33658767 C>T maps to ENST00000374316 I2369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:33658768 C>T maps to ENST00000374316 L2370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:33633650 C>A maps to ENST00000374316 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:33659605 G>A maps to ENST00000374316 R2453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr6:33638302 C>G maps to ENST00000374316 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr6:33660554 C>T maps to ENST00000374316 I2503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr10:106075038 G>A maps to NM_033397.2 C257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr10:106074552 C>T maps to NM_033397.2 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:106074456 C>T maps to NM_033397.2 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr2:96993391 C>G maps to ENST00000420728 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr16:19126187 C>A maps to NM_001034841.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr21:35190746 C>G maps to NM_003024.2 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:35257785 C>T maps to NM_003024.2 N1601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:24484449 A>T maps to NM_006277.2 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr2:24432686 C>T maps to NM_006277.2 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:24484539 T>A maps to NM_006277.2 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr2:24484593 T>A maps to NM_006277.2 V791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:24433774 G>A maps to NM_006277.2 S1377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:152883949 G>T maps to NM_005547.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:152883938 C>T maps to NM_005547.2 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:152882572 A>G maps to NM_005547.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:152882593 G>A maps to NM_005547.2 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr1:185277929 A>G did not map to a codon.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:128262664 G>A maps to NM_017969.2 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr2:128262821 A>G maps to NM_017969.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr6:150710599 C>G maps to NM_203395.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr20:10626067 G>A maps to NM_000214.2 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr20:10653369 C>G maps to NM_000214.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr20:10625899 G>A maps to NM_000214.2 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:10653357 G>A maps to NM_000214.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:10620403 C>T maps to NM_000214.2 T1133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr20:10632824 A>G maps to NM_000214.2 Y320Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr20:10622311 G>A maps to NM_000214.2 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:10625547 G>A maps to NM_000214.2 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:105612754 G>A maps to NM_002226.3 C892C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr14:105609912 G>A maps to NM_002226.3 I1049I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr14:105618507 G>C maps to NM_002226.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr14:105609256 C>T maps to NM_002226.3 A1164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr1:65300340 C>T did not map to a codon.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:65332749 C>T maps to NM_002227.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:65301897 C>T maps to NM_002227.2 W1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr1:65303625 G>A maps to NM_002227.2 S1043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:5029861 C>T maps to NM_004972.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr9:5065040 G>A did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr19:17942158 G>T maps to NM_000215.3 A952A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:17941380 G>A maps to NM_000215.3 D1009D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:17950352 C>T maps to NM_000215.3 W458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr19:17951089 G>A maps to NM_000215.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr4:6082015 C>T maps to NM_001099433.1 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:6114559 C>G maps to NM_001099433.1 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr4:6082003 C>T maps to NM_001099433.1 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr5:147012313 G>T maps to NM_014790.3 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr5:147040882 C>A maps to NM_014790.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr5:147020327 G>T maps to NM_014790.3 S447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:133946814 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:133930804 C>G maps to NM_001105521.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr10:133966475 G>A maps to NM_001105521.2 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:27078351 T>C maps to NM_021219.2 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr21:27062253 C>T maps to NM_021219.2 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr11:134014828 C>A maps to NM_032801.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:15468902 G>T maps to NM_004973.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr6:15501414 A>T maps to NM_004973.2 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr7:139796487 G>A maps to NM_030647.1 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr10:64975453 T>C maps to NM_032776.1 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:27221929 A>G maps to NM_001145348.1 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr16:27221653 G>A maps to NM_001145348.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:74720007 G>A maps to NM_001081461.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:42132976 C>T maps to NM_005090.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:42133452 C>T maps to NM_005090.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:42134774 G>A maps to NM_005090.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:42138473 C>T maps to NM_005090.3 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr15:42133426 A>G did not map to a codon.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr15:42135876 G>A maps to NM_005090.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr5:78585954 G>A maps to NM_152405.4 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr5:78610396 A>G maps to NM_152405.4 E794E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr22:39085049 C>T maps to NM_014876.5 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr19:51009450 G>A maps to NM_138334.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr8:75157338 C>A maps to NM_020647.2 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:75227562 G>C maps to NM_020647.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr16:87678467 G>A maps to NM_020655.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr16:87724056 C>T maps to NM_020655.2 F697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr16:87678389 C>T maps to NM_020655.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr14:24045141 G>A maps to NM_032452.2 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:24040172 G>A maps to NM_032452.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:143746148 C>T maps to NM_003724.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:2254198 C>T maps to NM_144616.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr14:23451249 G>A maps to NM_032876.4 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr14:23451382 G>A maps to NM_032876.4 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr14:23451168 G>A maps to NM_032876.4 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr14:23447603 G>A maps to NM_032876.4 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr14:23450640 C>A maps to NM_032876.4 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr14:23450598 G>A maps to NM_032876.4 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr14:23451168 G>A maps to NM_032876.4 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr14:23445918 G>A maps to NM_032876.4 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr14:23444313 C>A did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr14:23447576 G>A maps to NM_032876.4 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr14:23444270 G>A maps to NM_032876.4 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr14:23444313 C>G did not map to a codon.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:12903301 C>T maps to NM_002229.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr19:18391913 C>T maps to NM_005354.4 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr17:39921283 G>A maps to NM_021991.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr23:8521999 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:8503690 C>T did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:8536378 G>A did not map to a codon.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr3:124207130 C>T maps to NM_001024660.3 A1453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr3:124418864 C>T maps to NM_001024660.3 R2661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr3:124418864 C>T maps to NM_001024660.3 R2661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr3:124157745 C>G maps to NM_001024660.3 V1018V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:123987645 G>A maps to NM_001024660.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:124053323 C>T maps to NM_001024660.3 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr3:124103784 C>T maps to NM_001024660.3 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr3:124390516 G>A maps to NM_001024660.3 S2237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr3:124418864 C>T maps to NM_001024660.3 R2661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:124114061 G>C maps to NM_001024660.3 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr3:124418864 C>T maps to NM_001024660.3 R2661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:738305 C>T maps to NM_015158.2 Q1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr9:713054 G>A maps to NM_015158.2 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:11283761 G>A maps to NM_015493.6 Y710Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr19:11280801 G>A maps to NM_015493.6 C786C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:11304260 T>C maps to NM_015493.6 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr19:11280794 C>A maps to NM_015493.6 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr19:11304608 G>A maps to NM_015493.6 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr19:8387791 A>T maps to NM_198471.2 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:8389335 G>T maps to NM_198471.2 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr19:8389621 C>T maps to NM_198471.2 Q725Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:62740601 G>A maps to NM_181712.4 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr1:62740511 G>A maps to NM_181712.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:62728767 C>T maps to NM_181712.4 E845E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:62703987 C>T maps to NM_181712.4 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:75665699 C>T maps to NM_001130089.1 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr17:40269509 C>T maps to NM_021078.2 K511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr17:40272334 G>A maps to NM_021078.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr3:20082193 C>T maps to NM_003884.4 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:20113934 T>C maps to NM_003884.4 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr11:65482117 C>T maps to NM_182710.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:65486585 C>G maps to NM_182710.1 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr6:149944271 T>C maps to NM_007044.2 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr6:149918670 C>T maps to NM_007044.2 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:30804673 G>A maps to NM_032116.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr16:57786824 C>T maps to NM_005886.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr16:57785853 C>G maps to NM_005886.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:15392163 G>A maps to NM_201628.2 K379K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:14925657 C>T maps to NM_201628.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:15287294 C>T maps to NM_201628.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr1:15287306 C>G maps to NM_201628.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:127642956 G>A maps to NM_207335.2 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr3:127703067 C>T maps to NM_207335.2 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:65370406 C>T maps to NM_001101362.2 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:32908968 T>C maps to NM_015483.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr7:32909364 G>A maps to NM_015483.2 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr11:47594880 C>T maps to NM_018095.4 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:47595030 A>G maps to NM_018095.4 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr3:42727526 C>T maps to NM_152393.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr3:67049504 C>G maps to NM_032505.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:67058733 G>T maps to NM_032505.2 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:67058493 T>C maps to NM_032505.2 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:85280507 T>C maps to NM_020122.4 N374N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr12:5021956 C>G maps to NM_000217.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:5021761 C>T maps to NM_000217.2 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr1:111146156 G>A maps to NM_004974.2 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr1:111147062 C>T maps to NM_004974.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:111217038 G>T maps to NM_002232.3 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr1:111217011 G>A maps to NM_002232.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:111216579 G>A maps to NM_002232.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:111217119 C>T maps to NM_002232.3 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:30033430 G>T maps to NM_002233.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:30034072 G>C maps to NM_002233.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr11:30033733 G>A maps to NM_002233.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr11:30032995 G>C maps to NM_002233.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:30033106 G>A maps to NM_002233.2 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr11:30032605 G>A maps to NM_002233.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr12:5153735 C>T maps to NM_002234.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:5154797 C>T maps to NM_002234.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:5155094 G>A maps to NM_002234.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr12:4920107 T>C maps to NM_002235.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:4919507 C>T maps to NM_002235.3 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr12:4919816 C>T maps to NM_002235.3 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:4919518 C>A maps to NM_002235.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr19:49575539 C>T maps to NM_031886.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr19:49573903 G>T maps to NM_031886.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr3:155838564 C>G maps to NM_172160.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:7831113 G>T maps to NM_004732.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr20:47991214 G>A maps to NM_004975.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr20:47991217 G>A maps to NM_004975.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:47991508 G>A maps to NM_004975.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr20:47990323 G>A maps to NM_004975.2 F591F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr8:73480043 G>T maps to NM_004770.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr8:73480478 C>A maps to NM_004770.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr8:73849914 G>T maps to NM_004770.2 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:73848927 C>T maps to NM_004770.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr8:73479974 A>T maps to NM_004770.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr8:73849152 C>T maps to NM_004770.2 H521H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:73848741 T>C maps to NM_004770.2 Y384Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr8:73849038 C>T maps to NM_004770.2 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:73849533 C>T maps to NM_004770.2 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr8:73849809 C>T maps to NM_004770.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:73480223 C>T maps to NM_004770.2 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr8:73848456 C>T maps to NM_004770.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr11:17793669 C>T maps to NM_001112741.1 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr11:17793573 C>T maps to NM_001112741.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:17793576 C>T maps to NM_001112741.1 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr11:17757968 C>T maps to NM_001112741.1 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr12:75601538 G>A maps to NM_139137.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr12:75444701 G>T maps to NM_139137.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr12:75436119 C>T maps to NM_139136.2 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:75601706 G>A maps to NM_139137.2 H19H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:75444682 G>A maps to NM_139137.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:75436911 A>G maps to NM_139137.2 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:75601547 G>A maps to NM_139137.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:75444617 C>T maps to NM_139137.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr19:50831718 G>A maps to NM_004977.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:110765815 C>T maps to NM_004978.4 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:48822581 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:48826246 G>T did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:48826592 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:48826200 G>A did not map to a codon.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:120386012 T>C maps to NM_012281.2 H549H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr7:120373043 T>A maps to NM_012281.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr7:119915021 C>T maps to NM_012281.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:119915561 C>T maps to NM_012281.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:112524370 G>A maps to ENST00000315987 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr11:74168572 C>T maps to NM_005472.4 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr2:223918015 C>T maps to NM_080671.2 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr2:11053826 C>T maps to NM_002236.4 H425H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr20:49626746 C>T maps to NM_002237.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:49620944 G>A maps to NM_002237.3 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr18:77659521 C>T maps to NM_012283.1 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr18:77623924 C>T maps to NM_012283.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr18:77659746 G>A maps to NM_012283.1 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr2:42671136 A>G maps to NM_133329.5 Y416Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr16:84256344 G>A maps to NM_172347.2 Y346Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K0-01B-21D-A31L-08 chr16:84255939 G>A maps to NM_172347.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:84256560 G>A maps to NM_172347.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr16:84255843 G>A maps to NM_172347.2 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:211192355 G>A maps to NM_172362.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr1:210857105 G>A maps to NM_172362.2 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:150644573 G>A maps to NM_000238.2 F998F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr7:150648845 G>A maps to NM_000238.2 Y545Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:150648076 G>A maps to NM_000238.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr12:49942696 C>T maps to NM_012284.1 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:49942876 C>T maps to NM_012284.1 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr12:49934899 C>T maps to NM_012284.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:49943927 G>A maps to NM_012284.1 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:49951476 C>G maps to NM_012284.1 S998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr12:49934892 G>A maps to NM_012284.1 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr17:40315276 C>T maps to NM_012285.2 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr17:40322230 C>T maps to NM_012285.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:40315718 G>A maps to NM_012285.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr17:40318342 G>C maps to NM_012285.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:40315820 G>A maps to NM_012285.2 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:63174447 G>A maps to NM_139318.3 H915H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr14:63174642 C>T maps to NM_139318.3 E850E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr14:63453788 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:63269169 G>A maps to NM_139318.3 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:63269170 G>A maps to NM_139318.3 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:63417205 C>T maps to NM_139318.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr17:61613163 G>A maps to NM_030779.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr17:61621725 C>T maps to NM_030779.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:61611638 C>T maps to NM_030779.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:163280004 A>T maps to NM_033272.2 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:163292053 G>T maps to NM_033272.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr3:19295144 G>C did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr3:19554769 G>A maps to NM_144633.2 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:19575323 G>A maps to NM_144633.2 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr3:19479725 G>A maps to NM_144633.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr5:170148873 C>T maps to NM_001034837.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr10:103587991 C>G maps to NM_014591.4 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr4:20852191 G>A maps to ENST00000382152 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:20884282 G>A maps to ENST00000382152 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:20734305 G>A maps to ENST00000382152 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:128709439 T>A maps to NM_000220.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr11:128710111 G>A maps to NM_000220.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:17409545 C>T maps to NM_000525.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr17:21319814 C>T maps to NM_021012.4 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:21318731 G>C maps to NM_021012.4 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr17:21319865 C>T maps to NM_021012.4 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:21318737 C>T maps to NM_021012.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr17:21319643 G>T maps to NM_021012.4 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr17:21319682 G>A maps to NM_021012.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr21:39671930 C>T maps to NM_170736.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr21:39671653 G>A maps to NM_170736.1 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr17:68129079 T>C maps to NM_018658.1 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr17:68172220 T>G maps to NM_000891.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr17:68171809 G>A maps to NM_000891.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:155566302 C>T maps to NM_002239.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:155555718 C>A maps to NM_002239.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:155555406 G>A maps to NM_002239.2 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:155566131 G>A maps to NM_002239.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr2:155711566 C>A maps to NM_002239.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr22:38823813 C>T maps to NM_152868.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr22:38824020 C>T maps to NM_152868.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:38823411 G>A maps to NM_152868.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:38823924 G>C maps to NM_152868.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr11:128782055 G>A maps to NM_000890.3 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:128781746 C>G maps to NM_000890.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr11:128782076 C>T maps to NM_000890.3 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr11:128781854 C>T maps to NM_000890.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr21:39086694 C>T maps to NM_002240.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr12:21918776 G>A maps to NM_004982.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr12:21918865 G>A maps to NM_004982.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr12:21918982 C>A maps to NM_004982.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr12:21919121 C>T maps to NM_004982.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:233750264 C>T maps to NM_002245.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:233807017 T>C maps to NM_002245.3 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr1:233802461 C>T maps to NM_002245.3 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr14:88658718 G>T maps to NM_138318.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:88707124 C>A maps to NM_138318.2 G148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr14:88658748 C>T maps to NM_138318.2 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr14:90651010 G>C maps to NM_022054.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr20:43379004 C>T maps to ENST00000372861 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:43374745 G>A maps to ENST00000372861 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:43378791 T>C maps to ENST00000372861 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:39272354 G>C maps to NM_031460.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr10:118969310 C>G maps to NM_181840.1 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr10:118969464 T>C maps to NM_181840.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr10:118969449 C>T maps to NM_181840.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:215345467 C>T maps to NM_001017425.2 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr1:215408400 C>T maps to NM_001017425.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:64067023 C>A maps to ENST00000422670 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr11:64067044 C>T maps to ENST00000422670 N368N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:65360634 G>C maps to NM_033347.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr8:140631106 G>A maps to NM_016601.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr8:140630758 G>A maps to NM_016601.2 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr8:140630971 C>T maps to NM_016601.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr8:140631259 C>T maps to NM_016601.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr8:140631259 C>T maps to NM_016601.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:78669855 T>C did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:78846272 G>A maps to NM_001161352.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:78729806 G>C maps to NM_001161352.1 S762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr10:79163661 C>A maps to NM_001161352.1 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr10:78708932 C>T maps to NM_001161352.1 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:169812328 G>A maps to NM_004137.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr5:169810823 C>A maps to NM_004137.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr5:169805749 C>T maps to NM_004137.2 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:169805800 G>A maps to NM_004137.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr5:169805869 T>A maps to NM_004137.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr3:178543543 G>A maps to NM_005832.3 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr3:178968831 C>T maps to NM_014407.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr5:113831872 T>C maps to NM_021614.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr5:113699623 C>T maps to NM_021614.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr5:113829156 G>A maps to NM_021614.2 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:113831599 C>T maps to NM_021614.2 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr5:113798814 C>G maps to NM_021614.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr5:113740538 C>T maps to NM_021614.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:113822856 C>T maps to NM_021614.2 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:154841648 T>C maps to NM_002249.4 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:2604771 A>T maps to NM_000218.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr11:2594161 C>T maps to NM_000218.2 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:62038283 C>A maps to NM_172107.2 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr8:133144492 G>C maps to NM_004519.2 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:133142132 C>A maps to NM_004519.2 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr8:133196523 G>T maps to NM_004519.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr6:73904677 C>T maps to NM_001160133.1 V799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr6:73787198 A>G maps to NM_001160133.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr20:43726836 C>T maps to NM_002251.3 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr8:99441163 G>A maps to NM_020697.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr2:18112571 C>T maps to NM_002252.3 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr2:18113211 C>T maps to NM_002252.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:138662903 G>T maps to ENST00000298480 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:138667191 C>T maps to ENST00000298480 I760I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:138662201 G>T maps to ENST00000298480 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr1:196205129 C>T maps to NM_198503.2 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:196309571 G>T maps to NM_198503.2 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:196309632 G>A maps to NM_198503.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:196197395 G>T maps to NM_198503.2 C1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr1:196309632 G>A maps to NM_198503.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:196342280 G>A maps to NM_198503.2 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:196434490 A>G maps to NM_198503.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:196461470 C>T maps to NM_198503.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr8:36673193 C>G maps to NM_001031836.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr8:36766905 G>A maps to NM_001031836.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:110980589 G>A maps to NM_014379.2 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr8:110980373 C>T maps to NM_014379.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr8:110984517 C>A maps to NM_014379.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:110984838 G>T maps to NM_014379.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:110980753 C>A maps to NM_014379.2 G356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:110980737 G>C maps to NM_014379.2 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr8:110980397 C>A maps to NM_014379.2 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr9:2718221 C>G maps to NM_133497.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr9:2718572 G>A maps to NM_133497.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr9:2717792 G>A maps to NM_133497.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:24035850 C>T maps to NM_001142730.1 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr13:77460091 G>A maps to NM_138444.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:29934633 G>C maps to NM_178863.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:29923280 C>T maps to NM_178863.2 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr16:29937219 C>T maps to NM_178863.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr5:143586984 T>A maps to NM_020768.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr16:67325247 G>A maps to NM_001100915.1 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr16:67335718 G>C maps to NM_001100915.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr16:67338384 C>T maps to NM_001100915.1 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:67328008 C>T maps to NM_001100915.1 K552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr16:67327849 A>G maps to NM_001100915.1 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr6:36449468 G>C maps to NM_173562.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:215752340 A>G did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr1:215777531 G>A maps to NM_016121.3 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr7:66103259 G>A maps to ENST00000451741 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr4:44449817 G>A maps to NM_198353.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr4:44450255 C>T maps to NM_198353.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr4:44177040 T>A maps to NM_198353.2 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:44450345 G>C maps to NM_198353.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:44176944 C>T maps to NM_198353.2 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr4:44177256 C>T maps to NM_198353.2 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr13:103441562 A>C maps to NM_024089.2 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr11:108350192 G>T maps to NM_153705.4 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr11:108348423 T>C maps to NM_153705.4 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:48887691 C>T maps to NM_006801.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:23385656 A>G maps to NM_001009999.2 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr6:18207750 C>T maps to ENST00000388870 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr6:18160203 C>T maps to ENST00000388870 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:66985218 C>T maps to NM_012308.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:66985206 C>T maps to NM_012308.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:66986771 T>C maps to NM_012308.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:121881865 C>T maps to ENST00000377071 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr12:122012497 C>T maps to ENST00000377071 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:121947474 C>T maps to ENST00000377071 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr12:121880093 G>T maps to ENST00000377071 P1050P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:121986849 C>T maps to ENST00000377071 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr12:121880318 C>T maps to ENST00000377071 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr12:121880534 C>T maps to ENST00000377071 K903K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:86716519 C>G maps to NM_001146688.1 V1131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr2:86705090 T>A maps to NM_001146688.1 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:137754820 G>A maps to NM_016604.3 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:137727660 G>A maps to NM_016604.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:137726868 G>A maps to NM_016604.3 Q516Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr5:137727715 C>T maps to NM_016604.3 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr5:137762665 C>T maps to NM_016604.3 R1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:44156524 G>T maps to NM_014663.2 G683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr1:44133691 T>C did not map to a codon.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr19:5133892 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:5082395 G>T maps to NM_015015.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr19:5047506 C>T maps to NM_015015.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:94731016 C>T maps to NM_018039.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr12:475138 G>C maps to NM_001042603.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:438015 C>T maps to NM_001042603.1 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr12:427288 C>T maps to NM_001042603.1 K960K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:459894 G>A maps to NM_001042603.1 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:202702866 G>A maps to ENST00000367264 Q1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:202710589 C>A maps to ENST00000367264 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr1:202698873 G>A maps to ENST00000367264 I1522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr1:202698922 G>T maps to ENST00000367264 S1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr23:53246349 C>G did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:53230782 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr23:53239930 C>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:53225147 C>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:53243983 C>T did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:53239926 C>A did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr23:53224436 T>C did not map to a codon.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr23:53223010 C>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr24:21869832 T>A did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr24:21877709 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr24:21869119 G>T did not map to a codon.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr23:44929601 G>T did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr23:44870204 G>A did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr23:44938389 G>C did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:44949093 T>A did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr23:44942703 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr23:44910974 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:44929077 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:44929078 G>T did not map to a codon.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr23:44918552 C>T did not map to a codon.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr23:44942797 A>G did not map to a codon.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr23:44879904 G>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:44969462 A>G did not map to a codon.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr23:44922693 C>T did not map to a codon.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr23:44922693 C>T did not map to a codon.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr23:44913195 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr23:44945194 C>A did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:44928825 G>A did not map to a codon.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr17:7755571 G>A maps to NM_001080424.1 V1462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr17:7751610 C>T maps to NM_001080424.1 R669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:7752017 C>G maps to NM_001080424.1 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:7753195 G>A maps to NM_001080424.1 V1166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr17:7752800 G>A maps to NM_001080424.1 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr17:7750718 T>C maps to NM_001080424.1 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:7755267 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr4:55968136 G>A maps to NM_002253.2 D731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr4:55970954 G>T maps to NM_002253.2 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr18:61027013 C>A maps to NM_002035.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr18:61018258 G>A maps to NM_002035.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr19:10602731 C>T maps to NM_203500.1 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:10610148 G>A maps to NM_203500.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr19:10610309 C>A maps to NM_203500.1 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr19:10610553 G>A maps to NM_203500.1 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:142640670 G>T maps to NM_000420.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr7:142638422 G>A maps to NM_000420.2 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:73952216 G>A maps to ENST00000370385 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr6:73951451 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:62604605 C>A maps to NM_152688.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr6:62604556 C>A maps to NM_152688.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:62442585 C>A did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr19:6416662 T>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:6416878 A>C maps to NM_003685.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr1:19577910 A>G maps to NM_015047.1 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:19559126 C>T maps to NM_015047.1 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr1:19547304 C>T maps to NM_015047.1 K875K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr17:26962071 G>A maps to NM_014680.2 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:26942795 G>A maps to NM_014680.2 D2137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr17:26960317 G>A maps to NM_014680.2 N1189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr17:26962165 C>A maps to NM_014680.2 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr17:26948138 G>A maps to NM_014680.2 I1703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr17:26955287 G>T maps to NM_014680.2 S1530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr17:26960083 G>A maps to NM_014680.2 V1227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr5:141316761 G>T did not map to a codon.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr8:48309051 G>C maps to NM_001080394.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr8:48353026 G>C maps to NM_001080394.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr17:73481510 C>T maps to ENST00000375248 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr8:126059560 G>A maps to ENST00000377985 Q803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr8:126062853 G>A maps to ENST00000377985 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:126061385 G>A maps to ENST00000377985 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:126059446 A>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:126059483 T>C maps to ENST00000377985 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr3:197402347 C>T maps to NM_014687.1 Q895Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:197427592 G>A maps to NM_014687.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:197432013 G>A maps to NM_014687.1 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr6:42796800 C>T maps to NM_015349.1 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7593-01A-11D-2229-08 chr14:105349546 T>C maps to ENST00000453495 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:105353440 C>T maps to ENST00000453495 D956D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:75150017 G>A maps to NM_001039479.1 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr14:75142546 C>T maps to NM_001039479.1 W312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:24570135 G>A maps to NM_014809.3 H662H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr6:24566859 G>A maps to NM_014809.3 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:24596342 G>A maps to NM_014809.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr6:24572863 C>T maps to NM_014809.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:35917292 G>T maps to NM_024874.4 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:35921703 G>A maps to NM_024874.4 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:35907887 G>A maps to NM_024874.4 A943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:35944660 G>A maps to NM_024874.4 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr1:35900554 G>C maps to NM_024874.4 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:35936544 G>A maps to NM_024874.4 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr19:34843625 C>T maps to NM_014686.3 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:114134892 G>A maps to NM_001080398.1 I1626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr14:35593113 C>T maps to NM_014672.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr14:35592828 A>G maps to NM_014672.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr14:35593230 A>C maps to NM_014672.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:35595979 C>T maps to NM_014672.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr20:36631032 C>T maps to NM_014657.1 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:36641078 G>A maps to NM_014657.1 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr6:127771047 T>C did not map to a codon.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr6:127768851 T>C maps to NM_014702.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr6:127767858 A>G maps to NM_014702.4 N535N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr6:127768623 C>T maps to NM_014702.4 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:4830307 G>A maps to ENST00000450194 W1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr7:4828506 C>T maps to ENST00000450194 A1255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr7:4820886 C>T maps to ENST00000450194 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr16:15718916 C>T maps to NM_014647.3 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr16:15694393 G>C maps to NM_014647.3 L1568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:15715621 G>A maps to NM_014647.3 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:15705497 G>A maps to NM_014647.3 Q1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr16:15694387 G>T maps to NM_014647.3 L1570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:43907766 G>A maps to NM_015284.2 R1714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:43909377 G>A maps to NM_015284.2 L2013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:43900071 G>A maps to NM_015284.2 E1041E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr1:43907988 C>T maps to NM_015284.2 R1743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:43895743 C>T maps to NM_015284.2 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:47182006 G>C maps to NM_014774.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr1:3662747 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr16:85112591 G>A maps to NM_014732.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:22676468 C>A maps to ENST00000446597 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr16:27789276 C>T maps to NM_015202.2 S1596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr16:27765492 G>A did not map to a codon.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr16:27751396 C>T maps to NM_015202.2 Y593Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:27752187 C>G maps to NM_015202.2 S857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr16:27788941 C>T maps to NM_015202.2 D1521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr16:27777776 C>T maps to NM_015202.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:3754056 G>C maps to NM_014704.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr13:42293869 C>T maps to NM_015058.1 P991P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:42393494 G>A maps to NM_015058.1 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr13:42295520 T>A maps to NM_015058.1 I983I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:42352180 C>T maps to NM_015058.1 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr13:42335295 G>C maps to NM_015058.1 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:42440145 A>G maps to NM_015058.1 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:42393506 G>A maps to NM_015058.1 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:59014612 A>T maps to ENST00000354386 A1618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr14:58909588 G>A maps to ENST00000354386 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr9:138377301 G>T maps to NM_014811.3 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr9:138377933 C>T maps to NM_014811.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr9:138376706 C>T maps to NM_014811.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr9:138379124 C>A maps to NM_014811.3 G923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr9:138376658 C>T maps to NM_014811.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr9:138378032 G>A maps to NM_014811.3 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr9:138377642 G>A maps to NM_014811.3 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr11:46690951 A>T did not map to a codon.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:2604100 G>A maps to NM_015229.3 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:2604688 G>A maps to NM_015229.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr17:2604760 C>A maps to NM_015229.3 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr17:2597271 G>C maps to NM_015229.3 Y1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr17:2600085 C>T maps to NM_015229.3 E666E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:55367304 T>C did not map to a codon.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr17:6498367 G>A maps to NM_014804.2 Y788Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:39878081 T>C maps to NM_015038.1 C715C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr1:39876600 C>T maps to NM_015038.1 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr6:96984252 G>A maps to NM_015323.4 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr6:97000465 C>G maps to NM_015323.4 T698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr6:96997423 T>C maps to NM_015323.4 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:96996133 G>A maps to NM_015323.4 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr6:96971058 T>C maps to NM_015323.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:8819103 C>A maps to ENST00000456698 I1320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr18:8825950 A>T maps to ENST00000456698 P1800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr18:8825332 G>A maps to ENST00000456698 E1594E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr18:8784807 G>C maps to ENST00000456698 G926G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr18:8828904 G>A did not map to a codon.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr18:8784582 G>A maps to ENST00000456698 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr14:55878477 C>A maps to NM_014924.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr16:67213450 C>G maps to NM_001040715.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr1:155887349 C>T maps to NM_014949.2 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:75560117 C>G maps to NM_015037.2 T1638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:154556599 C>T maps to NM_001131007.1 A1478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:154553966 G>A maps to NM_001131007.1 Q1435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:5461060 G>A maps to NM_015325.1 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:5463277 C>A maps to NM_015325.1 C1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr5:5460624 C>G maps to NM_015325.1 S393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr5:5461755 C>G maps to NM_015325.1 S770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr5:5486870 A>T maps to NM_015325.1 P2186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr18:29450922 T>C maps to NM_014939.3 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr15:79760680 C>T maps to NM_015206.2 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr15:79750589 A>T maps to NM_015206.2 K701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:79749049 C>T maps to NM_015206.2 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:79750222 G>A maps to NM_015206.2 K578K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr15:79750300 C>T maps to NM_015206.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:105536969 T>C maps to NM_015275.1 Y653Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:105515901 G>A maps to NM_015275.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr9:34976156 C>T maps to NM_015297.1 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr4:123270378 C>T maps to NM_015312.3 I4449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:123267826 C>T maps to NM_015312.3 L4261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:123155981 A>G maps to NM_015312.3 K1126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:123159466 G>A maps to NM_015312.3 E1265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr4:123249347 G>C maps to NM_015312.3 V3695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr4:123230491 A>G maps to NM_015312.3 A3375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr4:123176338 T>C maps to NM_015312.3 V2093V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr3:44795847 G>A maps to NM_020696.3 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr9:34371651 G>A maps to NM_020702.3 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr15:81188375 C>T maps to NM_018689.1 C462C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr23:118217057 T>C did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:118219355 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:118220823 C>T did not map to a codon.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr23:118284510 G>A did not map to a codon.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr23:118221838 C>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:118221771 G>T did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr23:118220734 C>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:118220796 G>T did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr23:118222747 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:118281445 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:118281446 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:118220903 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:118220997 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr23:118220566 T>C did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:118221720 C>G did not map to a codon.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr23:118220812 A>T did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:57190343 A>G maps to NM_020722.1 P1151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:57190421 G>A maps to NM_020722.1 T1177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr4:57182511 C>T maps to NM_020722.1 H948H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:57181221 G>A maps to NM_020722.1 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr4:57180309 G>A maps to NM_020722.1 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr4:57179361 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:24802316 A>T maps to NM_019590.3 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr10:24762686 G>A maps to NM_019590.3 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr10:24832953 C>T maps to NM_019590.3 L1585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr10:24722042 A>T maps to NM_019590.3 K225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:138584502 C>G maps to NM_020340.4 S628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:138615204 G>A maps to NM_020340.4 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:138576846 C>A maps to NM_020340.4 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:138655328 G>A maps to NM_020340.4 R1782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr6:138657565 C>T maps to NM_020340.4 R2159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:138584500 G>T maps to NM_020340.4 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:128712027 C>T maps to NM_020741.2 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr17:44109630 G>A maps to NM_015443.3 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:44248385 G>C maps to NM_015443.3 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr17:44110823 C>T maps to NM_015443.3 W890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr17:44110826 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr17:44144913 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr17:44248548 G>A maps to NM_015443.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr10:72324151 G>A maps to NM_014431.2 R765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr10:72294535 G>C maps to NM_014431.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr10:70775626 G>T maps to NM_015634.3 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr2:97274402 T>C did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:97278596 G>A maps to ENST00000421845 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr1:109730881 G>C maps to NM_020775.3 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:86544176 C>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:86569410 T>G maps to NM_001142749.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr7:86556202 G>A maps to NM_001142749.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr7:86537764 A>G maps to NM_001142749.2 Y818Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr18:34647274 A>G maps to NM_020776.1 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:52905992 C>T maps to NM_019600.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr11:101815011 C>T maps to NM_020802.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:101834192 T>C maps to NM_020802.2 N809N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr1:232942445 T>C maps to NM_019090.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:232943747 G>A maps to NM_019090.2 V993V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:232943333 C>T maps to NM_019090.2 F855F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr3:113697716 C>T maps to NM_020817.1 Q816Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-F7-A624-01A-22D-A30E-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-QK-A6IJ-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:113729642 C>T maps to NM_020817.1 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr14:94088225 A>G maps to ENST00000393153 R1571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr14:94089059 C>T maps to ENST00000393153 S1849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr14:94120289 G>C maps to ENST00000393153 G2128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr14:94060061 G>A maps to ENST00000393153 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr14:94083610 G>A maps to ENST00000393153 R1417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr14:94088413 C>G maps to ENST00000393153 S1634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:94044270 G>A maps to ENST00000393153 R765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr14:94158123 C>T maps to ENST00000393153 F2495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr14:94088399 G>C maps to ENST00000393153 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:94041486 G>A maps to ENST00000393153 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr14:94069642 C>A maps to ENST00000393153 I1211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr14:94156478 G>T maps to ENST00000393153 E2429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:95508621 T>C maps to NM_015496.3 K1439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr8:95531704 C>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:95500995 T>G maps to NM_015496.3 R1793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:186111711 A>G maps to NM_020827.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr9:5763585 A>G maps to ENST00000414202 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr9:5762632 C>T maps to ENST00000414202 D695D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:5754838 A>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:5757414 T>C maps to ENST00000414202 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr9:5765454 T>A maps to ENST00000414202 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr10:30318245 C>T maps to NM_020848.2 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:30316178 G>A maps to NM_020848.2 D966D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr10:30316131 G>C maps to NM_020848.2 S982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:30315989 C>G maps to NM_020848.2 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr10:30317651 C>T maps to NM_020848.2 W475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr12:13221563 C>T maps to NM_020853.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:13224218 C>T maps to NM_020853.1 Y471Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:13224191 T>A maps to NM_020853.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr18:59888729 G>A maps to NM_020854.3 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr18:59928748 A>G maps to NM_020854.3 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:59912004 C>T maps to NM_020854.3 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr18:59854899 G>A maps to NM_020854.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:226447437 C>T maps to NM_020864.1 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr2:226447503 C>T maps to NM_020864.1 Y457Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:226447443 C>A maps to NM_020864.1 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:226446801 G>A maps to NM_020864.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:226447563 C>T maps to NM_020864.1 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:226446753 C>T maps to NM_020864.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr2:226273607 C>G maps to NM_020864.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:33237515 G>A maps to NM_020888.2 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:33236756 C>G maps to NM_020888.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:33236190 G>T maps to NM_020888.2 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:33236813 G>A maps to NM_020888.2 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:33235952 C>T maps to NM_020888.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:33235676 C>G maps to NM_020888.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:33235550 C>T maps to NM_020888.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:33237215 C>G maps to NM_020888.2 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr1:33236051 C>T maps to NM_020888.2 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr1:33237578 G>A maps to NM_020888.2 A933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr3:108278851 C>T maps to NM_020890.2 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr9:100090305 G>T maps to ENST00000375206 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:100092788 C>T maps to ENST00000375206 Q855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:100070393 C>T maps to ENST00000375206 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr9:100137789 C>A maps to ENST00000375206 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr9:100080768 C>T maps to ENST00000375206 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:100080852 C>T maps to ENST00000375206 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:100074393 G>T did not map to a codon.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr9:100122337 T>C maps to ENST00000375206 L1161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr4:1360142 C>T maps to NM_020894.2 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr4:1379682 C>T maps to NM_020894.2 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr4:1369263 C>G maps to NM_020894.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr9:35107971 C>T maps to NM_025182.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr9:35107863 C>T maps to NM_025182.2 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr19:7671399 G>C maps to NM_001080429.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr19:7677136 C>A maps to NM_001080429.2 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr7:138524925 C>T maps to NM_001164665.1 G1850G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr7:138579165 G>A maps to NM_001164665.1 I1318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:138583772 G>A maps to NM_001164665.1 L1259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr7:138602130 A>G maps to NM_001164665.1 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr7:138603486 G>A maps to NM_001164665.1 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:138603405 G>A maps to NM_001164665.1 Y322Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:138602190 G>A maps to NM_001164665.1 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr7:138529059 A>G did not map to a codon.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr7:138603741 C>T maps to NM_001164665.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr7:138604074 G>A maps to NM_001164665.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr6:56917578 C>T maps to NM_020931.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr16:84520477 G>T maps to NM_020947.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr16:84520501 G>A maps to NM_020947.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr16:84529447 C>G maps to NM_020947.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:180885979 C>T maps to NM_020950.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr18:43467784 G>A maps to NM_020964.2 V1680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr18:43460093 G>A maps to NM_020964.2 S1871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr18:43469793 C>A maps to NM_020964.2 E1641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:43464701 G>A maps to NM_020964.2 S1728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:43534458 T>C maps to NM_020964.2 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr18:43514832 C>T maps to NM_020964.2 E733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr18:43438565 G>T maps to NM_020964.2 L2397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr22:44692709 G>A maps to NM_001099294.1 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:44681333 C>T maps to NM_001099294.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:18368202 C>T maps to NM_001145304.1 P1297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:18368175 G>A maps to NM_001145304.1 A1306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr19:18368529 G>A maps to NM_001145304.1 P1188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr19:18376099 T>C maps to NM_001145304.1 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:18368451 T>A maps to NM_001145304.1 T1214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr19:18368706 C>T maps to NM_001145304.1 A1129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr13:45580366 T>C maps to NM_018559.2 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr14:77576296 C>T maps to NM_033426.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr20:36850903 G>T maps to NM_001029864.1 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr20:36869728 G>A maps to NM_001029864.1 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:36855594 C>T maps to NM_001029864.1 K671K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr20:36841584 A>G maps to NM_001029864.1 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr20:36869161 A>G maps to NM_001029864.1 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr20:36869476 G>A maps to NM_001029864.1 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr20:36870320 G>C maps to NM_001029864.1 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr20:36850870 C>T maps to NM_001029864.1 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr20:36855588 C>T maps to NM_001029864.1 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:20820387 C>G maps to NM_017794.3 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr9:20944733 C>T maps to NM_017794.3 H1172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr9:20986312 C>G maps to NM_017794.3 V1585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:233489591 C>T maps to NM_032435.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr2:61336369 C>G maps to NM_001129993.1 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:111588222 C>G maps to NM_153369.2 Y486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr6:111583599 C>A maps to NM_153369.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr9:115422153 C>T maps to NM_133465.2 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr9:139701273 C>T maps to NM_001039374.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:139701234 C>T maps to NM_001039374.4 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr9:139700964 C>T maps to NM_001039374.4 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr1:11985514 G>A maps to ENST00000376576 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:11983376 G>A maps to ENST00000376576 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr3:113377776 G>A maps to NM_001009899.2 Q918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr3:113378749 G>C maps to NM_001009899.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr3:113376842 G>C maps to NM_001009899.2 S1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:73961160 A>G did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:73962429 T>C did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr23:73962995 C>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:73961333 C>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:73963449 A>G did not map to a codon.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr23:73962240 G>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:73960812 C>G did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:73963605 C>G did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:73963606 T>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr23:73962847 G>T did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr23:73962344 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr23:73962752 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:73960448 C>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:73964111 C>T did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:73960703 C>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:73963236 G>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr23:73962129 G>T did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:73962021 C>A did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr23:73962795 G>C did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:73962134 G>T did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr23:73964208 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:73964194 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr23:73963133 G>T did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:73960498 A>G did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:73960758 T>A did not map to a codon.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr23:73963629 G>A did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:5920394 G>A maps to NM_001017969.2 F1867F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:6007496 G>A maps to NM_001017969.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr9:5922221 C>T maps to NM_001017969.2 Q1258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr9:5922608 C>T maps to NM_001017969.2 Q1129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:5922658 G>A maps to NM_001017969.2 Q1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr9:5968205 G>A maps to NM_001017969.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:6007475 G>A maps to NM_001017969.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr9:5923142 C>T maps to NM_001017969.2 K951K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr9:5929141 C>T maps to NM_001017969.2 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr9:5922662 C>G maps to NM_001017969.2 V1111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr2:8931277 G>A maps to NM_020738.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:8871437 C>G maps to NM_020738.2 A1576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:8871879 G>C maps to NM_020738.2 S1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:94369263 T>C maps to NM_004523.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr10:94405302 G>A maps to NM_004523.3 Q817Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr9:116857598 G>A maps to ENST00000259410 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:17764820 C>T maps to NM_022113.4 P1646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:17772180 C>T maps to NM_022113.4 K1478K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:17781110 G>A maps to NM_022113.4 S1232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr6:17837132 C>T maps to NM_022113.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:17790141 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:17809130 T>C maps to NM_022113.4 K677K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:29037626 C>T maps to NM_015254.3 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:28974434 G>A maps to NM_015254.3 I1250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:29033587 G>C maps to NM_015254.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:200550375 T>C maps to NM_014875.2 E1096E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr1:200550380 G>A maps to NM_014875.2 Q1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:200522869 G>A maps to NM_014875.2 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr3:44852483 G>A maps to NM_020242.2 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr3:44856476 G>T maps to NM_020242.2 E820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr20:16496214 G>C maps to NM_024704.4 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:21031009 G>A maps to NM_020816.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:20992740 G>A maps to NM_020816.2 S959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr1:21013937 G>A maps to NM_020816.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:21042075 C>T maps to NM_020816.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:43003860 T>C maps to ENST00000438933 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr17:72348367 G>T maps to NM_153209.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr17:72349697 G>A maps to NM_153209.3 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:72348996 C>G maps to NM_153209.3 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr17:72341018 C>T maps to NM_153209.3 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr17:72322499 C>T maps to NM_153209.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:241661289 C>T maps to ENST00000373308 L1567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:241657474 C>T maps to ENST00000373308 G1783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:241710441 G>A maps to ENST00000373308 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr2:241659321 C>T maps to ENST00000373308 R1638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:10364176 C>T maps to NM_183416.3 I978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:10434487 C>T maps to ENST00000377086 L1687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:10328245 C>T maps to ENST00000377086 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:10355163 C>T maps to ENST00000377086 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:10356658 C>T maps to ENST00000377086 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr1:10397555 C>T maps to ENST00000377086 I1129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:4923829 C>T maps to NM_006612.5 N598N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr17:4907159 C>T maps to NM_006612.5 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr10:91532578 A>G maps to ENST00000416354 S1822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr10:91518640 T>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:39720118 T>C maps to ENST00000395670 V1116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:39713803 G>C maps to ENST00000395670 S1228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr12:39696847 G>A maps to ENST00000395670 T1551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr12:39756910 G>A maps to ENST00000395670 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr12:39751239 C>A did not map to a codon.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:39726144 C>T maps to ENST00000395670 E974E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:39763620 G>A maps to ENST00000395670 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr12:39745658 G>A maps to ENST00000395670 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:39726013 A>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:200954075 G>C maps to NM_017596.2 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:200959777 G>A maps to NM_017596.2 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr1:200956236 G>A maps to NM_017596.2 S1167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:200948799 G>T maps to NM_017596.2 I1328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:200944710 G>A maps to NM_017596.2 L1497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:200944026 C>T maps to NM_017596.2 A1530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:200969699 G>A maps to NM_017596.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:200971388 C>T maps to NM_017596.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:200954078 T>A maps to NM_017596.2 T1237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr1:200959460 C>T did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:200943885 G>A maps to NM_017596.2 I1577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:200944632 G>A maps to NM_017596.2 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr16:29816600 C>G maps to NM_007317.1 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr16:29814095 A>G maps to NM_007317.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr16:29810640 G>A maps to NM_007317.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr16:29809784 G>A maps to NM_007317.1 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr15:69737349 C>T maps to NM_138555.1 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:34290295 G>A maps to NM_194313.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr9:34255734 C>T maps to NM_194313.2 A1290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:168434600 C>T maps to NM_030615.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:104642400 G>A maps to NM_015656.1 E1092E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:104639753 C>T maps to NM_015656.1 R591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr1:245850064 G>A maps to NM_018012.3 P1260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:245848772 C>T maps to NM_018012.3 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:245775204 C>T maps to NM_018012.3 D675D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr1:245582993 C>T maps to NM_018012.3 C371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:245849149 G>A maps to NM_018012.3 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr1:245847603 G>A maps to NM_018012.3 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr9:86518412 G>A maps to NM_017576.1 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr9:86495229 C>T maps to NM_017576.1 R875R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr17:51901020 G>C maps to NM_032559.4 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:51901497 G>A maps to NM_032559.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:51900744 G>A maps to NM_032559.4 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr1:45206651 A>C maps to NM_006845.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:45218849 G>A maps to NM_006845.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr20:30897726 G>A maps to NM_004798.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr20:30915387 C>G maps to NM_004798.3 S631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr20:30898674 C>G maps to NM_004798.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr2:26204036 G>A maps to NM_002254.6 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:26203808 G>C maps to NM_002254.6 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:26204429 G>C maps to NM_002254.6 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr2:26203811 C>T maps to NM_002254.6 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:69626749 C>T did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:69563609 G>T did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:69595997 G>A did not map to a codon.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr23:69510346 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:69606537 G>A did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:69622515 A>G did not map to a codon.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr5:154393919 T>C maps to NM_001099293.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:154393877 C>A maps to NM_001099293.1 C153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr5:154393631 G>A maps to NM_001099293.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:154394891 G>A maps to NM_001099293.1 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr5:154396520 T>C maps to NM_001099293.1 F1034F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr5:154396625 T>C maps to NM_001099293.1 D1069D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr5:154396652 C>T maps to NM_001099293.1 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr5:154396703 G>A maps to NM_001099293.1 G1095G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr5:154396892 C>T maps to NM_001099293.1 N1158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr5:154396895 T>C maps to NM_001099293.1 P1159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K0-01B-21D-A31L-08 chr5:154394711 C>T maps to NM_001099293.1 N431N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr5:154393829 A>G maps to NM_001099293.1 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr5:154396173 G>T maps to NM_001099293.1 E919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:57974824 G>A maps to NM_004984.2 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr12:57975222 C>T maps to NM_004984.2 Y927Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr12:57963438 G>T maps to NM_004984.2 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr12:57958725 C>T maps to NM_004984.2 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr10:32311167 C>T maps to NM_004521.2 K644K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr10:32321666 C>T maps to NM_004521.2 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr2:149868126 G>A maps to NM_004522.1 T937T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr2:149806901 C>A maps to NM_004522.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:149840153 G>A maps to NM_004522.1 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:149853787 C>T maps to NM_004522.1 H678H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:39507890 G>A maps to NM_145027.4 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr15:90172249 C>G maps to NM_198525.2 L1207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr15:90176167 C>T maps to NM_198525.2 R926R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr15:90190894 G>T maps to NM_198525.2 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:169941739 C>G did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:170015865 T>A maps to NM_014970.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr1:169890825 A>G maps to NM_014970.2 Y790Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:33371887 C>T maps to NM_002263.3 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:145698667 G>T maps to NM_145754.2 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr16:57829030 G>C maps to NM_005550.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr16:57803505 C>G did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr10:7822112 G>A maps to NM_012311.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr19:55281316 C>T maps to ENST00000291633 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr19:55286878 G>A maps to ENST00000291633 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr19:55258837 G>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:55340900 C>G maps to NM_013289.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:55340876 C>A maps to NM_013289.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:55363639 C>A maps to NM_006737.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr19:55378184 A>G maps to ENST00000355608 *456W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr19:55377999 G>A maps to ENST00000355608 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr19:55378163 C>A maps to ENST00000355608 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:55239224 T>C maps to NM_153443.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:55246765 C>T maps to NM_153443.3 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr1:158047872 G>T maps to ENST00000368173 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:36357324 C>T maps to NM_199180.2 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:36357123 T>C maps to NM_199180.2 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:36351462 A>T maps to NM_199180.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr19:36357105 G>A maps to NM_199180.2 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:36353413 G>A maps to NM_199180.2 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr19:36353393 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:126343308 C>T maps to NM_032531.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr11:126314916 G>T maps to NM_032531.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:126432786 C>A maps to NM_032531.3 G26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:204159794 G>T maps to ENST00000306118 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:55603418 G>A maps to NM_000222.2 E925E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr4:55594177 G>T maps to NM_000222.2 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:55604671 C>A maps to NM_000222.2 V960V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr4:55565906 C>G maps to NM_000222.2 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr4:55599288 C>A maps to NM_000222.2 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr4:55575700 G>C maps to NM_000222.2 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr13:33638295 G>A maps to NM_004795.3 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr13:33635738 C>G maps to NM_004795.3 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:33635744 T>C maps to NM_004795.3 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr13:33591183 C>T maps to NM_004795.3 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:39448238 G>A maps to NM_175737.3 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:104129087 C>T maps to ENST00000445352 Y379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:104142024 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr6:43030738 G>T maps to NM_201523.1 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr19:12997870 G>A maps to NM_006563.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr8:103664139 G>A maps to NM_005655.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr8:103664556 C>T maps to NM_005655.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr3:126070937 G>C maps to NM_014079.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr3:126071726 C>A maps to NM_014079.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:44595383 C>T maps to NM_173484.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:44596219 C>G maps to NM_173484.3 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:38691483 C>T maps to NM_016531.5 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:38690407 C>G maps to NM_016531.5 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr4:38690368 C>A maps to NM_016531.5 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr9:110249792 G>A maps to NM_004235.4 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:73636024 G>C maps to NM_001730.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr10:3823968 C>G maps to NM_001300.5 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr10:3827191 G>A maps to NM_001300.5 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:207989095 C>G maps to NM_003709.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:56296752 A>T did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:56310805 A>T did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:56310858 G>C did not map to a codon.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr9:73002723 G>A maps to NM_001206.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr14:50159965 C>G maps to NM_172193.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr6:42986848 C>T maps to NM_057161.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr16:87782312 G>A maps to NM_017566.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr16:87782313 G>A maps to NM_017566.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr16:87782280 G>A maps to NM_017566.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr12:27950646 G>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr22:50987659 C>T maps to NM_138433.3 Y355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr22:50987548 A>G maps to NM_138433.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:205306714 G>A maps to NM_018203.1 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:205312507 G>A maps to NM_018203.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr1:205307703 G>A maps to NM_018203.1 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:161069389 G>A maps to NM_152366.4 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr13:70549921 G>A maps to NM_020866.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr13:70456524 C>A maps to NM_020866.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr13:70549882 A>G maps to NM_020866.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr13:70549903 A>C maps to NM_020866.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr13:70275854 C>T maps to NM_020866.2 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:39994345 G>A maps to NM_152467.3 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:202861735 G>A maps to NM_021633.2 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr23:117043644 G>A did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr23:117033237 C>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:117079425 T>C did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr23:117043396 G>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:117106770 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:117033122 G>T did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr18:30350278 C>T maps to NM_020805.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr18:30260291 T>C did not map to a codon.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr18:30260492 G>A maps to NM_020805.1 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr23:24024380 C>T did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr23:24006506 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:900537 C>T maps to NM_198317.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr1:900540 G>A maps to NM_198317.2 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:47378139 C>T maps to NM_025010.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:166231783 C>T maps to NM_001161521.1 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr4:166184407 A>G maps to NM_001161521.1 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr4:166232679 T>C maps to NM_001161521.1 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:6659378 G>A maps to NM_014851.2 Y385Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr22:20843368 G>T maps to NM_032775.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr22:20800822 C>T maps to NM_032775.3 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr3:183381263 G>A maps to NM_017644.3 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr3:183381385 C>G maps to NM_017644.3 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:183368284 C>T maps to NM_017644.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:86312263 C>A maps to NM_022480.3 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr15:86312711 G>A maps to NM_022480.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr15:86312315 C>T maps to NM_022480.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:18779736 C>T maps to NM_018316.1 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:136964010 G>A maps to NM_017415.2 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:137028127 G>A maps to NM_017415.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:137045499 C>T maps to NM_017415.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:53519581 C>T maps to NM_001003760.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:53519395 T>C maps to NM_001003760.4 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:97562023 C>A maps to NM_052904.3 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:97562041 C>T maps to NM_052904.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:21675293 G>C did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:21674707 G>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:21675185 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:21675203 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:21674748 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:21675712 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:21675147 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:21674051 C>T did not map to a codon.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr23:21675272 G>T did not map to a codon.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr23:21675043 C>T did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:75139658 T>G maps to NM_001039548.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr11:75139523 G>A maps to NM_001039548.2 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr16:84695243 C>T maps to NM_024731.2 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr8:124664956 C>T maps to NM_001081675.2 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr8:124658218 G>C maps to NM_001081675.2 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:86919783 C>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:86877359 G>T did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:86773075 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr23:86890597 G>T did not map to a codon.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr23:86890581 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:86890738 C>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:86773056 G>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:86919889 G>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:86773131 G>T did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:86888819 G>A did not map to a codon.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr23:86877395 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:86773014 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:86887298 G>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:86873047 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr23:86919899 G>C did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:86773150 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:86873068 C>T did not map to a codon.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr23:86880612 C>A did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr23:86869563 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:86919874 C>A did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr23:86888859 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:86887270 G>A did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:86919927 G>A did not map to a codon.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr23:86887359 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr3:183210453 G>A maps to NM_130446.2 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:183225975 G>A maps to NM_130446.2 N260N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:183217504 C>T maps to NM_130446.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr3:183217408 G>A maps to NM_130446.2 C372C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr7:23213805 C>T maps to NM_001031710.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:88116484 G>A maps to NM_020803.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr19:51532605 A>G maps to NM_019598.2 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:51563853 C>T maps to NM_015596.1 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:51379787 G>A maps to NM_005551.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:51379883 C>G maps to NM_005551.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:51361524 G>A maps to NM_001648.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:51411650 G>T maps to NM_004917.3 C192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:51410249 A>C maps to NM_004917.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:51503432 G>A maps to NM_144505.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr4:187172683 A>G maps to ENST00000511608 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr4:187175917 G>A did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:187173204 A>G maps to ENST00000511608 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr4:187179173 G>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr4:187177144 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:48698495 C>T maps to NM_001135629.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:48687278 C>T maps to NM_001135629.2 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:48681850 C>T maps to NM_001135629.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:48734517 T>G maps to NM_001135629.2 Y693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:9751249 C>G did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:10587971 G>T maps to NM_002260.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:10569333 C>T maps to NM_007333.2 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr12:10570963 A>T maps to NM_007333.2 C155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:9162051 C>A maps to NM_005810.3 C163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:10531150 A>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:135012523 G>T maps to ENST00000368572 E838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr10:135015083 C>T maps to ENST00000368572 D1025D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:135024219 G>T maps to ENST00000368572 T1302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:135011839 G>T did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:135020756 C>T maps to ENST00000368572 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:135015068 G>A maps to ENST00000368572 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:135015188 C>T maps to ENST00000368572 G1060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr10:135024222 G>A maps to ENST00000368572 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr10:135015257 C>T maps to ENST00000368572 P1083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:186450324 C>T maps to NM_001102416.2 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:186450367 G>T maps to NM_001102416.2 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:186450366 G>T maps to NM_001102416.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr12:123082439 G>A maps to NM_014708.4 T1506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr12:123061461 C>G maps to NM_014708.4 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr12:123019278 A>G maps to NM_014708.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:123102941 C>G maps to NM_014708.4 S2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:123019326 C>T maps to NM_014708.4 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:123089935 C>T maps to NM_014708.4 L1824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr12:123054274 C>G maps to NM_014708.4 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr12:123067337 C>T maps to NM_014708.4 H1023H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:123089165 A>G maps to NM_014708.4 L1719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr3:122172741 G>C maps to NM_002264.3 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr3:122145936 G>A maps to NM_002264.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr3:122145945 C>T maps to NM_002264.3 E501E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr3:122168492 G>C maps to NM_002264.3 S282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr17:66040030 A>G maps to NM_002266.2 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr13:50293955 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:160243623 T>A maps to NM_002268.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7100-01A-11D-2012-08 chr3:160239584 G>A maps to NM_002268.3 H295H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr3:160245807 C>G maps to NM_002268.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr3:160253594 C>T did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr6:117050815 T>C maps to NM_002269.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IF-01A-11D-A31L-08 chr1:32625008 T>G maps to NM_012316.4 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr1:152732579 C>T maps to NM_001025231.1 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr1:152732234 C>T maps to NM_001025231.1 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:152732721 C>T maps to NM_001025231.1 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr19:47986449 G>C maps to NM_007059.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:149430328 G>A maps to NM_032534.2 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:88327773 G>A maps to NM_016618.1 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:10675659 C>T maps to NM_023008.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr19:10664770 C>T maps to NM_023008.3 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr19:10675656 C>T maps to NM_023008.3 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:10670070 G>A maps to NM_023008.3 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:10671085 A>G maps to NM_023008.3 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:10673445 G>A maps to NM_023008.3 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:91870363 A>G maps to NM_194456.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:75905361 G>A maps to NM_007043.6 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:53072486 C>T maps to NM_006121.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr12:53069123 G>A maps to NM_006121.3 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr12:53069018 G>A maps to NM_006121.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:38978335 C>A maps to NM_000421.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:39019388 G>A maps to NM_000223.3 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:39019595 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:39019385 C>T maps to NM_000223.3 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:39659679 C>G maps to NM_153490.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr17:39659615 G>A maps to NM_153490.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr17:39743026 G>A maps to NM_000526.4 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr17:39740134 G>T maps to NM_000526.4 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:39740511 C>T maps to NM_000526.4 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:39740537 G>A maps to NM_000526.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr17:39739590 C>T maps to NM_000526.4 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr17:39740125 C>T maps to NM_000526.4 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:39780614 G>A maps to NM_000422.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr17:39780689 C>T maps to NM_000422.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:53343349 G>A maps to NM_000224.2 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:53346616 G>C maps to NM_000224.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr17:39684169 C>T maps to NM_002276.4 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:53045401 C>T maps to NM_000423.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr12:53044253 G>T maps to NM_000423.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:39084609 A>G maps to NM_015515.3 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:38906821 C>A maps to NM_181534.3 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:38935780 C>T maps to NM_181537.3 E315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:38938472 G>C maps to NM_181537.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:53187988 G>A maps to ENST00000309505 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr17:39616418 G>C maps to NM_002278.3 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:39503387 C>G maps to NM_004138.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:39502481 G>A maps to NM_004138.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr17:39522832 G>A maps to ENST00000394004 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr17:39521783 G>A maps to ENST00000394004 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr17:39522751 C>T maps to ENST00000394004 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr17:39643395 G>T maps to NM_003771.4 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:39580457 C>T maps to NM_003770.4 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:39580042 C>T maps to NM_003770.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr17:39580481 G>A maps to NM_003770.4 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:39577791 G>A maps to NM_003770.4 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:39580517 G>A maps to NM_003770.4 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:39596762 G>C maps to NM_006771.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr17:39594346 G>T maps to NM_006771.3 C413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:39596462 C>T maps to NM_006771.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:39596777 C>T maps to NM_006771.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:39122693 G>A maps to NM_213656.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr17:39118799 G>A maps to NM_213656.3 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:39122955 G>A maps to NM_213656.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr17:39120031 G>A maps to NM_213656.3 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr12:53201524 G>A maps to NM_002272.2 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr12:53201425 A>G did not map to a codon.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr12:53202523 G>A maps to NM_002272.2 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:39140174 C>T maps to NM_182497.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr12:52913990 G>A maps to NM_000424.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr12:52912853 C>A maps to NM_000424.3 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:52912866 C>T maps to NM_000424.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr12:52881536 G>A maps to NM_005554.3 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr12:52884659 C>T maps to NM_005554.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr12:52884358 C>T maps to NM_005554.3 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:52882329 G>A maps to NM_005554.3 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr12:52845430 G>A maps to NM_005555.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr12:52842694 C>T maps to NM_005555.3 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr12:52845355 G>A maps to NM_005555.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:52862854 G>A maps to NM_173086.4 Y562Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr12:52864969 G>C maps to NM_173086.4 Y341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr12:52627277 C>T maps to NM_005556.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:52639266 C>T maps to NM_005556.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr12:52639287 C>T maps to NM_005556.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr12:52629033 C>T maps to NM_005556.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr12:52942484 G>A maps to NM_033448.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr12:52943097 G>A maps to NM_033448.2 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr12:52994828 G>A maps to NM_080747.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:52979792 G>A maps to NM_080747.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:52992875 C>T maps to NM_080747.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr12:52986736 C>A did not map to a codon.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:53012017 C>T maps to NM_175068.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr12:53004409 G>A maps to NM_175068.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr12:52965208 C>A maps to NM_175053.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr12:52825419 G>A maps to ENST00000252245 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr12:52818393 G>A maps to ENST00000252245 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:52818531 G>A maps to ENST00000252245 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr12:53165949 G>T maps to NM_015848.4 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:53171042 A>G maps to NM_015848.4 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:53169246 G>C maps to NM_015848.4 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:53086202 A>G did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr12:53227876 G>C maps to NM_175834.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:53227939 T>C maps to NM_175834.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:53227933 C>T maps to NM_175834.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr12:53293762 G>A maps to NM_002273.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr12:52565208 G>A maps to NM_182507.2 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:52685168 G>A maps to NM_002281.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:52685195 G>A maps to NM_002281.3 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:52797672 C>T maps to NM_033033.3 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:52799719 C>T maps to NM_033033.3 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr12:52713010 C>T maps to NM_002282.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr12:52710275 G>A maps to NM_002282.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr12:52714969 A>G maps to NM_002282.3 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:52710789 T>C maps to NM_002282.3 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:52756640 G>T maps to NM_002283.3 C358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr17:39724517 G>A maps to NM_000226.3 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:39726122 C>T maps to NM_000226.3 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr17:39725791 C>T maps to NM_000226.3 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr17:39725675 A>G did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr17:39724873 G>A maps to NM_000226.3 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:39190614 G>A maps to NM_030966.1 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr17:39190830 G>T maps to NM_030966.1 C81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:39183230 A>G maps to NM_031957.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr21:45959217 G>A maps to NM_198691.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr21:45959991 G>A maps to NM_198691.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr21:46057495 G>A maps to NM_181688.1 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:46057660 T>C maps to NM_181688.1 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr21:46057585 C>T maps to NM_181688.1 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr21:46066854 C>T maps to NM_198692.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr21:45978217 G>A maps to NM_198696.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:45978295 C>T maps to NM_198696.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr21:45978004 G>C maps to NM_198696.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr21:46000227 C>T maps to NM_198694.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr21:46011579 G>T maps to NM_198688.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr21:46021342 C>T maps to ENST00000380102 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr21:46047690 C>G maps to NM_198690.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr21:32253774 C>T maps to NM_175858.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr21:46074246 G>A maps to NM_198698.1 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:31768436 C>T maps to NM_181599.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr21:31744288 G>T maps to NM_181621.3 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr21:31744003 T>A maps to NM_181621.3 *176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr21:31744359 C>A maps to NM_181621.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr21:31797759 C>T maps to NM_181622.1 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr21:31803000 C>A maps to NM_181600.1 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr21:31812665 T>A maps to NM_181623.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr21:31812938 A>T maps to NM_181623.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr21:31812858 C>T maps to NM_181623.1 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr21:31812773 G>T maps to NM_181623.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr21:31812701 G>A maps to NM_181623.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IF-01A-11D-A31L-08 chr17:39471806 G>A maps to NM_031964.1 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr21:31864055 C>A maps to ENST00000433652 G83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr21:31864134 G>T maps to ENST00000433652 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr21:31864176 G>C maps to NM_181609.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:31869218 C>T maps to NM_181610.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr21:32007778 G>A maps to NM_181616.1 *66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr21:32127483 G>T maps to NM_181619.1 C71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr21:31692053 A>G maps to NM_203405.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr21:31692244 C>A maps to NM_203405.1 G37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr21:31709485 G>A maps to NM_001077711.1 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr21:31709899 G>T maps to NM_001077711.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:39334272 C>G maps to ENST00000458321 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr17:39240643 C>A maps to ENST00000377731 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr17:39261861 T>C maps to NM_001146041.1 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr17:39262014 T>C maps to ENST00000377731 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr11:1606257 G>T maps to NM_001005922.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:1606149 G>A maps to NM_001005922.1 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:1605990 G>A maps to NM_001005922.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr11:1605716 G>A maps to NM_001005922.1 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr11:71293826 G>A maps to ENST00000376535 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr11:71293727 A>G maps to ENST00000376535 C52C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-A497-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CQ-6224-01A-11D-1912-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-HD-7229-01A-11D-2012-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-P3-A6T3-01A-11D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:1629199 G>C maps to ENST00000359229 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr11:1642820 G>C maps to NM_001012709.1 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:1643044 G>A maps to ENST00000359229 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:1643014 G>A maps to ENST00000359229 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:1643053 G>A maps to ENST00000359229 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr11:1642783 G>A maps to NM_001012709.1 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr11:1718849 C>A maps to NM_001012416.1 C125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr11:71238435 A>C maps to NM_001012503.1 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:71249136 C>T maps to ENST00000422553 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr21:31971007 A>G maps to NM_181604.1 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr21:31965095 G>A maps to NM_181605.3 *111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:39406205 A>G maps to NM_033191.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr17:39394317 T>C maps to NM_031963.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:39412083 C>A maps to ENST00000431129 C155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:155145306 C>T maps to NM_173852.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr17:25932785 G>T maps to ENST00000268763 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr17:25935032 C>T maps to ENST00000268763 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:25904582 G>T maps to ENST00000268763 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr17:25936333 C>G maps to ENST00000268763 S680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:118198937 C>T maps to ENST00000339824 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr12:117977626 C>T maps to ENST00000339824 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:118199102 C>T maps to ENST00000339824 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr12:117969468 A>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:118199072 C>T maps to ENST00000339824 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr12:117962952 C>T maps to ENST00000339824 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:52498548 C>A maps to NM_138417.2 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:52499424 G>A maps to NM_138417.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr3:134323140 G>A maps to NM_178554.4 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:143790865 C>G maps to NM_003937.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:143797995 G>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:143676238 C>A maps to NM_003937.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:143712376 A>G did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:143790808 G>A maps to NM_003937.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr2:143713794 A>G maps to NM_003937.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:153134344 C>A did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:153130402 G>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:153134315 C>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:153135905 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:153132809 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:153132823 G>C did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:153128176 C>T did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr23:153135916 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153130377 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153133364 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153133563 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153133564 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr23:153130125 G>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:153134303 A>T did not map to a codon.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr14:50736049 T>G did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr20:42157953 G>A maps to NM_032107.4 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr20:42164480 C>T maps to NM_032107.4 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr22:41613199 C>T maps to NM_031488.4 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr22:41623202 C>T maps to NM_031488.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr22:41623844 G>A maps to NM_031488.4 K620K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:41625592 G>A maps to NM_031488.4 K646K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr6:130415449 C>T maps to NM_032438.2 C558C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:130425590 C>G maps to NM_032438.2 S586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr6:130378575 G>T maps to NM_032438.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr18:6239846 G>A maps to NM_173464.3 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr18:6311561 G>A maps to NM_173464.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:6239846 G>A maps to NM_173464.3 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:108843528 C>T maps to NM_145315.3 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:63419874 G>A maps to NM_032857.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr1:201356296 G>A maps to NM_005558.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:201352258 G>A maps to NM_005558.3 H443H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:6886562 G>A maps to NM_002286.5 W397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr12:6883836 C>T maps to NM_002286.5 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:153706740 G>A did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:54868567 C>T maps to NM_002287.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:54872772 C>G maps to NM_002287.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr19:54868205 C>T maps to NM_002287.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:55019221 G>T maps to NM_002288.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr18:7016586 C>A maps to NM_005559.2 T964T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:6983141 C>A maps to NM_005559.2 E1918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr18:7050889 G>A maps to NM_005559.2 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr18:6978215 G>A maps to NM_005559.2 L2057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr18:6955458 C>T maps to NM_005559.2 Q2700Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:6950939 G>A maps to NM_005559.2 F2746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr18:6976040 C>T maps to NM_005559.2 R2128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:7032980 A>G did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr18:6978306 C>T maps to NM_005559.2 L2026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr18:6978336 C>T maps to NM_005559.2 T2016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr18:6985294 C>T maps to NM_005559.2 L1867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr6:129674410 C>T maps to NM_000426.3 V1542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr6:129475782 T>C maps to NM_000426.3 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr6:129774130 A>C did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:129802529 G>A maps to NM_000426.3 L2565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr6:129714274 G>T maps to NM_000426.3 E1774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr6:129588364 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:129634085 C>T maps to NM_000426.3 F1085F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr6:129649433 G>A maps to NM_000426.3 P1396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr6:129835642 G>A maps to NM_000426.3 E3038E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr6:129371199 C>T maps to NM_000426.3 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr18:21489241 A>C maps to ENST00000416669 R2383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr18:21419889 G>A maps to ENST00000416669 P1113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr18:21444831 G>A maps to ENST00000416669 P1558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr18:21478997 G>A maps to ENST00000416669 V1937V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr18:21422396 C>A maps to ENST00000416669 G1127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr18:21333767 T>C maps to ENST00000416669 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:112443311 G>A maps to NM_001105206.1 S1460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:112513042 G>A maps to NM_001105206.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:112575274 G>C maps to NM_001105206.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr6:112537670 C>T did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:112430785 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:112440462 G>A maps to NM_001105206.1 R1573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr6:112528289 G>T maps to NM_001105206.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr6:112480013 T>A maps to NM_001105206.1 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr6:112471740 G>A maps to NM_001105206.1 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr20:60900575 G>T maps to NM_005560.3 R1775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr20:60906172 G>A maps to NM_005560.3 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr20:60887106 C>T did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:60942118 G>A maps to NM_005560.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr20:60893706 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:60885588 G>A maps to NM_005560.3 L3496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr20:60890183 C>T maps to NM_005560.3 Q2649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr20:60913315 G>A maps to NM_005560.3 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr20:60908966 G>C maps to NM_005560.3 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:107601752 C>T maps to NM_002291.2 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:107638889 C>T maps to NM_002291.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr7:107626632 G>C maps to NM_002291.2 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:107576054 T>C maps to NM_002291.2 A1331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:49161039 C>T maps to NM_002292.3 E1274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr1:209803115 C>A maps to NM_000228.2 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:209791281 G>A maps to NM_000228.2 S1007S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CN-4734-01A-01D-1434-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:107746423 A>G maps to NM_007356.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr7:107752370 G>A maps to NM_007356.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr7:107704424 G>A maps to NM_007356.2 Q948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:183105650 T>G maps to NM_002293.3 A1415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:183093838 C>T maps to NM_002293.3 C825C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr1:182992965 G>T maps to NM_002293.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:183095287 G>A maps to NM_002293.3 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr1:183094592 G>A maps to NM_002293.3 G903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr1:183077529 T>G maps to NM_002293.3 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:183206611 C>G maps to NM_005562.2 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:183177136 G>A maps to NM_005562.2 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:183209188 G>A maps to NM_005562.2 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr1:183192456 C>T maps to NM_005562.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr1:183208565 C>T maps to NM_005562.2 I979I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:133945218 C>T maps to ENST00000355048 Y1017Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:133946977 G>A maps to ENST00000355048 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr9:133932454 G>A maps to ENST00000355048 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr9:133957543 G>T maps to ENST00000355048 L1354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr9:133957544 G>T maps to ENST00000355048 E1355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:113975726 T>C maps to NM_005561.3 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr23:119565262 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr3:182853619 C>T maps to NM_014398.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:182841970 C>A maps to NM_014398.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:182871532 G>A maps to NM_014398.3 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:182870194 G>A maps to NM_014398.3 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:182841989 G>T maps to NM_014398.3 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr7:55466317 C>T maps to NM_018697.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:37431411 A>T did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:37431413 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:37431156 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr23:37526543 A>G did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr23:37431382 C>T did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr4:17583957 A>G maps to NM_015907.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr2:20237148 G>A maps to NM_014713.4 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:20234790 G>A maps to NM_014713.4 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:31212768 G>A maps to NM_006762.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr22:33673129 C>G maps to NM_133642.3 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr22:34046370 C>A maps to NM_133642.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr22:33700300 G>A maps to NM_133642.3 N548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr22:33733712 C>T maps to NM_133642.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr22:33780179 G>A maps to NM_133642.3 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr22:33670598 G>A maps to NM_133642.3 F695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr22:34000497 G>A maps to NM_133642.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:154179520 G>T maps to ENST00000377643 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr5:154179560 G>T maps to ENST00000377643 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:154179305 C>T maps to ENST00000377643 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:154179272 C>T maps to ENST00000377643 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:154188022 G>A maps to ENST00000377643 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr5:154179149 G>T did not map to a codon.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr5:154173459 G>A maps to ENST00000377643 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:129043273 T>C maps to NM_018078.2 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr4:129012523 T>C maps to NM_018078.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr12:50855031 G>A maps to ENST00000429001 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr12:50869523 C>A maps to ENST00000429001 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr12:50829269 G>C did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr10:863816 G>A maps to NM_015155.1 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr10:931621 G>A maps to NM_015155.1 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr10:875360 C>A maps to NM_015155.1 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr15:71124777 C>A maps to NM_018357.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:145506096 T>A maps to NM_020117.9 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:64737986 C>T did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:150941484 G>A maps to NM_181746.2 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr1:150940945 C>T maps to NM_181746.2 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr15:100942944 G>A maps to ENST00000394113 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:8319400 G>A maps to NM_024552.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr19:8321560 G>A maps to NM_024552.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:169571585 C>T maps to ENST00000392687 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:28997454 G>C did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:149997416 T>A maps to NM_004690.2 T954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr6:150005728 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:150004896 G>C maps to NM_004690.2 S443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:150005092 G>A maps to NM_004690.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr13:21562739 G>A maps to NM_014572.2 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr13:21549413 G>A maps to NM_014572.2 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:21565461 G>A maps to NM_014572.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:21565462 G>A maps to NM_014572.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr13:21565492 G>A maps to NM_014572.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr2:30457288 G>C maps to NM_030915.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:30457342 C>T maps to NM_030915.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr20:36975002 C>T maps to NM_004139.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr10:102988515 C>T maps to NM_006562.4 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr10:102988335 G>C maps to NM_006562.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:74725407 G>A maps to NM_001009812.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:68118399 C>T maps to ENST00000380035 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr6:80197507 C>T maps to NM_181714.3 W436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:152800040 A>C maps to NM_178348.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:152800094 A>G maps to NM_178348.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:152671631 C>T maps to NM_178428.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:152659360 C>T maps to NM_014357.4 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:152659535 C>T maps to NM_014357.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:152648544 C>A maps to NM_178429.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:152595357 C>T maps to NM_178431.1 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:152681604 C>A maps to NM_178356.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:32745440 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:32742007 G>A maps to ENST00000373562 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr1:32740384 C>T maps to ENST00000373562 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr2:30682531 C>T maps to NM_182551.3 N18N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr16:25176023 C>T maps to ENST00000380963 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:43621175 C>T maps to NM_014793.4 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:139635722 C>T maps to NM_001001712.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr9:139634423 G>T maps to NM_001001712.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr9:139658428 T>C maps to NM_203347.1 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:139879315 C>T maps to NM_207510.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:98714868 G>A maps to NM_001170765.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr10:98711950 C>T maps to NM_001170765.1 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr13:46728937 A>T did not map to a codon.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr5:169701310 C>T maps to NM_005565.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr5:169675712 T>A maps to NM_005565.3 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr2:136566781 G>A maps to NM_002299.2 Y1045Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr2:136579615 C>A maps to NM_002299.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr2:136546022 G>A maps to NM_002299.2 Y1885Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr2:136561590 C>T maps to NM_002299.2 Q1524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:136567554 C>A maps to NM_002299.2 E788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:136566586 C>T maps to NM_002299.2 E1110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr2:136570328 G>A maps to NM_002299.2 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:136566156 G>A maps to NM_002299.2 R1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr2:136566640 C>T maps to NM_002299.2 R1092R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr15:66855886 G>A maps to NM_207338.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr10:103867954 G>A maps to NM_001113407.1 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr4:16760796 A>G maps to NM_001290.3 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr4:16590359 T>C maps to NM_001290.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr4:16510220 T>C maps to NM_001290.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:88446936 G>C maps to NM_001171610.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:18428862 C>T maps to NM_001165415.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr11:18500317 C>T maps to NM_144972.4 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr15:59499844 G>T maps to NM_033195.1 G236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr15:59499630 C>T maps to NM_033195.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr15:59499195 G>A maps to NM_033195.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr12:21794925 G>A maps to NM_002300.6 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr11:18467777 G>A maps to NM_017448.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr16:75146543 G>C maps to NM_153486.3 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:11233895 A>G maps to NM_000527.4 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:11227550 C>T maps to NM_000527.4 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:54483763 C>T did not map to a codon.
Sequencing variant TCGA-BA-A4IH-01A-11D-A25Y-08 chr1:22141023 C>T maps to NM_001013693.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr23:140270911 C>T did not map to a codon.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr23:140271159 T>C did not map to a codon.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr23:140271119 C>T did not map to a codon.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr23:140271068 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr22:44893382 C>T maps to NM_032287.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:226127191 C>T maps to NM_003240.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:226125197 C>A maps to NM_003240.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:156711003 G>T maps to NM_001004316.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr6:33740485 C>T maps to NM_181336.3 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr19:54969110 A>G did not map to a codon.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr19:54965697 C>T maps to ENST00000431846 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:54965652 C>A maps to ENST00000431846 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:54967629 G>A maps to ENST00000431846 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr19:54973653 C>T maps to NM_198988.1 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:52242002 A>T did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:66062269 C>A maps to NM_002303.5 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:66036307 G>T maps to NM_002303.5 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr1:66102650 C>T maps to NM_002303.5 Q1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:66058501 A>C maps to NM_002303.5 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:66036414 C>A maps to NM_002303.5 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:66081723 C>T maps to NM_002303.5 Q677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:66036243 C>T maps to NM_002303.5 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr1:66088606 G>A maps to NM_002303.5 W872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr1:66067601 C>T maps to NM_002303.5 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr1:66102289 G>A maps to NM_002303.5 E1030E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr3:189702337 C>T did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:6943183 G>T maps to NM_014262.3 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr12:6940503 C>A maps to NM_014262.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:6940434 G>A maps to NM_014262.3 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:6939087 G>C maps to NM_014262.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr8:38264943 C>A maps to ENST00000379957 S459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr7:2559806 C>T maps to NM_001040167.1 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr7:2552940 C>T maps to NM_001166355.1 Y66Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:2559920 G>A maps to NM_001040167.1 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr11:63283756 G>A maps to NM_001142535.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:40095318 G>C did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:40097948 C>A maps to NM_013268.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:40197265 T>C maps to NM_203471.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr22:37967897 G>C maps to NM_006498.2 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr14:55604801 C>T maps to NM_002306.3 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr17:76968227 G>C maps to NM_005567.3 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr17:76967897 G>A maps to NM_005567.3 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:76967753 C>T maps to NM_005567.3 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:39297124 G>A maps to NM_006149.3 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr17:20363738 C>T maps to ENST00000324290 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr10:95552568 C>A maps to NM_005097.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr4:25005705 G>A maps to NM_018176.3 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr4:25005441 C>T maps to NM_018176.3 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:35617861 G>A maps to NM_139284.2 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:35625001 G>A maps to NM_139284.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr14:93176021 G>A maps to NM_005606.6 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr14:93199104 G>A maps to NM_005606.6 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:93179216 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr11:27389779 G>A maps to NM_018490.2 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:202287785 C>G maps to NM_001017403.1 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:202287593 G>A maps to NM_001017403.1 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:202287122 C>T maps to NM_001017403.1 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:202287686 C>T maps to NM_001017403.1 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:202287896 C>G maps to NM_001017403.1 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:202245592 C>T maps to NM_001017403.1 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:202288299 C>T maps to NM_001017403.1 Q957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:63990489 A>G maps to NM_016571.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr6:63989943 G>A maps to NM_016571.2 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr6:63990177 G>A maps to NM_016571.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr6:63990432 C>T maps to NM_016571.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:206785671 G>C maps to NM_006893.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:49519456 G>A maps to NM_000894.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr13:39918177 G>A maps to NM_005780.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr23:111874750 G>C did not map to a codon.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr23:111914238 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:77805826 G>A maps to NM_005779.2 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr5:77805895 C>G maps to NM_005779.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:77805874 C>T maps to NM_005779.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr7:104377218 T>C maps to NM_199000.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:104377191 T>A maps to NM_199000.2 C172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:35773512 G>A maps to NM_182548.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:35773542 C>T maps to NM_182548.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr6:35773524 C>T maps to NM_182548.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:126172786 C>T maps to NM_022126.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr17:35299543 G>A maps to NM_005568.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr17:35297813 G>C did not map to a codon.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr17:35295562 C>T maps to NM_005568.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr17:35298159 C>A maps to NM_005568.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr17:35297709 C>T maps to NM_005568.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr9:126776322 G>T maps to NM_004789.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr9:126777640 G>A maps to NM_004789.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr9:139089572 C>T maps to NM_014564.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr9:139090819 G>A maps to NM_014564.3 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:139092510 G>C maps to NM_014564.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:180243596 G>C maps to NM_033343.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:180199672 G>A maps to NM_033343.3 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:180240978 C>T maps to NM_033343.3 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:180243575 G>A maps to NM_033343.3 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr1:180199675 T>C maps to NM_033343.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr12:113906036 C>T maps to NM_022363.2 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:75622594 T>C maps to NM_001001933.1 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:75622624 T>G maps to NM_001001933.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr1:197898182 G>T maps to NM_020204.2 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:197896917 T>C maps to NM_020204.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:197898130 G>C did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:197889214 G>A maps to NM_020204.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:197896779 C>T maps to NM_020204.2 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:197889130 C>T maps to NM_020204.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr1:197889124 G>A maps to NM_020204.2 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:38486047 G>A maps to NM_002310.5 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:38486029 C>T maps to NM_002310.5 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr5:38506106 A>G maps to NM_002310.5 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr19:48646857 T>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:33318805 G>A maps to NM_013975.3 K386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr17:33321375 C>T maps to NM_013975.3 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:108861663 G>A maps to NM_001098268.1 N651N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr13:108861731 T>A maps to NM_001098268.1 K629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr13:108861129 C>T maps to NM_001098268.1 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:55106643 C>A maps to NM_006863.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr19:55107879 C>G maps to NM_006863.1 Y395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr19:55106220 G>A maps to NM_006863.1 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:55106847 C>A maps to NM_006863.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr19:55107221 G>A maps to NM_006863.1 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr19:55107314 C>T maps to NM_006863.1 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr19:55087421 G>T maps to NM_001130917.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:55086048 G>T maps to NM_001130917.1 G118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr19:55098522 G>T maps to NM_001130917.1 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:55087019 G>T did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:55087310 G>T maps to NM_001130917.1 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:55087484 C>T maps to NM_001130917.1 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:55087565 C>T maps to NM_001130917.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:55086387 C>T maps to NM_001130917.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:54803658 C>T maps to ENST00000251375 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:54802122 G>A maps to ENST00000251375 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:54802684 G>A maps to ENST00000251375 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr19:54803280 G>A maps to ENST00000251375 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr19:54803070 C>T maps to ENST00000251375 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:54849457 G>C maps to NM_012276.3 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr19:54849883 G>C maps to NM_012276.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:54848373 G>T maps to NM_012276.3 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr19:54823883 C>T maps to NM_021250.2 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:54819016 G>C maps to NM_021250.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:54822642 G>A maps to NM_181879.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:54744216 G>A maps to ENST00000419410 Y397Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr19:54744755 G>A maps to ENST00000245620 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:54742903 G>T maps to NM_024318.2 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:54744932 G>A maps to ENST00000245620 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr19:55143425 C>T maps to ENST00000427581 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:55147976 G>C maps to ENST00000427581 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:55143680 G>C maps to ENST00000427581 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr19:54778551 G>A maps to ENST00000391747 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr19:54780727 C>G maps to ENST00000391747 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr19:54782208 G>C maps to ENST00000391747 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr19:54724539 G>A maps to NM_001081450.1 Y372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr19:54726839 G>A maps to NM_001081450.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:55177323 C>A maps to ENST00000391733 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr19:55175416 T>G maps to ENST00000391733 Y92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr19:54755937 G>A maps to NM_001081442.1 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:54758760 C>G maps to NM_001081442.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr19:54758781 C>T maps to NM_001081442.1 K357K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:54758763 G>A maps to NM_001081442.1 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:54761047 G>A maps to NM_001081442.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr19:54758895 C>G maps to NM_001081442.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:50616055 G>A maps to NM_001113546.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr4:41648831 T>C maps to NM_014988.2 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr3:45636952 A>G maps to NM_014240.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:45636826 G>A maps to NM_014240.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:73523308 C>G maps to NM_002314.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr7:73535346 C>T maps to NM_002314.2 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr22:31673038 C>T maps to NM_001031801.1 D658D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-7095-01A-21D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:128415075 G>A maps to NM_017980.4 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:128396882 G>A maps to NM_017980.4 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:128414993 C>A maps to NM_017980.4 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr12:81331468 C>A maps to NM_004664.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr12:81331432 G>C maps to NM_004664.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr12:81205333 T>C maps to NM_004664.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:226465499 G>A maps to ENST00000366807 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:77907917 C>A maps to NM_032808.5 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:77906817 G>A maps to NM_032808.5 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr9:27949844 C>G maps to NM_152570.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:27950477 G>A maps to NM_152570.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr9:27950060 G>T maps to NM_152570.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:151774475 G>T maps to NM_001004432.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr1:151774778 C>T maps to NM_001004432.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr15:101120723 G>A maps to NM_001040616.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr15:101112103 C>G maps to NM_001040616.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr19:42911575 C>T maps to NM_005357.2 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:42914527 G>C maps to NM_005357.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr19:42914581 C>A maps to NM_005357.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr19:42914536 C>T maps to NM_005357.2 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr10:90433491 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr18:47108774 C>T maps to NM_006033.2 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr18:47113115 A>G maps to NM_006033.2 K459K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr18:47110035 G>A maps to NM_006033.2 W423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr18:47107899 C>T maps to NM_006033.2 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr18:47101892 C>T maps to NM_006033.2 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr3:185252693 T>C maps to NM_139248.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr3:185252681 G>C maps to NM_139248.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr21:15525003 G>A maps to NM_198996.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr21:15538693 G>C maps to NM_198996.2 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr10:90521212 T>C maps to NM_001102469.1 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr5:96460171 G>A maps to NM_153234.4 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:96478235 G>A maps to NM_153234.4 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:145498679 C>T maps to NM_153713.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:18144787 C>T maps to NM_004140.3 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:73568021 C>A maps to NM_001031803.1 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr17:73569246 C>T maps to NM_001031803.1 G871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr15:75113084 C>G maps to NM_021819.2 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr15:75105239 C>G maps to NM_021819.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr15:75105353 C>T maps to NM_021819.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr15:75108778 C>A maps to NM_021819.2 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:97400155 C>G maps to NM_001142292.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr2:97377726 G>A maps to NM_001142292.1 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:49498290 G>A maps to NM_018113.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:70411788 G>A maps to NM_018368.3 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:70386389 G>A maps to NM_018368.3 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:70428851 G>C maps to NM_018368.3 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr6:70428940 C>T maps to NM_018368.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:8607272 A>C maps to NM_014583.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr3:8609124 G>A did not map to a codon.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr22:50943407 C>T maps to NM_033200.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr22:50941936 G>A maps to NM_033200.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr22:50943395 C>A maps to NM_033200.2 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:197687214 A>G maps to NM_001136049.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:156106746 G>A maps to NM_170707.2 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr1:156108382 C>T maps to NM_170707.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:2434808 G>A maps to NM_032737.2 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:2444430 C>G maps to NM_032737.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:2438402 G>A maps to NM_032737.2 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr13:76381900 A>G maps to ENST00000357063 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr13:76391320 C>T maps to ENST00000357063 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:201868532 G>A maps to NM_012134.2 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr1:201869121 G>C maps to NM_012134.2 S340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:201868901 C>T maps to NM_012134.2 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:123302482 G>A maps to NM_207163.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:69168974 T>C maps to NM_198271.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:97822446 T>C maps to NM_014916.3 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr7:97821069 G>A maps to NM_014916.3 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr7:97821897 C>T maps to NM_014916.3 H707H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr7:97832935 G>A maps to NM_014916.3 P1386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr7:97823364 C>T maps to NM_014916.3 D1196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr7:97833481 G>T maps to NM_014916.3 S1489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr7:97821552 C>G maps to NM_014916.3 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr19:49004335 G>A maps to NM_001080434.1 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:165218666 C>T maps to NM_177398.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:165322353 G>A maps to NM_177398.3 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:165173277 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr9:129377707 C>T maps to NM_001174147.1 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:96314944 T>C maps to NM_005575.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr5:96320873 C>A maps to NM_005575.2 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr4:54424119 G>A maps to NM_032622.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:54364927 G>C maps to NM_001126328.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr4:54362402 G>A maps to NM_001126328.1 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:54327108 G>A maps to NM_001126328.1 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:28155585 C>T maps to NM_153371.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:11350480 G>A maps to ENST00000252453 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:20824540 T>C maps to NM_030941.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:20856093 C>G maps to NM_030941.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr12:12514170 G>A maps to NM_058169.3 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr19:5699114 G>A maps to NM_004793.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr16:48382182 G>C maps to NM_031490.2 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr16:48333615 G>A maps to NM_031490.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr8:12583337 A>T maps to NM_152271.3 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:12595578 A>G maps to NM_152271.3 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:100916182 C>T maps to NM_198461.3 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:118124509 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:118124488 G>A did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:118108891 C>T did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:153233514 C>T maps to NM_000427.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:121411145 G>A maps to NM_002317.5 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr15:74241807 G>A maps to NM_005576.2 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr8:23190958 G>A maps to NM_002318.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr8:23179756 T>G maps to NM_002318.2 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:23217677 C>T maps to NM_002318.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:23156367 C>T maps to NM_002318.2 W742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr2:74777455 G>A maps to NM_032603.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:74763194 T>A maps to NM_032603.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:100012125 G>A maps to NM_032211.6 D645D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:100012155 C>T maps to NM_032211.6 E635E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:160977187 C>T maps to NM_005577.2 R1614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:161007652 G>C maps to NM_005577.2 T1319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:161071469 G>A maps to NM_005577.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr6:160999615 C>A maps to NM_005577.2 S1470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr9:113704007 C>T maps to NM_057159.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr9:113703977 C>T maps to NM_057159.2 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr19:19737970 G>C maps to NM_004720.5 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:85331149 G>A maps to NM_012152.2 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr23:78010406 C>G did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:78010387 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:78010698 C>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:78011269 C>A did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr23:78011179 T>G did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:78010706 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:78010776 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:78010771 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr23:78011320 C>T did not map to a codon.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr12:6729532 C>T maps to ENST00000435659 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr12:6729715 C>T maps to ENST00000435659 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:1488527 G>A maps to NM_024830.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:1474682 C>A maps to NM_024830.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:1489928 G>A maps to NM_024830.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr5:1463912 G>A maps to NM_024830.3 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:7086774 A>T maps to NM_005768.5 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr19:14262301 G>A maps to NM_001008701.2 R1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:14277831 C>T maps to NM_001008701.2 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr19:14273619 G>A maps to NM_001008701.2 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr1:82416119 A>T maps to ENST00000370717 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr1:82431760 C>A maps to ENST00000370717 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr1:82372825 G>T maps to ENST00000370717 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:82436122 G>A maps to ENST00000370717 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:62897306 C>T maps to ENST00000506720 F1190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr4:62935924 C>T maps to ENST00000506720 L1348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr4:62935974 C>T maps to ENST00000506720 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr4:62935974 C>T maps to ENST00000506720 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr4:62758431 G>A maps to ENST00000506720 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr2:11924027 G>A maps to ENST00000396099 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr2:11911610 C>T maps to ENST00000396099 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr2:11911568 G>A maps to ENST00000396099 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr2:11943119 C>T maps to ENST00000396099 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:2938025 T>A maps to NM_014646.2 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr18:2923795 T>A maps to NM_014646.2 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr20:39978494 C>T maps to NM_022896.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:19811806 C>T maps to NM_000237.2 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:56342210 C>G maps to NM_006151.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr17:56344746 G>A maps to NM_006151.2 Q577Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr17:56345267 C>T maps to NM_006151.2 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr17:56320354 C>G maps to NM_006151.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr3:188590461 G>T maps to NM_005578.3 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:188242515 T>C maps to NM_005578.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr3:188590550 G>A maps to NM_005578.3 E570E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:188123991 C>T maps to NM_005578.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:188590478 C>T maps to NM_005578.3 A546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr9:104071491 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr9:104048519 T>A did not map to a codon.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr19:11474441 C>G maps to NM_001170635.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:11470245 C>G maps to NM_022737.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:11470546 C>T maps to NM_001170635.1 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:11470231 C>T maps to NM_022737.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:813187 G>A maps to NM_024888.1 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr1:99762292 G>T did not map to a codon.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:99772406 C>T maps to NM_014839.4 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr1:99772514 T>C maps to NM_014839.4 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:99771257 G>A maps to NM_014839.4 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr1:99771527 G>A maps to NM_014839.4 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:99771296 A>G maps to NM_014839.4 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr1:99771684 C>T maps to NM_014839.4 Q471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:99418769 A>G maps to NM_001037317.1 Y159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr1:99422163 C>G did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr11:58322349 A>G maps to NM_004811.2 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:58317310 C>T maps to NM_004811.2 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:151682969 T>G maps to NM_006726.3 A1870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:151186874 C>A maps to NM_006726.3 *2864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:151509250 G>C maps to NM_006726.3 L2104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr4:151271209 C>G maps to NM_006726.3 V2443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:151773392 G>A maps to NM_006726.3 Q1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:47303004 C>T maps to NM_001164211.1 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr23:114357667 C>T did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr23:114357437 A>G did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:114357121 G>A did not map to a codon.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr3:197559097 C>T maps to ENST00000425562 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr3:197566208 A>G maps to ENST00000425562 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr7:100179490 G>A maps to NM_002319.3 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr11:802260 C>A maps to NM_145886.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:799972 G>C maps to NM_145886.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr11:803326 G>A maps to NM_145886.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:804232 G>A maps to NM_145886.3 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr11:800349 G>A maps to NM_145886.3 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:39805043 C>A maps to NM_020862.1 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:39804665 G>A maps to NM_020862.1 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:40399495 G>A maps to NM_020737.1 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:40359912 C>T maps to NM_020737.1 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr6:40399667 G>A maps to NM_020737.1 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr6:40400810 C>T maps to NM_020737.1 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr6:40399880 G>C maps to NM_020737.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr6:40360116 G>A maps to NM_020737.1 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:36431158 C>T maps to NM_024509.1 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:36430642 C>T maps to NM_024509.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:36430791 C>A maps to NM_024509.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:66626405 C>T maps to NM_024036.4 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr14:42355881 G>A maps to NM_152447.3 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr14:42360815 A>T maps to NM_152447.3 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr14:42356803 A>T maps to NM_152447.3 K326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr14:42360708 C>T maps to NM_152447.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr14:42360919 C>A maps to NM_152447.3 S618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr14:42356271 C>A maps to NM_152447.3 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:4538050 C>T maps to NM_052972.2 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr3:66457860 C>G maps to NM_015541.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr3:66501996 G>A maps to NM_015541.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr1:113636138 A>T maps to NM_014813.1 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr1:113616159 C>G maps to NM_014813.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:113666512 C>T maps to NM_014813.1 P996P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:113638609 A>G maps to NM_014813.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr1:113638915 G>A maps to NM_014813.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr12:59271320 C>T maps to NM_153377.3 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr12:59272719 C>A maps to NM_153377.3 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr12:59271287 G>A maps to NM_153377.3 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr12:59282175 G>A maps to NM_153377.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:85992309 C>A maps to NM_015613.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr10:86001138 G>T maps to NM_015613.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr10:85992183 A>G maps to NM_015613.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:85992039 G>T maps to NM_015613.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:85991727 G>T maps to NM_015613.2 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr10:85997336 G>T maps to NM_015613.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr10:85984194 G>T maps to NM_001017924.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:85984391 G>A maps to NM_001017924.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr4:110791581 G>A maps to NM_198506.2 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:110791476 G>T maps to NM_198506.2 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:25259892 G>T maps to ENST00000354454 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr12:57570908 C>T maps to NM_002332.2 Y1359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:57571368 C>T maps to NM_002332.2 D1452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:57573151 C>T maps to NM_002332.2 I1593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr12:57594937 T>C did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:57538854 G>A maps to NM_002332.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr12:57571374 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr12:57532246 A>T maps to NM_002332.2 K25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57554759 C>T maps to NM_002332.2 H688H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57569839 C>T maps to NM_002332.2 T1314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr12:57573658 C>A maps to NM_002332.2 A1687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr12:57556242 G>T maps to NM_002332.2 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr12:57550689 G>C maps to NM_002332.2 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:150174186 G>A maps to NM_032832.5 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:150164230 G>A maps to NM_032832.5 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr8:105503224 C>T maps to NM_013437.4 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr8:105503737 C>G maps to NM_013437.4 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:141083448 T>A did not map to a codon.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr2:141806555 A>G maps to NM_018557.2 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:140995761 C>A maps to NM_018557.2 G4507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr2:141032096 G>C maps to NM_018557.2 V4346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:141457817 C>A did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:141473633 A>T maps to NM_018557.2 I1977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr2:141625741 G>A maps to NM_018557.2 D1420D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:141533691 T>C maps to NM_018557.2 K1825K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:141072661 G>T maps to NM_018557.2 S4216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:141643800 T>A maps to NM_018557.2 T1290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:141130601 C>A maps to NM_018557.2 G3581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr2:142238094 C>T maps to NM_018557.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr2:142888280 G>C maps to NM_018557.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:141201896 A>C did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr2:141777552 C>G maps to NM_018557.2 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:141208160 C>A maps to NM_018557.2 G3345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:141771281 A>G maps to NM_018557.2 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:141986940 C>A maps to NM_018557.2 G221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr2:141267497 G>A maps to NM_018557.2 C2799C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr2:140992402 C>T maps to NM_018557.2 A4537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:141598640 G>A maps to NM_018557.2 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr2:141299369 A>T maps to NM_018557.2 A2455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:141081530 C>A maps to NM_018557.2 E4149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr2:141250262 C>G did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr2:141093260 C>T maps to NM_018557.2 L4013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr2:141128762 A>G maps to NM_018557.2 A3620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:141459359 C>T maps to NM_018557.2 T2119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr2:141201938 C>T maps to NM_018557.2 G3418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:141245233 G>T maps to NM_018557.2 P3065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr2:141762943 G>A maps to NM_018557.2 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr2:141457978 C>T maps to NM_018557.2 R2213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr2:141665505 C>A maps to NM_018557.2 E1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:141607800 A>G maps to NM_018557.2 P1603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:141773267 C>T maps to NM_018557.2 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr2:141272297 T>C maps to NM_018557.2 K2731K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr2:141643779 G>A maps to NM_018557.2 F1297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:141641477 G>A maps to NM_018557.2 I1359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr2:141072573 T>A maps to NM_018557.2 G4245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:170062966 G>A maps to NM_004525.2 V2421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:170115653 G>T maps to NM_004525.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr2:170103910 G>T maps to NM_004525.2 S962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:170136934 A>G maps to NM_004525.2 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:170063262 G>A maps to NM_004525.2 L2323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:170101260 C>T maps to NM_004525.2 K1124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:169989113 G>A maps to NM_004525.2 N4566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:170058312 G>T maps to NM_004525.2 R2759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:170096253 A>T maps to NM_004525.2 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:170013896 G>A maps to NM_004525.2 D4001D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:170101320 G>A maps to NM_004525.2 H1104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:170028585 A>G maps to NM_004525.2 P3734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr2:169989167 A>G maps to NM_004525.2 D4548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:170177350 G>A maps to NM_004525.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr2:170139443 C>G maps to NM_004525.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr2:170025079 G>A maps to NM_004525.2 G3868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:170053481 T>C maps to NM_004525.2 Q2879Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:170175356 C>T maps to NM_004525.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr2:170031766 C>T maps to NM_004525.2 P3568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr2:170113746 G>A maps to NM_004525.2 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr2:170068604 G>C maps to NM_004525.2 L2051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:186295606 C>T maps to ENST00000362004 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:33696632 C>T maps to NM_002333.3 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:33696503 G>T maps to NM_002333.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:33697257 C>T maps to NM_002333.3 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:33697064 T>C maps to NM_002333.3 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr11:46903410 G>A maps to ENST00000256991 R931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr11:46897148 G>A maps to ENST00000256991 L1306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr11:46898165 G>A maps to ENST00000256991 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr11:46890259 G>A maps to ENST00000256991 T1659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:68197130 C>G maps to NM_002335.2 V1242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:68181316 C>T maps to NM_002335.2 F888F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:68131337 G>A maps to NM_002335.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr11:68154174 G>A maps to NM_002335.2 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:68177398 C>T maps to NM_002335.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:68115390 C>T maps to NM_002335.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:68207317 C>T maps to NM_002335.2 D1474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr11:68115507 G>A maps to NM_002335.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr22:25755870 G>C maps to NM_001135772.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr22:25753224 G>A maps to NM_001135772.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr12:12315146 G>A maps to NM_002336.2 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr12:12334166 G>A maps to NM_002336.2 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:12274060 C>G maps to NM_002336.2 *1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:12318021 G>A maps to NM_002336.2 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr12:12419612 A>G did not map to a codon.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:53736920 G>C maps to NM_004631.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:53736706 C>T maps to NM_004631.3 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr1:53722975 G>A maps to NM_004631.3 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:3516630 T>A maps to NM_002337.2 K287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:3520616 C>T maps to NM_002337.2 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:44161340 C>T maps to NM_133259.3 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:44128663 C>G did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:44162017 C>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr2:44201420 G>A maps to NM_133259.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr2:44121769 T>C did not map to a codon.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr6:53747726 T>C maps to NM_018214.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:53787548 C>T maps to NM_018214.4 N511N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:70004348 C>A maps to NM_201550.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:145746351 G>A maps to NM_014665.2 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr5:192315 C>T maps to NM_001080478.1 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr5:195404 C>T maps to NM_001080478.1 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr5:195215 C>T maps to NM_001080478.1 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr5:192396 C>T maps to NM_001080478.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:194080602 G>T maps to NM_001135057.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr3:194081061 G>A maps to NM_001135057.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr3:194081301 G>A maps to NM_001135057.2 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr6:25600787 G>C maps to NM_017640.5 R1122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:25551135 A>T did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:25450577 C>T maps to NM_017640.5 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:25551232 C>T maps to NM_017640.5 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr14:24531702 C>G maps to NM_138360.3 S832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr7:102580024 C>T maps to NM_001031692.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:102580024 C>T maps to NM_001031692.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:46574373 G>C maps to NM_024512.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:46574322 A>G maps to NM_024512.3 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:7014884 G>T maps to NM_201650.2 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr10:134165109 G>A did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr21:45877294 G>T maps to NM_030891.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr18:7231915 C>T maps to NM_001105581.1 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr18:7231399 C>T maps to NM_001105581.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr18:7231432 G>A maps to NM_001105581.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:7231423 C>T maps to NM_001105581.1 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr18:7231852 C>G maps to NM_001105581.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr3:169557901 C>G maps to NM_024727.2 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:76372273 G>A maps to NM_001128922.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr11:76371158 A>T maps to NM_001128922.1 L493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:76370752 G>C maps to NM_001128922.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr11:76371961 C>T maps to NM_001128922.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:196387578 C>G maps to NM_198565.1 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr3:196388109 C>T maps to NM_198565.1 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:196388514 C>T maps to NM_198565.1 C667C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr3:196388067 C>T maps to NM_198565.1 L518L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-7245-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:67405000 G>A maps to NM_018296.5 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr16:67412490 G>A did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr16:67410681 G>A maps to NM_018296.5 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:44408470 C>A maps to NM_014834.4 T1276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr17:44632663 C>G maps to NM_001006607.2 S1643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr17:30348462 G>T maps to ENST00000327564 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:30349316 G>A maps to ENST00000327564 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr17:30349044 G>T maps to ENST00000327564 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr17:30372815 C>T maps to ENST00000327564 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr1:100618067 G>A maps to NM_144620.2 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr3:26751267 C>A maps to NM_052953.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr3:26751570 G>A maps to NM_052953.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr3:26751182 G>A maps to NM_052953.2 W7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:127669961 G>C maps to NM_022143.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:127670192 G>A maps to NM_022143.4 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:70618225 C>T maps to NM_017768.4 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:46745879 C>T maps to ENST00000254454 Q646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:46745254 C>T maps to ENST00000254454 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:46751226 T>C maps to ENST00000254454 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:54423864 C>A maps to NM_052940.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr17:79985311 G>A maps to NM_144999.2 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr17:79982594 C>T maps to NM_144999.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr1:3712428 G>C maps to NM_020710.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr1:3712632 G>T maps to NM_020710.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:17898416 C>A maps to NM_031294.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:17891327 G>A maps to NM_031294.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:71302303 C>T maps to NM_017691.3 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:71329517 G>A maps to NM_017691.3 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:51022333 G>A maps to NM_001080457.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:51022384 C>A maps to NM_001080457.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:51051873 C>T maps to NM_001080457.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:40136240 C>A maps to NM_020929.1 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr11:40137053 A>G maps to NM_020929.1 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr11:40136522 G>T maps to NM_020929.1 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr11:40137211 C>A maps to NM_020929.1 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:40137316 G>T maps to NM_020929.1 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr11:40137505 T>G maps to NM_020929.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:40136048 A>T maps to NM_020929.1 Y598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:40137316 G>A maps to NM_020929.1 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr11:40137482 G>A maps to NM_020929.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr11:40136231 T>A maps to NM_020929.1 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr16:84203861 A>G maps to NM_178452.4 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr16:84203864 G>A maps to NM_178452.4 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr16:84208328 G>C did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:84211374 C>G maps to NM_178452.4 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr16:84203678 C>A maps to NM_178452.4 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:84203765 T>C maps to NM_178452.4 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:165532976 C>T maps to NM_001005214.3 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr1:165533033 G>A maps to NM_001005214.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:56954743 C>A maps to NM_001005210.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:56950026 C>T maps to NM_001005210.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr3:120053966 G>A maps to NM_001099678.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr3:120053937 A>C maps to NM_001099678.1 Y226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:133622459 A>G maps to ENST00000250173 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr8:133622492 G>A maps to ENST00000250173 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr8:133596001 G>A maps to ENST00000250173 Q389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:133584729 T>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:133673703 A>T did not map to a codon.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr4:52862053 C>T maps to NM_001024611.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:52861042 G>A maps to NM_001024611.1 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:52869412 G>A maps to NM_001024611.1 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr4:52861474 A>G maps to NM_001024611.1 Y571Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:52861264 G>A maps to NM_001024611.1 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr8:67925255 C>T maps to ENST00000421742 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr8:67929967 G>T maps to ENST00000421742 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:67926686 G>C maps to ENST00000421742 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:70505166 G>C maps to NM_020794.2 V1182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:70504191 T>A maps to NM_020794.2 A857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:70518707 G>C did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:70555456 T>C maps to NM_020794.2 S1462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:70504980 G>A maps to NM_020794.2 V1120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:70502125 G>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr1:70488939 G>A maps to NM_020794.2 Q521Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr1:70505430 G>A maps to NM_020794.2 W1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr1:70541830 T>C maps to NM_020794.2 Y1396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr9:131670252 C>T maps to NM_001127244.1 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr9:131678562 C>T maps to NM_001127244.1 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr9:131670177 G>A maps to NM_001127244.1 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:90049933 G>T maps to NM_015350.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:90058600 G>A maps to NM_015350.2 *804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:90178612 C>T maps to NM_032270.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:90178872 C>T maps to NM_032270.4 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:90180457 C>T maps to NM_032270.4 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:90401041 G>A maps to NM_001134479.1 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:90400811 C>T maps to NM_001134479.1 Q729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr1:90398914 C>T maps to NM_001134479.1 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:7964964 C>T maps to NM_025061.3 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:7965434 A>T maps to NM_025061.3 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:7964150 C>T maps to NM_025061.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:37107712 A>G did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr12:85449884 C>T maps to NM_001079910.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:85500376 C>T maps to NM_001079910.1 Q1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:85434272 A>G maps to NM_001079910.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr12:85450283 G>A maps to NM_001079910.1 E571E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:85515604 C>T maps to NM_001079910.1 Q1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:85441136 C>T maps to NM_001079910.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:74507185 C>A maps to NM_001105659.1 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr1:74507186 T>C maps to NM_001105659.1 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:74492541 C>T maps to NM_001105659.1 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr1:74621484 C>G maps to NM_001105659.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:74507087 G>T maps to NM_001105659.1 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:74507573 G>T maps to NM_001105659.1 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:74649195 G>C maps to NM_001105659.1 S58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:169546665 G>T maps to NM_001080460.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:169540506 G>C maps to NM_001080460.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr3:169540269 C>G maps to NM_001080460.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr3:169540248 C>T maps to NM_001080460.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr3:169540506 G>A maps to NM_001080460.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr3:169540092 C>T maps to NM_001080460.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr3:169540080 G>A maps to NM_001080460.1 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr3:169540059 C>T maps to NM_001080460.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IH-01A-11D-A25Y-08 chr15:101598235 G>T maps to NM_024652.3 P1523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr15:101528986 G>A maps to NM_024652.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr15:101554518 A>C did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:101528995 C>T maps to NM_024652.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr15:101569221 G>A maps to NM_024652.3 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr15:101562618 T>C maps to NM_024652.3 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:40707844 G>C maps to NM_198578.3 S1536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:40631905 G>T did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr12:40692982 C>T maps to NM_198578.3 H1140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:40681306 T>C maps to NM_198578.3 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr12:40626085 C>G maps to NM_198578.3 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr12:40715963 A>T maps to NM_198578.3 T1766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:40734241 C>G maps to NM_198578.3 S2032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr12:40646774 C>T maps to NM_198578.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:40692914 A>T maps to NM_198578.3 K1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr12:40758832 C>T maps to NM_198578.3 V2457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr12:40631813 C>T maps to NM_198578.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:3886402 C>A maps to NM_020873.5 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:3887530 G>C maps to NM_020873.5 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:3888389 G>T maps to NM_020873.5 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:3887185 T>C maps to NM_020873.5 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:3887512 C>T maps to NM_020873.5 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr3:3886867 T>A maps to NM_020873.5 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:204587125 G>A maps to NM_201630.1 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr7:110762918 C>A maps to NM_018334.4 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr7:110764282 C>T maps to NM_018334.4 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:110762956 C>A maps to NM_018334.4 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr7:110763262 C>A maps to NM_018334.4 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr20:6021814 G>T maps to NM_152611.3 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr20:6031558 C>T maps to NM_152611.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr20:6031434 G>A maps to NM_152611.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr20:6032875 G>A maps to NM_152611.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:80529963 C>T maps to NM_178839.4 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr2:80530326 G>T maps to NM_178839.4 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr2:80529876 G>A maps to NM_178839.4 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:80530248 G>T maps to NM_178839.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:80530449 C>G maps to NM_178839.4 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:80530152 C>G maps to NM_178839.4 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:80530266 G>A maps to NM_178839.4 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr2:80530509 C>T maps to NM_178839.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:80530935 G>A maps to NM_178839.4 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:80530926 G>A maps to NM_178839.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr2:80530770 G>A maps to NM_178839.4 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr2:80529786 G>T maps to NM_178839.4 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:80529603 G>A maps to NM_178839.4 Y447Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:68687990 C>G maps to NM_178011.3 Y439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr10:68688014 G>C maps to NM_178011.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:68687294 C>G maps to NM_178011.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr10:68687180 G>A maps to NM_178011.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr10:68686992 G>T maps to NM_178011.3 G107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr10:68686346 T>C did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:77745731 T>C maps to NM_001134745.1 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:77745755 T>G maps to NM_001134745.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:77745761 A>T maps to NM_001134745.1 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:77745716 A>T maps to NM_001134745.1 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:77746580 C>T maps to NM_001134745.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:130263292 G>A maps to NM_001005374.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:1943842 G>T maps to NM_001163926.1 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:71804596 G>A maps to NM_145309.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:115805399 G>A maps to NM_002338.3 C53C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-F7-A624-01A-22D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:116163800 T>C maps to NM_002338.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:115571360 C>T maps to NM_002338.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr3:194362874 C>T maps to NM_018385.2 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:194362967 C>G maps to NM_018385.2 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:194390863 A>G maps to NM_018385.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:194380831 T>C maps to NM_018385.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr3:194390736 C>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:38033817 G>A maps to NM_014462.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:157181900 G>T maps to NM_173491.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr3:14223080 G>T maps to NM_014463.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr19:18420672 T>C did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr21:47635093 C>T maps to NM_002340.5 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr12:21196319 T>C maps to ENST00000381541 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:21242847 C>T maps to ENST00000381541 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:21207555 C>T maps to ENST00000381541 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr12:21201742 A>T maps to ENST00000381541 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr12:21201655 C>T maps to ENST00000381541 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:96394780 A>G maps to NM_000895.1 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr12:96409360 C>T maps to NM_000895.1 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:31548551 G>A maps to NM_002341.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr6:31548883 G>A maps to NM_002341.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr14:24785366 G>T maps to NM_181657.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:33488458 G>T maps to ENST00000354476 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:33540328 G>A maps to ENST00000354476 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr2:33412050 C>T maps to ENST00000354476 Q444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:33246015 C>T maps to ENST00000354476 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr14:74968147 G>A maps to NM_000428.2 C1772C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr14:75078170 C>T maps to NM_000428.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:74995354 C>T maps to NM_000428.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:75018992 C>G maps to NM_000428.2 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr11:65319551 G>A maps to NM_001130144.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:65314017 C>A maps to NM_001130144.2 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr11:65308357 G>A maps to NM_001130144.2 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:41125250 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:41135436 C>A maps to ENST00000308370 P1618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:46482937 C>A maps to NM_002343.3 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:46479620 C>A did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:41804996 C>T maps to NM_002344.5 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:41804372 G>C maps to NM_002344.5 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr15:41804948 C>T maps to NM_002344.5 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr6:144178464 C>T maps to NM_032860.3 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr16:242963 C>T maps to NM_201412.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr12:91502198 G>C maps to NM_002345.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr1:23418369 G>A maps to NM_001142546.1 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr11:24750789 A>C maps to NM_001009909.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:114540828 G>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:114540769 G>T did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr23:114536557 C>T did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr23:114540928 A>G did not map to a codon.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr23:114537942 C>T did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:114540823 G>C did not map to a codon.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr8:143866645 G>A maps to NM_003695.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr6:31646944 G>A maps to NM_025262.3 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:143783129 G>C maps to ENST00000292430 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr2:160709781 A>G did not map to a codon.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:160690587 G>A maps to NM_001198759.1 Q1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr2:160673379 G>C maps to NM_001198759.1 L1439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:160663607 G>C maps to NM_001198759.1 V1622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:6589095 G>A maps to NM_004271.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:160769733 C>T maps to ENST00000263285 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:160784327 G>A maps to ENST00000263285 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:160793528 G>A maps to ENST00000263285 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr8:74922284 C>A maps to NM_015364.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr8:74922332 C>T maps to NM_015364.4 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr8:74922332 C>T maps to NM_015364.4 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr8:74941281 C>G maps to NM_015364.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:56879419 G>T maps to NM_002350.2 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:56879310 C>T maps to NM_002350.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:143832541 C>A maps to NM_205545.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr2:150305596 C>G maps to NM_194317.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr2:150061850 T>C maps to NM_177964.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr1:24119249 G>A maps to NM_007260.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:219384872 C>T maps to NM_138794.3 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:219347231 G>A did not map to a codon.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr1:219366441 A>G maps to NM_138794.3 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr1:219383943 A>G maps to NM_138794.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr16:20927014 G>A maps to NM_020424.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr5:89814774 G>T maps to NM_198273.1 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:100269707 T>A maps to NM_152449.2 K172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr15:100269525 G>A maps to NM_152449.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr1:235922443 G>A maps to NM_000081.2 Q2237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:235915331 G>A maps to NM_000081.2 Q2534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr1:235940476 G>A maps to NM_000081.2 S1782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:235904811 G>A maps to NM_000081.2 H2756H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr1:235972998 A>G maps to NM_000081.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:235966292 A>G maps to NM_000081.2 C1209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr1:235993527 G>A maps to NM_000081.2 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:29581595 C>T maps to NM_032517.4 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr10:29599072 C>T maps to NM_032517.4 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr10:30900883 T>A maps to NM_183058.2 *195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr10:30915091 G>A maps to NM_183058.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr22:21349205 G>A maps to NM_006767.3 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:102762579 C>T maps to NM_032429.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:102763320 C>T maps to NM_032429.2 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:9095068 T>C maps to NM_002355.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:9098991 A>G maps to NM_002355.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr13:36049603 C>T maps to NM_005584.4 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr13:36050181 G>T maps to NM_005584.4 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr13:36050071 G>A maps to NM_005584.4 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr4:151504952 C>A maps to NM_006439.4 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:151504654 C>G maps to NM_006439.4 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:151504975 C>A maps to NM_006439.4 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr7:20198240 G>A maps to NM_182762.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:20198915 C>T maps to NM_182762.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:20199824 G>A maps to NM_182762.3 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr1:39907691 C>G maps to ENST00000361689 L4188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:39792904 G>A maps to ENST00000361689 E1503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:39753029 C>T maps to ENST00000361689 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:39749132 G>A maps to ENST00000361689 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:39763348 A>T maps to ENST00000361689 K810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:39826463 G>C did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:39854050 T>A maps to ENST00000361689 S3117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:39854051 G>T maps to ENST00000361689 E3118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:39806364 C>T maps to ENST00000289893 F1909F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr1:39800392 A>G maps to ENST00000289893 K1151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr1:39806218 G>T maps to ENST00000289893 E1861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr1:39838216 T>C maps to ENST00000361689 L2326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr1:39806525 G>A maps to ENST00000289893 L1934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:63767134 C>T maps to NM_014067.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr20:15967445 G>T maps to ENST00000310348 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr20:15412048 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:2265107 C>A maps to NM_003550.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr7:2188860 G>A maps to NM_003550.2 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:11736194 G>C maps to ENST00000376669 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:47330540 A>G maps to NM_003682.3 K1293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr11:47298326 G>C maps to NM_003682.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:47345331 C>T maps to NM_003682.3 C1496C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr11:47310954 G>A maps to NM_003682.3 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:166974631 A>T maps to NM_032858.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:166987196 G>T did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr8:145160606 G>A maps to NM_032272.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr20:39317052 C>A maps to NM_005461.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr7:1579887 C>T maps to NM_002360.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:35804287 A>G maps to NM_002361.3 K604K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:35786780 C>G maps to NM_002361.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:35790469 C>T maps to NM_002361.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:35800951 G>T maps to NM_002361.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:35791164 C>T maps to NM_002361.3 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:35786322 C>G maps to NM_002361.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:35786520 C>T maps to NM_002361.3 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr19:35800999 C>T maps to NM_002361.3 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr23:152483001 A>T did not map to a codon.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr23:151303807 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:151303505 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr23:151303719 C>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:151303999 G>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:151303038 T>A did not map to a codon.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr23:151303171 C>A did not map to a codon.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr23:151303874 T>C did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:151303323 C>T did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:151303695 C>G did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:151304049 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:148798246 G>C did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:148797304 G>T did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr23:148798057 T>C did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:148798377 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:148797756 G>A did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr23:148794916 T>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:151900744 T>C did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:151900412 A>T did not map to a codon.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr23:151900172 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr23:151899860 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:151935814 G>T did not map to a codon.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr23:151935539 G>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:151935916 A>T did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:151935917 G>T did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:151935757 C>A did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:151935674 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:151935643 A>C did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:151092702 C>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:151092985 T>A did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr23:151092295 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:151092750 C>T did not map to a codon.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr23:151283637 T>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:151283932 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:151283933 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:151283786 C>T did not map to a codon.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr23:151283858 C>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:151869845 C>G did not map to a codon.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr23:151869580 G>A did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:151870208 C>A did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:151870253 G>C did not map to a codon.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr23:151870026 C>G did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:149013597 C>T did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:149013284 G>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:149013785 A>G did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:30269380 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:30269431 G>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:30268766 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:30269233 C>A did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr23:30268841 G>T did not map to a codon.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr23:30269039 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:30269582 C>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:30269596 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:30269431 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr23:30269431 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr23:30268813 C>A did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:30269281 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr23:30269419 C>A did not map to a codon.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr23:27840149 G>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:27839500 A>T did not map to a codon.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr23:27839868 T>A did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:35821251 G>C did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:35820839 C>G did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:35820840 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:35821009 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr23:26157864 G>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:26157129 C>A did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:26158076 T>C did not map to a codon.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr23:26158051 G>C did not map to a codon.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr23:26157440 G>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:26158122 C>A did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr23:26157204 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr23:26157625 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr23:26157127 T>C did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr23:26157728 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr23:30236704 G>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr23:30237174 C>A did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr23:30237075 A>G did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:30237575 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:30254195 A>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:30254122 G>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:30254945 C>G did not map to a codon.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr23:30254047 C>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:30254264 T>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:30254264 T>C did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:30254870 C>G did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:30254628 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:30260671 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:30260336 C>T did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:30260455 C>G did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:30260833 C>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:30261231 C>T did not map to a codon.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr23:30260590 G>A did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:26212045 C>A did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:26212046 C>T did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr23:26212224 G>T did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr23:26212372 G>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:26212207 C>A did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr23:26212040 G>C did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:26212350 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:26212254 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:26212472 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:26212746 T>C did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr23:26213016 C>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr23:140993926 T>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:140993367 G>T did not map to a codon.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr23:140994008 C>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:140994993 G>A did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:140995038 C>G did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:140995931 G>C did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:140994506 C>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:140994308 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:140995491 G>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:140995642 C>A did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:140995989 A>G did not map to a codon.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr23:140996235 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr23:140996181 C>A did not map to a codon.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr23:140994878 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:140994190 C>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:140995681 T>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:140996135 C>A did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr23:140995559 T>C did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr23:140995928 C>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr23:140995749 C>T did not map to a codon.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr23:140994301 C>T did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr23:140995472 G>A did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:140995217 C>A did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:140995218 C>A did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr23:140995292 A>T did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr23:140994921 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:140996584 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:140996139 T>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:140994338 C>A did not map to a codon.
Sequencing variant TCGA-CV-A6K0-01B-21D-A31L-08 chr23:140995348 C>A did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr23:140993499 G>C did not map to a codon.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr23:140994644 C>T did not map to a codon.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr23:140994682 C>A did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:140995784 C>G did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:140994720 C>A did not map to a codon.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr23:140994456 A>C did not map to a codon.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr23:140994649 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr23:140994656 C>T did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:140994836 T>A did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr23:140994101 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr23:140996368 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:141291251 G>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:141291341 C>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:141290918 C>G did not map to a codon.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr23:141291580 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:141291746 G>A did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:141290745 C>G did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:141291673 C>T did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:141291307 A>G did not map to a codon.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr23:140984943 T>G did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr23:140985530 C>A did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:140984629 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:140984863 T>C did not map to a codon.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr23:140985589 T>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:140926156 G>T did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:140926142 T>C did not map to a codon.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr23:140985504 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:140969433 A>G did not map to a codon.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr23:140983073 G>A did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:140969549 G>A did not map to a codon.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr23:51640124 G>A did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr23:51639729 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:51638489 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:51643372 T>G did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:51641679 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr23:54841144 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:54837731 C>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:75648801 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr23:75648933 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:75650101 G>A did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:75649320 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:75650772 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:75648904 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:75648905 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:75649269 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:75650683 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:75650599 G>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:75649386 C>T did not map to a codon.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr23:75003749 G>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:75004400 G>T did not map to a codon.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr23:75004844 C>G did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr23:75004021 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:75004089 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr23:75004818 C>G did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:55479235 A>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr15:23890798 G>T maps to NM_019066.4 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr15:23889925 A>G maps to NM_019066.4 S988S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr15:23890015 C>T maps to NM_019066.4 W958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr3:65425584 C>T maps to NM_001033057.1 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr3:65350390 G>A maps to NM_001033057.1 T1100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr3:65367600 G>A maps to NM_001033057.1 A884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr3:65376847 C>T maps to NM_001033057.1 W795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr7:79082342 G>A maps to NM_012301.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:79082486 G>T maps to NM_012301.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr7:78150786 C>T maps to NM_012301.3 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:78131060 C>T maps to NM_012301.3 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:114193671 G>T maps to NM_001142782.1 E762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr1:114193779 C>T maps to NM_001142782.1 R798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr1:114215338 A>G maps to NM_001142782.1 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:114216017 G>A maps to NM_001142782.1 E1040E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr1:114165594 C>T maps to NM_001142782.1 Q447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr1:114128118 C>T maps to NM_001142782.1 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:49021377 G>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:49022441 C>G did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:53692755 G>A maps to NM_002370.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr23:77131008 C>T did not map to a codon.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr23:77126358 G>C did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr23:77112871 G>A did not map to a codon.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr23:77131008 C>T did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:77130964 A>T did not map to a codon.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr6:10818167 A>G maps to NM_005906.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr9:72723127 C>T maps to NM_153267.4 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr9:72758536 C>A maps to NM_153267.4 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr9:139748461 C>T maps to ENST00000392881 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr9:139754407 G>A maps to ENST00000392881 V1171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr9:139749722 G>A maps to ENST00000392881 Q405Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr5:179201800 C>T maps to NM_014757.4 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr5:179193110 C>G maps to NM_014757.4 S367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:179192839 G>T maps to NM_014757.4 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr11:95826264 G>A maps to NM_032427.1 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:95825904 T>A maps to NM_032427.1 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr4:140811146 G>A maps to ENST00000509479 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:140810675 C>T maps to ENST00000509479 Q638Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:140640737 G>A maps to ENST00000509479 S1052S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr4:140811122 T>C maps to ENST00000509479 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:140810660 C>T maps to ENST00000509479 Q643Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr23:149639238 G>T did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:149639447 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr23:149639634 A>T did not map to a codon.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:119501046 G>A maps to NM_005907.2 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr6:119611872 G>C maps to NM_005907.2 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:117984890 C>G maps to NM_006699.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr9:139990686 A>C did not map to a codon.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr9:139995565 C>G maps to NM_016219.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr9:139994164 C>T maps to NM_016219.3 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr9:140002087 C>T maps to NM_016219.3 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:25944443 C>G maps to NM_020379.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr1:26104777 G>A maps to NM_020379.2 Q480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:25944780 C>T maps to NM_020379.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:26012974 G>A maps to NM_020379.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr5:109152985 C>G maps to NM_002372.2 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr15:91454653 C>T maps to NM_006122.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr15:91448551 C>T maps to NM_006122.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:91448543 G>T maps to NM_006122.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr15:91461608 C>G maps to NM_006122.2 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:12767761 C>G did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:12763059 G>A maps to NM_000528.3 N651N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:12776598 C>T maps to NM_000528.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:6606981 G>A maps to NM_015274.1 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:6612991 C>T maps to NM_015274.1 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr15:75660448 G>A maps to NM_006715.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:103585970 C>T maps to NM_005908.3 W452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:96034605 A>G maps to NM_024641.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:96053863 T>C maps to NM_024641.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr23:43601195 G>C did not map to a codon.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr23:43590579 C>T did not map to a codon.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr23:43698133 G>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:43652759 C>A did not map to a codon.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr15:43818932 C>T maps to ENST00000382031 D1992D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr15:43816967 C>A maps to ENST00000382031 V1337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr15:43821896 C>T maps to ENST00000382031 L2933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr15:43820774 C>T maps to ENST00000382031 N2606N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:43820399 C>T maps to ENST00000382031 L2481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:43815392 G>A maps to ENST00000382031 Q812Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr15:43815350 T>C maps to ENST00000382031 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr5:71494371 G>A maps to NM_005909.3 P1730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr5:71495355 C>A maps to NM_005909.3 S2058S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:71482445 C>A maps to NM_005909.3 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr5:71492943 G>A maps to NM_005909.3 S1254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:71482526 C>T maps to NM_005909.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr5:71482571 C>T maps to NM_005909.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr2:172942596 T>C maps to NM_199227.1 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:172926265 C>T maps to NM_199227.1 Y27Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:117013806 C>G maps to NM_001085481.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:242159635 G>A maps to NM_001004343.2 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:17845128 C>T maps to NM_018174.4 Y1024Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:210574636 G>T did not map to a codon.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr2:210543347 C>T maps to NM_002374.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr2:210518096 C>G maps to NM_002374.3 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:210559486 G>T maps to NM_002374.3 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr2:210558198 T>A maps to NM_002374.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr2:210560328 G>A maps to NM_002374.3 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr2:210594940 T>A maps to NM_002374.3 A1768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:210558822 T>C maps to NM_002374.3 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr2:210594682 C>T maps to NM_002374.3 V1755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr2:210588336 A>T maps to NM_001039538.1 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr2:210559486 G>T maps to NM_002374.3 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:66782907 C>T maps to NM_002755.3 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:4101136 C>G maps to NM_030662.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr19:4110620 C>T maps to NM_030662.3 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:21208406 C>T maps to NM_145109.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:21205549 C>A maps to NM_145109.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr17:12032583 C>T maps to ENST00000415385 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:67873099 C>T maps to NM_145160.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr17:67513735 G>C maps to NM_002758.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:7968930 C>T maps to ENST00000425613 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr19:7976016 G>A maps to ENST00000425613 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr19:7976463 G>T did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:7975004 C>T maps to ENST00000425613 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:7975450 C>A maps to ENST00000425613 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:56152465 C>T maps to NM_005921.1 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr5:56167805 A>T maps to NM_005921.1 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr5:56167858 G>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:56180609 G>A maps to NM_005921.1 T1313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr19:40715067 C>T maps to NM_002446.3 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:40704315 C>T maps to NM_002446.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:40704300 C>T maps to NM_002446.3 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:65380699 G>T maps to NM_002419.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:65375489 G>C maps to NM_002419.3 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr12:53878058 C>T maps to NM_001193511.1 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr12:53876954 C>T maps to NM_001193511.1 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr12:53876789 C>T maps to NM_001193511.1 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:185161245 C>T maps to NM_004721.3 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr3:185191116 C>T maps to NM_004721.3 C666C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr3:185183640 G>T maps to NM_004721.3 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr3:185184676 C>T maps to NM_004721.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:43364680 C>A maps to ENST00000344686 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr17:43348458 C>T maps to ENST00000344686 W595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:19380882 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:19443773 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr23:19379652 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr23:19398255 C>T did not map to a codon.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr23:19425375 A>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:19449571 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:19449586 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr23:19410510 C>G did not map to a codon.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr23:19389132 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr23:19443724 C>T did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr17:61767678 C>T maps to NM_203351.1 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:161470019 C>G maps to NM_005922.2 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr6:161508787 T>C maps to NM_005922.2 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr6:161470316 C>G maps to NM_005922.2 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:136888995 G>A maps to NM_005923.3 F1178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:136977516 T>C maps to NM_005923.3 Q536Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:137019685 G>A maps to NM_005923.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:136990453 G>A maps to NM_005923.3 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr6:136913454 A>G maps to NM_005923.3 D1027D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:27686010 C>A maps to NM_004672.3 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr1:27690422 G>A maps to NM_004672.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:27684363 C>A maps to NM_004672.3 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr1:27682187 G>A maps to NM_004672.3 R1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:27682580 G>C maps to NM_004672.3 S1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:27690467 G>A maps to NM_004672.3 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:27687447 G>A maps to NM_004672.3 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr1:27688595 G>C maps to NM_004672.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:91226339 C>G maps to NM_145331.1 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr10:30749692 C>T maps to NM_005204.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr14:71205083 G>A maps to NM_033141.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr3:47957726 G>A maps to ENST00000426837 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr3:47912431 C>T maps to ENST00000426837 S2055S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr3:47951011 G>A maps to ENST00000426837 L1650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr3:47958458 C>T maps to ENST00000426837 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:39103306 G>A maps to NM_001042600.1 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:39100272 G>C maps to NM_001042600.1 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr19:39103291 C>A maps to NM_001042600.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr19:39108454 C>T maps to NM_001042600.1 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:39103252 G>A maps to NM_001042600.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:39108019 G>A maps to NM_001042600.1 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:39485696 G>A maps to NM_003618.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr2:102476319 G>T maps to NM_145686.2 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:102483018 C>T maps to NM_145686.2 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr2:102456448 C>T maps to NM_145686.2 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr14:50912807 G>A maps to NM_198794.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr11:75316986 C>T maps to NM_033063.1 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:75299191 G>A maps to NM_033063.1 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr3:183535850 C>T maps to NM_024871.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:136687110 C>T maps to NM_001198609.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr23:20033404 T>G did not map to a codon.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr23:20043129 G>T did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr23:20082894 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:20134902 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr23:20062587 T>A did not map to a codon.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr23:135303032 C>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:135323384 C>G did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr23:135314214 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:135323337 C>T did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:135313730 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:135314193 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:156289866 T>A maps to NM_001039580.1 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr4:156277011 C>T maps to NM_001039580.1 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr22:22127163 C>A maps to NM_138957.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr22:50705585 G>A maps to NM_002751.5 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr22:50703899 G>A maps to NM_002751.5 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr22:50693900 C>T maps to NM_002969.3 L277L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-6477-01A-11D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr6:36020562 C>T maps to NM_139012.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr6:36020565 C>T maps to NM_139012.2 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr6:36043719 G>A maps to NM_139012.2 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr18:48252450 C>T maps to NM_002747.3 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr18:48255617 G>A maps to NM_002747.3 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr15:52338809 T>C maps to NM_002748.3 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr17:19284198 G>A maps to NM_139034.2 W226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr11:45926321 C>G maps to NM_005456.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr16:1811305 G>A maps to NM_015133.3 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:1816350 C>A maps to NM_015133.3 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr16:1815177 C>T maps to NM_015133.3 P814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:179666939 T>C maps to NM_002752.4 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr9:128201269 G>A maps to NM_001006617.1 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:128268676 C>T maps to NM_001006617.1 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr9:128347841 C>T maps to NM_001006617.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr9:128206806 A>G maps to NM_001006617.1 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:128321982 G>A maps to NM_001006617.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:206858717 C>G maps to NM_032960.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:50681874 C>T maps to NM_004635.3 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr12:112318261 G>A maps to NM_139078.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr15:42116701 C>T maps to NM_001128608.1 Q1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:42104153 G>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:42117603 C>T maps to NM_001128608.1 A1505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr15:42111557 G>A maps to NM_001128608.1 K808K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr15:42109604 C>T maps to NM_001128608.1 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr15:42114546 C>A maps to NM_001128608.1 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:31434485 G>A maps to NM_012325.2 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr18:32650270 G>T maps to NM_014268.2 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr17:44061063 C>G maps to NM_001123066.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:44049300 A>T maps to NM_001123066.3 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:164534560 A>G maps to NM_017923.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr4:164506924 C>T maps to ENST00000514618 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:16067873 A>T maps to NM_001102562.1 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:16067783 C>A maps to NM_001102562.1 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr5:16177894 G>T maps to NM_001102562.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr5:16177930 G>T maps to NM_001102562.1 C199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:8491642 C>T maps to NM_016496.4 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:217124225 C>A maps to NM_020814.2 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:217148395 A>G maps to NM_020814.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:10414542 A>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:10415711 G>A maps to NM_005885.2 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:10405686 C>T maps to NM_005885.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr5:10407239 G>A maps to NM_005885.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr2:160585575 C>T maps to NM_022826.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr12:58152382 C>T maps to NM_138396.4 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr6:114181713 G>T maps to NM_002356.5 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr6:114181118 C>T maps to NM_002356.5 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr2:119739967 G>T maps to NM_006770.3 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr2:119726796 G>A maps to NM_006770.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:220791839 C>T maps to NM_018650.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr11:63668101 G>A maps to NM_001039469.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:63666241 A>G maps to NM_001039469.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:103923476 A>G did not map to a codon.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr19:45768122 G>A maps to NM_031417.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:45783692 G>A maps to NM_031417.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:45790801 C>T maps to NM_031417.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr19:45774926 C>T maps to NM_031417.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:45769535 G>A maps to NM_031417.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr19:45805656 G>A maps to NM_031417.3 R676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr19:45774875 C>T maps to NM_031417.3 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr12:57908983 C>G maps to NM_004990.2 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:198570719 C>G maps to NM_138395.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr2:198571571 G>A maps to NM_138395.3 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:198570155 G>T maps to NM_138395.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:68715436 C>G maps to NM_001038603.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr16:71674672 C>T maps to NM_001017967.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr16:71668180 G>A maps to NM_052858.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:71674608 C>T maps to NM_001017967.2 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr6:160328943 C>T maps to NM_002377.2 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr6:29454872 C>T maps to NM_052967.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:29454572 G>A maps to NM_052967.1 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:186944201 G>T maps to NM_001879.5 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:186953611 G>A maps to NM_139125.3 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr3:186943238 G>A maps to NM_001879.5 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr3:186954355 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:11106733 C>A maps to NM_006610.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:11090259 C>A maps to NM_006610.2 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:12976158 C>T maps to NM_014975.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:12958690 C>G maps to NM_014975.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr19:12984813 G>A maps to NM_014975.2 A1281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:12958434 C>T maps to NM_014975.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr19:12969219 C>T maps to NM_014975.2 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr19:12975623 C>T maps to NM_014975.2 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:12979964 C>T maps to NM_014975.2 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:12985308 G>A maps to NM_014975.2 K1446K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr19:12954372 G>A maps to NM_014975.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:12984813 G>C maps to NM_014975.2 A1281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:46471916 C>G maps to NM_015112.2 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:46500249 C>T maps to NM_015112.2 S1303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr1:46496347 C>T maps to NM_015112.2 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:18254653 G>A maps to NM_015016.1 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:18242830 C>T maps to NM_015016.1 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr19:18232696 G>A maps to NM_015016.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr19:18235531 C>T maps to NM_015016.1 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:18252810 G>A maps to NM_015016.1 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr19:18232572 G>A maps to NM_015016.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr19:18248157 C>A maps to NM_015016.1 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:66456299 C>G maps to NM_001164664.1 S1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr5:66460511 G>C maps to NM_001164664.1 V1835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:66460112 C>T maps to NM_001164664.1 L1702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:66461495 G>A maps to NM_001164664.1 P2163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr5:66429470 A>G maps to NM_001164664.1 K741K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr5:66459359 G>A maps to NM_001164664.1 S1451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr10:82039991 G>A maps to NM_000429.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:85769462 G>A maps to NM_005911.4 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:31187157 G>A maps to NM_002379.3 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:31194584 C>T maps to NM_002379.3 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:31191678 C>T maps to NM_002379.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:98943557 C>T maps to ENST00000254898 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:99039680 C>T maps to ENST00000254898 I660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr20:43933063 C>T maps to ENST00000372754 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr20:43933165 C>G maps to ENST00000372754 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr20:43929778 C>T maps to ENST00000372754 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr5:138657675 G>T maps to ENST00000394800 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr5:138657714 G>A maps to ENST00000394800 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr20:3845296 G>A maps to NM_020746.3 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr20:3845383 C>T maps to NM_020746.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr20:3846448 C>A maps to NM_020746.3 S426S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-TN-A7HJ-01A-12D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr16:29821458 A>G maps to NM_002383.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr18:47806251 C>T did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr18:47799235 T>C maps to ENST00000424334 K609K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr19:1585083 G>A maps to NM_003926.5 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:1581179 G>C maps to NM_003926.5 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:1585104 C>T maps to NM_003926.5 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:1585074 G>A maps to NM_003926.5 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:1582648 C>T maps to NM_003926.5 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr2:149226534 A>G maps to ENST00000404807 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:149247785 C>T maps to ENST00000404807 R1529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:149227842 C>T maps to ENST00000404807 N777N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr2:149226942 A>T maps to ENST00000404807 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:149226999 A>T maps to ENST00000404807 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr2:149247889 C>G maps to ENST00000404807 V1563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:57918501 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr12:57919662 G>T maps to NM_052897.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57919368 G>A maps to NM_052897.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:57920550 G>A maps to NM_052897.3 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr12:57921680 C>T maps to NM_052897.3 Q763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr12:57919494 T>C maps to NM_052897.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr14:36783736 A>G maps to NM_016586.2 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:54529050 G>C maps to NM_000242.2 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:152173352 C>T maps to NM_021038.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:131526278 G>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr6:20102579 T>C maps to NM_001080480.1 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr6:20124637 C>T did not map to a codon.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:9008677 A>G maps to NM_138799.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:9022663 G>A maps to NM_138799.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:54692108 G>C maps to NM_024298.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr19:54691099 C>A maps to NM_024298.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:54678112 G>A maps to NM_024298.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:54692189 C>T maps to NM_024298.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr16:84093016 C>T maps to NM_003791.2 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr16:84104309 T>C maps to NM_003791.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr16:84132847 C>A maps to NM_003791.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:21863308 T>G did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr23:21869683 A>T did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr23:21896225 C>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:21886679 G>C did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr16:89986163 G>A maps to ENST00000304984 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr16:89986382 C>T maps to ENST00000304984 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr18:13885286 C>T maps to NM_000529.2 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr18:13884800 G>T maps to NM_000529.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr18:13885390 G>A maps to NM_000529.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr18:13885466 A>G maps to NM_000529.2 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr18:13884785 G>A maps to NM_000529.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:13884842 G>A maps to NM_000529.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr18:13885016 G>T maps to NM_000529.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr20:54824312 C>T maps to ENST00000371389 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr20:54824141 G>A maps to ENST00000371389 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr18:58038901 A>T maps to NM_005912.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr18:58038765 G>A maps to NM_005912.2 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr18:58039414 G>T maps to NM_005912.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr18:13826438 C>A maps to NM_005913.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr18:13826448 C>A maps to NM_005913.2 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:119185720 G>A maps to NM_006500.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:119181848 G>A maps to NM_006500.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr18:29340270 A>G maps to NM_001034172.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr5:112458452 G>A maps to NM_001085377.1 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr5:112676269 C>T maps to NM_001085377.1 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:112406804 C>T maps to NM_001085377.1 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:112403780 G>A maps to NM_001085377.1 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr5:112363034 C>T maps to NM_001085377.1 E1008E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr3:182759448 A>C maps to NM_020166.3 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:70898413 G>A maps to NM_022132.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr5:70952609 C>T maps to NM_022132.4 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr5:70948525 G>T maps to NM_022132.4 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:70927997 T>C maps to NM_022132.4 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr23:138698571 G>A did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:138714491 A>T did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr23:138714554 T>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:138708351 C>A did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr23:138724624 A>T did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:138686865 T>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:138670520 G>T did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr23:138680606 G>C did not map to a codon.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr23:138699731 C>A did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr23:138687073 C>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:138667262 T>C did not map to a codon.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr23:138711910 A>T did not map to a codon.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr23:138664651 G>A did not map to a codon.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr23:138689863 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr23:138687060 C>T did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr13:113728843 G>A maps to NM_001112732.1 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr13:113748881 C>G maps to NM_001112732.1 S1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr13:113730377 C>T maps to NM_001112732.1 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:182923662 C>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:182924002 C>A did not map to a codon.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr3:183017858 G>A maps to NM_015078.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr3:183059381 G>A maps to NM_015078.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr3:182897936 G>A maps to NM_015078.2 S1009S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr22:41077103 C>A maps to NM_005297.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:100390919 C>A maps to NM_032503.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:13222600 G>T maps to NM_182751.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr10:13234262 C>T maps to NM_182751.2 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr10:13240696 G>T maps to NM_182751.2 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr10:13251294 G>C maps to NM_182751.2 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:127338054 G>A maps to NM_004526.2 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:127327233 C>T maps to NM_004526.2 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr3:127323892 G>A maps to NM_004526.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr6:52138595 G>C maps to ENST00000419835 S543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:52133881 A>G did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:52141937 T>A maps to ENST00000419835 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr6:52129418 G>T maps to ENST00000419835 V843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr21:47660828 C>T maps to NM_003906.3 G1843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr21:47700471 A>G maps to NM_003906.3 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr21:47697543 G>A maps to NM_003906.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr21:47678977 G>A maps to NM_003906.3 V1203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr21:47692668 G>A maps to NM_003906.3 H757H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr21:47662744 C>T maps to NM_003906.3 T1799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:48882490 A>C maps to NM_182746.1 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr8:48887406 T>A maps to NM_182746.1 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr8:48874748 C>G maps to NM_182746.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:35817334 C>T maps to NM_006739.3 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr22:35802583 C>T maps to NM_006739.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr22:35809933 C>G maps to NM_006739.3 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:99696308 G>A maps to NM_005916.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:99696749 A>G maps to NM_005916.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr20:5948560 G>A maps to NM_032485.4 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:119245036 G>C maps to ENST00000316316 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:119252639 G>A maps to ENST00000316316 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:7595341 C>T maps to NM_020533.2 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr1:85506781 G>A maps to NM_018298.9 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:6303034 G>T maps to NM_024596.3 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:94204082 A>G maps to NM_024717.4 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr5:94043230 T>A maps to NM_024717.4 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr15:94910963 C>T maps to NM_018349.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr15:94841760 C>T maps to NM_018349.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:119738099 G>C did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:30672318 G>C maps to NM_014641.2 V1547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr6:30681829 G>A maps to NM_014641.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:30671661 G>A maps to NM_014641.2 S1766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr6:30673793 G>A maps to NM_014641.2 Q1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:30675571 G>A maps to NM_014641.2 C928C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr6:30673818 G>A maps to NM_014641.2 A1047A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr6:41621180 C>T maps to NM_005586.3 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:37606333 G>A maps to ENST00000297153 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:37623649 C>A maps to ENST00000297153 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr14:47426687 G>A maps to NM_001113498.2 Q660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr14:47504385 C>A maps to NM_001113498.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr14:47426670 G>A maps to NM_001113498.2 Y665Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:47504487 A>T maps to NM_001113498.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr14:47530569 T>C maps to NM_001113498.2 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr14:47426703 C>T maps to NM_001113498.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:207615716 C>T maps to NM_001039845.1 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:207619850 C>T maps to NM_001039845.1 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:75687335 C>T maps to NM_005918.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr12:68724992 A>G maps to NM_017440.4 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr12:68720539 G>T maps to NM_017440.4 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr6:90385184 G>A maps to NM_014611.1 L4253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:90411327 G>A maps to NM_014611.1 F2792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:90402455 C>T maps to NM_014611.1 R3431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr6:90392898 C>T maps to NM_014611.1 L4018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr6:90425373 G>A maps to NM_014611.1 F2286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:90382060 G>C maps to NM_014611.1 S4551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr6:90434919 G>A maps to NM_014611.1 Q1890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:90402812 C>T maps to NM_014611.1 K3312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:90384309 T>C did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr6:90482424 G>A maps to NM_014611.1 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:90440562 C>T maps to NM_014611.1 K1674K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:90380681 G>A maps to NM_014611.1 L4638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr6:90440540 G>A maps to NM_014611.1 Q1682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:90402572 G>A maps to NM_014611.1 F3392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:90364053 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr6:90409882 G>A maps to NM_014611.1 H2923H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr6:90455080 G>A maps to NM_014611.1 I1363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:48465979 T>C maps to NM_002396.4 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:48439272 G>T maps to NM_002396.4 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr18:48447541 T>G maps to NM_002396.4 Y347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr3:168838940 G>T maps to NM_004991.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr3:168834350 C>A maps to NM_004991.3 G437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr3:168838895 C>A maps to NM_004991.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:168833802 G>A maps to NM_004991.3 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr3:168838946 G>T maps to NM_004991.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr3:168838958 G>A maps to NM_004991.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr3:168807815 C>A maps to NM_004991.3 E1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr23:153296807 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153296669 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:29533364 C>T maps to NM_016011.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:29557400 G>A maps to NM_016011.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:37564042 C>T maps to NM_004774.3 Q1477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr17:37571362 G>C maps to NM_004774.3 S472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:37565431 C>T maps to NM_004774.3 K1014K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr17:37565023 C>T maps to NM_004774.3 G1150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:37599806 G>C maps to NM_004774.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr17:37566454 G>A maps to NM_004774.3 S673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr5:6374522 G>T maps to NM_032286.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:4635167 G>A maps to NM_001001683.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:70349994 T>C did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:70342149 C>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:70357670 G>T did not map to a codon.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr23:70356302 G>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:70340888 G>T did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:70351427 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr23:70346842 G>C did not map to a codon.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr23:70338615 C>G did not map to a codon.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr23:70356762 A>G did not map to a codon.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr23:70339728 T>G did not map to a codon.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr23:70342192 G>A did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:70347741 G>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:70338649 C>G did not map to a codon.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr23:70350029 A>G did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:70347859 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:70349585 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:70349586 C>T did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:70345276 G>T did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:70353024 A>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:70349192 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:70348163 C>G did not map to a codon.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr23:70347217 G>A did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:70357475 G>C did not map to a codon.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr3:151082799 T>C maps to NM_053002.4 Y962Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:151072984 C>G maps to NM_053002.4 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:151078366 C>T maps to NM_053002.4 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:151105632 G>A maps to NM_053002.4 P1673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr3:150903226 G>A maps to NM_053002.4 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr3:151112628 C>T maps to NM_053002.4 Q1897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:150840607 G>A maps to NM_053002.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr3:151095915 T>A maps to NM_053002.4 L1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:150873976 C>T maps to NM_053002.4 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr3:151100524 C>T maps to NM_053002.4 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:60088193 G>A maps to NM_005121.2 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr12:116409988 G>A maps to NM_015335.4 L1928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:116457050 G>A maps to NM_015335.4 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr12:116445305 A>G maps to NM_015335.4 Y716Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr12:116444183 A>G maps to NM_015335.4 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr23:40522376 G>A did not map to a codon.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr23:40541115 G>A did not map to a codon.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr23:40571487 G>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr23:40513655 G>A did not map to a codon.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr23:40511064 C>T did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:40534537 A>T did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:40534569 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr23:40572267 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr22:20909265 G>A maps to NM_001003891.1 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:880110 G>A maps to NM_005481.2 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:873568 G>C maps to NM_005481.2 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr19:889661 C>T maps to NM_005481.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr19:881688 G>C maps to NM_005481.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr19:879972 C>T maps to NM_005481.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:93523942 G>A maps to NM_004268.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:93529597 G>A maps to NM_004268.4 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr6:41884613 C>T maps to NM_004275.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr6:131917291 C>T maps to ENST00000403834 E936E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:131946090 A>G maps to ENST00000403834 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr6:131917141 T>C maps to ENST00000403834 V986V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr17:38189605 G>A maps to NM_014815.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr17:38189380 G>A maps to NM_014815.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:16687956 C>T maps to NM_004831.3 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr4:17616297 T>G maps to NM_025205.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:39882004 G>A maps to NM_017592.1 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr19:39888290 C>T maps to NM_017592.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:39882004 G>A maps to NM_017592.1 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr8:118552147 G>A maps to NM_080651.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:118533123 C>T maps to NM_080651.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr14:71058033 C>A maps to ENST00000430055 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:43853230 G>A maps to NM_052877.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr5:88047710 A>T maps to NM_002397.4 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:88047671 A>T did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:88018741 T>C maps to NM_002397.4 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:88057135 T>A maps to NM_002397.4 K90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr5:88056882 T>C maps to NM_001193347.1 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr5:88027716 C>T maps to NM_002397.4 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr5:88056903 G>A maps to NM_001193347.1 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:156450661 G>T maps to NM_005920.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr16:3304352 G>A maps to NM_000243.2 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr16:3293433 C>A maps to NM_000243.2 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:3304449 G>A maps to NM_000243.2 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:3306442 T>G maps to NM_000243.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:3296523 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr16:3304455 G>T maps to NM_000243.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr5:126753413 C>T maps to NM_032446.2 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr5:126732332 G>T maps to NM_032446.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr15:66220799 G>A maps to NM_032445.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:66257436 G>A maps to NM_032445.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:3427383 G>A maps to ENST00000452816 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:3418408 C>G maps to ENST00000452816 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr19:42839479 C>T maps to ENST00000251268 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr19:42873016 G>A maps to ENST00000251268 G2168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:42847638 G>A maps to ENST00000251268 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr19:42853778 C>G maps to ENST00000251268 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr19:42839326 C>T maps to ENST00000251268 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr19:42866709 G>T maps to ENST00000251268 E2007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr2:66739353 T>C maps to ENST00000407092 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:66775127 C>T maps to ENST00000407092 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr2:66691248 G>A maps to ENST00000407092 W213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:37388488 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr15:37184421 A>G maps to NM_170675.2 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:47910190 G>A maps to NM_020160.1 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr19:47920457 C>T maps to NM_020160.1 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr19:47920460 C>T maps to NM_020160.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:36677295 A>T maps to NM_014791.2 R640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr9:36599429 C>T maps to NM_014791.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr11:64577226 T>A maps to NM_130804.2 K119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr11:64572116 G>A maps to NM_130804.2 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:41738515 G>A maps to NM_004527.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr7:15652167 C>T maps to NM_005924.4 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:15725556 C>T maps to NM_005924.4 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:15725703 G>T maps to NM_005924.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:15666369 C>T did not map to a codon.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr7:15652016 A>G maps to NM_005924.4 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr6:46802420 C>G maps to NM_005588.2 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:46793144 G>A maps to NM_005588.2 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:46806749 G>A maps to NM_005588.2 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr6:46787387 C>G maps to NM_005588.2 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr18:29793352 G>A maps to NM_005925.2 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr4:88755892 C>T maps to ENST00000395102 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr2:112786350 C>T maps to NM_006343.2 S970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:112779061 C>T maps to NM_006343.2 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr15:81294797 C>T maps to NM_022566.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr15:81282114 C>T maps to NM_015154.1 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr7:116340199 C>T maps to NM_001127500.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr7:116397690 G>T maps to ENST00000436117 G666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr12:95887870 A>G maps to NM_006838.3 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr12:95869845 G>A did not map to a codon.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr17:81043035 A>G maps to NM_001004431.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:2323538 C>A maps to NM_024086.3 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:2323365 G>A maps to NM_024086.3 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr14:21464756 C>T maps to NM_001029991.1 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr11:28318420 C>T maps to NM_001113528.1 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr11:28311782 C>T maps to NM_001113528.1 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr10:126454033 C>T maps to NM_212554.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:62434252 G>A maps to NM_001043229.1 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:171753397 G>A maps to NM_015935.4 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr17:60501346 G>T maps to NM_181725.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:60525119 C>T maps to NM_181725.3 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr7:128119443 G>A maps to NM_018396.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr7:128138150 C>T maps to NM_018396.2 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr14:21971905 A>T maps to NM_019852.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr14:21971932 G>A maps to NM_019852.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr14:21971720 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:2547410 C>T maps to NM_022840.3 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr18:2539046 G>C maps to NM_022840.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr1:156046532 G>A maps to NM_001093725.1 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr15:82336834 C>A maps to NM_032246.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr15:82336382 G>A maps to NM_032246.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr15:82337812 G>A maps to NM_032246.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:82336880 G>C maps to NM_032246.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr19:1556194 G>A maps to NM_001174118.1 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr19:1556344 G>A maps to NM_001174118.1 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr19:1556839 C>T maps to NM_001174118.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr5:153429536 G>A maps to NM_005927.4 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr5:153432558 C>T maps to NM_005927.4 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:170913347 C>G maps to NM_021647.6 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr17:19288008 G>C maps to NM_001198695.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr15:89450551 G>A maps to NM_005928.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr15:89449093 G>A maps to NM_005928.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr8:8748456 G>A maps to NM_004225.2 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr8:8749413 G>A maps to NM_004225.2 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:8750010 C>T maps to NM_004225.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr8:8747706 G>A maps to NM_004225.2 T954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr3:196746660 G>A maps to NM_033316.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr3:196753555 C>T maps to NM_005929.5 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr3:196746672 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr3:196736528 C>T maps to NM_005929.5 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:179095130 G>A did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:179103460 G>A maps to NM_033540.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:179096139 G>A maps to NM_033540.2 K447K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr3:179082964 C>T maps to NM_033540.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr3:179082099 C>T maps to NM_033540.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:179104302 G>A maps to NM_033540.2 W633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:179104303 G>A maps to NM_033540.2 W633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:179103448 A>T maps to NM_033540.2 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:179080156 A>G maps to NM_033540.2 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:12062112 G>A maps to NM_014874.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:12067147 C>T maps to NM_014874.3 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr22:37882098 G>T maps to NM_002405.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr22:37870702 G>A maps to NM_002405.3 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr3:158531857 T>C did not map to a codon.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr17:74734466 C>T maps to NM_024311.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:74774349 G>T maps to NM_024311.2 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:40422866 C>T maps to NM_001136493.1 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:40434074 C>T maps to NM_001136493.1 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr1:40434297 G>A maps to NM_001136493.1 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr1:40421044 G>T maps to NM_001136493.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:24247129 G>T maps to ENST00000338315 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr8:145734847 G>A maps to NM_138431.1 K44K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:53647819 C>A maps to NM_001170790.1 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:191362378 C>G maps to NM_017694.3 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:8700952 G>A maps to NM_152599.3 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr17:8701979 G>A maps to NM_152599.3 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:8701400 A>G maps to NM_152599.3 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:680329 G>A maps to ENST00000404286 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:103347527 C>A did not map to a codon.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr15:42041117 G>A maps to ENST00000219905 R1881R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr15:42041777 G>A maps to ENST00000219905 K2040K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr15:41961253 G>A maps to ENST00000219905 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr15:42019555 C>T maps to ENST00000219905 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr15:41961827 C>T maps to ENST00000219905 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr15:42041055 C>T maps to ENST00000219905 L1861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr15:42003183 C>T maps to ENST00000219905 F907F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:141803073 G>A maps to ENST00000475668 T2674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:141797391 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:141752581 A>G did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:141719027 G>A maps to ENST00000475668 W119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:141794548 G>T maps to ENST00000475668 T2449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr7:141764208 G>C maps to ENST00000475668 L1457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr7:141727027 G>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:141765159 C>T maps to ENST00000475668 R1504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr7:141754630 G>A maps to ENST00000475668 E1079E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:141763321 C>T maps to ENST00000475668 F1427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:180218666 C>A maps to NM_001114617.1 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr5:180219179 G>A maps to NM_001114617.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:50088060 G>A maps to NM_002408.3 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr22:39883966 G>A maps to NM_001098270.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr22:39883474 C>T maps to NM_001098270.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr2:99279520 G>T maps to NM_012214.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr5:179225170 C>G maps to NM_054013.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:86373114 T>G maps to ENST00000393205 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr17:74928763 C>T maps to NM_198955.1 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:74902122 G>C maps to NM_198955.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr7:88423629 G>C maps to NM_152706.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:88423572 T>G maps to NM_152706.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr7:88423890 T>C maps to NM_152706.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr5:43280500 G>C maps to NM_153361.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr7:22534407 C>A maps to ENST00000441815 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:103558943 A>C maps to NM_012215.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:103558655 C>T maps to NM_012215.3 W584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr10:103557836 G>C maps to NM_012215.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:131565173 A>T maps to NM_002412.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:131565233 G>A maps to NM_002412.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:15035946 G>A maps to NM_001190839.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:15035940 G>T maps to NM_001190839.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr12:15038674 A>C maps to NM_001190839.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr16:4715152 G>T did not map to a codon.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:4714766 G>T maps to NM_015246.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:4700381 G>A maps to NM_015246.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:41281723 C>T maps to NM_006533.2 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr14:39721979 G>A maps to NM_054024.3 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr14:39716524 C>T maps to NM_054024.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:39716594 C>T maps to NM_054024.3 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:39717157 C>T maps to NM_054024.3 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr18:19378061 C>T maps to NM_020774.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr18:19427047 C>T maps to NM_020774.2 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:19429230 C>G maps to NM_020774.2 S823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:19359502 T>C maps to NM_020774.2 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr1:1563209 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:31379008 C>T maps to NM_000247.1 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:109771219 C>T maps to NM_022765.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:12263801 C>G maps to NM_014632.2 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:12248644 C>G maps to NM_014632.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:12229645 C>T maps to NM_014632.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr11:12281412 C>A maps to NM_014632.2 A1101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr11:12278372 C>T maps to NM_014632.2 S999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr11:12247784 C>T maps to NM_014632.2 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:12257761 G>A maps to NM_014632.2 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:12241953 G>A maps to NM_014632.2 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr22:18301235 C>T maps to NM_015241.2 E1397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr22:18364024 G>A maps to NM_001136004.1 I762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:18387473 G>A maps to NM_015241.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:18387599 G>A maps to NM_015241.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr22:18384650 G>A maps to NM_015241.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr22:18304794 C>A did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr11:12345522 A>G did not map to a codon.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr11:12379875 G>A maps to NM_032867.2 E646E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr22:38336827 C>T maps to NM_033386.2 D861D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr22:38323541 G>A maps to NM_033386.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:38318041 C>A maps to NM_033386.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr22:38327855 C>T maps to NM_033386.2 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:1479681 C>T maps to NM_182924.3 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:1486398 C>G maps to NM_182924.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:1477793 C>T maps to NM_182924.3 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr6:31477568 C>T maps to NM_005931.3 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr23:10437742 C>T did not map to a codon.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr23:10535568 C>A did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:10463667 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:10442738 G>A did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:38664679 C>G did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:107084401 G>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:107169921 C>A did not map to a codon.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr23:107159286 G>C did not map to a codon.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr23:107084608 A>G did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr23:107169396 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:107148728 G>C did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:107097875 G>C did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr23:107170194 C>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:1254428 C>T maps to NM_177401.4 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr19:1255541 G>A maps to NM_177401.4 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr19:327203 G>T maps to NM_017550.1 S141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr19:312209 G>A maps to NM_017550.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr19:307339 G>A maps to NM_017550.1 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr17:73264169 G>T maps to NM_020679.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:12091354 G>A maps to NM_021933.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:4799023 G>T maps to NM_153827.4 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:4788778 G>A maps to NM_153827.4 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:89264701 G>T maps to NM_004897.4 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr10:89265178 C>T maps to NM_004897.4 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr7:7628163 A>G maps to NM_019005.3 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:7622857 G>A maps to NM_019005.3 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:7612633 A>G maps to NM_019005.3 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr7:7635886 G>C did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:50927675 C>T maps to NM_017584.5 Q180*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-7568-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr14:37777651 G>A maps to NM_001195296.1 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:37754563 G>T maps to NM_001195296.1 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:5392533 C>T maps to NM_024039.1 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:70014320 C>T maps to ENST00000448226 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:129913711 T>C maps to NM_002417.4 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr10:129906869 T>A maps to NM_002417.4 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr10:129905569 T>A maps to NM_002417.4 K1512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr10:129906284 G>A maps to NM_002417.4 I1273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr20:10393769 G>C maps to NM_170784.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr20:10393970 G>C maps to NM_170784.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr20:10393946 G>A maps to NM_170784.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr22:40816945 G>T maps to NM_020831.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr22:40817049 C>A maps to NM_020831.3 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr22:40815259 A>G maps to NM_020831.3 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:14312824 A>G maps to NM_014048.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr7:131012744 C>T maps to NM_013255.4 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:47025907 C>T maps to NM_003684.4 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:2037828 C>A did not map to a codon.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr7:140158911 G>A maps to NM_013446.3 C222C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr3:12623355 G>T maps to NM_014160.3 G340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr3:12616299 T>C maps to NM_014160.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:23812140 G>A maps to NM_005664.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr15:23811462 T>G maps to NM_005664.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:23811592 G>T maps to NM_005664.3 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr15:23811611 C>A maps to NM_005664.3 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:23811399 G>A maps to NM_005664.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:23811309 C>G maps to NM_005664.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr15:23811474 C>T maps to NM_005664.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr15:23812437 C>T maps to NM_005664.3 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr15:23811186 G>T maps to NM_005664.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr15:23811018 G>A maps to NM_005664.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:56285487 G>A maps to NM_017777.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr17:56291136 T>C maps to NM_017777.3 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr17:56290378 C>T maps to NM_017777.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:28023598 G>T maps to NM_173576.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:28030396 C>T maps to NM_173576.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:50500059 G>A maps to NM_015166.3 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr22:50500012 C>T maps to NM_015166.3 *378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr22:50502549 G>A maps to NM_015166.3 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr12:121125272 G>T maps to NM_014730.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:37081680 C>T maps to NM_000249.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:37048547 G>A maps to NM_000249.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:37042541 G>T maps to NM_000249.3 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr14:75513214 G>A maps to NM_001040108.1 F1048F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr14:75509148 G>A maps to NM_001040108.1 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:74716631 C>G maps to NM_152649.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr11:118376146 C>T maps to NM_001197104.1 I3180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:118352584 C>T maps to NM_001197104.1 R1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr11:118362544 C>T maps to NM_001197104.1 R1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr11:118342476 A>G maps to NM_001197104.1 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr11:118347647 C>T maps to NM_001197104.1 A1095A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr11:118376893 C>T maps to NM_001197104.1 I3429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:118347535 C>A maps to NM_001197104.1 S1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:118375348 C>A maps to NM_001197104.1 V2914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr11:118377361 G>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:118390381 C>T maps to NM_001197104.1 F3732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr11:118307580 C>G maps to NM_001197104.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:49425940 G>A maps to NM_003482.3 Q4183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:49425941 C>A maps to NM_003482.3 G4182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr12:49433006 G>A maps to NM_003482.3 S2788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr12:49434324 G>A maps to NM_003482.3 R2410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:49434543 G>A maps to NM_003482.3 Q2337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr12:49434414 G>A maps to NM_003482.3 Q2380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr12:49440157 C>A maps to NM_003482.3 E1490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:49435774 T>C did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr12:49445125 G>T maps to NM_003482.3 C780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:49443898 C>A maps to NM_003482.3 E1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr12:49436572 G>T maps to NM_003482.3 T1911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:49438544 C>A maps to NM_003482.3 E1649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr12:49428363 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr12:49447021 C>A maps to NM_003482.3 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr12:49443702 G>C maps to NM_003482.3 S1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr12:49448534 C>T did not map to a codon.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr12:49436601 C>A maps to NM_003482.3 E1902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:49434414 G>A maps to NM_003482.3 Q2380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr12:49438594 G>C maps to NM_003482.3 S1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr12:49448692 G>A maps to NM_003482.3 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:49434306 G>A maps to NM_003482.3 Q2416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr12:49428449 C>G did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:49420594 G>A maps to NM_003482.3 L5052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr12:49433387 G>A maps to NM_003482.3 R2687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr12:49415845 G>A maps to NM_003482.3 R5501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr12:49424104 T>A maps to NM_003482.3 K4653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:49443616 G>A maps to NM_003482.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:49435982 G>A maps to NM_003482.3 Q2000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:49435963 C>T maps to NM_003482.3 W2006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:49438748 C>G did not map to a codon.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr12:49433279 C>A maps to NM_003482.3 E2723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:49425037 G>A maps to NM_003482.3 R4484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:49432222 C>T maps to NM_003482.3 E2972E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr12:49443616 G>A maps to NM_003482.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr12:49445625 C>A maps to NM_003482.3 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr12:49438646 G>A maps to NM_003482.3 R1615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:49433934 G>A maps to NM_003482.3 Q2540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr12:49423199 G>A maps to NM_003482.3 Q4687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:49448119 C>T maps to NM_003482.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr12:49438184 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr12:49427257 G>A maps to NM_003482.3 Q3744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr7:151868381 T>C maps to ENST00000355193 E3140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr7:151945265 A>G maps to ENST00000355193 D751D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr7:151835943 C>T maps to ENST00000355193 V4917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:151884561 C>A did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:151900144 C>T maps to ENST00000355193 W1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr7:151891213 C>G did not map to a codon.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr7:151845931 C>T maps to ENST00000355193 W4417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr7:152055755 G>A maps to ENST00000355193 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr7:151859793 G>C maps to ENST00000355193 S3623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:152012252 G>C maps to ENST00000355193 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:151845955 C>T maps to ENST00000355193 W4409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr7:151960215 C>A did not map to a codon.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr7:151917677 C>T maps to ENST00000355193 V1214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:151849900 G>A maps to ENST00000355193 R4196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:151880196 T>C maps to ENST00000355193 V1709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:151877082 C>T maps to ENST00000355193 E2426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr7:151849997 G>A maps to ENST00000355193 H4163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr7:151873544 G>C maps to ENST00000355193 S2998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr7:151962120 A>T did not map to a codon.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr19:36214908 G>T did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr19:36215988 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:36223500 C>T maps to NM_014727.1 H2017H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr19:36211938 C>T maps to NM_014727.1 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr19:36217141 T>C maps to NM_014727.1 C1297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr19:36212435 C>T maps to NM_014727.1 N729N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:36228843 G>C did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr19:36210687 C>T maps to NM_014727.1 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:36214840 C>T maps to NM_014727.1 F1089F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:36210696 C>T maps to NM_014727.1 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr19:36211784 C>T maps to NM_014727.1 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:104717781 A>G maps to NM_182931.2 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr7:104752437 C>G maps to NM_182931.2 S1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:104753005 A>G maps to NM_182931.2 G1601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr10:22024157 C>T maps to NM_004641.3 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr9:20346500 C>A maps to NM_004529.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr9:20414312 G>A maps to NM_004529.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:168276154 C>G maps to ENST00000400822 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr6:168352491 G>A maps to ENST00000400822 R1478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr6:168351916 G>T maps to ENST00000400822 E1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:168319464 G>A maps to ENST00000400822 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr6:168315998 G>T maps to ENST00000400822 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr17:36864100 C>T maps to NM_005937.3 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:36876643 G>C maps to NM_005937.3 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr17:36868951 G>A maps to NM_005937.3 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr13:49796404 G>A maps to NM_001507.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:238449172 G>T maps to NM_024101.5 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr16:2258606 C>T maps to NM_022372.4 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:2256573 G>A maps to NM_022372.4 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr12:122622099 C>G maps to NM_014938.3 S706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:122620139 G>T maps to NM_014938.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr12:122625502 C>T maps to NM_014938.3 F837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr12:122617947 C>T maps to NM_014938.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:73008628 G>A maps to NM_032951.2 Y805Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:83948559 G>C did not map to a codon.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr16:83945884 C>T maps to NM_012213.2 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr4:146567273 A>T maps to NM_172250.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr2:150426655 A>T maps to NM_015702.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:53471829 G>A maps to NM_012329.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:154802865 C>G maps to NM_007289.2 S60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr3:154802022 C>T maps to NM_007289.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:154834750 G>A maps to NM_007289.2 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:154886356 C>A maps to NM_007289.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr3:154855961 C>T maps to NM_007289.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:2522994 C>T did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:135047294 T>C did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:135047199 C>T did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:102663348 G>A maps to NM_002421.3 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr11:102668111 C>G maps to NM_002421.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:102646042 C>T maps to NM_002425.2 W314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr11:102650334 G>A maps to NM_002425.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr22:24122900 G>A maps to NM_005940.3 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:102738032 G>C maps to ENST00000326227 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr11:102736638 A>C maps to ENST00000326227 L358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:102818642 C>G maps to NM_002427.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr14:23311708 G>T maps to NM_004995.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr14:23313956 C>T maps to NM_004995.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:23313039 C>T maps to NM_004995.2 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:23312535 C>T maps to NM_004995.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:23313941 T>G maps to NM_004995.2 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr14:23311906 C>G maps to NM_004995.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr14:23311834 G>A maps to NM_004995.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr16:58076193 C>T maps to NM_002428.2 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr16:58076154 C>T maps to NM_002428.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr8:89180108 T>A maps to NM_005941.4 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:89128828 G>A maps to NM_005941.4 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr8:89053868 A>G maps to NM_005941.4 D548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:89068363 C>T maps to NM_005941.4 K455K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr8:89058939 C>A maps to NM_005941.4 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:89053769 A>G maps to NM_005941.4 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr12:132323154 A>G did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:132326313 C>T maps to NM_016155.4 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr16:55530840 C>T maps to NM_004530.4 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr16:55517035 G>A maps to NM_004530.4 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr16:55519217 C>T maps to NM_004530.4 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr16:55522554 G>A maps to NM_004530.4 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr11:102480738 G>A maps to NM_004771.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:102465487 C>T maps to NM_004771.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr10:127462418 G>T maps to NM_147191.1 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:33862273 G>A maps to NM_006690.3 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr16:3100515 C>T maps to NM_022468.4 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr16:3100317 T>C maps to NM_022468.4 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:5012646 C>T maps to NM_021801.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr11:102564692 G>A maps to NM_022122.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:102709883 G>A maps to NM_002422.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr11:102593221 G>A maps to NM_002424.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr20:44641954 C>A maps to NM_004994.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr20:44641090 G>A maps to NM_004994.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr20:44640843 A>T maps to NM_004994.2 K356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr4:90857471 A>T maps to NM_007351.2 K881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:90857797 G>A maps to NM_007351.2 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr4:90848949 G>A maps to NM_007351.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:90874517 C>A maps to NM_007351.2 A1212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:90857708 C>T maps to NM_007351.2 Q960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:90857092 T>C maps to NM_007351.2 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:90857466 C>A maps to NM_007351.2 S879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr10:88705125 C>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr22:28194071 G>A maps to NM_002430.2 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr22:28193870 G>A maps to NM_002430.2 A887A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr22:28193510 C>T maps to NM_002430.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:158812161 A>G maps to NM_002432.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:158815618 C>A maps to NM_002432.1 Y271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:158812149 C>A maps to NM_002432.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:158817561 T>C maps to NM_002432.1 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr1:158817522 C>T maps to NM_002432.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr1:158817651 G>A maps to NM_002432.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr1:158815705 C>T maps to NM_002432.1 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr15:56748689 G>T maps to NM_018365.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr17:2298242 T>G maps to NM_020310.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:2290452 G>C maps to NM_020310.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr7:156798411 C>T maps to NM_005515.3 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr11:1491581 G>C maps to NM_001172223.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr11:1501644 G>A maps to NM_001172223.1 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr4:71835699 C>T maps to ENST00000396051 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr4:71840891 G>T maps to ENST00000396051 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:74399788 A>G maps to NM_018221.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:27359211 G>A maps to NM_024761.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr9:27455166 G>A maps to NM_024761.3 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr2:198400318 C>G maps to NM_015387.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:39543700 T>C maps to ENST00000311042 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr18:33828963 G>T did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr18:33795645 C>T maps to NM_017947.2 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:39893452 C>T maps to ENST00000425303 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:49575405 C>A maps to NM_014484.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:29638475 A>G did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:223554123 A>T maps to NM_058165.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:100839227 T>A maps to NM_178176.2 *342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr2:74688528 C>T maps to NM_006302.2 W796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr3:49948974 G>A maps to NM_032355.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:49948246 C>T maps to NM_032355.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr3:49947691 G>A maps to NM_032355.3 F510F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr3:49948252 C>T maps to NM_032355.3 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr16:77228544 G>T maps to NM_014940.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:62938683 C>T maps to ENST00000393630 Q826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr12:62943489 T>C maps to ENST00000393630 V933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:108822765 T>A did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:108746687 G>A maps to NM_014429.3 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr3:108773722 G>A maps to NM_014429.3 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr3:108773581 G>T maps to NM_014429.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr3:108818258 C>T maps to NM_014429.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:31333849 G>A maps to ENST00000397641 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr22:31330914 G>C maps to ENST00000397641 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:31338231 A>G maps to ENST00000397641 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr22:31335615 G>C maps to ENST00000397641 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr21:37742036 C>T maps to ENST00000290384 Q792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr21:37741536 C>G maps to ENST00000290384 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7391-01A-11D-2012-08 chr23:106186358 G>C did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:106200164 C>G did not map to a codon.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr23:106229363 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:79186492 G>A maps to NM_206839.1 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr23:102931248 C>G did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr23:102931660 G>A did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:102931677 T>A did not map to a codon.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr23:102931679 G>A did not map to a codon.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr12:122097168 G>A maps to NM_173855.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:99376133 G>A maps to NM_001098831.1 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr8:57025629 G>A maps to NM_005372.1 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:57025647 G>A maps to NM_005372.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:220986690 G>C maps to NM_022746.3 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:220936310 G>A maps to NM_017898.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:134033179 G>T did not map to a codon.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr23:14927077 A>G did not map to a codon.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:113240919 C>T maps to NM_020963.3 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:113232687 C>G maps to NM_020963.3 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr22:50591607 G>A maps to NM_018995.2 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:50599149 C>T maps to NM_018995.2 R1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:50591517 G>A maps to NM_018995.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr6:132649649 G>A maps to NM_015529.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:132722445 G>T maps to NM_015529.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr9:13188968 A>C maps to ENST00000319217 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr11:58979530 G>A maps to NM_001039396.1 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr11:58979417 G>C maps to NM_001039396.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr16:129428 C>T maps to NM_002434.2 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:82182458 G>A maps to NM_005792.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr13:20240583 C>G maps to ENST00000414242 S680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:123651317 G>A maps to NM_022782.2 D673D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:123687372 G>A maps to NM_022782.2 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:123705974 T>C maps to NM_022782.2 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr15:75185034 C>T maps to NM_002435.1 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:75189513 C>G maps to NM_002435.1 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr1:43812538 G>A maps to NM_005373.2 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:43803900 C>A maps to NM_005373.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr1:43804212 G>A maps to NM_005373.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr19:4359197 C>T maps to ENST00000262967 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:4345869 G>A maps to ENST00000262967 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr17:56356774 C>A maps to ENST00000340482 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:56349014 C>T did not map to a codon.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr17:56352926 C>T maps to ENST00000340482 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:56355307 G>A maps to ENST00000340482 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:56349242 G>T maps to ENST00000340482 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr23:154019322 C>T did not map to a codon.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr23:154033629 C>T did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:154013397 C>T did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:154019309 A>C did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:154033633 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:154014571 A>T did not map to a codon.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr17:41958920 G>A maps to NM_005374.3 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr17:41956729 C>A maps to NM_005374.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr17:41955243 G>A maps to NM_005374.3 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr17:41903171 G>A maps to ENST00000398393 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:202550740 C>T maps to NM_033066.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:67768784 G>T maps to NM_022474.2 G251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr14:67787834 G>A maps to NM_022474.2 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:24703279 G>A maps to ENST00000409253 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr7:24720063 G>A maps to ENST00000409253 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr10:28413007 G>A maps to NM_173496.3 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:11888678 C>T maps to ENST00000344987 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr18:11893496 G>T maps to ENST00000344987 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:43898629 C>A maps to NM_001044370.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr22:43870808 C>T maps to NM_001044370.1 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:43831034 G>A maps to NM_001044370.1 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr22:43821158 G>A maps to NM_001044370.1 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:17030065 G>A maps to NM_015134.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:17079759 A>G maps to NM_015134.2 E910E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:17061835 G>A maps to NM_015134.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr17:17077274 G>A maps to NM_015134.2 E825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr17:17062108 C>T maps to NM_015134.2 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:17045964 T>C maps to NM_015134.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr2:27534803 G>A maps to ENST00000405983 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:15501679 G>A did not map to a codon.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr11:118107897 T>C maps to NM_198275.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:118111018 C>T maps to NM_198275.1 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:33671365 G>A maps to ENST00000445271 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr21:33671365 G>A maps to ENST00000445271 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr10:17875800 G>A maps to NM_002438.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr10:17865309 G>A maps to NM_002438.2 W100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:60758227 G>A maps to NM_006039.3 A847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:60755932 G>T maps to NM_006039.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:60755896 G>A maps to NM_006039.3 K695K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:60757607 C>T maps to NM_006039.3 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:60757608 C>T maps to NM_006039.3 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr17:60767595 G>T maps to NM_006039.3 R1274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr17:60766301 C>T maps to NM_006039.3 F1105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:94179019 G>C maps to NM_005591.3 S608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr4:6711284 G>A maps to NM_203462.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:3249861 G>A maps to ENST00000328215 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:18956205 C>T maps to NM_147199.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:18955509 G>A maps to NM_147199.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:19077742 G>T maps to NM_054030.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:19077628 A>G maps to NM_054030.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:18158886 G>A maps to NM_054031.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:18158850 G>A maps to NM_054031.3 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr11:18159570 C>T maps to NM_054031.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr18:48331679 G>C maps to NM_001127176.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr18:48333166 G>A maps to NM_001127176.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr4:78815400 C>T maps to NM_020236.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:45906031 C>A maps to NM_145255.3 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr17:45901756 C>T maps to NM_145255.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr11:6704512 G>C maps to NM_022061.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:43022194 G>A maps to NM_015950.3 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:1341263 G>C maps to NM_017971.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr11:68658834 C>T maps to NM_181514.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr11:68665461 G>T maps to NM_181514.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr5:154330429 C>T maps to NM_014180.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr17:48447948 T>A did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:48450507 C>T maps to NM_016504.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr3:131219332 G>A maps to ENST00000425847 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:28002381 G>T maps to NM_145330.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr2:28002300 G>T maps to NM_004891.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr2:86433352 C>T maps to NM_016622.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr21:26960032 G>A maps to NM_080794.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:93873223 G>C maps to NM_172177.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:89010391 G>A maps to NM_022163.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr3:179311659 T>C maps to NM_020409.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:73555874 G>T maps to NM_016055.5 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:64893284 C>A maps to NM_004927.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr12:6602124 C>T maps to NM_016497.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr2:74699248 G>A maps to NM_053050.3 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:151734859 C>A maps to NM_031420.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr1:151735514 C>T maps to NM_031420.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:89015920 G>A maps to NM_022839.3 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:36929440 G>C maps to NM_031280.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:36921786 C>G did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr10:75011545 G>C maps to NM_016065.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr7:56022708 G>C maps to ENST00000426595 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr7:56020971 G>C maps to ENST00000426595 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr6:43639526 G>C maps to ENST00000372118 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr9:138395633 C>T maps to NM_016034.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:43906548 G>A maps to NM_032014.2 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:44815100 C>T maps to NM_016640.3 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr7:140710223 G>C maps to NM_053035.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr12:27908239 G>T maps to NM_021821.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:73258703 G>A maps to NM_015971.3 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:105665723 G>A maps to NM_182640.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr2:105708869 C>T maps to NM_182640.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr9:125047559 C>T maps to NM_138777.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:10648010 C>T maps to NM_001098579.1 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr11:60234504 G>A maps to NM_152866.2 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr11:60230542 C>T maps to NM_152866.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:60230539 G>A maps to NM_152866.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr11:60561572 C>A maps to NM_206893.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:60182999 G>T maps to NM_032597.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr11:60164122 T>A maps to NM_032597.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr11:60170535 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:60184304 C>T maps to NM_032597.3 Q622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr11:60531292 G>T maps to NM_001098835.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr11:59860321 G>C did not map to a codon.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:59857260 G>A maps to NM_000139.4 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr11:59860934 C>T maps to NM_000139.4 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr11:59857235 C>G maps to NM_000139.4 S43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:59829988 C>T maps to NM_006138.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:59829951 C>A maps to NM_006138.4 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:59828722 T>C maps to NM_006138.4 N30N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr11:60059778 A>T maps to NM_148975.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr11:60068505 A>T maps to NM_148975.1 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7593-01A-11D-2229-08 chr11:60048156 G>A maps to NM_148975.1 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:60215207 T>C maps to NM_023945.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:60107352 G>C maps to NM_139249.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:60156974 C>G maps to NM_206939.1 S151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr11:60474520 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr8:72756404 C>T maps to NM_005098.3 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:72754901 G>T maps to NM_005098.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:72756323 G>A maps to NM_005098.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:17998363 G>A maps to NM_001105569.1 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:47707856 G>A maps to NM_000251.1 G827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:80168933 G>T did not map to a codon.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr5:79965952 C>G maps to NM_002439.3 S206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr5:80057394 G>A maps to NM_002439.3 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:76365378 G>T maps to NM_002440.2 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:76288148 A>T maps to NM_002440.2 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:76365338 C>G maps to NM_002440.2 S856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:76363683 T>C maps to NM_002440.2 H816H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr6:31729647 C>T maps to ENST00000375742 C762C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:48026376 C>T maps to NM_000179.2 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr17:55339538 C>T maps to NM_138962.2 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:38289862 C>T maps to ENST00000398532 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:135870600 C>T maps to NM_018133.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr23:11783733 C>A did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:11786729 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr23:11790284 G>A did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr2:234775834 C>G did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr16:815613 G>A maps to NM_013404.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr16:823206 G>T maps to NM_001025190.1 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr16:823221 C>A maps to NM_001025190.1 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr16:830538 C>T maps to NM_001025190.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:819553 C>T maps to NM_001025190.1 G1012G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:830221 C>T maps to NM_001025190.1 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:819430 G>C maps to NM_001025190.1 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:64959589 G>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:64957171 G>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:64959703 G>T did not map to a codon.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr8:16026257 G>C maps to ENST00000445506 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr3:49724468 G>A maps to NM_020998.3 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:49936567 C>T maps to NM_002447.2 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr3:49933238 C>T maps to NM_002447.2 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:49934738 G>A maps to NM_002447.2 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:131207016 G>C did not map to a codon.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr23:131205198 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr23:131197494 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:190927052 C>G maps to NM_005259.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr2:190927172 A>C maps to NM_005259.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr1:155582073 C>T maps to NM_018116.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr4:4864758 G>T maps to NM_002448.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr4:4864701 G>A maps to NM_002448.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr16:56660852 G>T maps to NM_175617.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr14:105932763 G>A maps to NM_004689.3 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr14:105930440 G>T maps to NM_004689.3 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr14:105916416 G>A maps to NM_004689.3 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr14:105920570 G>A maps to NM_004689.3 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:62364200 C>A maps to NM_004739.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:62365498 C>A maps to NM_004739.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr11:62363554 G>A maps to NM_004739.2 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:42936240 G>A maps to NM_020744.2 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr2:42935133 A>T maps to ENST00000405094 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr9:21854751 G>A maps to NM_002451.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:21818160 C>T maps to NM_002451.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr9:21861973 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr8:121500540 G>A maps to NM_022045.3 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:121475946 T>C maps to NM_022045.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr8:121468866 C>G maps to NM_022045.3 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr8:121502757 G>A maps to NM_022045.3 Q465Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:36938201 G>A maps to ENST00000373627 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:47650567 G>A maps to NM_014342.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr23:154294264 C>T did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:154292276 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:154290192 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:154290184 G>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:91503288 C>G maps to NM_006980.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr8:97263141 C>T maps to NM_015942.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr8:97269220 A>G maps to NM_015942.3 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr2:242038874 C>T maps to NM_182501.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:107371511 T>A maps to NM_025198.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:93576130 C>T maps to NM_007358.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr15:65319318 G>C maps to NM_139242.3 S90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:65297256 G>A maps to NM_139242.3 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:66605982 A>T maps to NM_014637.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:135212702 G>C maps to NM_138384.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:64891612 C>T maps to NM_005956.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr14:64908854 C>G maps to NM_005956.3 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr14:64894129 C>T maps to NM_005956.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:64892911 T>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:64906956 A>G maps to NM_005956.3 K596K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr6:151265716 G>A maps to NM_015440.3 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr2:74441281 G>A maps to NM_006636.3 K322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:11854026 G>A maps to ENST00000376585 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr1:11855276 C>T maps to ENST00000376585 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr15:80181636 T>C maps to NM_006441.3 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr16:86585793 G>A maps to NM_001159378.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:86565691 G>A maps to NM_001159377.1 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr16:86575787 G>A maps to NM_001159377.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr13:28011270 G>A maps to NM_152912.4 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr11:68506203 G>C maps to NM_004923.3 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:68517756 G>A maps to NM_004923.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:149807466 G>T did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:149809803 T>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:149839964 G>A did not map to a codon.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr23:149898675 C>G did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:149905308 G>A maps to NM_001145862.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr1:149902779 C>T maps to NM_001145862.1 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:149901585 G>A maps to NM_001145862.1 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:149906926 C>A maps to NM_001145862.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:32243654 C>A maps to NM_001040446.1 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr3:9695336 G>T maps to NM_001077525.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr3:9691416 C>A maps to NM_001077525.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr3:9712818 G>A maps to NM_001077525.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr3:9739526 G>A maps to NM_001077525.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr15:31218128 C>T maps to NM_014967.4 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:31197879 G>A maps to NM_014967.4 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr15:31197066 T>C maps to NM_014967.4 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:31210384 C>T maps to NM_014967.4 H610H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr15:31210381 G>A maps to NM_014967.4 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr11:95569428 G>A maps to NM_016156.5 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:30412530 G>A maps to NM_021090.3 Q506Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr22:30421780 T>A maps to NM_021090.3 T1196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:30408419 G>A maps to NM_021090.3 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr13:25825792 T>C maps to NM_004685.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr13:25840347 G>C maps to NM_004685.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr8:17206460 C>T did not map to a codon.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr23:63488488 G>T did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:63488476 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:63569919 C>A did not map to a codon.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr23:63557244 A>T did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr23:63555986 T>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:63551560 T>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:63563519 T>G did not map to a codon.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr23:63579361 C>T did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:63490947 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:63565034 G>T did not map to a codon.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr23:63548720 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:63548660 T>C did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:63576112 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr8:11152789 G>A maps to NM_015458.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr8:11172548 C>T maps to NM_015458.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr4:187454890 C>T maps to NM_005958.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr4:187455655 C>T maps to NM_005958.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:92715106 C>T maps to NM_005959.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr11:92714994 G>A maps to NM_005959.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr11:92715441 C>T maps to NM_005959.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:92714937 C>T maps to NM_005959.3 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr6:74190512 G>A maps to NM_001123226.1 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:11294217 G>A maps to NM_004958.3 Y771Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr1:11319339 C>A maps to NM_004958.3 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr22:30824463 C>T maps to ENST00000439838 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr10:30638177 C>T maps to NM_018109.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr1:237044135 G>A maps to NM_000254.2 V892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr1:237060419 T>C did not map to a codon.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr1:237037071 G>A did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr13:41826841 C>T maps to NM_004294.2 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr5:7870927 A>G maps to NM_024010.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:7897180 A>G maps to NM_024010.2 K618K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:7869266 C>T maps to NM_024010.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr16:70713745 C>A maps to NM_138383.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:100534245 C>T maps to ENST00000511045 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr4:100543977 G>A maps to ENST00000511045 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr4:100534245 C>T maps to ENST00000511045 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr8:17611495 G>T maps to NM_001001924.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:17611495 G>C maps to NM_001001924.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr13:29599329 G>A maps to NM_001033602.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr13:29599503 C>T maps to NM_001033602.2 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:29599353 G>A maps to NM_001033602.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr13:29599099 C>T maps to NM_001033602.2 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr1:155180165 G>T maps to NM_002455.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:177194098 G>A maps to NM_006554.4 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:155160216 C>T maps to ENST00000425082 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:124646818 G>C maps to NM_033049.3 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:124646390 G>A maps to NM_033049.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:124641064 C>T maps to NM_033049.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:124646508 A>G maps to NM_033049.3 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr11:26587443 C>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:9007502 G>T maps to NM_024690.2 P13155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:9075388 G>A maps to NM_024690.2 D4019D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr19:9059461 A>T maps to NM_024690.2 S9328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:9002555 G>A maps to NM_024690.2 H13420H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:9060523 G>A maps to NM_024690.2 T8974T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr19:8976758 C>A maps to NM_024690.2 E14103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:9062945 G>C maps to NM_024690.2 S8167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr19:9064690 T>A maps to NM_024690.2 T7585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:9088914 C>T maps to NM_024690.2 W967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:9067135 C>T maps to NM_024690.2 Q6770Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:9058237 C>A maps to NM_024690.2 T9736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:9008171 C>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:8987084 G>A maps to NM_024690.2 L13969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:9086083 G>A maps to NM_024690.2 R1911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr19:9059812 C>A maps to NM_024690.2 L9211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr19:9088536 G>C maps to NM_024690.2 S1093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:9011001 G>A maps to NM_024690.2 F12972F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr19:9084377 G>T maps to NM_024690.2 V2479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr19:9085092 G>T maps to NM_024690.2 S2241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr19:9011325 G>A maps to NM_024690.2 V12969V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:9084695 C>T maps to NM_024690.2 L2373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:9085595 C>T maps to NM_024690.2 L2073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:9059668 G>T maps to NM_024690.2 P9259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:9074422 G>T maps to NM_024690.2 T4341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr19:9056572 G>A maps to NM_024690.2 T10291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:9069583 A>T maps to NM_024690.2 A5954A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:9085507 G>A maps to NM_024690.2 Q2103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr19:9048093 G>T maps to NM_024690.2 T11179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:9003691 T>A maps to ENST00000380951 T1T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:9048497 G>A maps to NM_024690.2 L11045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:9012851 G>T maps to NM_024690.2 T12864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr19:9066781 C>A maps to NM_024690.2 A6888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:9071926 A>G maps to NM_024690.2 G5173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr19:9088748 G>C maps to NM_024690.2 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:9011340 C>T maps to NM_024690.2 R12964R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:9071209 T>C maps to NM_024690.2 T5412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr19:9045869 C>A maps to NM_024690.2 E11921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:9065155 T>C maps to NM_024690.2 Q7430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:9062671 G>A maps to NM_024690.2 S8258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:9089072 G>A maps to NM_024690.2 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:9068842 G>A maps to NM_024690.2 N6201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:9069844 A>G maps to NM_024690.2 P5867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:9009596 C>A maps to NM_024690.2 L13043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:9047025 C>G maps to NM_024690.2 T11535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:9077257 G>A maps to NM_024690.2 T3396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:9033702 G>A maps to NM_024690.2 L12078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr19:9046407 C>T maps to NM_024690.2 E11741E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:9049323 G>A maps to NM_024690.2 V10769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:9068059 C>T maps to NM_024690.2 W6462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:9090941 G>T maps to NM_024690.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:9045666 G>A maps to NM_024690.2 A11988A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr19:9008206 G>T maps to NM_024690.2 P13115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr19:9060889 A>G maps to NM_024690.2 P8852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:9085572 G>C maps to NM_024690.2 S2081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:9020780 T>G maps to NM_024690.2 R12441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:9088991 G>A maps to NM_024690.2 H941H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr19:9057046 C>A maps to NM_024690.2 V10133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:9020057 C>T maps to NM_024690.2 E12479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:9073348 T>C maps to NM_024690.2 S4699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:9088667 T>C maps to NM_024690.2 E1049E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr19:9076138 G>A maps to NM_024690.2 I3769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr19:9090794 G>A maps to NM_024690.2 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:9091808 C>T maps to NM_024690.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:9065167 G>C maps to NM_024690.2 L7426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr19:9009653 A>T maps to NM_024690.2 Y13024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr19:9066223 G>A maps to NM_024690.2 L7074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr19:8993421 G>A maps to NM_024690.2 I13889I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:100678728 C>G maps to NM_001040105.1 V1344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:100685697 C>A maps to NM_001040105.1 I3667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr7:100696278 G>A maps to NM_001040105.1 T4372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr7:100684914 C>T maps to NM_001040105.1 V3406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr7:100684955 C>G maps to NM_001040105.1 S3420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr7:100685697 C>T maps to NM_001040105.1 I3667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:100679094 G>C maps to NM_001040105.1 P1466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:100683465 T>C maps to NM_001040105.1 P2923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:100684032 C>G maps to NM_001040105.1 V3112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr7:100681269 T>C maps to NM_001040105.1 P2191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:100681212 G>T maps to NM_001040105.1 V2172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr7:100676142 G>A maps to NM_001040105.1 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr7:100684365 A>G maps to NM_001040105.1 P3223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:100685078 C>G maps to NM_001040105.1 S3461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:100676772 T>C maps to NM_001040105.1 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:100685832 C>T maps to NM_001040105.1 S3712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr7:100677783 T>C maps to NM_001040105.1 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:100686711 G>A maps to NM_001040105.1 V4005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:100686942 G>A maps to NM_001040105.1 T4082T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:100678876 G>T maps to NM_001040105.1 G1394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:100686756 C>A maps to NM_001040105.1 G4020G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr7:100679244 A>G maps to NM_001040105.1 L1516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr7:100684620 C>A maps to NM_001040105.1 T3308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr7:100681341 T>C maps to NM_001040105.1 P2215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr7:100676291 C>A maps to NM_001040105.1 S532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:1087950 C>T maps to ENST00000441003 F1142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr11:1075750 C>T maps to ENST00000441003 C59C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr11:1098724 G>C maps to ENST00000441003 S2365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:1093907 G>A maps to ENST00000441003 P1909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr11:1093643 G>A maps to ENST00000441003 T1821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr11:1093790 G>A maps to ENST00000441003 T1870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr11:1075768 C>T maps to ENST00000441003 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:195451994 C>G maps to ENST00000447234 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr3:195452895 C>G maps to ENST00000447234 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr6:30954440 C>T maps to NM_001010909.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:195486031 G>A maps to NM_018406.5 F4983F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:195479979 G>A maps to NM_018406.5 A5150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:195496023 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:195501147 G>A maps to NM_018406.5 G4324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr3:195491937 G>A maps to NM_018406.5 G4618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr11:1271399 G>A maps to ENST00000447027 T4433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:1255444 C>A maps to ENST00000447027 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:1261155 G>A maps to ENST00000447027 A1240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr11:1263374 C>T maps to ENST00000447027 T1758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:1264976 C>T maps to ENST00000447027 S2292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:1268747 C>T maps to ENST00000447027 S3549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:1263791 G>A maps to ENST00000447027 T1897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:1266767 C>T maps to ENST00000447027 P2889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr11:1268525 T>G maps to ENST00000447027 T3475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr11:1262588 C>T maps to ENST00000447027 V1496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr11:1266020 C>A maps to ENST00000447027 T2640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr11:1268885 C>T maps to ENST00000447027 G3595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr11:1268537 G>A maps to ENST00000447027 S3479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:1279558 G>A did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr11:1268339 A>T maps to ENST00000447027 P3413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr11:1264577 T>A maps to ENST00000447027 T2159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr11:1264580 C>T maps to ENST00000447027 P2160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr11:1267340 C>T maps to ENST00000447027 T3080T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr11:1031901 G>C maps to NM_005961.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr11:1028715 G>T maps to NM_005961.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr11:1018366 T>A maps to NM_005961.2 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:1017713 G>T maps to NM_005961.2 S1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:1016424 G>A maps to NM_005961.2 Q2126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:1017583 T>C maps to NM_005961.2 S1739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:1017982 T>C maps to NM_005961.2 S1606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr4:71347024 C>A maps to NM_152291.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr4:71346527 C>T maps to NM_152291.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr4:71346724 C>T maps to NM_152291.2 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr4:71346802 G>A maps to NM_152291.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr14:57749706 C>T maps to ENST00000431972 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr19:1360486 G>T maps to NM_032853.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr23:105450641 G>A did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:105451292 T>C did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr23:105450866 G>C did not map to a codon.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr23:105451254 G>A did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:103340679 C>T maps to NM_001018116.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr11:65631091 G>C maps to NM_025128.4 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:65631359 C>T maps to NM_025128.4 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:65633308 C>T maps to NM_025128.4 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr9:113563103 C>T maps to ENST00000189978 R822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr9:113562628 C>A maps to ENST00000189978 Y663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:52867432 C>T maps to ENST00000504329 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr3:52867390 C>T maps to ENST00000504329 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr6:49425486 C>A maps to NM_000255.3 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:45797202 G>A maps to NM_001128425.1 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:29845166 C>T maps to NM_017458.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:29853077 C>T maps to NM_017458.3 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr16:29858622 G>T maps to NM_017458.3 E791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr16:29858705 G>A maps to NM_017458.3 Q818Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr21:42754439 C>T maps to NM_002463.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr10:111988080 T>C did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:3228111 C>A did not map to a codon.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr23:3241327 C>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:3235194 G>T did not map to a codon.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr23:3228387 C>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:3235180 T>A did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:3238065 C>A did not map to a codon.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr23:3241943 C>T did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr23:3241680 C>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:3229298 C>T did not map to a codon.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr23:3241207 C>A did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr23:3238515 G>A did not map to a codon.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr23:3239736 A>G did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:3239483 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:3239246 G>A did not map to a codon.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr23:3235366 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:3240600 T>C did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:3228539 C>T did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:3228713 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:74679981 G>A maps to NM_001008529.1 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:4442814 C>G maps to NM_001105538.1 A1294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:4457188 C>G maps to NM_001105538.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr17:4446339 G>A maps to NM_001105538.1 A920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:42328422 C>T maps to NM_002466.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:42310476 C>T maps to NM_002466.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr20:42343841 C>G maps to NM_002466.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr12:102036247 G>A maps to NM_002465.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr12:102030482 C>T maps to NM_002465.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:102025392 C>T maps to NM_002465.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:102069094 G>A maps to NM_002465.2 V945V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr19:50958902 T>C did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:50957534 C>T maps to NM_004533.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:50962563 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:50962507 G>T maps to NM_004533.3 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr11:47372994 G>A maps to ENST00000399249 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:203144776 G>C maps to NM_004997.2 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:203140616 G>C maps to NM_004997.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr1:203144533 C>G maps to NM_004997.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:109839459 G>A maps to NM_001010985.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:128753113 G>A maps to NM_002467.4 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr13:77870790 A>G maps to NM_015057.4 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr13:77715010 G>C maps to NM_015057.4 V2457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr13:77792088 T>C maps to NM_015057.4 G981G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr13:77754438 G>T maps to NM_015057.4 I1652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:48601146 T>A did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:48586067 A>G maps to NM_032133.4 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:16082734 C>T maps to NM_005378.4 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr6:153043079 C>T maps to NM_025107.2 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr3:38180478 G>A maps to NM_001172567.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr15:48443708 C>A maps to NM_016132.3 G423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:48460948 A>T maps to NM_016132.3 Y83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:69063225 T>A maps to NM_138768.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr11:69062838 C>A maps to NM_138768.2 C6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:69063360 G>T maps to NM_138768.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:241069333 C>T maps to NM_138336.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr12:81112189 C>A maps to NM_005593.2 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr12:81110931 C>T maps to NM_005593.2 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:81101863 C>T maps to NM_002469.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:10408505 C>A maps to NM_005963.3 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:10415429 G>A maps to NM_005963.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr17:10418212 C>G did not map to a codon.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr17:10400463 G>C maps to NM_005963.3 R1526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr17:10398331 C>T maps to NM_005963.3 V1794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:10406201 A>G maps to NM_005963.3 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:10399766 C>A maps to NM_005963.3 E1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:10412810 G>C maps to NM_005963.3 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:10408141 T>C maps to NM_005963.3 Q892Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr17:10415995 A>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr17:10419285 G>A maps to NM_005963.3 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10408288 G>T maps to NM_005963.3 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr17:10399803 C>T maps to NM_005963.3 K1573K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr17:10399293 A>G maps to NM_005963.3 S1714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr17:8383507 G>T maps to ENST00000360416 V1839V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr17:8438759 C>T maps to ENST00000360416 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr17:8422109 C>G did not map to a codon.
Multiple mappings detected for codon TCGA-CV-7254-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr17:8411914 G>A maps to ENST00000360416 A1057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr16:15818248 C>T maps to NM_001040114.1 K1385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:15917114 G>A maps to NM_001040114.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr16:15797862 G>A maps to NM_001040114.1 T1975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr17:10222178 C>T maps to NM_003802.2 E1222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:10227484 A>G maps to NM_003802.2 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr17:10248894 G>A maps to NM_003802.2 Y434Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr17:10209913 T>C maps to NM_003802.2 E1776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:10248870 G>A maps to NM_003802.2 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:10248843 G>T maps to NM_003802.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr17:10253891 C>G maps to NM_003802.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10205017 C>T maps to NM_003802.2 E1890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr17:10219336 G>A maps to NM_003802.2 N1248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:10216004 C>T maps to NM_003802.2 S1417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr17:10253942 C>G maps to NM_003802.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr17:10209850 C>T maps to NM_003802.2 L1797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:50721023 G>T maps to NM_001145809.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr19:50713684 C>T maps to NM_001145809.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:50805051 C>T maps to NM_001145809.1 A1868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:50766676 G>A maps to NM_001145809.1 K898K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:50804958 C>T maps to NM_001145809.1 F1837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:50780154 G>A maps to NM_001145809.1 R1274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:108159996 C>T maps to NM_014981.1 E942E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:108147436 G>A maps to NM_014981.1 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr3:108211973 C>A maps to NM_014981.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:108147551 G>A maps to NM_014981.1 F1183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr3:108117635 C>A maps to NM_014981.1 E1681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr3:108100407 T>G did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:108218299 A>G did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr17:10426818 C>T maps to NM_017534.5 E1822E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr17:10436834 C>T maps to NM_017534.5 G765G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-4723-01A-01D-1434-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr17:10440763 G>C maps to NM_017534.5 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr17:10442662 G>A maps to NM_017534.5 N425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:10440652 C>T maps to NM_017534.5 E598E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10432159 G>A maps to NM_017534.5 T1197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10450896 G>A maps to NM_017534.5 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr17:10448711 C>T maps to NM_017534.5 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr17:10432119 C>A maps to NM_017534.5 E1211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:10429084 C>T maps to NM_017534.5 E1432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr17:10427800 A>G maps to NM_017534.5 V1719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:10545559 G>A maps to NM_002470.2 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr17:10555772 G>A maps to NM_002470.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:10547748 G>A maps to NM_002470.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr17:10554922 G>T maps to NM_002470.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:10549117 C>G maps to NM_002470.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr17:10533200 C>T maps to NM_002470.2 L1872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr17:10543902 G>A maps to NM_002470.2 Q756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr17:10351236 C>T maps to NM_017533.2 K1621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:10360800 C>A maps to NM_017533.2 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr17:10364245 T>A maps to NM_017533.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr17:10368798 G>A maps to NM_017533.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:10364259 C>A maps to NM_017533.2 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:10366497 T>C maps to NM_017533.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:10353771 G>T maps to NM_017533.2 A1393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr17:10354167 G>A maps to NM_017533.2 Q1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:10352201 C>T maps to NM_017533.2 K1448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:10354159 G>T maps to NM_017533.2 S1306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr17:10351338 G>A maps to NM_017533.2 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr17:10363394 C>T maps to NM_017533.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr17:10369588 C>A did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr17:10369619 G>A maps to NM_017533.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr17:10362565 A>T did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:10362663 G>A maps to NM_017533.2 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10358388 G>A maps to NM_017533.2 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10369996 C>T maps to NM_017533.2 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr17:10360893 G>A maps to NM_017533.2 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:10359161 C>G maps to NM_017533.2 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr17:10358337 T>C maps to NM_017533.2 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:10364305 G>A maps to NM_017533.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr17:10346787 C>T maps to NM_017533.2 E1908E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr14:23855642 G>A maps to NM_002471.3 L1614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr14:23866796 G>A maps to NM_002471.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:23855232 C>T maps to NM_002471.3 E1689E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:23862230 G>A maps to NM_002471.3 R1047R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr14:23871947 G>A maps to NM_002471.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr14:23855802 G>T maps to NM_002471.3 I1560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr14:23884667 G>A maps to NM_000257.2 S1735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr14:23886824 G>A maps to NM_000257.2 L1414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr14:23884361 C>A maps to NM_000257.2 E1801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr14:23894525 G>A maps to NM_000257.2 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:23882970 C>G maps to NM_000257.2 T1929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr14:23884263 G>A maps to NM_000257.2 N1833N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr14:23887504 A>C maps to NM_000257.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr14:23897711 C>T maps to NM_000257.2 E525E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr14:23887504 A>C maps to NM_000257.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr14:23887504 A>C maps to NM_000257.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr14:23886112 C>T maps to NM_000257.2 E1536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr14:23902405 G>A maps to NM_000257.2 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:33567490 C>T maps to NM_020884.3 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr20:33577924 G>T maps to NM_020884.3 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:33568427 C>T maps to NM_020884.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:33582099 T>C maps to NM_020884.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:33588930 G>A maps to NM_020884.3 G1857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:10304047 G>T maps to NM_002472.2 R1132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:10318850 G>A maps to NM_002472.2 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:10304006 T>C maps to NM_002472.2 E1145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr17:10296299 C>A maps to NM_002472.2 E1771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:10301954 G>A maps to NM_002472.2 A1328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr17:10318815 C>T maps to NM_002472.2 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:10304952 C>T maps to NM_002472.2 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr17:10293782 G>T maps to NM_002472.2 I1934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr22:36722648 C>T maps to NM_002473.4 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:36708219 G>A maps to NM_002473.4 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr22:36685214 C>T maps to NM_002473.4 Q1491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:36684375 G>A maps to NM_002473.4 D1618D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr22:36688142 C>A maps to NM_002473.4 L1411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr22:36701123 G>T maps to NM_002473.4 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr22:36745143 G>C maps to NM_002473.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr22:36745251 G>C maps to NM_002473.4 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr22:36708153 G>A maps to NM_002473.4 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr22:36681375 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr2:211179748 G>A maps to NM_079420.2 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr7:101266280 C>A maps to NM_138403.4 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr17:45291172 C>T maps to NM_002476.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:56548974 G>A maps to NM_002475.4 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr20:35173440 G>T maps to NM_006097.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:16141927 G>T maps to NM_013262.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr6:16143385 G>T maps to NM_013262.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:123333077 G>A maps to NM_053025.3 C1873C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr3:123451755 G>T maps to NM_053025.3 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr3:123419395 C>T maps to NM_053025.3 P973P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:123451899 G>T maps to NM_053025.3 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr3:123456282 C>T maps to NM_053025.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:123427704 C>A maps to NM_053025.3 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr3:123512631 C>T maps to NM_053025.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr3:123419830 G>A maps to NM_053025.3 C828C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr3:123452807 G>A maps to NM_053025.3 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:123419194 G>A maps to NM_053025.3 N1040N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:123471337 T>C maps to NM_053025.3 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr3:123452939 C>T maps to NM_053025.3 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:30411358 T>C maps to NM_033118.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:46763018 G>A maps to NM_182493.2 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr16:46771726 C>T maps to NM_182493.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:46741675 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr16:46762976 G>A maps to NM_182493.2 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:46771855 C>T maps to NM_182493.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:2675331 G>C maps to NM_001012418.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr6:2685585 G>T maps to NM_001012418.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:169492265 C>G maps to NM_018657.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr3:169496708 A>G maps to NM_018657.4 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:16694553 G>A maps to NM_012334.2 R1242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:16676205 G>A maps to NM_012334.2 R1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:16877786 G>T maps to NM_012334.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr5:16674966 C>T maps to NM_012334.2 L1653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr5:16682097 C>T maps to NM_012334.2 T1357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr5:16701456 G>C maps to NM_012334.2 S1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:16701599 G>A maps to NM_012334.2 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:16668424 G>A maps to NM_012334.2 I2012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr17:18022344 C>T maps to ENST00000205890 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr17:18022713 C>T maps to ENST00000205890 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr17:18022215 G>T maps to ENST00000205890 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:18023724 G>T maps to ENST00000205890 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr17:18039774 C>T maps to ENST00000205890 S1547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:18045515 C>T maps to ENST00000205890 L1925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr17:18057107 G>A maps to ENST00000205890 L2662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:18030102 A>G did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:18070959 C>T maps to ENST00000205890 S3335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:18062989 G>A maps to ENST00000205890 L3100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr17:18075504 C>T maps to ENST00000205890 S3417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr17:18066631 C>T maps to ENST00000205890 C3229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:18045391 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:18023547 C>T maps to ENST00000205890 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr17:18035780 G>A maps to ENST00000205890 R1407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr17:18061114 C>T maps to ENST00000205890 F2956F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:109817247 G>C did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr13:109792670 C>A maps to NM_015011.1 R1349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr13:109496714 C>T maps to NM_015011.1 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr13:109661379 T>C maps to NM_015011.1 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr13:109707434 G>A maps to NM_015011.1 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr13:109793137 C>T maps to NM_015011.1 P1504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr13:109535432 A>T maps to NM_015011.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr13:109318468 C>T maps to NM_015011.1 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr13:109318414 G>A maps to NM_015011.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr13:109475563 C>A maps to NM_015011.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr17:27421763 G>A maps to NM_078471.3 A1538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr17:27423780 C>T maps to NM_078471.3 R1461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr17:27442706 C>T maps to NM_078471.3 E734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:27421968 C>T maps to NM_078471.3 L1498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr22:26423400 G>C maps to ENST00000407587 G2489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr22:26159337 C>T maps to ENST00000407587 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr22:26423550 T>A maps to ENST00000407587 G2539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr22:26423370 G>A maps to ENST00000407587 T2479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr22:26242186 C>A maps to ENST00000407587 T1165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:26343754 G>C maps to ENST00000407587 L1905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr22:26164179 T>C maps to ENST00000407587 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr22:26242141 C>G maps to ENST00000407587 G1150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:26423574 G>A maps to ENST00000407587 R2547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr22:26317306 C>T maps to ENST00000407587 L1818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:57430773 C>T maps to NM_005379.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:192225421 C>T maps to NM_001130158.1 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:192225453 C>T maps to NM_001130158.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr2:192278878 G>A maps to NM_001130158.1 V993V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:192228947 C>T maps to NM_001130158.1 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr17:1387007 G>A maps to NM_001080779.1 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr17:1375217 G>A maps to NM_001080779.1 Y668Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:1387540 G>A maps to NM_001080779.1 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:59553687 T>C maps to NM_004998.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr15:59494581 C>T maps to NM_004998.2 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr19:8592315 G>T maps to NM_012335.3 R794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:8618293 C>G maps to NM_012335.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:8606806 C>G maps to NM_012335.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr19:8618064 G>A maps to NM_012335.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr19:8601168 C>T maps to NM_012335.3 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr12:109872839 A>G did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:109834317 G>A maps to NM_001101421.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:109849745 G>C maps to NM_001101421.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr10:26463413 G>A maps to NM_017433.4 K1407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr10:26377305 G>T maps to NM_017433.4 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr10:26409612 T>C maps to NM_017433.4 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr10:26377302 C>T maps to NM_017433.4 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr2:171240290 T>A maps to NM_138995.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:171248953 A>G maps to NM_138995.3 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr15:52672047 G>A maps to ENST00000358212 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr15:52606035 G>A maps to ENST00000358212 R1834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:52609405 G>A maps to ENST00000358212 Q1750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr15:52664413 G>C maps to ENST00000358212 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr15:52725428 C>T maps to ENST00000358212 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr15:52659264 G>C maps to ENST00000358212 L1041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr15:52620116 G>A maps to ENST00000358212 L1548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr18:47421487 G>C maps to NM_001080467.2 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr18:47373591 C>T maps to NM_001080467.2 R1461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:47527717 G>T maps to NM_001080467.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr18:47527696 G>A maps to NM_001080467.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:52515860 C>T maps to NM_018728.3 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr15:52497339 C>T maps to NM_018728.3 P1514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:76551079 A>T maps to ENST00000428345 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:76624543 G>T maps to ENST00000428345 E1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:76527374 A>G maps to ENST00000428345 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr6:76591500 G>A maps to ENST00000428345 K794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr6:76572370 T>G maps to ENST00000428345 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr6:76558165 A>G maps to ENST00000428345 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr11:76919560 C>T maps to NM_000260.3 D1981D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:76870541 G>C maps to NM_000260.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr11:76916512 C>T maps to NM_000260.3 S1829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr11:76891460 G>A maps to NM_000260.3 E876E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:76873900 C>T maps to NM_000260.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr11:76877186 C>A maps to NM_000260.3 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:76872096 A>T maps to NM_000260.3 K427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:128394475 C>A maps to ENST00000389524 C2080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr2:128351212 C>T maps to ENST00000389524 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:128366311 G>A maps to ENST00000389524 Q891Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:128354095 C>T maps to ENST00000389524 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr2:128350409 G>A maps to ENST00000389524 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr2:128387388 G>A maps to ENST00000389524 S1572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:128394184 C>T maps to ENST00000389524 L2038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:128324381 G>A maps to ENST00000389524 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr2:128354095 C>G maps to ENST00000389524 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:128322842 C>G maps to ENST00000389524 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:128366401 C>T maps to ENST00000389524 F921F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr2:128331591 G>C maps to ENST00000389524 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr15:72190745 T>C maps to ENST00000424560 K1366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr15:72193585 G>C maps to ENST00000424560 V1032V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:72141212 G>T maps to ENST00000424560 T2341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr15:72208800 C>G maps to ENST00000424560 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:72189933 G>C maps to ENST00000424560 S1637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr15:72119039 G>A maps to ENST00000424560 Q2581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:17213219 G>A maps to NM_004145.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:17291807 C>T maps to NM_004145.3 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr19:17320427 G>A maps to NM_004145.3 R1886R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr19:17256214 A>T maps to NM_004145.3 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr17:12639604 C>T maps to NM_001146312.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr17:12618890 G>A maps to NM_001146312.1 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:12655997 C>T maps to NM_001146312.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:12620738 G>T did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:12642623 A>T maps to NM_001146312.1 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr11:17741385 T>G maps to NM_002478.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr10:95111311 A>T maps to NM_013451.3 L1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr10:95069803 G>A maps to NM_013451.3 F2040F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:95079640 G>A maps to NM_013451.3 I1862I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr10:95168666 G>A maps to NM_013451.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr10:95169455 G>A maps to NM_013451.3 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr18:3129466 C>A maps to NM_003803.3 G853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr18:3116424 C>T maps to NM_003803.3 P1069P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:2056621 G>A did not map to a codon.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr8:2020521 C>G maps to NM_003970.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:2044189 G>T maps to NM_003970.2 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr8:2024314 G>A maps to NM_003970.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr8:2088644 G>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr8:2033443 C>A maps to NM_003970.2 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:2021530 C>T maps to NM_003970.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr8:2054044 C>T maps to NM_003970.2 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:24409085 G>A maps to ENST00000330966 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:24384111 C>T maps to ENST00000330966 L1355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:24434493 G>A maps to ENST00000330966 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr5:137206630 C>G maps to NM_006790.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:69881285 G>T maps to NM_032578.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr10:69957118 C>A maps to NM_032578.2 R1057R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:69961673 C>A maps to NM_032578.2 R1194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr10:69925474 G>A maps to NM_032578.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:40275390 C>A maps to NM_015460.2 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr3:40085594 G>A maps to NM_015460.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:40231678 C>A maps to NM_015460.2 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:40231704 G>A maps to NM_015460.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:40223838 G>A maps to NM_015460.2 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr3:40293460 G>T maps to NM_015460.2 E840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr1:59147829 G>A maps to NM_001085487.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr17:47886545 C>T maps to NM_007067.4 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr17:47895327 C>T maps to NM_007067.4 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr8:41791309 C>T maps to NM_006766.3 A1476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:41798737 G>C maps to NM_006766.3 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:41792080 T>C maps to NM_006766.3 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr8:41791630 G>A maps to NM_006766.3 T1369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:41798869 A>G maps to NM_006766.3 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:76789240 C>T maps to NM_012330.2 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:76788995 G>T maps to NM_012330.2 E1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr10:76602905 A>G maps to NM_012330.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr20:62839235 C>T maps to NM_004535.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr20:62837125 G>T maps to NM_004535.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:62848554 T>C maps to NM_004535.2 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:1914019 G>A maps to ENST00000399161 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:1914013 G>A maps to ENST00000399161 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:1926708 C>A maps to ENST00000399161 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:1805524 C>T maps to ENST00000399161 K1073K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:1843126 C>A maps to ENST00000399161 G958G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:1796223 C>A maps to ENST00000399161 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:1893174 G>A maps to ENST00000399161 C786C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr2:1926595 C>G maps to ENST00000399161 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr19:59073762 G>A maps to NM_198055.1 C627C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:48596100 C>T maps to NM_153029.3 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:48595295 C>A maps to NM_153029.3 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr16:48595683 A>G maps to NM_153029.3 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:48596172 C>A maps to NM_153029.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:48596193 G>A maps to NM_153029.3 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr13:32977299 G>A maps to NM_052818.2 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr13:32981422 G>A maps to NM_052818.2 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr13:33016825 C>T maps to NM_033111.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr13:33091953 G>T maps to NM_014887.2 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:33017614 T>C maps to NM_033111.3 E353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr5:177548576 C>T maps to NM_015111.1 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr21:30255314 A>C maps to NM_013240.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr13:21331599 C>T maps to NM_174928.1 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:153195467 C>A did not map to a codon.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr4:80247010 C>T maps to NM_032693.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr4:140272759 G>T maps to NM_057175.3 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:140265371 T>C maps to NM_057175.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr4:140309171 G>A maps to NM_057175.3 E845E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr4:140264023 A>T maps to NM_057175.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:140297592 T>C maps to NM_057175.3 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr4:140262202 C>T maps to NM_057175.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr4:140291480 C>T maps to NM_057175.3 Q624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:41894878 C>G maps to NM_024561.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:41891056 G>T maps to NM_024561.4 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr20:20013235 A>T maps to NM_016100.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr12:112492279 G>A maps to NM_024953.3 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:112512521 G>A maps to NM_024953.3 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:112506763 T>A maps to NM_024953.3 K357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr12:112481475 C>A maps to NM_024953.3 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr14:57857725 T>G maps to NM_001011713.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr14:57857968 C>G maps to NM_001011713.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr14:57857977 C>G maps to NM_001011713.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:117828388 C>T maps to NM_016200.4 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:113440618 C>T maps to NM_025146.2 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr4:76861952 G>A maps to NM_014435.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:89892473 G>T maps to NM_005467.3 G320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:89902134 T>A maps to NM_005467.3 Y439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:89902143 G>C maps to NM_005467.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:89885503 C>T maps to NM_005467.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:64825882 G>T maps to ENST00000340252 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr3:175293827 G>C did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr3:175520960 G>A maps to NM_207015.2 V786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr3:174974309 G>A maps to NM_207015.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr3:175293953 C>T maps to NM_207015.2 Y593Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:175520801 C>G maps to NM_207015.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:191524147 C>T maps to NM_005966.3 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:57484985 C>A maps to NM_005967.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr12:57106905 G>C maps to NM_001113203.1 V2013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr12:57111164 A>T maps to NM_001113203.1 A1383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:57106605 C>T maps to NM_001113203.1 L2062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:57108148 C>A maps to NM_001113203.1 R1940R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:57112996 C>A maps to NM_001113203.1 E773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr12:57112436 C>T maps to NM_001113203.1 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr12:57112022 T>C maps to NM_001113203.1 P1097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:13247197 G>T maps to NM_052876.2 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr1:1686105 C>T maps to ENST00000344463 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr1:1686839 G>A maps to ENST00000344463 Q366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:1685534 C>T maps to ENST00000344463 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr11:71185568 C>T maps to NM_018161.4 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:71175156 C>T maps to NM_018161.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr11:71164410 G>A maps to NM_018161.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr16:66847749 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr4:164061529 G>A maps to NM_138386.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:164069512 G>C maps to NM_138386.2 S205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr22:42461813 C>T maps to NM_000262.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr22:42461762 C>T maps to NM_000262.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:71305523 G>A maps to NM_017567.4 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr17:40693135 C>T maps to NM_000263.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr16:5077277 C>T did not map to a codon.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr17:42083544 G>A maps to NM_153006.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:130828915 G>A maps to NM_197956.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr13:101759853 G>A maps to NM_052867.2 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr13:101997661 C>A maps to NM_052867.2 G252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr13:101759892 G>A maps to NM_052867.2 R842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr13:101910913 C>T maps to NM_052867.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45T-01A-11D-A24D-08 chr13:101720362 G>A maps to NM_052867.2 S1451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr13:102047707 G>A maps to NM_052867.2 H39H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr13:101944607 G>T maps to NM_052867.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr13:101881862 C>A maps to NM_052867.2 G503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr13:101721053 C>A maps to NM_052867.2 L1441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:105894878 T>C maps to NM_005746.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr20:25604530 G>A maps to NM_152667.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr12:76453585 C>A maps to NM_139207.2 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:72433919 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr23:72432953 C>A did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:92927286 G>C did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:92928012 C>T did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:92927423 C>G did not map to a codon.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr23:92927420 G>T did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:92927455 C>G did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr23:92927030 C>T did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:92928296 C>G did not map to a codon.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr23:92927519 C>A did not map to a codon.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr23:92927175 T>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:92927641 T>C did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:92926977 G>C did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:89618773 A>G maps to NM_153757.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:47996259 C>T maps to NM_003827.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr19:48018173 C>T maps to NM_003827.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:144658322 C>A maps to ENST00000276844 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr8:144658292 G>A maps to ENST00000276844 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:50864943 T>C maps to NM_004851.1 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr16:786323 C>G maps to NM_022493.1 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:780841 C>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:60745948 T>A maps to NM_024611.4 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:78279725 C>A maps to NM_024678.4 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:78176975 T>C maps to NM_024678.4 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr11:78285431 G>A maps to NM_024678.4 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:46073528 G>T maps to NM_002482.3 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:46073824 C>G maps to NM_002482.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:50334678 C>A maps to NM_012191.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:50334272 G>A maps to NM_012191.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:73868551 G>A maps to NM_003960.3 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr17:72767907 G>A maps to NM_015654.3 H193H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:72768369 C>G maps to NM_015654.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr1:201751709 A>T maps to ENST00000367296 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:201687751 G>A maps to ENST00000367296 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:201789045 C>T maps to ENST00000367296 Q1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr1:201763687 C>G maps to ENST00000367296 S1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr11:20119157 A>T maps to ENST00000396087 L2075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr11:20067213 C>A maps to ENST00000396087 R1323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:20065573 T>C maps to ENST00000396087 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:20066745 C>T maps to ENST00000396087 S1167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr11:20119262 G>A maps to ENST00000396087 E2110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:20136232 C>T maps to ENST00000396087 P2411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr11:20119139 C>G maps to ENST00000396087 V2069V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr11:20139696 C>T maps to ENST00000396087 L2454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr11:20129231 C>T maps to ENST00000396087 C2347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr12:78598822 C>T maps to NM_014903.4 R2293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr12:78516169 C>T maps to NM_014903.4 L1400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:78400832 G>A maps to NM_014903.4 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:78562545 T>A maps to NM_014903.4 L1627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:78400499 G>C maps to NM_014903.4 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:78531083 T>G maps to NM_014903.4 S1523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr12:78400844 C>A maps to NM_014903.4 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:78400889 C>G maps to NM_014903.4 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:78400817 C>T maps to NM_014903.4 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr12:78573384 T>C maps to NM_014903.4 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr12:78362440 G>A maps to NM_014903.4 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:78553042 C>T maps to NM_014903.4 L1616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr12:78582050 G>A maps to NM_014903.4 L1916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr12:78522566 C>T maps to NM_014903.4 D1454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr12:78591041 C>T maps to NM_014903.4 L2081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr2:15557649 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:15519751 G>C maps to NM_015909.2 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:15374712 C>T maps to NM_015909.2 K2034K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr2:15319195 C>T maps to NM_015909.2 L2252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr2:15415922 C>T maps to NM_015909.2 L1803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr2:15468388 T>C maps to NM_015909.2 E1465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:15607789 G>A maps to NM_015909.2 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr2:15555747 T>C maps to NM_015909.2 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:15470865 G>A maps to NM_015909.2 S1401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr2:15694236 C>A maps to NM_015909.2 G79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr13:36229031 C>T maps to ENST00000400445 L2671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr13:36241641 C>T maps to ENST00000400445 R2845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr13:36229803 C>T maps to ENST00000400445 I2739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr13:35619135 G>A maps to ENST00000400445 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr13:35751192 C>T maps to ENST00000400445 Q1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr13:35630238 T>C maps to ENST00000400445 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr2:204032067 C>T maps to NM_001114132.1 L1965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr2:204000971 A>G maps to NM_001114132.1 Q1433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr2:204039941 G>T maps to NM_001114132.1 A2103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr2:204073439 C>T maps to NM_001114132.1 I2500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr3:47041665 C>A maps to NM_015175.1 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:47045663 C>T maps to NM_015175.1 I1993I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:47037918 C>T maps to NM_015175.1 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:47049353 C>G maps to NM_015175.1 S2519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:47037516 C>T maps to NM_015175.1 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:90965507 G>A maps to NM_002485.4 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:90958430 G>A maps to NM_002485.4 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:16890587 T>A maps to NM_017940.3 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr1:16895571 T>A maps to NM_017940.3 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:16893672 C>A did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:16907925 T>A maps to NM_017940.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:16895700 G>A maps to NM_017940.3 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:16918492 C>T maps to NM_017940.3 W8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr1:16890530 G>A maps to NM_017940.3 I1110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:145368571 C>G maps to NM_001039703.4 S3517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:145368629 G>A maps to NM_001039703.4 L3536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:145368590 C>T maps to NM_001039703.4 I3523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:145368632 G>T maps to NM_001039703.4 T3537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:145296494 C>T maps to NM_001039703.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:145293580 G>T did not map to a codon.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr1:145368467 A>G maps to NM_001039703.4 E3482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:145304608 A>G maps to NM_001039703.4 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr1:145293464 C>T maps to NM_001039703.4 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr1:145304641 C>T maps to NM_001039703.4 H525H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:148004598 C>A maps to ENST00000310701 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:21808092 C>A maps to NM_032264.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:21800025 C>T maps to NM_032264.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:102701557 C>T maps to NM_032041.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:113076801 C>A maps to ENST00000316851 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr11:113105875 G>A maps to ENST00000316851 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr21:22656565 A>T maps to NM_004540.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr21:22746286 A>C maps to NM_004540.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr21:22696775 C>T maps to NM_004540.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr21:22804479 G>A maps to NM_004540.2 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr21:22710815 A>T maps to NM_004540.2 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:22841079 G>A maps to NM_004540.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr21:22804470 G>A maps to NM_004540.2 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr21:22658659 C>A maps to NM_004540.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:19356216 C>T maps to NM_004386.2 N1196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:19356186 G>A maps to NM_004386.2 V1186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr19:19338828 G>C maps to NM_004386.2 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr19:19330001 C>A maps to NM_004386.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:19337497 C>T maps to NM_004386.2 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr11:134062789 G>A maps to NM_015261.2 C613C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr11:134038397 G>A maps to NM_015261.2 F1113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:158445167 C>T maps to NM_017760.5 K917K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr7:158454899 G>A maps to NM_017760.5 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr7:158449249 C>T maps to NM_017760.5 Q736Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:97035189 C>G maps to NM_015341.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:97024781 G>A did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr22:50960668 C>T maps to NM_001185011.1 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr9:100424348 G>A maps to NM_002486.4 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr9:100412849 C>T maps to NM_002486.4 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr3:196669323 C>T maps to NM_007362.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr19:39691034 C>T maps to NM_001001414.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:36031041 C>T maps to NM_001014839.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr1:36030831 T>G maps to NM_001014839.1 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr3:172365793 G>C maps to NM_001146276.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:74193714 C>T maps to NM_000265.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:183532570 C>T maps to NM_001127651.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr22:37273816 G>C maps to NM_000631.4 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:136667113 C>G maps to NM_006153.4 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:106498396 C>T maps to NM_001004720.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:106497976 C>T maps to NM_001004720.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:106498357 A>G maps to NM_001004720.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr2:106498120 G>A maps to NM_001004720.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6017-01A-11D-1683-08 chr2:183888620 T>C maps to NM_205842.1 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr2:183790480 C>G maps to NM_205842.1 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:54932699 G>A maps to NM_005337.4 Q1072Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:54936369 G>A maps to NM_005337.4 E1095E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr12:54925050 G>A maps to NM_005337.4 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:54936456 C>T maps to NM_005337.4 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr12:54914561 G>T maps to NM_005337.4 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:133541611 C>T maps to NM_207363.2 V924V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr2:133543009 C>A maps to NM_207363.2 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:133540564 G>A maps to NM_207363.2 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr2:133543009 C>G maps to NM_207363.2 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:133489550 C>T maps to NM_207363.2 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:133721319 C>T maps to NM_207363.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr12:50189494 C>G maps to NM_001037806.3 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr12:50186312 G>A maps to NM_001037806.3 F1236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:50189929 G>A maps to NM_001037806.3 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:50186686 G>A maps to NM_001037806.3 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr12:50189158 A>T maps to NM_001037806.3 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:48719786 G>A maps to NM_016453.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:48717524 G>A maps to NM_016453.2 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:3207204 G>A maps to NM_020170.3 E503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:3192540 C>T maps to NM_020170.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:3192651 C>T maps to NM_020170.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr19:3198879 C>T maps to NM_020170.3 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr19:3207442 C>T maps to NM_020170.3 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:24905932 C>G maps to NM_003743.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:24928093 C>T maps to NM_003743.4 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:24985572 G>A maps to NM_003743.4 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr2:24929929 C>A maps to NM_003743.4 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr2:24985572 G>A maps to NM_003743.4 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr8:71071825 A>G maps to NM_006540.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr20:46281791 T>C maps to NM_181659.2 S1413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr20:46277840 G>A maps to NM_181659.2 Q1213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr10:51581332 T>C maps to NM_001145260.1 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr20:44690979 G>A maps to NM_020967.2 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr20:44691088 G>A maps to NM_020967.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr20:33315171 T>A maps to NM_014071.2 P2013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr20:33337510 G>A maps to NM_014071.2 V829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr20:33329652 T>C maps to NM_014071.2 K1469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr20:33356327 T>A maps to NM_014071.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:33329792 G>A maps to NM_014071.2 Q1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr20:33328668 C>T maps to NM_014071.2 L1797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr20:33329071 G>T maps to NM_014071.2 S1663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr20:33331001 G>A maps to NM_014071.2 Q1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr20:33345722 C>T maps to NM_014071.2 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:126203621 G>A maps to NM_181782.4 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:126199425 C>T maps to NM_181782.4 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:16005051 G>A maps to ENST00000395857 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:16024583 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr17:16012156 G>A maps to ENST00000395857 Q709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:16024503 G>A maps to ENST00000395857 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr12:124957521 C>T maps to NM_006312.4 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr12:124839419 G>A maps to NM_006312.4 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr12:124832753 G>T maps to NM_006312.4 R1324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:124862848 C>A maps to NM_006312.4 E701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:124824682 G>A maps to NM_006312.4 S1859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:124824852 G>A maps to NM_006312.4 P1832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:124819763 G>A maps to NM_006312.4 Q2117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:55417663 T>A maps to NM_004829.5 C14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:41318600 G>A maps to NM_004828.3 *277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:41303864 G>A maps to NM_004828.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr9:132988726 C>T maps to NM_014286.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr18:2589201 G>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:23931617 G>A maps to NM_002487.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr15:23931752 G>T maps to NM_002487.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:23932094 C>T maps to NM_002487.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:23931732 C>T maps to NM_002487.2 W211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:23932304 G>A maps to NM_002487.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:140109352 C>T maps to NM_001144026.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:43817842 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:43809194 G>C did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr14:21487853 G>A maps to NM_201537.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr14:21486368 C>A maps to NM_201537.1 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr20:35299788 C>G maps to ENST00000373803 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr20:35293460 T>G maps to ENST00000373803 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr5:149901142 C>T maps to NM_001543.4 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr10:75567372 A>G maps to NM_003635.3 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr4:119059258 G>T maps to NM_004784.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr4:119026255 T>C maps to NM_004784.2 H355H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:118975166 C>T maps to NM_004784.2 Y34Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr4:119148126 C>A maps to NM_004784.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr4:119059243 G>T maps to NM_004784.2 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr4:119059213 C>T maps to NM_004784.2 H410H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr4:115997943 G>A maps to NM_022569.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr4:115751019 G>A maps to NM_022569.1 Q809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr4:115891639 G>A maps to NM_022569.1 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr4:115858650 T>A maps to NM_022569.1 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr4:115858476 G>T maps to NM_022569.1 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:115858512 A>T maps to NM_022569.1 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:119007335 G>A did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr7:123185710 A>C maps to NM_005000.2 L68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr22:42482285 T>C maps to NM_002490.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr19:8385741 G>A maps to NM_005001.2 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr12:4796252 G>C maps to NM_005002.4 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:41688683 C>A did not map to a codon.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr3:49059931 C>A maps to NM_199069.1 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr14:92588013 G>T maps to NM_004545.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:47002065 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr3:120320070 C>A maps to NM_004547.5 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr1:161183706 C>T maps to NM_004550.4 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:39500166 G>C maps to NM_004552.2 *107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:67803772 C>T maps to NM_002496.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:67378580 C>T maps to NM_007103.3 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr21:44324334 G>T maps to NM_021075.3 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr21:44324168 G>T maps to NM_021075.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr21:44324288 C>T maps to NM_021075.3 H389H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr2:152580788 G>C maps to NM_001164507.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr2:152522032 G>A maps to NM_001164507.1 F1684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr2:152394686 G>C maps to NM_001164507.1 V6988V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:152507243 G>A maps to NM_001164507.1 F2357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr2:152521101 C>T maps to NM_001164507.1 W1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:152539187 G>A maps to NM_001164507.1 D977D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr2:152534282 G>A maps to NM_001164507.1 N1190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:152423804 G>A maps to NM_001164507.1 A6011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr2:152383455 G>C maps to NM_001164507.1 L7307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr2:152580788 G>A maps to NM_001164507.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr2:152420375 G>T maps to NM_001164507.1 P6180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:152536300 T>C maps to NM_001164507.1 G1063G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr2:152423810 G>C maps to NM_001164507.1 V6009V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr10:21108394 C>T maps to ENST00000430741 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:21108418 C>T maps to ENST00000430741 K663K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr10:21141500 A>G maps to ENST00000430741 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr10:21098747 G>C maps to ENST00000430741 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:91937822 C>T maps to NM_022351.4 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:91929758 A>T maps to NM_022351.4 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:91929770 A>T maps to NM_022351.4 K137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:91940499 G>A maps to NM_022351.4 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr8:91929768 T>A maps to NM_022351.4 L136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:91929727 A>G maps to NM_022351.4 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:8244401 G>A maps to NM_015509.3 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:16774624 G>A maps to NM_018090.4 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr12:97337516 G>T maps to NM_001135175.1 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr15:56140619 T>G maps to ENST00000508342 R917R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:56207862 G>A maps to ENST00000508342 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr22:29885767 G>A maps to NM_021076.3 K713K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr22:29886349 G>A maps to NM_021076.3 E907E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr22:29885176 C>A maps to NM_021076.3 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr8:24813612 G>C maps to ENST00000221169 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr8:24775398 A>G maps to NM_005382.2 K677K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:24771548 G>T maps to NM_005382.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:24771437 G>A maps to NM_005382.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr1:72400875 T>G maps to NM_173808.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr15:75641449 C>G maps to NM_024608.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:178283594 G>T maps to NM_018248.2 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr4:178272609 A>T maps to NM_018248.2 K316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr3:130947447 G>A maps to NM_024800.4 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr3:130889681 C>T maps to NM_024800.4 H450H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr3:130799386 T>C maps to NM_024800.4 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr3:130799419 G>T maps to NM_024800.4 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:211842542 G>A maps to NM_002497.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr3:52797517 C>T maps to NM_003157.4 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr9:127089615 G>A did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:198233295 C>T maps to NM_133494.2 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr1:198288544 C>T maps to NM_133494.2 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:27068132 C>T maps to NM_178170.2 H590H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr17:27068429 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr14:75553753 C>T maps to NM_033116.4 Q928Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:20939792 A>G maps to NM_006157.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:21581765 C>T maps to NM_006157.3 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr11:21592398 C>T maps to NM_006157.3 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr11:21556010 C>T maps to NM_006157.3 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr11:21592314 C>T maps to NM_006157.3 G662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr12:44913862 G>A maps to NM_001145107.1 D825D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr12:44917199 G>A maps to NM_001145107.1 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr15:73575380 C>T maps to NM_002499.3 G1113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr15:73581579 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr15:73562573 G>A maps to NM_002499.3 K906K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr1:156640277 C>T maps to NM_006617.1 G1234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr1:156642170 C>G maps to NM_006617.1 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:5495244 C>T maps to NM_001047160.1 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr10:5498680 G>A maps to NM_001047160.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr18:70461639 C>G did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr18:70526310 T>A did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr18:70461477 C>T maps to NM_153181.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr18:70532112 T>C maps to NM_153181.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr18:70417496 G>A maps to NM_153181.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr16:47117172 G>A maps to NM_018092.3 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr16:47117200 C>T maps to NM_018092.3 E503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr6:31828218 G>A maps to NM_000434.3 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:31829147 G>A maps to NM_000434.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr2:233899355 C>T maps to NM_005383.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:233899031 G>A maps to NM_005383.2 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:233899487 C>T maps to NM_005383.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr11:74716672 G>A maps to NM_006656.5 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr10:105330707 C>T maps to NM_004210.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:105349975 C>T maps to NM_004210.4 C524C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:105330707 C>T maps to NM_004210.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr20:44519213 T>C maps to NM_080749.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:7230538 C>T maps to NM_032442.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:7221174 G>T maps to NM_032442.2 A1379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr17:7220819 G>A maps to NM_032442.2 A1426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:182543548 C>T maps to NM_002500.2 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr2:182542609 G>A maps to NM_002500.2 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:37761718 C>A maps to NM_006160.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr17:37762278 G>A maps to NM_006160.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr7:31378056 C>A maps to NM_022728.2 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:31378426 G>A maps to NM_022728.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr7:31378674 C>A maps to NM_022728.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:31378345 G>A maps to NM_022728.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr4:113436580 T>C maps to NM_024019.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:113436007 G>A maps to NM_024019.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:71332388 T>C maps to NM_020999.3 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr1:78392265 C>G maps to NM_144573.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:78390877 G>A maps to NM_144573.3 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr17:29557871 A>G maps to NM_001042492.2 V1042V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr17:29556272 G>A maps to NM_001042492.2 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr17:29657374 C>T maps to NM_001042492.2 Q1891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr17:29663705 T>C maps to NM_001042492.2 P2067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:29548870 C>T maps to NM_001042492.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr17:29508729 A>G maps to NM_001042492.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr17:29528440 C>T maps to NM_001042492.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr22:30051657 C>T maps to NM_181832.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr22:30061030 C>G maps to NM_181832.2 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr22:30051609 G>T maps to NM_181832.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr22:30077426 G>A did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:204931254 G>A maps to NM_001160331.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:204943328 G>A maps to ENST00000367172 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:204966433 C>A maps to ENST00000367172 T1080T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:204955120 C>T maps to ENST00000367172 R890R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr1:204957854 C>T maps to ENST00000367172 Y1003Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr1:204948661 C>T maps to ENST00000367172 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr16:69681024 C>T maps to NM_138713.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr16:69711218 C>T maps to NM_138713.2 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr16:69689630 C>A maps to NM_138713.2 C375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr16:69725770 G>A maps to NM_138713.2 Q681Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr16:69726981 C>G maps to NM_138713.2 S1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr18:77246596 C>T maps to NM_172387.1 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:77170880 G>A maps to NM_172387.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr18:77208871 C>T maps to NM_172387.1 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr18:77246755 G>A maps to NM_172387.1 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr20:50133388 G>A maps to NM_012340.3 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr20:50158921 C>T maps to NM_012340.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:50140071 C>T maps to NM_012340.3 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:50140539 G>A maps to NM_012340.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:50049029 G>A maps to NM_012340.3 Q766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr20:50048637 C>T maps to NM_012340.3 Q896Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr20:50048820 C>T maps to NM_012340.3 E835E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr16:28967618 C>T maps to NM_032815.3 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr16:68156550 G>T maps to NM_173165.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:68200871 T>C maps to NM_173165.2 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr14:24845707 A>G maps to NM_001136022.1 P818P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr12:54686718 G>A maps to NM_001136023.1 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr17:46128845 C>T maps to ENST00000362042 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:46135824 G>T maps to ENST00000362042 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr17:46136576 C>T maps to ENST00000362042 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr17:46136933 C>T maps to ENST00000362042 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr2:178095968 G>A maps to NM_006164.3 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr2:178095545 G>A maps to NM_006164.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:26225150 T>C maps to NM_004289.6 C611C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:26224728 G>T maps to NM_004289.6 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr7:26224793 A>G maps to NM_004289.6 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr9:14150262 C>T maps to ENST00000397581 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:3452480 G>T maps to ENST00000269778 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr19:13136139 G>A maps to ENST00000397661 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr19:13192669 G>T did not map to a codon.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr4:103518734 C>T maps to NM_003998.3 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:104161252 C>A maps to NM_001077494.1 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr10:104157125 C>T maps to NM_001077494.1 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:35872922 G>A maps to NM_020529.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr14:35873702 G>A maps to NM_020529.2 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:39398346 G>C maps to NM_001001716.1 *307Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:39398082 C>A maps to NM_002503.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr19:36386968 G>C maps to ENST00000352614 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:36381393 T>A did not map to a codon.
Multiple mappings detected for codon TCGA-CQ-5326-01A-01D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:31525603 G>A maps to NM_005007.3 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr8:145661382 C>T maps to NM_013432.4 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:145661199 G>A maps to NM_013432.4 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:145662238 T>C maps to NM_013432.4 E597E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr8:145655882 G>A maps to NM_013432.4 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr3:101572574 C>G maps to NM_031419.3 S402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:129734649 C>T maps to NM_006165.3 P1315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr20:34262285 G>T maps to NM_021100.4 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr2:69627579 G>A maps to NM_001002755.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr4:47853952 G>A maps to NM_152995.4 Q810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr4:47857089 T>A maps to NM_152995.4 K803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr4:47898590 G>A maps to NM_152995.4 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr6:41065109 C>T maps to NM_002505.4 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:41235026 G>A did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr1:41213249 G>A maps to ENST00000308733 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr14:23940185 G>A maps to NM_001042635.1 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr14:23944384 C>T maps to NM_001042635.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr2:233759518 G>A maps to NM_019850.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:115828837 G>A maps to NM_002506.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:47589373 G>A maps to NM_002507.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr17:47579543 C>A maps to NM_002507.3 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr17:47583778 C>T maps to NM_002507.3 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:102632527 C>A did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr3:25773839 C>T maps to NM_018297.3 W465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr4:103822450 G>A maps to NM_139173.3 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr4:103949912 G>A maps to NM_178833.4 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr2:219942054 C>A maps to NM_024782.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:160340724 C>T maps to NM_005598.3 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:116380886 G>T maps to NM_005599.3 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:18121916 C>T maps to NM_198586.2 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr10:115618362 C>T maps to NM_198514.3 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr22:42070975 G>T maps to ENST00000402458 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:17739578 G>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:17745087 G>C did not map to a codon.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr23:17710475 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:17743957 G>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:17746378 G>T did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:17744772 G>A did not map to a codon.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr23:17744145 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:17744916 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr23:17746840 T>G did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr23:71359915 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:71359606 C>A did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr23:71358840 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:49463813 G>A maps to NM_032316.3 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr1:236228282 C>A maps to NM_002508.2 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:236195923 C>A maps to NM_002508.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr1:236205525 G>A maps to NM_002508.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:236180535 C>T maps to NM_002508.2 G722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr14:52534596 G>A maps to NM_007361.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr14:52481132 G>T maps to NM_007361.3 R1098R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr14:52477628 C>T maps to NM_007361.3 V1229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:201757019 G>A maps to NM_001136039.2 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr14:51224284 G>A maps to NM_020921.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr14:51204923 T>C maps to NM_020921.3 Q1903Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:51259516 G>A maps to NM_020921.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr12:675229 G>A maps to NM_016533.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr20:25472103 C>T maps to NM_025176.4 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr20:25477375 C>T maps to NM_025176.4 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr20:25478943 C>A maps to NM_025176.4 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr20:25457598 C>T maps to NM_025176.4 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr20:25472024 C>A maps to NM_025176.4 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr20:25436401 C>T maps to NM_025176.4 L1288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr16:69374141 G>A maps to NM_016101.4 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr15:23006378 G>A maps to NM_030922.6 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:48036924 C>T maps to NM_207330.1 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr4:48037978 G>C maps to NM_207330.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr5:156895763 C>T maps to NM_001099287.1 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:156899364 G>A maps to NM_001099287.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr5:36985987 A>G maps to NM_133433.3 K902K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr5:36986386 A>G maps to NM_133433.3 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr5:37006526 G>A maps to NM_133433.3 A1308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr5:37051936 G>A maps to NM_133433.3 K2337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr5:37027508 C>T maps to NM_133433.3 Q1953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr5:37008755 T>G maps to NM_133433.3 L1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:37003450 T>C did not map to a codon.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr5:37049396 A>G maps to NM_133433.3 P2316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr5:37008731 C>G maps to NM_133433.3 S1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr5:37064094 G>A maps to NM_015384.4 R2688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr5:37052592 C>G maps to NM_133433.3 Y2396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr5:37044526 G>T maps to NM_133433.3 E2063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr5:36955631 C>G maps to NM_133433.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr9:107531142 G>C did not map to a codon.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:124676414 T>C maps to NM_001040214.1 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr8:63492236 T>C did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:63492129 C>T maps to NM_173688.2 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:119077277 C>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:119077486 G>T did not map to a codon.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr23:119070344 C>T did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr23:119066102 C>G did not map to a codon.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr23:119077226 C>T did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:119066121 G>A did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:119059237 A>G did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:119077436 C>A did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr6:28227977 T>C maps to NM_001007531.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr16:50667325 C>A maps to NM_033119.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr16:50659472 C>T maps to NM_033119.3 N148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:1033580 G>A maps to NM_033120.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr5:1034965 C>T maps to NM_033120.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr3:23942310 T>C maps to NM_020345.3 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:40175776 G>T maps to ENST00000316082 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr23:118723941 C>A did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr23:118723932 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr23:118724261 A>C did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:118723981 A>T did not map to a codon.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr23:118723978 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:118723540 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr23:118723884 A>G did not map to a codon.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr3:42660539 G>C maps to NM_005385.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr3:42679133 C>T maps to NM_005385.3 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:36988379 G>A maps to NM_001079668.2 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr20:21494271 G>A maps to NM_002509.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr20:21376611 C>T maps to NM_033176.1 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr5:172659655 G>A maps to NM_004387.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:23538826 G>C maps to NM_006167.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr4:13545813 G>A maps to NM_001189.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr4:85414576 G>A maps to NM_006168.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:85414621 C>G maps to NM_006168.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:134598891 G>T maps to NM_177400.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:33469077 G>A maps to NM_018096.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr3:173993198 C>T maps to NM_014932.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr3:173998975 C>T maps to NM_014932.2 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:173997335 C>A maps to NM_014932.2 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr3:173998385 G>T maps to NM_014932.2 G589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr3:173997143 C>A maps to NM_014932.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr3:173996852 A>T maps to NM_014932.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:7317750 A>T maps to NM_020795.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr17:7320706 C>A maps to NM_020795.2 Y699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:70389689 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr23:70384130 T>C did not map to a codon.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr23:70367762 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:70389886 C>T did not map to a codon.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr23:70387116 C>G did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:70375175 C>G did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:6069248 G>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:6069471 C>T did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr23:5821253 G>T did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr23:6069194 G>T did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr23:5821899 G>C did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:5821197 G>T did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:5821172 C>T did not map to a codon.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr23:5811510 A>G did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:6069123 A>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:5811025 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr23:5811432 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr23:5811299 T>A did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:5810947 C>T did not map to a codon.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr17:26488203 G>A maps to NM_016231.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr5:65084005 G>A maps to NM_020726.4 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr5:65077117 T>A maps to NM_020726.4 L231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr5:65118739 G>A maps to NM_020726.4 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:3614574 G>T maps to ENST00000448023 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr16:3614103 G>A maps to ENST00000448023 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr16:3614337 G>A maps to ENST00000448023 H247H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr16:3614472 C>T maps to ENST00000448023 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:3606979 G>A maps to ENST00000448023 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:3613074 G>A maps to ENST00000448023 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:3614247 G>A maps to ENST00000448023 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:32474681 G>A maps to NM_021209.4 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:32475966 C>T maps to NM_021209.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr2:32474718 C>A maps to NM_021209.4 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr16:57088720 C>T maps to NM_032206.3 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:57067575 G>A maps to NM_032206.3 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr16:57101665 C>T maps to NM_032206.3 L1475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:57088698 C>T maps to NM_032206.3 F1181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr16:57104530 G>A did not map to a codon.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr16:57074582 C>G maps to NM_032206.3 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr16:57075483 C>A maps to NM_032206.3 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:5486122 C>T maps to NM_033004.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr17:5462453 C>T maps to NM_033004.3 W521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr17:5445208 C>G maps to NM_033004.3 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr17:5462998 C>T maps to NM_033004.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:7981598 G>T maps to NM_176821.3 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr11:7981898 C>A maps to NM_176821.3 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr11:7982198 C>T maps to NM_176821.3 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:56307531 G>A maps to NM_145007.3 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:56300306 T>A maps to NM_145007.3 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:56321435 G>A maps to NM_145007.3 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr19:56303837 C>A did not map to a codon.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr19:54327176 G>A maps to ENST00000391773 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:54314438 G>T maps to ENST00000391773 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:54314432 G>T maps to ENST00000391773 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:54327404 G>A maps to ENST00000391773 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:54327416 G>A maps to ENST00000391773 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:54318202 G>C maps to ENST00000391773 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr19:54313274 G>C maps to ENST00000391773 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:54313979 G>T maps to ENST00000391773 C311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:54297341 C>A maps to ENST00000391773 A1050A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr19:54314024 G>A maps to ENST00000391773 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr19:54313427 G>C maps to ENST00000391773 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:54308535 A>G maps to ENST00000391773 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:54313631 C>T maps to ENST00000391773 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr19:54313274 G>A maps to ENST00000391773 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr19:54314150 C>T maps to ENST00000391773 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr19:56422071 G>A maps to NM_176810.2 H713H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:56423802 G>A maps to NM_176810.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:56436022 C>T maps to NM_176810.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:56423844 C>T maps to NM_176810.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:56413453 G>C maps to NM_176810.2 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:56423610 C>T maps to NM_176810.2 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:56423072 C>A maps to NM_176810.2 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:7064474 C>T maps to NM_176822.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr11:7079660 A>G maps to NM_176822.3 Q871Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:7068025 G>T maps to NM_176822.3 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:7091525 C>A maps to NM_176822.3 Y995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr11:7064663 C>T maps to NM_176822.3 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:55494890 C>T maps to NM_017852.3 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr19:55493830 G>C maps to NM_017852.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:55494908 G>T maps to NM_017852.3 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr19:55501498 G>T maps to NM_017852.3 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:55493545 C>A maps to NM_017852.3 C160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:55493546 A>C maps to NM_017852.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:247608039 G>T maps to NM_004895.4 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr1:247608111 G>C maps to NM_004895.4 L1000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr1:247588448 C>T maps to NM_004895.4 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:247599292 A>G maps to NM_004895.4 T840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:247599409 C>A maps to NM_004895.4 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr1:247597515 C>T maps to NM_004895.4 F813F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:247587341 C>T maps to NM_004895.4 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:56370016 C>A maps to NM_134444.4 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:56372753 C>A maps to NM_134444.4 S620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:56373415 C>T maps to NM_134444.4 Q693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:56373426 G>A maps to NM_134444.4 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:56370045 C>T maps to NM_134444.4 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr19:56552434 C>A maps to NM_153447.4 P978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr19:56515381 G>T maps to NM_153447.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:56552286 G>T did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr19:56539099 C>T maps to NM_153447.4 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:56539845 C>T maps to NM_153447.4 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:56549453 C>T maps to NM_153447.4 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:56515258 C>T maps to NM_153447.4 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr19:56539107 C>T maps to NM_153447.4 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr19:56539107 C>T maps to NM_153447.4 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:280966 G>A maps to NM_138329.1 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:280492 C>A maps to NM_138329.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:280493 C>T maps to NM_138329.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr11:284295 C>A maps to NM_138329.1 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:55451292 C>G maps to ENST00000446217 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr19:55450491 C>G maps to ENST00000446217 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:55451376 G>A maps to ENST00000446217 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr19:55435179 C>T maps to ENST00000446217 K1042K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr19:55450944 C>T maps to ENST00000446217 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr19:55435236 C>T maps to ENST00000446217 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:56466302 T>A maps to NM_176811.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:56487624 G>T maps to NM_176811.2 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr19:56490772 C>T maps to NM_176811.2 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr19:56466410 G>A maps to NM_176811.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr19:56485170 T>A maps to NM_176811.2 C896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:56466996 C>T maps to NM_176811.2 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr19:56473486 T>C maps to NM_176811.2 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr19:56244752 C>T maps to NM_176820.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr19:56244124 C>A maps to NM_176820.2 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:56243714 G>A maps to NM_176820.2 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:119052949 C>T maps to NM_024618.2 N834N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr15:85201311 G>A maps to NM_205858.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:142409720 C>T maps to NM_002511.2 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr3:160942822 C>T maps to ENST00000472947 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:160968691 G>C maps to NM_015938.3 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:160964155 A>G maps to ENST00000472947 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr3:160942781 C>T maps to ENST00000472947 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr17:49237411 A>G maps to ENST00000393198 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:48336721 C>T maps to NM_005793.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr1:169267910 T>C maps to NM_013330.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr1:169256565 A>G maps to NM_013330.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:152138557 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr1:10042518 G>A maps to NM_022787.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:183230438 C>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:183387390 G>C maps to NM_015039.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr16:4519401 C>T maps to NM_020677.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr2:101087009 A>G maps to NM_001011717.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:101096983 C>T maps to NM_001011717.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr2:101097598 G>A maps to NM_001011717.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:43171125 C>G maps to NM_021079.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:43159089 G>A maps to NM_021079.3 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr17:43173653 G>C did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:232393431 G>A maps to NM_006056.4 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:232393152 G>A maps to NM_006056.4 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr2:232393434 G>C maps to NM_006056.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:151784434 G>A maps to NM_020167.4 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:43659376 C>T maps to NM_182977.2 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:43651922 C>T maps to NM_182977.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:43704469 G>C maps to NM_182977.2 A1075A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr5:43659397 C>T maps to NM_182977.2 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:144096937 G>T maps to ENST00000467773 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr1:891547 T>A maps to NM_015658.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:887965 C>A maps to NM_015658.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:96093936 G>A maps to NM_022451.9 H800H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr10:96106180 C>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:132636124 C>T maps to NM_024078.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr7:30492294 G>A maps to NM_006092.2 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:30485797 G>A maps to NM_006092.2 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr7:30485827 G>A maps to NM_006092.2 N794N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:50763773 G>T maps to NM_022162.1 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:50745594 C>T maps to NM_022162.1 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr16:50745418 C>T maps to NM_022162.1 Q533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr16:50733834 C>T maps to NM_022162.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr16:50744967 C>T maps to NM_022162.1 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr16:50746257 T>A maps to NM_022162.1 P812P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:54671878 G>T maps to NM_005450.4 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr2:10803139 G>A maps to NM_024894.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr2:10712232 C>T maps to NM_024894.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:10729398 C>T maps to NM_024894.2 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:65722657 G>A maps to NM_015462.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr17:65717546 G>A maps to NM_015462.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:65714140 G>A maps to NM_015462.3 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:65735666 G>A maps to NM_015462.3 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr18:31684008 A>G did not map to a codon.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr18:31538214 C>T maps to NM_003787.4 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr18:31538229 A>T maps to NM_003787.4 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:31803103 C>T maps to NM_003787.4 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:33467448 G>A maps to NM_022917.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr10:103921944 G>A maps to ENST00000405356 E683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr10:103917060 C>T maps to ENST00000405356 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr7:156762309 C>T maps to NM_138400.1 H832H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:14989417 C>T maps to ENST00000456867 R1195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:70514196 C>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:70514350 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:70514362 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr23:70517747 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:2956204 C>T maps to NM_003703.1 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr12:6666428 T>A maps to ENST00000382421 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr12:6672620 G>A maps to ENST00000382421 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:203157550 C>T maps to NM_015934.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:162337110 G>T maps to NM_014697.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:162326886 C>G maps to NM_014697.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:162337155 G>T maps to NM_014697.2 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr17:26089929 G>A maps to NM_000625.4 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr17:26091111 G>A maps to NM_000625.4 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:26107911 C>T maps to NM_000625.4 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:26114729 G>A maps to NM_000625.4 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr17:26108076 G>A maps to NM_000625.4 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr17:26115876 G>A maps to NM_000625.4 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr17:26114708 G>A maps to NM_000625.4 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:150696316 C>A maps to NM_000603.4 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr7:150710424 C>T maps to NM_000603.4 G1071G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr19:50060442 G>A maps to NM_015953.3 Q108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:169699617 C>T maps to NM_001171631.1 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr2:169690789 T>C maps to NM_001171631.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:169718497 A>G maps to NM_001171631.1 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr9:139393349 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr9:139417629 G>T maps to NM_017617.3 C138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr9:139412696 C>A maps to NM_017617.3 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr9:139407989 C>T did not map to a codon.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr9:139404311 C>A maps to NM_017617.3 E948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr9:139401755 C>T did not map to a codon.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr9:139413946 G>A maps to NM_017617.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr9:139396304 G>A maps to NM_017617.3 Q1845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr9:139407979 G>T maps to NM_017617.3 C739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr9:139412234 C>T maps to NM_017617.3 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr9:139402561 C>A maps to NM_017617.3 G1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:139391122 G>A maps to NM_017617.3 A2356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:139392010 C>T did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:139399999 C>A maps to NM_017617.3 E1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr9:139402770 G>A maps to NM_017617.3 Q1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:139395017 G>A maps to NM_017617.3 Q1974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:139402541 C>G maps to NM_017617.3 A1125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr9:139418286 C>A maps to NM_017617.3 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr9:139393695 G>A maps to NM_017617.3 R1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr9:139397640 G>A maps to NM_017617.3 A1720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr9:139407532 G>A maps to NM_017617.3 Q803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr9:139401393 G>T maps to NM_017617.3 C1225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr9:139405240 G>A maps to NM_017617.3 V868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:139402741 C>T maps to NM_017617.3 W1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:139411741 G>A maps to NM_017617.3 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr9:139410436 C>T maps to NM_017617.3 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:139395186 G>A maps to NM_017617.3 G1917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr9:139410451 G>T maps to NM_017617.3 Y550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr9:139409769 G>C maps to NM_017617.3 Y662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr9:139413261 C>A maps to NM_017617.3 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr9:139396247 G>A maps to NM_017617.3 Q1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:120462867 C>G maps to NM_024408.2 V1821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:120548095 G>A maps to NM_024408.2 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:120539833 A>T maps to NM_024408.2 C179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:120539637 C>A maps to NM_024408.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:120467944 C>T maps to NM_024408.2 G1498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr1:120491109 G>A maps to NM_024408.2 G893G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr1:120462964 C>T maps to NM_024408.2 W1789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:120479961 G>A maps to NM_024408.2 S1155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:145281459 A>G maps to ENST00000454606 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr1:145273376 G>C maps to ENST00000454606 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:145273250 G>A maps to ENST00000454606 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:15299971 G>A maps to NM_000435.2 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr19:15295220 G>A maps to NM_000435.2 P817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr19:15302415 G>T maps to NM_000435.2 C285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr19:15308353 C>A maps to NM_000435.2 G52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:15292502 C>G maps to NM_000435.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr19:15290214 G>A maps to NM_000435.2 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:15291044 A>G maps to NM_000435.2 C1055C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:15272482 C>A maps to NM_000435.2 E1986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr19:15299866 C>T maps to NM_000435.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr19:15302801 G>A maps to NM_000435.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:32188356 G>A maps to NM_004557.3 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:32166456 G>C maps to NM_004557.3 S1529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:32169063 C>G maps to NM_004557.3 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:32172088 T>A maps to NM_004557.3 G981G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:32166500 C>T maps to NM_004557.3 L1514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr6:32169899 T>C maps to NM_004557.3 E1236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr6:32163522 C>G maps to NM_004557.3 S1901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:79916265 G>A maps to NM_178493.5 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr8:120429125 C>G maps to NM_002514.3 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:120430511 A>T maps to NM_002514.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr8:120431404 C>G maps to NM_002514.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr14:26917689 A>G maps to ENST00000449198 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr14:26939670 C>A maps to NM_006491.2 *182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr19:46444041 G>A maps to NM_002516.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr19:46444161 G>A maps to NM_002516.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:46444140 C>G maps to NM_002516.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:100117441 A>G did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:100098949 T>G did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:100125790 C>T did not map to a codon.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr23:100099013 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:100117395 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr23:100117562 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:155750156 G>A maps to NM_015718.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr6:155764442 G>A maps to NM_015718.2 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:89070671 C>T maps to NM_016931.3 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:89135492 C>A did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr15:69335138 G>T maps to NM_024505.3 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:69347809 C>T maps to NM_024505.3 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr15:69348930 G>A maps to NM_024505.3 K731K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr9:140327702 C>T maps to NM_006647.1 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:140323431 C>T maps to NM_006647.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr19:47548509 C>A maps to NM_002517.2 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:101607325 G>A maps to NM_002518.3 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr2:101609898 G>A maps to NM_002518.3 Q734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr14:34269099 C>T maps to NM_001164749.1 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr14:34145430 C>G maps to NM_001164749.1 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr14:34269117 G>A maps to NM_001164749.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:33684489 T>A maps to NM_001164749.1 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:34269384 C>A maps to NM_001164749.1 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr11:66190202 C>T maps to NM_178864.3 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr11:66192179 G>T maps to NM_178864.3 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:66190250 A>T maps to NM_178864.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr11:66192496 C>T maps to NM_178864.3 D712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:66192178 C>T maps to NM_178864.3 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr11:66192685 G>A maps to NM_178864.3 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr11:66191815 G>A maps to NM_178864.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr11:66192412 G>C maps to NM_178864.3 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:108031918 G>A maps to NM_002519.2 D1298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr11:108044178 G>T maps to NM_002519.2 S511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr20:62737248 G>A maps to NM_005286.2 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr20:62738004 C>G maps to NM_005286.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr18:21140391 G>A maps to NM_000271.4 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr7:44578579 G>A maps to NM_013389.2 Y472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:44555447 G>A maps to NM_013389.2 G1277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:44556433 G>A maps to NM_013389.2 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:44578909 C>T maps to NM_013389.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr7:44579404 G>A maps to NM_013389.2 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:44579281 C>T maps to NM_013389.2 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr7:44560391 C>A maps to NM_013389.2 V1036V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr7:44571798 G>A maps to NM_013389.2 V809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr14:74951162 G>A maps to ENST00000434013 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr9:139934262 C>T maps to ENST00000371600 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:57268860 C>T maps to NM_024663.3 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr20:57269533 C>T maps to NM_024663.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr17:45673779 C>T maps to NM_006310.3 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr10:72020481 G>A maps to ENST00000277942 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr10:72020460 G>A maps to ENST00000277942 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr4:73013162 C>G maps to NM_004885.2 Y401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr4:73012693 G>C did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr2:110917742 G>A maps to NM_000272.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:110927449 G>T maps to NM_000272.3 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:132408076 C>T maps to ENST00000393156 W908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr3:132423040 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr3:132437922 G>A maps to ENST00000393156 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:6007208 G>A maps to NM_015102.2 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:5993283 G>A maps to NM_015102.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr1:5923970 C>T maps to NM_015102.2 R1373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr1:5925254 G>A maps to NM_015102.2 V1241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr1:5950981 G>A maps to NM_015102.2 D750D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr1:5934608 G>T maps to NM_015102.2 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:5965749 G>A maps to NM_015102.2 Q569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:36341872 G>A maps to NM_004646.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:36335329 C>T maps to NM_004646.3 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr19:36342481 G>A maps to NM_004646.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:36338957 G>A maps to NM_004646.3 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr1:179544753 C>T maps to NM_014625.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr16:15045812 C>G maps to NM_006985.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr17:79589282 G>A maps to NM_017921.2 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr5:170819712 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:21891773 G>A maps to NM_182795.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:11907496 C>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:11918860 C>A maps to NM_002521.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:153661437 C>T maps to NM_000906.3 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:153660622 G>A maps to NM_000906.3 Q781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr5:32724822 C>T maps to ENST00000265074 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:32712158 C>T maps to ENST00000265074 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:32774848 C>T maps to ENST00000265074 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr16:169168 G>A maps to ENST00000399953 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:129347782 G>T maps to NM_001030013.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr7:34724267 C>T maps to NM_207172.1 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:34724285 G>A maps to NM_207172.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr7:34851446 C>T maps to NM_207172.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr15:73862515 C>T maps to NM_012428.3 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr15:73925475 G>C maps to NM_012428.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr17:78444753 C>T maps to NM_002522.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr7:98248962 C>G maps to NM_002523.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:98256640 C>A maps to NM_002523.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr7:98256571 C>T maps to NM_002523.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr22:39222540 C>T maps to NM_014293.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr7:25267993 G>C maps to NM_022150.3 S22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:24324888 C>T maps to NM_000905.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr7:24325047 G>A did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:164247553 G>T maps to NM_000909.4 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr4:164271638 C>T maps to NM_006174.2 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr4:164271505 C>T maps to NM_006174.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr4:164272648 C>T maps to NM_006174.2 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr16:69746948 G>A maps to NM_000903.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:30326411 G>T did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr23:30322941 T>A did not map to a codon.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr23:30326445 C>A did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr23:30326946 C>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:30326618 G>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:30327198 C>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:30326347 T>G did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr23:30327171 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:30327462 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:30326380 T>C did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:30327210 C>T did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr3:24018765 C>T maps to NM_005126.4 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:24003915 C>T maps to NM_005126.4 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr19:50881484 C>T maps to NM_007121.4 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:47283483 G>A maps to NM_005693.2 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr12:100955660 A>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:100955673 G>T maps to ENST00000392986 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr12:100904823 G>A maps to ENST00000392986 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:119528934 G>A maps to NM_022002.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr3:119534275 C>G maps to NM_022002.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:161199673 C>G maps to NM_001077482.1 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr12:95442957 G>A maps to NM_003297.2 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr6:108501524 A>G did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:92929547 G>C maps to NM_005654.4 *424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:92923836 G>C maps to NM_005654.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:92923998 C>T maps to NM_005654.4 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr5:92929487 C>T maps to NM_005654.4 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr15:96880845 C>T maps to NM_021005.3 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr15:96875681 C>A maps to NM_021005.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr15:96877671 G>T maps to NM_021005.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:149357709 T>C maps to ENST00000511528 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr4:149357541 C>T maps to ENST00000511528 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:149357049 C>A maps to ENST00000511528 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr4:149357811 T>C maps to ENST00000511528 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:52448879 G>C maps to ENST00000360284 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:52451147 C>A maps to ENST00000360284 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr12:52451242 C>G maps to ENST00000360284 S544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:157182273 C>T maps to NM_006186.3 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:127253384 G>C maps to NM_004959.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:127245258 G>A maps to NM_004959.4 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:200017864 G>T maps to NM_205860.1 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr1:200017504 A>G maps to NM_205860.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:200017720 G>T maps to NM_205860.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:127289142 G>A maps to NM_033334.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr10:115393948 G>A maps to ENST00000369358 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr10:115389478 G>A maps to ENST00000369358 N644N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:115365939 A>G maps to ENST00000369358 S1276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:115372034 C>T maps to ENST00000369358 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr2:27657997 A>T did not map to a codon.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr2:27662653 C>T maps to ENST00000379863 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr7:107875085 A>G maps to ENST00000379032 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr7:107823214 C>T maps to ENST00000379032 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr7:107880401 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr7:107800848 C>T maps to ENST00000379032 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr1:52281982 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:52305984 T>C maps to NM_002525.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr1:52260185 C>G maps to NM_002525.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr1:52305984 T>C maps to NM_002525.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:52280400 A>G maps to NM_002525.2 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr8:32620825 T>A maps to NM_001160004.1 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr8:32621346 G>A maps to NM_013956.3 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr10:83635833 C>A maps to ENST00000404547 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr10:83635735 G>T maps to ENST00000404547 G214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:84498356 C>A maps to ENST00000404547 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:84711270 C>T maps to ENST00000404547 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr10:84745219 C>T maps to ENST00000404547 Y674Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr10:83635272 G>C maps to ENST00000404547 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:76254224 A>G maps to NM_138573.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr21:16340480 C>T maps to NM_003489.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:16338608 T>C maps to NM_003489.3 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr21:16338837 G>C maps to NM_003489.3 S559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr11:9009123 G>A maps to NM_020645.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:9007291 G>A maps to NM_020645.2 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:105149321 C>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:105132385 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:105152867 C>A did not map to a codon.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr23:105153046 C>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:105179292 G>T did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr23:105178436 G>T did not map to a codon.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr23:105153549 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:105075065 C>G did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:105153230 G>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:105153084 G>T did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr23:105179221 T>C did not map to a codon.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr23:105183933 G>A did not map to a codon.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr23:105153469 G>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:105153193 C>T did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:105168849 G>T did not map to a codon.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr6:6002626 C>T maps to NM_016588.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr16:67919691 C>T maps to NM_198443.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:206659495 G>A maps to NM_201266.1 W837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:206562313 C>T maps to NM_201266.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr2:206608072 C>T maps to NM_201266.1 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr2:206590641 C>T maps to NM_201266.1 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr6:24145807 C>A maps to NM_080723.4 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr20:333906 C>T maps to NM_024958.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:5824274 C>T maps to NM_004558.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:51254949 G>A maps to ENST00000404971 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:50847322 T>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:50573943 C>A maps to NM_138735.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr2:50149207 G>A maps to ENST00000404971 D1506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr2:50723067 G>T maps to ENST00000404971 A1055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:50779851 C>T maps to ENST00000404971 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:50780106 T>A maps to ENST00000404971 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr2:50149200 G>A maps to ENST00000404971 R1509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:51255102 G>A maps to ENST00000404971 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:50847189 G>T maps to ENST00000404971 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:50765423 C>A maps to ENST00000404971 G744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:51255054 G>A maps to ENST00000404971 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:51254988 C>T maps to ENST00000404971 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr2:50280429 C>G maps to ENST00000404971 P1409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr2:51255024 G>A maps to ENST00000404971 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr2:51255255 G>A maps to ENST00000404971 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr2:50850744 C>A maps to ENST00000404971 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr2:50724789 C>A maps to ENST00000404971 E894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr2:51254856 A>T maps to ENST00000404971 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr2:51255183 G>T maps to ENST00000404971 C76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr11:64418040 G>C maps to NM_015080.3 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:64398030 C>T maps to NM_015080.3 V1200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr11:64418740 G>T maps to NM_015080.3 I968I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr14:80328222 C>T maps to NM_004796.4 N1034N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr14:80328090 C>T maps to NM_004796.4 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr14:79933657 C>T maps to NM_004796.4 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr14:79933567 C>T maps to NM_004796.4 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr14:80130177 G>T maps to NM_004796.4 E795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:79423681 C>T maps to NM_004796.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:79432617 G>A maps to NM_004796.4 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr14:80328175 C>T maps to NM_004796.4 Q1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr5:176637761 C>T maps to NM_022455.4 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:176637519 C>G maps to NM_022455.4 S707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr5:176678811 G>T maps to NM_022455.4 E1575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr5:176638613 C>T maps to NM_022455.4 R1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr5:176638367 G>T maps to NM_022455.4 E990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:176638274 G>T maps to NM_022455.4 G959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:176707724 G>T maps to NM_022455.4 G1928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:176666860 A>T maps to NM_022455.4 K1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:176637630 C>G maps to NM_022455.4 S744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr5:176665486 G>T maps to NM_022455.4 E1391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr5:176710872 G>A maps to NM_022455.4 W2032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr5:176719159 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr5:176675184 G>T maps to NM_022455.4 E1501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr5:176638878 G>A maps to NM_022455.4 W1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr5:176638399 C>T maps to NM_022455.4 S1000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr5:176637434 C>T maps to NM_022455.4 Q679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:176709507 G>T maps to NM_022455.4 E1979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr5:176687120 C>T maps to NM_022455.4 R1700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:176709537 C>T maps to NM_022455.4 Q1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr5:176673716 C>T maps to NM_022455.4 R1473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:176709522 C>T maps to NM_022455.4 R1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:176675283 G>T maps to NM_022455.4 E1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:176665391 C>A maps to NM_022455.4 S1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr5:176638856 C>T maps to NM_022455.4 Q1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:176637775 C>A maps to NM_022455.4 C792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:176721511 C>A maps to NM_022455.4 P2381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:176637200 A>T maps to NM_022455.4 K601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:176665273 C>T maps to NM_022455.4 R1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr5:176675229 G>T maps to NM_022455.4 E1516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr5:176700719 G>T maps to NM_022455.4 E1853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:152036164 G>A did not map to a codon.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr23:152037562 G>C did not map to a codon.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr23:152018843 C>T did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr17:44770321 C>T maps to NM_006178.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:1424428 G>A maps to ENST00000476071 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr20:1424537 G>A maps to ENST00000476071 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:59522252 T>C maps to NM_001144772.1 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr8:59512351 T>C maps to NM_001144772.1 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr16:27237110 G>A maps to NM_145080.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:123730453 T>A maps to NM_017615.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr10:123722761 G>A maps to NM_017615.2 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr5:6625744 G>T maps to NM_017755.5 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:6609986 T>A maps to NM_017755.5 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr5:6620226 G>T maps to NM_017755.5 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:93781973 C>T maps to NM_022072.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:72717962 T>A maps to NM_148956.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:72718296 C>A maps to NM_148956.2 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:72717905 G>A maps to NM_148956.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr10:18905211 T>A maps to NM_182543.2 K108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr10:18903501 A>T maps to NM_182543.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr4:40778127 C>G maps to NM_024677.4 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:73127367 C>T maps to NM_014595.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:40129050 G>C maps to NM_032526.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:18767630 C>T maps to ENST00000455492 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:18765359 G>A maps to ENST00000455492 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr2:18765458 G>A maps to ENST00000455492 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr2:18766139 C>T maps to ENST00000455492 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:104860860 T>C did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:33066515 G>A maps to NM_001002010.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:39991345 G>A maps to NM_052935.4 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr17:39983814 C>A maps to NM_052935.4 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr6:116565107 C>G maps to NM_152729.2 S430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:52562240 G>A maps to NM_001134231.1 H243H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:104186973 A>G maps to NM_001031701.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr6:86197161 C>T maps to NM_002526.2 C353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:86176944 A>G maps to NM_002526.2 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr6:86197161 C>T maps to NM_002526.2 C353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:17248202 C>T maps to ENST00000379552 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:15141944 T>C maps to NM_173474.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:5603697 G>A maps to NM_001102654.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:49564711 G>A maps to NM_006179.4 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr16:2089925 C>T maps to NM_002528.5 *313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr11:132081942 C>G maps to NM_001144058.1 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:132180114 G>A maps to NM_001144058.1 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr11:132016252 G>A maps to NM_001144058.1 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:132016340 C>T maps to NM_001144058.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr17:8926248 C>A maps to NM_004822.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr16:2522265 C>T maps to NM_006181.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr16:2522373 C>G maps to NM_006181.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:2522334 C>G maps to NM_006181.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr1:107691214 G>A did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:107691397 G>A maps to NM_001113226.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr9:135073846 G>A maps to NM_032536.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr9:135073813 C>T maps to NM_032536.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:156845367 T>C maps to NM_002529.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:156849867 C>T maps to NM_002529.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:87482317 C>T maps to NM_006180.3 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:87325653 G>A maps to NM_006180.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr9:87636300 C>G maps to NM_006180.3 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr15:88472442 G>C maps to NM_001012338.1 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr15:88483889 G>T maps to NM_001012338.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr15:88799154 G>C maps to NM_001012338.1 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:88669547 G>A maps to NM_001012338.1 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:88420303 G>A maps to NM_001012338.1 V794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:11802336 G>A maps to NM_012344.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:106461452 G>T maps to NM_014840.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:106464624 G>A maps to NM_014840.2 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:106466567 C>G maps to NM_014840.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr12:106461044 C>T maps to NM_014840.2 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:205272901 G>A maps to ENST00000441520 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:10851748 C>T maps to NM_002484.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr16:1838663 C>A maps to NM_012225.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr16:1837973 G>A maps to NM_012225.2 L174L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CQ-7071-01A-12D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr1:205687511 C>A maps to NM_022731.4 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:27272171 G>A maps to NM_006600.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr8:110255386 C>A maps to NM_032869.3 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:110305699 T>C maps to NM_032869.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr7:44524877 G>A maps to NM_015332.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:51075948 C>G did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:51239211 G>T did not map to a codon.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr23:51238819 C>T did not map to a codon.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr5:102895787 T>G maps to NM_031438.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr3:131100764 C>T maps to NM_152395.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:21965719 A>T maps to NM_024815.3 C100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr8:21965083 G>A maps to NM_024815.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr8:21965791 C>T maps to NM_024815.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:33183420 C>G maps to NM_001105570.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:33183198 G>A maps to NM_001105570.1 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr9:34343281 G>A maps to NM_147173.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr11:63996765 C>T maps to NM_032344.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr12:93789269 A>G maps to NM_199040.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr4:123814216 G>A maps to NM_007083.3 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:123814171 C>A maps to NM_007083.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr4:88370347 T>C maps to NM_024047.3 H195H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr1:163295849 T>A maps to NM_145697.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:163317626 C>T maps to NM_145697.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr13:45563304 C>T maps to NM_012345.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr11:71725760 G>A maps to ENST00000393695 Q936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr11:71717270 C>T maps to ENST00000393695 S1840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr11:71725191 G>A maps to ENST00000393695 G1125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:71716365 C>A maps to ENST00000393695 L1920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:71724873 G>A maps to ENST00000393695 S1231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:71723444 A>G did not map to a codon.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr11:71721848 G>A maps to ENST00000393695 Q1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr11:71732292 G>A maps to ENST00000393695 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr14:73743878 G>A maps to NM_001005743.1 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr14:73745998 G>A maps to NM_001005743.1 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:41188692 G>A maps to NM_004756.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr12:69083343 T>C maps to NM_020401.2 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr12:69115631 C>T maps to NM_020401.2 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr6:17669741 G>C maps to ENST00000430136 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:17629210 T>C maps to ENST00000430136 E1104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr6:17626392 G>A maps to ENST00000430136 Q1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr6:17688741 G>A maps to ENST00000430136 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr5:37363994 C>T maps to NM_153485.1 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:37302929 G>C maps to NM_153485.1 S1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:37331894 C>G maps to NM_153485.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr5:37303482 G>A maps to NM_153485.1 R1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr5:37327822 A>C maps to NM_153485.1 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr5:37348605 C>G did not map to a codon.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr5:37301541 A>G maps to NM_153485.1 T1186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr11:47833635 A>G maps to NM_015231.1 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr11:47814400 G>T maps to NM_015231.1 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr9:131768857 G>A maps to NM_015354.1 S1717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr9:131735479 C>G maps to NM_015354.1 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:135289086 G>C did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr7:135272677 C>T maps to NM_015135.2 Q471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr7:135292095 C>T maps to NM_015135.2 Q1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr3:13370374 C>T maps to NM_024923.2 V1394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:13407499 G>A maps to NM_024923.2 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:153973461 G>A maps to NM_207308.2 Y1752Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr1:154029335 C>T maps to NM_207308.2 K1065K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:153982538 G>T maps to NM_207308.2 L1613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr1:154031151 A>T maps to NM_207308.2 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:154072542 T>C maps to NM_207308.2 T632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr9:134016057 C>T maps to ENST00000451030 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr9:134073596 G>T maps to ENST00000451030 T1573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:102492897 G>A maps to NM_024057.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr12:102471260 A>G maps to NM_024057.2 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr22:45574200 C>T maps to NM_007172.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr22:45571833 A>G maps to NM_007172.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:45574764 C>T maps to NM_007172.3 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr22:45574293 G>A maps to NM_007172.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:77039259 G>A maps to ENST00000458189 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:77057368 G>A maps to ENST00000458189 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr4:77057544 G>A maps to ENST00000458189 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:77053824 G>C maps to ENST00000458189 S254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr19:50412641 C>T maps to NM_012346.4 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:50412134 C>A maps to NM_012346.4 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:50412008 G>A maps to NM_012346.4 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr23:106391015 C>T did not map to a codon.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:73227441 C>T maps to NM_024844.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:73230730 G>A did not map to a codon.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr17:73230759 C>T maps to NM_024844.3 Y548Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr17:73221839 G>A maps to NM_024844.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr17:5312066 G>A maps to NM_002532.3 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:5290431 T>C did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr16:56878442 C>G maps to NM_014669.3 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr16:56875618 C>A maps to NM_014669.3 I741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr16:56875738 C>T maps to NM_014669.3 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr16:56865769 G>T maps to NM_014669.3 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:56839413 A>T did not map to a codon.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr16:56878496 G>A maps to NM_014669.3 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr16:56875705 G>A maps to NM_014669.3 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr16:56868677 C>T maps to NM_014669.3 D590D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:3784170 G>C maps to NM_016320.4 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:3716750 C>T maps to NM_016320.4 W1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr11:3697544 A>G maps to NM_016320.4 D1749D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr11:3727720 G>C maps to NM_016320.4 S960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr13:25881994 A>C maps to NM_014089.3 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr13:25914136 C>T maps to NM_014089.3 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr13:25875964 C>T maps to NM_014089.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr7:23240135 G>C maps to ENST00000413919 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr6:118015290 G>A maps to NM_138459.3 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr15:41641366 G>A maps to NM_016359.3 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr19:16860196 C>T maps to ENST00000438489 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:16875992 C>A maps to ENST00000438489 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:16861003 G>A maps to ENST00000438489 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:16860799 G>C maps to ENST00000438489 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr11:62567850 G>A maps to NM_006362.4 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr11:62561860 C>T maps to NM_006362.4 E543E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:101581423 C>T did not map to a codon.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr23:101623789 T>C did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:102332650 A>T did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:102332614 C>T did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:102337968 C>T did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr23:102337276 C>T did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr23:102337235 A>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:102339349 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr23:102337233 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:102332635 G>A did not map to a codon.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr23:101092615 C>T did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr23:101092465 C>G did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:101095786 G>C did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr23:101092762 T>A did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:101096679 A>G did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr7:8791052 C>A maps to NM_152745.2 S157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr7:8790657 G>A maps to NM_152745.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:8790657 G>A maps to NM_152745.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr2:139429082 G>A maps to NM_007226.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr17:47656377 C>T maps to ENST00000513748 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:57619421 C>A maps to NM_007224.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr12:57619052 C>T maps to NM_007224.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr14:24878575 C>T maps to NM_025081.2 Q526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:24886198 C>T maps to NM_025081.2 F1748F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:24884815 C>G maps to NM_025081.2 P1287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:24884422 C>T maps to NM_025081.2 S1156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:24884779 C>T maps to NM_025081.2 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr11:120082136 G>A maps to NM_178507.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr12:113445709 C>T maps to NM_016817.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr12:113442854 C>A maps to NM_016817.2 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr12:113444281 A>G maps to NM_016817.2 K511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:113384760 T>C maps to NM_006187.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr10:126100542 T>C maps to NM_000274.3 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr19:2271953 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr15:64982655 G>A maps to ENST00000403937 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56622939 C>T maps to NM_024068.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr1:228480266 C>T maps to NM_001098623.1 A3549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:228566494 G>A maps to NM_001098623.1 *7969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr1:228433260 C>G maps to NM_001098623.1 S1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr1:228437859 C>T maps to NM_001098623.1 Q1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr1:228468012 C>T maps to NM_001098623.1 N2599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:228476581 C>T maps to NM_001098623.1 T3444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:228432255 C>T maps to NM_001098623.1 F1155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:228521392 C>T maps to NM_001098623.1 S5322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:228556502 A>G maps to NM_001098623.1 P6616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:228468381 C>T maps to NM_001098623.1 F2694F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:228548416 C>T maps to NM_052843.2 I6608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:228553778 C>T maps to NM_001098623.1 P6356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:228559547 C>T maps to NM_001098623.1 S7023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:228565247 C>T maps to NM_001098623.1 Q7780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:228495221 C>G maps to NM_001098623.1 L4152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:228563712 C>A maps to NM_001098623.1 G7597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr1:228433258 C>T maps to NM_001098623.1 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr1:228505638 C>T maps to NM_001098623.1 S4632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:228462510 C>T maps to NM_001098623.1 G1974G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:228464949 G>A maps to NM_001098623.1 A2230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:228475446 T>C maps to NM_001098623.1 G3199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:228494169 A>T maps to NM_001098623.1 T3919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr1:228402695 C>T maps to NM_001098623.1 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr2:220422716 C>T maps to NM_015311.2 W1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr2:220435108 C>T maps to NM_015311.2 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:220422981 G>A maps to NM_015311.2 H1142H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr2:220419304 C>T maps to NM_015311.2 S1589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:220424010 C>T maps to NM_015311.2 E1054E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:220422770 C>T maps to NM_015311.2 G1188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:133041344 C>A maps to ENST00000262283 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr15:28326954 C>T maps to NM_000275.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr15:28235775 C>A maps to NM_000275.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:28116343 G>A maps to NM_000275.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:28090151 C>G maps to NM_000275.2 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr15:28234813 T>A did not map to a codon.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr15:28326984 G>A maps to NM_000275.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr19:17339664 G>A maps to NM_024578.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr4:48894853 G>A maps to NM_001014446.1 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:186370310 G>C maps to NM_022375.3 *45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:97617810 G>A maps to NM_006188.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr23:128692623 G>C did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr23:128710496 C>T did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:128696644 C>G did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:128724192 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr23:128709135 G>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr4:71068635 T>C did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:71068543 C>T maps to NM_017855.3 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:103564143 C>G maps to NM_024410.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr8:103564041 C>T maps to NM_024410.3 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr9:131260796 G>A maps to NM_153435.1 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:131233666 C>T maps to NM_153435.1 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr9:131221863 G>A maps to NM_153435.1 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr9:131221881 C>T maps to NM_153435.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr9:131254733 C>G maps to NM_153435.1 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr11:198283 A>G maps to NM_053280.3 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr23:123699279 G>T did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:123514645 C>G did not map to a codon.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr23:123517883 T>C did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:123554209 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:123839066 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:123839067 A>G did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:124097569 A>T did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr23:123518697 A>T did not map to a codon.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr23:123519781 G>A did not map to a codon.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr23:123587206 A>G did not map to a codon.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr23:123517612 C>T did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr23:123775673 C>T did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr23:123775762 C>A did not map to a codon.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr23:124097536 A>T did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr23:123615798 G>T did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:123779051 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr23:123554625 G>C did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:123657441 G>C did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:123518064 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:123805603 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:123805536 T>A did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr23:123870837 C>G did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr23:123515058 T>C did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:123615698 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:123805603 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:123517858 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:123518365 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:123630899 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr23:123657345 C>G did not map to a codon.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr23:123554572 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:123554340 C>T did not map to a codon.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr23:123780596 T>G did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:123630880 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:124029908 A>G did not map to a codon.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr23:123657465 G>A did not map to a codon.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr23:123538974 G>A did not map to a codon.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr23:123556318 T>A did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:124029891 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:123779069 G>A did not map to a codon.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr23:123514614 G>A did not map to a codon.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr23:123654609 G>A did not map to a codon.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr23:123515049 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr23:123514959 A>G did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:123516635 C>G did not map to a codon.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr23:123514621 C>A did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr5:167674087 C>T maps to NM_001122679.1 V2039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr5:167689097 C>G maps to NM_001122679.1 A2527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:167419990 C>T maps to NM_001122679.1 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:167645221 G>A maps to NM_001122679.1 E1433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:167674246 A>G maps to NM_001122679.1 A2092A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr5:167642272 G>A maps to NM_001122679.1 P1349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr5:167689328 C>T maps to NM_001122679.1 I2604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr4:183601502 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:183659599 G>A maps to NM_001080477.1 W1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr11:78369840 A>G maps to NM_001098816.2 C2524C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr11:78413295 G>A maps to NM_001098816.2 D1454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:78413271 G>T maps to NM_001098816.2 A1462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr23:13778323 A>T did not map to a codon.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr23:13762638 G>T did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:13769429 A>G did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:13757118 A>T did not map to a codon.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr23:13767611 A>T did not map to a codon.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr23:13776516 T>C did not map to a codon.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr7:44715627 C>A maps to ENST00000444676 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr7:44737218 C>T maps to ENST00000444676 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr7:44739835 C>A maps to ENST00000444676 R858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr7:44747332 C>G maps to ENST00000444676 V998V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr7:44721371 G>A maps to ENST00000444676 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr10:50946287 C>T maps to NM_018245.2 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr10:50954858 G>A maps to NM_018245.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr10:50960021 G>T maps to NM_018245.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:56503928 G>A maps to NM_018233.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr6:72006454 G>A maps to NM_024576.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr3:9798303 G>A maps to NM_016821.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr3:9792850 C>T maps to NM_016821.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:70776820 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:70787354 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr23:70776890 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:70776892 C>G did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:70787879 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:70787525 G>A did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:70775081 T>G did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:41624609 G>C maps to NM_007280.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:41602044 C>G maps to NM_007280.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr10:74673201 C>G maps to NM_152635.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:175006585 C>G maps to ENST00000409546 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr10:15106497 A>T maps to NM_018324.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:15115167 G>A maps to NM_018324.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr9:137998598 C>T maps to NM_014279.4 C209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr9:138011606 C>T maps to NM_014279.4 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:9967506 C>T maps to NM_058164.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:102270396 C>A maps to ENST00000338858 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr1:102290780 G>A maps to ENST00000338858 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:102270140 G>A maps to ENST00000338858 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr1:102296365 C>T maps to ENST00000338858 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:102290582 T>A maps to ENST00000338858 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr13:53624257 A>T maps to NM_006418.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr13:53624562 C>G maps to NM_006418.3 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:53603066 C>G maps to NM_006418.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr13:53616046 G>A maps to NM_006418.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:127572375 C>T maps to NM_182487.2 I548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr9:127549501 G>A maps to NM_182487.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr9:127563739 G>T maps to NM_182487.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr9:127549483 G>A maps to NM_182487.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr1:161993073 C>T maps to ENST00000451379 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:161953755 C>T maps to ENST00000451379 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:161953787 C>A maps to ENST00000451379 E645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr1:161954031 G>A maps to ENST00000451379 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr21:34442896 G>A maps to NM_138983.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:137814641 C>T maps to NM_175747.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:137814986 G>A maps to NM_175747.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:137815022 C>T maps to NM_175747.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr6:137814788 G>A maps to NM_175747.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:10319425 C>T maps to NM_002543.3 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr12:10319440 T>A maps to NM_002543.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:59002203 G>T maps to NM_145243.3 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr9:95179153 A>G maps to NM_005014.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr11:76814247 C>T maps to NM_006189.1 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr11:76813989 C>T maps to NM_006189.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr15:53050033 C>T maps to NM_004498.1 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr15:53081730 T>G maps to NM_004498.1 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr18:55103823 G>C maps to NM_004852.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr18:55143900 C>T maps to NM_004852.2 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr6:74079425 C>T maps to NM_001080507.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr3:193332568 A>T maps to NM_130837.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:193366586 G>T maps to NM_130837.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr3:193382667 G>A did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:46032621 G>A maps to NM_001017989.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr10:98105698 C>T maps to NM_033207.3 *142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:132306620 C>T maps to NM_002545.3 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr11:132527153 G>A maps to NM_002545.3 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:132306094 G>A maps to NM_002545.3 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:132307218 C>T maps to NM_002545.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:132527054 G>A maps to NM_002545.3 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr23:67430101 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:67283998 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:67316709 A>G did not map to a codon.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr23:67421523 C>A did not map to a codon.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr8:145107417 G>A maps to ENST00000360660 N1079N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr8:145112801 G>A maps to ENST00000360660 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr8:145111063 G>A maps to ENST00000360660 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr23:153421949 A>T did not map to a codon.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr23:153420102 C>A did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr23:153416181 C>A did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:153496184 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:241761197 C>T maps to NM_014322.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:241767852 C>A maps to NM_014322.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:88418244 C>T maps to NM_001030015.2 C154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr6:47762986 C>T maps to ENST00000489301 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:47775956 C>A maps to ENST00000489301 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:29189479 C>T maps to NM_000911.3 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr8:54163408 C>G maps to NM_000912.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:54142036 G>T maps to NM_000912.3 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:54147343 G>A maps to NM_000912.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:54147355 G>T maps to NM_000912.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:54147380 C>T maps to NM_000912.3 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr8:54142364 A>T maps to NM_000912.3 L212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr20:62729633 G>T maps to NM_000913.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:203472811 C>T maps to NM_014359.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:6891365 T>A maps to NM_001004460.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:6891449 C>T maps to NM_001004460.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:7960500 A>G maps to NM_001003745.1 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:7960206 C>T maps to NM_001003745.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:6898645 C>A maps to NM_207186.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:6898759 G>A maps to NM_207186.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:6898651 C>T maps to NM_207186.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:6898069 C>T maps to NM_207186.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:6866954 C>T maps to ENST00000379831 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:6867338 G>T maps to ENST00000379831 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr11:6867254 C>T maps to ENST00000379831 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr12:55615023 T>C maps to NM_001005280.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr12:48596946 G>T maps to NM_001004134.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:48596793 G>A maps to NM_001004134.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:55735897 G>A maps to NM_001005491.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr11:55735540 A>G maps to NM_001005491.1 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:29407902 C>G maps to NM_013941.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:29408400 C>A maps to NM_013941.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr6:29407953 C>A maps to NM_013941.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:29408337 T>A maps to NM_013941.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:29407890 C>T maps to NM_013941.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:29408427 C>T maps to NM_013941.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr14:22102497 C>T maps to NM_001005466.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr14:22102113 C>T maps to NM_001005466.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr14:22038629 G>A maps to NM_001005465.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr11:123886379 C>T maps to ENST00000375021 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr11:123886727 C>A maps to NM_001004462.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:123886937 C>A maps to NM_001004462.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:123887147 G>A maps to NM_001004462.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr11:123886370 G>T maps to ENST00000375021 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:123908970 C>A maps to NM_001004463.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr11:123909618 C>A maps to NM_001004463.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr11:123908940 G>A maps to NM_001004463.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:123900616 C>T maps to NM_001004464.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:123900445 G>A maps to NM_001004464.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:123901243 A>T maps to ENST00000375021 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:123900457 C>T maps to NM_001004464.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr11:123901132 T>C maps to ENST00000375021 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr11:123894150 C>T maps to NM_001001953.1 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:123894351 C>T maps to NM_001001953.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:123894261 G>A maps to NM_001001953.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:123894354 G>A maps to NM_001001953.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr11:123893847 C>T maps to NM_001001953.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr11:123893808 G>T maps to NM_001001953.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:15918352 G>A maps to NM_013940.2 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:15918181 G>A maps to NM_013940.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:15918703 G>A maps to NM_013940.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr19:15839710 C>G maps to NM_013939.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr19:15839059 C>T maps to NM_013939.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr19:15852273 C>G maps to NM_013938.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr19:15905406 T>C maps to NM_001004466.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:15905709 C>A maps to NM_001004466.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr1:159410357 C>G maps to NM_012351.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:159410396 G>C maps to NM_012351.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:159410090 T>C maps to NM_012351.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:159409808 C>T maps to NM_012351.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:159410405 G>A maps to NM_012351.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr1:159410018 G>T maps to NM_012351.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:159284020 G>A maps to NM_001004467.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr1:159505569 G>C maps to NM_001004469.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:158435518 T>C maps to NM_001004473.1 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:158435443 C>T maps to NM_001004473.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:158389858 G>A maps to NM_001004476.1 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:158390344 G>A maps to NM_001004476.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:158390341 G>T maps to NM_001004476.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:158390305 G>A maps to NM_001004476.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:56031283 C>A maps to NM_206899.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56031406 C>T maps to NM_206899.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:57996164 G>C maps to NM_001004471.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr11:57995516 G>A maps to NM_001004471.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr11:57995837 C>A maps to NM_001004471.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr11:57995714 C>A maps to NM_001004471.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr1:158450101 C>T maps to NM_001004472.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:123847810 G>T maps to NM_001004474.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr11:123847522 G>T maps to NM_001004474.1 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr11:123847714 G>A maps to NM_001004474.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr11:123848323 G>A maps to NM_001004474.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:158368956 G>A maps to NM_001004475.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:59480700 G>A maps to NM_001005324.1 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr11:59480655 G>A maps to NM_001005324.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr11:58034970 C>T maps to NM_207374.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr1:158549569 C>T maps to NM_001004477.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr1:158549197 A>C maps to NM_001004477.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr1:158576473 C>T maps to NM_001004478.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:29394965 G>C maps to NM_013937.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr6:29394620 G>T maps to NM_013937.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr6:29394829 G>A maps to NM_013937.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr14:20666108 C>A maps to NM_001005503.1 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:20666321 C>T maps to NM_001005503.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:20665862 C>T maps to NM_001005503.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr22:16449113 C>A maps to NM_001005239.1 G231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr14:19378015 C>A maps to NM_001013354.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr14:19378042 C>T maps to NM_001013354.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:20711093 C>T maps to NM_001004479.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr14:20692281 T>A maps to NM_001004480.1 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr14:20692713 A>T maps to NM_001004480.1 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr14:20692041 A>G maps to NM_001004480.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr1:248004730 G>A maps to NM_001001959.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:248004601 G>A maps to NM_001001959.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:248004559 C>A maps to NM_001001959.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr1:248004706 G>A maps to NM_001001959.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6017-01A-11D-1683-08 chr6:29365003 C>G maps to NM_013936.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr6:29364550 C>T maps to NM_013936.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:29364490 C>G maps to NM_013936.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr10:45799189 C>T maps to NM_001004297.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr10:45799762 C>T maps to NM_001004297.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr10:45799804 A>G maps to NM_001004297.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:107298344 G>A maps to NM_001001961.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr9:107298662 A>G maps to NM_001001961.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr9:107298665 C>G maps to NM_001001961.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr9:107289109 A>G maps to NM_001001919.1 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr9:107331474 G>C maps to NM_001004483.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr9:107379600 G>A maps to NM_001001956.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:107379789 C>T maps to NM_001001956.1 E232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:107379975 C>T maps to NM_001001956.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr9:107457532 G>C maps to NM_001004484.1 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:107457095 C>T maps to NM_001004484.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:107267226 C>A maps to NM_001004485.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr9:107267256 T>C maps to NM_001004485.1 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr9:107267403 T>C maps to NM_001004485.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:107266938 C>T maps to NM_001004485.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr23:130678200 G>A did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:130678613 T>G did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr9:35869555 G>T maps to NM_001004487.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr9:35869981 C>G maps to NM_001004487.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:35870044 C>A maps to NM_001004487.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr9:35870143 G>A maps to NM_001004487.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:247978845 C>T maps to NM_001001966.1 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:247978413 G>A maps to NM_001001966.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr1:247978593 A>T maps to NM_001001966.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:248512789 C>G maps to NM_001001918.1 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr1:248513011 G>A maps to NM_001001918.1 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7391-01A-11D-2012-08 chr1:248844911 G>A maps to NM_001004734.1 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:29274873 C>G maps to NM_030946.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:29274828 C>T maps to NM_030946.1 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:3119609 C>T maps to NM_014565.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:3118955 C>T maps to NM_014565.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:3119394 C>T maps to NM_014565.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:3101342 C>T maps to NM_012352.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr17:3101366 G>C maps to NM_012352.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr9:125391589 T>G maps to NM_001004450.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:125391640 G>A maps to NM_001004450.1 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:247921357 C>A maps to NM_012353.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:247921165 G>A maps to NM_012353.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:3301356 C>T maps to NM_003553.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr17:3030083 A>T maps to ENST00000381953 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr9:125273991 C>A maps to NM_054107.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr9:125281469 C>T maps to ENST00000444856 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr9:125282153 C>T maps to NM_001004452.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:125281823 C>T maps to ENST00000444856 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr9:125563198 A>T maps to NM_080859.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:125438028 G>A maps to NM_001005234.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr9:125438163 T>A maps to NM_001005234.1 Y252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr9:125486387 G>A maps to NM_001005235.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr9:125487199 C>G maps to NM_001005235.1 S311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr9:125486858 G>A maps to NM_001005235.1 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr9:125512512 C>T maps to ENST00000373684 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr9:125330735 G>T maps to NM_001004454.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr19:9204510 C>T maps to ENST00000305465 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:9204175 C>T maps to ENST00000305465 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr19:9203972 C>G maps to ENST00000305465 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr9:125289434 G>A maps to ENST00000359439 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr9:125288893 G>A maps to ENST00000359439 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr9:125315717 C>T maps to NM_001004457.1 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr9:125316289 C>G maps to NM_001004457.1 S281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr9:125315510 G>C maps to NM_001004457.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:125315732 C>T maps to NM_001004457.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr11:57982335 C>G maps to NM_001004458.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:57982932 G>A maps to NM_001004458.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr11:57983028 G>T maps to NM_001004458.1 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr11:57982299 G>T maps to NM_001004458.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:57971377 G>A maps to NM_001004459.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:143793099 A>G maps to NM_001004135.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr7:143826963 C>T maps to NM_001001659.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr7:143806860 C>T maps to NM_001005480.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:143807022 G>A maps to NM_001005480.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:143806845 C>A maps to NM_001005480.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr7:143806749 C>G maps to NM_001005480.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:143747688 G>T maps to NM_012365.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr7:143955989 G>A maps to NM_001005328.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr7:143956022 C>T maps to NM_001005328.1 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:143955983 C>A maps to NM_001005328.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr7:99474425 G>A maps to NM_001005276.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr7:99474187 G>A maps to NM_001005276.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:6806471 C>A maps to NM_001004489.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr11:6806381 C>A maps to NM_001004489.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr11:6806399 A>G maps to NM_001004489.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr11:6790059 A>G maps to NM_001004490.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr11:6789726 C>T maps to NM_001004490.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr11:6789861 G>A maps to NM_001004490.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr1:248128890 C>T maps to NM_001004491.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:74799888 G>C maps to NM_001005285.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:247614633 G>A maps to NM_001004492.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:247614690 C>T maps to NM_001004492.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:27879440 A>G maps to NM_033057.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr6:29054605 G>A maps to NM_001005226.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr6:29054371 A>G maps to NM_001005226.2 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:27925494 G>A maps to NM_012367.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr6:27925695 G>A maps to NM_012367.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:27925413 C>A maps to NM_012367.1 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:27925795 C>T maps to NM_012367.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:27925717 C>T maps to NM_012367.1 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr16:3406176 C>G maps to NM_012368.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr1:247695696 C>G maps to NM_198074.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:247695519 A>T maps to NM_198074.4 C98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:247694955 C>G maps to NM_198074.4 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr1:247695054 G>A maps to NM_198074.4 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:6913476 C>A maps to NM_003700.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr11:6913227 G>A maps to NM_003700.1 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:143657596 C>T maps to NM_012369.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr7:143633044 G>T maps to NM_001004685.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr7:143632930 T>G maps to NM_001004685.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:247751828 C>A maps to NM_001001915.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:247752566 G>C maps to NM_001001915.1 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:247752500 C>T maps to NM_001001915.1 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:247752020 G>A maps to NM_001001915.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:247752272 G>A maps to NM_001001915.1 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:247752083 C>T maps to NM_001001915.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:247769129 C>G maps to NM_001001914.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:247769111 T>C maps to NM_001001914.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr1:247769354 C>T maps to NM_001001914.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:247769225 C>T maps to NM_001001914.1 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr1:247769657 C>T maps to NM_001001914.1 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:248685813 C>A maps to NM_001013355.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr1:248685627 G>A maps to NM_001013355.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr1:248685294 C>T maps to NM_001013355.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:248685672 G>A maps to NM_001013355.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr6:29429638 T>A maps to NM_030883.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr6:29430085 A>G maps to NM_030883.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr6:29429614 G>A maps to NM_030883.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr6:29556071 T>C maps to NM_007160.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:29556101 C>T maps to NM_007160.3 P127P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-F7-A61V-01A-11D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr6:29141561 A>T maps to NM_030905.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr6:29141531 G>A maps to NM_030905.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr6:29141421 A>T maps to NM_030905.2 K4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr6:29080239 G>A maps to NM_001005216.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:29080329 T>A maps to NM_001005216.2 Y221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:114090188 G>A maps to ENST00000374428 H204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:114090370 G>A maps to ENST00000374428 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr1:248263540 C>A maps to NM_175911.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:248201601 C>T maps to NM_001004686.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:248223986 G>T maps to NM_001004687.1 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:248224180 C>G maps to NM_001004687.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:248224348 C>T maps to NM_001004687.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:248224879 C>A maps to NM_001004687.1 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:248224261 C>T maps to NM_001004687.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:248224681 G>A maps to NM_001004687.1 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr1:248343475 C>T maps to NM_001004688.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:248366389 C>T maps to NM_001004689.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:248366773 C>G maps to NM_001004689.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr1:248367253 G>A maps to NM_001004689.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:248402848 C>T maps to NM_017504.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr1:248402919 T>C maps to NM_017504.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:248402521 G>T maps to NM_017504.1 G98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr1:248402322 C>T maps to NM_017504.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:248309364 G>T maps to NM_001004690.1 G306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:248308464 C>T maps to NM_001004690.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:248487681 G>A maps to NM_001004691.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr1:248487597 G>T maps to NM_001004691.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr1:248487819 G>T maps to NM_001004691.1 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:248570266 C>T maps to NM_030904.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr1:248570302 C>T maps to NM_030904.1 N336N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:248569513 C>A maps to NM_030904.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:248569507 G>A maps to NM_030904.1 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:248569861 G>T maps to NM_030904.1 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:248570263 C>T maps to NM_030904.1 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:248756313 A>G maps to NM_001004693.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:248756556 G>A maps to NM_001004693.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:248790415 G>C maps to NM_001001964.1 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:248790264 G>A maps to NM_001001964.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:248790381 C>T maps to NM_001001964.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr1:248790243 C>T maps to NM_001001964.1 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr1:248789964 C>T maps to NM_001001964.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:248458697 C>T maps to NM_001004692.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr1:248458472 C>T maps to NM_001004692.1 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:248458274 C>T maps to NM_001004692.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:248616313 C>A maps to NM_001004136.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:248616451 C>T maps to NM_001004136.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr1:248616202 C>A maps to NM_001004136.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr1:248813330 G>C maps to NM_001001824.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:248636986 G>T maps to NM_001005495.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr1:248636947 G>T maps to NM_001005495.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:248637568 G>A maps to NM_001005495.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr1:248436657 G>A maps to NM_001004695.1 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:248436630 C>A maps to NM_001004695.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:248437008 G>T maps to NM_001004695.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr1:248436657 G>A maps to NM_001004695.1 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr1:248436935 G>A maps to NM_001004695.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:248737449 G>T maps to NM_001001821.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:248737332 G>A maps to NM_001001821.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:248525532 G>A maps to NM_001004696.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:248525118 T>C maps to NM_001004696.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:248525601 C>A maps to NM_001004696.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr1:248525490 C>T maps to NM_001004696.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:248551580 A>T maps to NM_001005471.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:248551736 C>A maps to NM_001005471.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr1:248551196 C>A maps to NM_001005471.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:248551745 C>T maps to NM_001005471.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr1:248550956 G>A maps to NM_001005471.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:248084354 C>T maps to NM_001005522.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:248084546 G>T maps to NM_001005522.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr6:29012394 C>T maps to NM_030903.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr6:29012232 G>C maps to NM_030903.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:248059076 C>T maps to NM_001001957.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr1:248059226 G>T maps to NM_001001957.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:248059404 G>T maps to NM_001001957.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr1:248059007 A>C maps to NM_001001957.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:247655014 G>T maps to NM_001004698.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:247655079 C>T maps to NM_001004698.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr1:247654617 T>G maps to NM_001004698.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:180166536 A>G maps to NM_001001657.1 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr19:8841623 C>T maps to NM_001004699.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr17:3195525 C>T maps to ENST00000397187 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr17:3182211 G>A maps to NM_002551.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:55135909 C>A maps to NM_001005275.1 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:55135370 G>A maps to NM_001005275.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:55135811 C>A maps to NM_001005275.1 Y151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:55135799 C>T maps to NM_001005275.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:55110930 T>A maps to NM_001005274.1 C85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr11:55110790 G>T maps to NM_001005274.1 G39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:55110909 A>G maps to NM_001005274.1 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:55111113 C>A maps to NM_001005274.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:51411716 G>A maps to NM_001005272.3 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:51411501 G>C maps to NM_001005272.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:51411543 A>G maps to NM_001005272.3 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:48239278 A>T maps to NM_001005470.1 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr11:48238858 C>T maps to NM_001005470.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr11:48238784 C>T maps to NM_001005470.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:55371369 C>A maps to NM_001004700.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:55371480 G>A maps to NM_001004700.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:50003784 G>A maps to NM_001005270.2 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:49974252 T>C maps to NM_001001955.2 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr11:49974681 T>A maps to NM_001001955.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:55322552 G>T maps to NM_001001920.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:55322573 C>T maps to NM_001001920.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr11:55322861 G>C maps to NM_001001920.1 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr11:55322162 A>T maps to NM_001001920.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:55340088 G>T maps to NM_001004701.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:55339626 T>C maps to NM_001004701.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:55339627 G>T maps to NM_001004701.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:55340172 C>A maps to NM_001004701.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr11:48346828 G>T maps to NM_001004702.1 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:48346906 C>T maps to NM_001004702.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:48346809 C>A maps to NM_001004702.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr11:48347157 G>T maps to NM_001004702.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr11:48346917 G>T maps to NM_001004702.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:51515475 C>T maps to NM_001004703.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:51515815 C>T maps to NM_001004703.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr11:51515640 C>T maps to NM_001004703.1 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr11:51516006 C>T maps to NM_001004703.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr11:51515884 G>T maps to NM_001004703.1 G202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr11:51515280 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr11:55433355 C>A maps to NM_001004704.1 C238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr11:55433373 G>T maps to NM_001004704.1 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:55433551 G>T maps to NM_001004704.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr11:55432770 T>C maps to NM_001004704.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr11:55433283 G>A maps to NM_001004704.1 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:55432836 C>A maps to NM_001004704.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr11:55433283 G>A maps to NM_001004704.1 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr11:55433331 G>A maps to NM_001004704.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr17:56233092 C>T maps to NM_012374.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr17:56232954 C>T maps to NM_012374.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:59244958 G>A maps to NM_001004705.1 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr11:59245408 C>T maps to NM_001004705.1 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:59245072 G>T maps to NM_001004705.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:59271773 C>T maps to NM_001004706.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr11:59271950 G>A maps to NM_001004706.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:56247543 C>T maps to NM_001004707.3 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr11:123811174 T>C maps to NM_001001965.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr11:123811144 A>G maps to NM_001001965.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr11:59224762 A>G maps to NM_001004708.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:59224906 C>T maps to NM_001004708.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:59224882 G>C maps to NM_001004708.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:59283059 G>C maps to NM_001004711.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:22133981 C>G maps to NM_001001912.1 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr14:22133625 C>T maps to NM_001001912.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr15:102358821 T>C maps to NM_001001674.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr19:110699 C>T maps to NM_001005240.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:102462359 A>G maps to NM_001004195.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr15:102462371 C>T maps to NM_001004195.2 W297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr1:69560 G>A maps to NM_001005484.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr14:20403894 C>T maps to NM_001004063.2 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr14:20404664 C>A maps to NM_001004063.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:20404103 C>T maps to NM_001004063.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20502833 G>A maps to NM_001004714.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:20482728 G>C maps to NM_001004712.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20482420 C>T maps to NM_001004712.1 *311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20482830 C>T maps to NM_001004712.1 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:20482638 G>T maps to NM_001004712.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20443770 C>A maps to NM_001005486.1 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr14:20444507 A>T maps to NM_001005486.1 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:20586437 G>A maps to NM_001004715.1 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr14:20586095 G>T maps to NM_001004715.1 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr14:20344869 C>A maps to NM_001005501.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr14:20345328 G>C maps to NM_001005501.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20344869 C>T maps to NM_001005501.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr14:20389481 G>T maps to NM_001005483.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr14:20389062 C>T maps to NM_001005483.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:20389262 G>T maps to NM_001005483.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr14:20389325 T>G maps to NM_001005483.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr14:20528934 C>T maps to NM_001004717.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr14:20528871 C>A maps to NM_001004717.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr14:20528634 T>C maps to NM_001004717.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr14:20529069 G>A maps to NM_001004717.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:20528985 A>G maps to NM_001004717.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr14:20529066 C>A maps to NM_001004717.1 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr14:20528493 C>T maps to NM_001004717.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr14:20528442 G>A maps to NM_001004717.1 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr14:20249098 C>A maps to NM_001005500.1 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:20248501 C>A maps to NM_001005500.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr14:20248699 C>G maps to NM_001005500.1 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr14:20248858 C>T maps to NM_001005500.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:22368757 C>T maps to NM_001004719.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr15:22369189 G>T maps to NM_001004719.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr15:22369132 G>T maps to NM_001004719.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr14:20295738 C>T maps to NM_001004723.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr14:20296314 C>A maps to NM_001004723.1 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr14:20296392 C>T maps to NM_001004723.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr14:20295660 C>A maps to NM_001004723.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:20295630 G>A maps to NM_001004723.1 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr14:20295759 A>G maps to NM_001004723.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr15:22382663 C>A maps to NM_001005241.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr15:22382711 G>A maps to NM_001005241.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr15:22382702 G>T maps to NM_001005241.1 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:22382672 C>A maps to NM_001005241.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr14:20612590 A>T maps to NM_001004724.1 K233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr14:20612329 T>C maps to NM_001004724.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr14:20612781 T>A maps to NM_001004724.1 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr11:55406477 T>C maps to NM_001004124.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr14:20216209 T>C maps to NM_172194.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr14:20216404 C>A maps to NM_172194.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:20216206 G>C maps to NM_172194.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr11:48328703 A>G maps to NM_001004725.1 *310W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:48327914 C>A maps to NM_001004725.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:55418943 G>T maps to NM_001004059.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:48285516 T>G maps to NM_001004726.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:48266855 C>T maps to NM_001004727.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr11:48267104 A>G maps to NM_001004727.1 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:4976783 C>A maps to NM_001004748.1 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:4967898 G>A maps to NM_001005329.1 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr11:4929489 A>G maps to NM_001004749.1 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr11:5344900 A>G maps to NM_033180.4 C209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr11:5322798 T>C maps to NM_033179.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:5364442 T>A maps to NM_001005567.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:5364184 G>T maps to NM_001005567.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr11:5363938 G>A maps to NM_001005567.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:5373441 C>G maps to NM_001004750.1 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:5373627 T>C maps to NM_001004750.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:5373013 G>T maps to NM_001004750.1 G93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr11:4661697 C>T maps to NM_001004751.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr11:4703254 G>A maps to NM_030774.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr11:4790427 G>A maps to ENST00000380383 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr11:4843391 C>A maps to NM_001004753.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:4842794 G>C maps to NM_001004753.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:4843541 G>A maps to NM_001004753.1 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:4945554 A>C maps to NM_001005237.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:4945473 G>T maps to NM_001005237.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:4945220 G>A maps to NM_001005237.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr11:4944866 C>A maps to NM_001005237.1 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:4935986 G>A maps to NM_001005238.1 Q303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr11:4936269 G>A maps to NM_001005238.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr11:4936674 C>T maps to NM_001005238.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr11:5462198 G>C maps to NM_001005288.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr11:5474873 G>A maps to NM_001004754.2 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:5474909 C>A maps to NM_001004754.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr11:5475068 C>T maps to NM_001004754.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:5020433 G>C maps to NM_001004755.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:5020493 C>T maps to NM_001004755.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:5020607 G>A maps to NM_001004755.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr11:5020811 T>A maps to NM_001004755.1 Y200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:5411011 C>T maps to NM_001004756.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:5444059 C>T maps to NM_001004757.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:5443498 G>A maps to NM_001004757.2 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr11:5444248 G>A maps to NM_001004757.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:4903749 C>A maps to NM_001004759.1 Y234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr11:4903236 C>G maps to NM_001004759.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr11:4903512 C>T maps to NM_001004759.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr11:5221654 C>T maps to NM_001004760.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:5221711 G>A maps to NM_001004760.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:5221754 C>T maps to NM_001004760.2 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:5173295 G>A maps to NM_012375.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:5172864 A>G maps to NM_012375.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr11:5172786 G>T maps to NM_012375.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:5172714 A>G maps to NM_012375.2 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:5142421 C>T maps to NM_001005222.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr11:5142406 C>A maps to NM_001005222.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:5142451 C>A maps to NM_001005222.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr11:5142745 G>A maps to NM_001005222.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:5153038 G>A maps to NM_001005160.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr11:5153245 G>T maps to NM_001005160.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:6191433 G>A maps to NM_001004052.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr11:6190884 G>A maps to NM_001004052.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr11:6191144 G>A maps to NM_001004052.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:6191433 G>T maps to NM_001004052.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:5602861 C>A maps to NM_001005162.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr11:5602504 C>A maps to NM_001005162.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:5602244 C>T maps to NM_001005162.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:5510655 T>C maps to NM_001005163.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:5510562 C>A maps to NM_001005163.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr11:5509983 C>T maps to NM_001005163.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:5080617 G>T maps to NM_001005164.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:5079888 C>G maps to NM_001005164.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr11:5906085 G>A maps to NM_001005165.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr11:5862347 G>A maps to ENST00000379946 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr11:5878253 G>A maps to NM_001005168.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:4615654 C>T maps to ENST00000450052 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:4616128 C>T maps to ENST00000450052 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:4608359 G>C maps to NM_001005170.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:4608506 C>T maps to NM_001005170.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr11:4608713 C>G maps to NM_001005170.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr11:5068240 C>G maps to NM_001001916.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr11:4510852 G>A maps to NM_001005171.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:4510411 C>A maps to NM_001005171.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:4470787 G>T maps to NM_001005172.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr11:6008145 A>G maps to NM_001005173.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:6007719 G>T maps to NM_001005173.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr11:5809392 G>A maps to NM_001001913.1 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr11:5809419 C>A maps to NM_001001913.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:5809560 A>C maps to NM_001001913.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:5799429 G>C maps to NM_001001922.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr11:5799294 G>A maps to NM_001001922.2 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:5799486 G>A maps to NM_001001922.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:5799573 A>G maps to NM_001001922.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:4825604 C>T maps to ENST00000380382 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:6220866 T>A maps to NM_001005178.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr11:6220872 G>T maps to NM_001005178.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr11:6048724 G>A maps to NM_001001917.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:6048914 G>T maps to NM_001001917.2 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr11:6048160 G>A maps to NM_001001917.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:5969346 C>T maps to NM_001003443.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:5968692 C>T maps to NM_001003443.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr11:5968671 C>T maps to NM_001003443.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:6024018 G>A maps to NM_001005179.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr11:6023445 C>A maps to NM_001005179.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:6024282 G>A maps to NM_001005179.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr11:6023760 C>T maps to NM_001005179.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr11:5758255 G>T maps to NM_001005180.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:5758675 C>T maps to NM_001005180.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:6129217 C>A maps to NM_001005181.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:6129109 C>T maps to NM_001005181.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr11:6129877 A>G maps to NM_001005181.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:6129823 G>A maps to NM_001005181.1 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:59211186 C>T maps to NM_001004728.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:59189574 G>T maps to NM_001001954.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:59189604 C>A maps to NM_001001954.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr11:59190018 G>A maps to NM_001001954.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr11:59190240 G>A maps to NM_001001954.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:97806282 C>T maps to NM_054106.1 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:97806801 G>T maps to NM_054106.1 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr3:97806441 C>G maps to NM_054106.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:56756813 C>T maps to NM_001005323.1 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr11:56756942 T>G maps to NM_001005323.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:59132215 T>C maps to NM_001004729.1 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr11:59132569 A>G maps to NM_001004729.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:59132055 G>A maps to NM_001004729.1 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:56431877 C>A maps to NM_001004730.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr11:56431940 G>C maps to NM_001004730.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr11:56432081 A>G maps to NM_001004730.1 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr11:56431505 G>C maps to NM_001004730.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:56431805 C>T maps to NM_001004730.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr11:55798823 T>C maps to NM_001001921.1 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:55798049 T>C maps to NM_001001921.1 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:55798562 C>T maps to NM_001001921.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:55798250 T>C maps to NM_001001921.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:21623848 G>A maps to NM_001004731.1 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:58206943 G>C maps to NM_001004733.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr11:58207048 G>A maps to NM_001004733.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:58206859 A>G maps to NM_001004733.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr11:58207324 G>A maps to NM_001004733.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr11:58125893 G>A maps to NM_001005489.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:58126449 G>A maps to NM_001005489.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr11:58189993 G>T maps to NM_001005566.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr11:58189873 G>T maps to NM_001005566.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr9:125551231 C>A maps to NM_001001923.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr11:55541467 A>T maps to NM_001001967.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr11:55541561 C>T maps to NM_001001967.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:55541281 C>T maps to NM_001001967.1 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:55563456 C>T maps to NM_001004735.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr11:55563924 C>T maps to NM_001004735.1 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:55563126 G>A maps to NM_001004735.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:55606808 T>A maps to NM_001005496.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr11:55606643 C>G maps to NM_001005496.1 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr11:55606667 G>A maps to NM_001005496.1 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:55606283 C>T maps to NM_001005496.1 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:55606466 T>A maps to NM_001005496.1 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:55606516 C>G maps to NM_001005496.1 S97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr11:55606556 A>G maps to NM_001005496.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr11:55606886 T>A maps to NM_001005496.1 Y220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr11:55587491 C>T maps to ENST00000395203 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr11:55587579 G>T maps to ENST00000395203 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr11:55587566 C>G maps to ENST00000395203 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr11:55587458 G>A maps to ENST00000395203 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:55587920 C>T maps to ENST00000395203 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr11:55761627 G>C maps to NM_003697.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr11:55761645 C>A maps to NM_003697.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr11:55761663 G>A maps to NM_003697.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:55761639 C>T maps to NM_003697.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:97868306 C>A maps to NM_001005514.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:97868270 C>T maps to NM_001005514.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr3:97868948 C>A maps to NM_001005514.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:97887665 G>C maps to NM_001005515.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:97887884 C>G maps to NM_001005515.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:98001946 C>G maps to NM_001005482.1 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr3:98002138 A>G maps to NM_001005482.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:55703378 A>G maps to NM_006637.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:55703120 G>T maps to NM_006637.1 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:55944603 C>T maps to NM_001005492.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr11:55944827 G>T maps to NM_001005492.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:55944655 C>A maps to NM_001005492.1 S188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:55944827 G>A maps to NM_001005492.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:98188839 C>T maps to NM_001004736.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:98217105 C>T maps to NM_001004737.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr3:98109748 G>A maps to NM_001005516.1 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:98073044 G>T maps to NM_001005517.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:55579556 G>A maps to NM_001004738.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:55579652 C>T maps to NM_001004738.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr11:55595191 C>A maps to NM_001004739.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr11:55594820 C>T maps to NM_001004739.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:55595554 C>A maps to NM_001004739.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr11:56380882 A>C maps to NM_001004740.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr11:56380888 T>C maps to NM_001004740.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr11:56380078 G>A maps to NM_001004740.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr11:56345152 T>C maps to NM_001004741.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr11:56344939 G>A maps to NM_001004741.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:56344726 G>A maps to NM_001004741.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:56344918 G>A maps to NM_001004741.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr11:56310670 C>T maps to NM_001005245.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:56309851 T>C maps to NM_001005245.1 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:56309823 G>A maps to NM_001005245.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:56309824 G>A maps to NM_001005245.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:56310643 C>A maps to NM_001005245.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr11:56237424 G>A maps to NM_001004742.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:56237805 G>T maps to NM_001004742.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr11:56237826 G>C maps to NM_001004742.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr11:56237208 G>A maps to NM_001004742.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:56258411 C>A maps to NM_001005282.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:56257932 G>C maps to NM_001005282.1 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:56258069 G>A maps to NM_001005282.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr11:56258303 T>A maps to NM_001005282.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr11:56258615 A>G maps to NM_001005282.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:56258723 G>A maps to NM_001005282.1 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:56230772 G>A maps to NM_001004743.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:56230730 G>A maps to NM_001004743.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:56230000 T>A maps to NM_001004743.1 K293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr11:56230394 A>G maps to NM_001004743.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:56230517 C>T maps to NM_001004743.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr11:7818033 A>G maps to NM_153444.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:7846616 C>T maps to NM_153445.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:7846841 C>T maps to NM_153445.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr11:56185276 C>A maps to NM_001004744.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:56185378 A>T maps to NM_001004744.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr11:56185141 G>A maps to NM_001004744.1 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:56184847 G>A maps to NM_001004744.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr11:56185585 G>T maps to NM_001004744.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr11:56043908 G>C maps to NM_001004745.1 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr11:56044040 A>G maps to NM_001004745.1 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr11:56000385 G>A maps to NM_001004746.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:56000379 G>A maps to NM_001004746.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:56000427 G>A maps to NM_001004746.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:55999740 C>T maps to NM_001004746.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:56020199 C>T maps to NM_001004747.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:56019806 G>A maps to NM_001004747.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr6:29323419 G>A maps to NM_030876.5 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:55681515 G>T maps to NM_001001960.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr11:6816909 C>G maps to NM_003696.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr11:6816033 G>T maps to NM_003696.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:143701562 G>A maps to NM_001005281.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:143701433 G>C maps to NM_001005281.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr2:240969459 C>T maps to NM_001005853.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr2:240969561 G>T maps to NM_001005853.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr2:240969702 G>A maps to NM_001005853.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:240985468 G>C maps to NM_173351.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr2:240984615 G>A maps to NM_173351.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr12:55714667 C>A maps to NM_001005182.1 C95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr12:55714811 T>G maps to NM_001005182.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr12:55714856 C>G maps to NM_001005182.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:55726161 G>T maps to NM_054104.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr12:55945873 T>C maps to NM_001005494.1 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr12:55945681 G>T maps to NM_001005494.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:55688557 G>A maps to NM_001005493.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:55794383 G>A maps to NM_001005518.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr12:55886851 C>T maps to NM_001005519.1 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr12:55887078 T>A maps to NM_001005519.1 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:55863388 G>A maps to NM_001005499.1 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr12:55863562 G>A maps to NM_001005499.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr12:55759092 C>T maps to NM_001005497.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:55820375 C>T maps to NM_001005183.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr12:55820729 A>G maps to NM_001005183.1 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:55820432 C>A maps to NM_001005183.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr12:55820444 G>A maps to NM_001005183.1 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:247875238 A>C maps to NM_001005286.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:247875868 C>G maps to NM_001005286.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:158669836 G>C maps to NM_001005279.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr1:158669773 C>A maps to NM_001005279.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:158669656 G>A maps to NM_001005279.1 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:158669806 C>T maps to NM_001005279.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:158669572 G>T maps to NM_001005279.1 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:158687611 G>T maps to ENST00000368146 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:158724700 G>A maps to NM_001005184.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr11:123676664 C>A maps to NM_001005325.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr11:123676379 G>A maps to NM_001005325.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr11:123676226 C>A maps to NM_001005325.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr11:123676214 G>A maps to NM_001005325.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:158735617 G>A maps to NM_001005185.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr1:158735783 G>C maps to NM_001005185.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:158746810 G>A maps to NM_001005278.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr14:21109085 A>G maps to NM_001001968.1 Y255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr14:21109808 G>A maps to NM_001001968.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr11:123813816 C>T maps to NM_001005187.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr11:123813777 G>A maps to NM_001005187.1 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:142749509 C>T maps to NM_001001667.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:142750109 C>A maps to NM_001001667.1 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr11:123625127 G>A maps to NM_001005188.1 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:123624752 C>T maps to NM_001005188.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:14952227 C>G maps to NM_001005190.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:14991891 G>A maps to NM_030901.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr19:14938942 G>C maps to NM_017506.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr19:15052713 C>A maps to NM_012377.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:9297145 C>G maps to NM_175883.2 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:9296834 C>G maps to NM_175883.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:9325342 G>A maps to NM_001005191.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr19:9324826 G>A maps to NM_001005191.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr19:9361988 T>G maps to NM_001079935.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:9226034 G>A maps to ENST00000293614 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr19:9213868 C>T maps to NM_001005193.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:9237044 G>A maps to NM_001001958.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr11:124440374 C>T maps to NM_001005194.1 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr11:124413210 G>A maps to NM_001005195.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:124413187 G>C maps to NM_001005195.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:124412749 G>C maps to NM_001005195.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:124252329 G>A maps to NM_001005468.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:124252317 G>A maps to NM_001005468.1 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:124252579 G>A maps to NM_001005468.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:124266425 A>T maps to NM_001005467.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:124267067 G>A maps to NM_001005467.1 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr11:124266602 G>A maps to NM_001005467.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr11:124294277 G>A maps to NM_001005196.1 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:124310450 G>A maps to NM_012378.1 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:124180473 G>A maps to NM_001002917.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:124180026 T>C maps to NM_001002917.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:124189697 G>T maps to NM_001002918.1 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr11:124189433 G>A maps to NM_001002918.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:123777944 C>T maps to NM_001005197.1 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr11:56058148 A>G maps to NM_001005199.1 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr11:56058166 A>C maps to NM_001005199.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr11:56057818 A>G maps to NM_001005199.1 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:55872802 G>T maps to NM_001005200.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:55872553 C>T maps to NM_001005200.1 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr11:55872943 C>T maps to NM_001005200.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:55872955 T>G maps to NM_001005200.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr11:55873273 T>C maps to NM_001005200.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:55890009 C>A maps to NM_001005201.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr11:55861496 C>A maps to NM_001003750.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:56128007 G>T maps to NM_001005205.1 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr11:56127817 G>C maps to NM_001005205.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr11:56128168 C>T maps to NM_001005205.1 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:56127928 T>C maps to NM_001005205.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr11:55904528 A>T maps to NM_001004064.1 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:55904597 G>T maps to NM_001004064.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:55904672 G>T maps to NM_001004064.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:56114035 C>T maps to NM_001002907.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:56113723 A>G maps to NM_001002907.1 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:56113936 C>T maps to NM_001002907.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:56114158 C>T maps to NM_001002907.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:56085892 C>A maps to NM_001005202.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:56086375 A>T maps to NM_001005202.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:56085944 T>C maps to NM_001005202.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr11:56085985 C>T maps to NM_001005202.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:55927514 G>C maps to NM_001004058.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:55927361 C>G maps to NM_001004058.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr11:55927528 G>A maps to NM_001004058.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:55927655 G>A maps to NM_001004058.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:48919764 G>T maps to NM_001005203.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:48919587 C>T maps to NM_001005203.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:48921858 G>A maps to NM_001005203.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr7:142724129 G>A maps to NM_001001658.1 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr7:142724093 C>T maps to NM_001001658.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:142723571 G>A maps to NM_001001658.1 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:141619409 C>T maps to NM_001001656.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr7:141618782 G>A maps to NM_001001656.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:56468408 C>T maps to NM_001013358.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:56510759 G>A maps to NM_001005284.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:56511254 G>A maps to NM_001005284.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr11:56511134 C>T maps to NM_001005284.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:56510690 C>T maps to NM_001005284.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:57886520 A>G maps to NM_001005211.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:57886289 G>T maps to NM_001005211.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:57886445 G>T maps to NM_001005211.1 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:57947761 C>A maps to NM_001005212.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr11:57946990 C>T maps to NM_001005212.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr11:57958039 T>A maps to NM_001005283.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr12:122079194 G>T maps to NM_032790.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr12:122079386 G>C maps to NM_032790.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr12:122079044 C>T maps to NM_032790.3 H136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr7:102087372 C>G maps to NM_032831.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IF-01A-11D-A31L-08 chr16:30960831 C>T maps to NM_152288.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr1:52841199 G>A maps to NM_004153.3 F735F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:52854209 C>T maps to NM_004153.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:52847411 G>A maps to NM_004153.3 Q679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:52841196 G>A maps to NM_004153.3 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr2:201791526 G>T maps to NM_006190.4 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr2:201798697 C>T did not map to a codon.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:201798643 G>C maps to NM_006190.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr6:88315720 C>T maps to NM_181837.2 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:103835693 T>C maps to NM_002553.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:58088660 G>A maps to NM_006812.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:59377943 G>A maps to NM_002556.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr11:59376072 G>A maps to NM_002556.2 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:31091252 C>T maps to NM_030758.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr22:31266527 C>T maps to NM_030758.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr22:31091273 G>A maps to NM_030758.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr22:31266542 C>T maps to NM_030758.3 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr22:31302301 G>A maps to NM_030758.3 W909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:31871624 G>A maps to NM_017784.4 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr18:21745030 C>T maps to NM_080597.2 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr18:21892034 G>A maps to NM_080597.2 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:60838713 C>T maps to NM_144498.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:24905838 G>A maps to NM_015550.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:24874173 G>A maps to NM_015550.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:3121472 C>T maps to NM_020896.3 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr11:3109524 C>G maps to NM_020896.3 P850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr2:179197684 A>T maps to ENST00000392505 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:179259093 G>A maps to ENST00000392505 E901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:45891042 C>A maps to NM_145798.2 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:45886705 G>A maps to NM_145798.2 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr12:76767186 A>G maps to NM_020841.4 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:52242581 G>A maps to ENST00000428468 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:54598533 A>G maps to NM_130771.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr1:36904425 G>A maps to ENST00000356637 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr14:20917163 G>A maps to NM_017807.3 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:83999317 C>T maps to NM_013370.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr8:90926440 G>A maps to NM_001126111.1 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr8:90937309 C>G maps to NM_001126111.1 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr22:30660369 C>T maps to NM_020530.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:30660006 G>A maps to NM_020530.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:38933398 T>C maps to NM_003999.2 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:38904531 A>G maps to NM_003999.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr2:19553233 G>C maps to NM_145260.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:19552945 G>A maps to NM_145260.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr9:77755828 G>A maps to NM_012383.4 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr6:108395462 T>A maps to NM_014028.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:190930353 C>T maps to NM_198184.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr3:195955138 C>T maps to NM_152672.5 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr3:195955066 G>T maps to NM_152672.5 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr3:195953917 C>T maps to NM_152672.5 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:38262912 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr23:38240681 G>A did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr16:21693073 G>T maps to ENST00000286149 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:21698870 C>T maps to ENST00000286149 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr16:21742217 C>T maps to ENST00000286149 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr2:26717899 C>T maps to NM_194248.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:26696030 T>G maps to NM_194248.2 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:26688664 C>A maps to NM_194248.2 T1558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr2:26682978 A>G maps to NM_194248.2 L1970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:26702479 G>T maps to NM_194248.2 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:26687857 G>A maps to NM_194248.2 S1613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:26707343 C>T maps to NM_194248.2 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr2:26750725 G>A maps to NM_194248.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr2:26706497 C>T maps to NM_194248.2 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr3:161214757 G>T maps to NM_001080440.1 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr4:4199804 A>G maps to NM_177998.1 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr4:4199750 G>A maps to NM_177998.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:72929558 C>T maps to NM_178160.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr17:72923777 A>T maps to NM_178160.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:72945429 C>T maps to NM_178233.1 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr11:63764861 C>T maps to ENST00000422031 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr14:94510930 G>A did not map to a codon.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr4:146059379 G>A maps to ENST00000447906 G849G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:48783268 C>G did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr23:48780922 G>T did not map to a codon.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr23:48792041 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr23:48781241 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:69282985 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:69282813 C>T did not map to a codon.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr23:69283069 C>A did not map to a codon.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr15:31947301 C>A maps to ENST00000382902 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr15:31794040 C>G maps to ENST00000382902 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr15:31776456 C>T maps to ENST00000382902 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr15:31818595 G>A maps to ENST00000382902 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:149916875 G>C maps to NM_020205.2 S471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr2:63283435 G>T maps to NM_014562.3 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr17:1945364 G>A maps to NM_080822.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:29597151 A>G maps to NM_183378.2 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:29631792 T>C maps to NM_183378.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:29649500 T>C maps to NM_183378.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:7718105 C>T maps to NM_198185.2 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr1:111965616 C>T maps to ENST00000369728 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr20:18022340 C>A maps to NM_021220.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr5:41862852 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:40235541 G>A maps to NM_022120.1 C462C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr2:42991085 G>A maps to NM_148962.4 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr8:107719170 A>G maps to NM_001198533.1 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr3:25832846 C>T maps to NM_017897.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:38266072 G>A maps to NM_005109.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr20:3052919 C>T maps to NM_000915.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr20:3052339 C>T maps to NM_000915.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr3:8809324 G>A maps to NM_000916.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr3:8794893 G>A maps to NM_000916.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:133195569 C>T maps to NM_170683.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:57118348 C>T maps to NM_002559.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:57118258 C>T maps to NM_002559.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:121670828 C>T maps to NM_002560.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:121670849 C>G maps to NM_002560.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:21377466 C>T maps to NM_005446.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:21377814 C>T maps to NM_005446.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:121605310 G>A maps to NM_002562.5 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr12:121615008 C>T maps to NM_002562.5 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:152554041 C>T maps to NM_002563.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr23:78216655 C>T did not map to a codon.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr23:78217000 C>T did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr23:78216633 G>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:78216596 G>T did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:78216841 C>A did not map to a codon.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr23:78217017 G>C did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:78216232 C>G did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:151046054 G>A maps to NM_176894.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr3:151045838 C>T maps to NM_176894.2 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr3:151046792 C>T maps to NM_176894.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr11:72945650 C>T maps to NM_176071.1 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr11:72945506 C>T maps to NM_176071.1 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr23:1584401 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:1584919 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:1584750 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr10:74831831 C>A maps to NM_000917.3 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:74770750 A>G maps to NM_000917.3 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:131530706 A>C maps to NM_001142599.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr5:131531173 C>A did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr17:79804355 C>T maps to NM_000918.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr17:79813068 G>A maps to NM_000918.3 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56504216 G>T maps to NM_006191.2 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:101733736 C>G maps to NM_002568.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr8:101717844 G>A maps to NM_002568.3 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr20:43559285 C>T maps to NM_001124756.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr13:25670473 G>A maps to NM_030979.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr13:25671149 C>A maps to NM_030979.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:90690742 G>T did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:90690748 C>T did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr23:90690654 C>A did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr23:90690655 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:90691136 G>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:90691162 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr23:90691200 G>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:90690735 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:90690669 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:90691154 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:90691536 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:90691044 G>T did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:90691440 G>C did not map to a codon.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr23:90691384 A>G did not map to a codon.
Alternatively spliced codon TCGA-UF-A7JS-01A-11D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr6:163510333 C>G maps to NM_152410.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:163735915 T>A maps to NM_152410.2 L263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr6:163483324 C>A maps to NM_152410.2 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:66003367 G>A did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr14:105848854 C>G maps to ENST00000458164 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr6:34499520 C>T maps to NM_020804.3 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:34498109 C>T maps to NM_020804.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:34496435 C>T maps to NM_020804.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:43287097 G>T maps to NM_001184970.1 S103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr22:43275153 G>A maps to NM_001184970.1 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr22:43272155 C>T maps to NM_001184970.1 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr22:43308052 C>A maps to NM_001184970.1 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:47201008 A>G maps to NM_016223.4 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr11:47199929 C>A maps to NM_016223.4 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:17552555 G>C maps to NM_013358.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:17609456 C>G maps to NM_016233.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:17597415 C>T maps to NM_016233.2 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr1:17603148 C>G maps to NM_016233.2 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr1:17603148 C>G maps to NM_016233.2 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:17662721 G>A did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:17668882 G>A maps to NM_012387.2 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:39880373 C>T maps to NM_019088.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:39879806 C>A maps to NM_019088.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr11:117038339 C>T maps to NM_002572.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr1:26303186 C>T maps to NM_000437.3 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr8:81905366 G>A maps to NM_018440.3 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr8:81897256 C>G maps to NM_018440.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr8:81899629 C>T maps to NM_018440.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr8:81897091 C>A maps to NM_018440.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr23:49454128 C>T did not map to a codon.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr23:55117015 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:55102483 C>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:49597192 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:49597226 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:55248197 A>C did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:55247871 T>C did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:103248920 G>A maps to NM_000277.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:103288645 C>T maps to NM_000277.1 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr12:103260441 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr12:103234268 C>A maps to NM_000277.1 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr5:43539097 T>C maps to NM_006451.4 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:77048408 A>G maps to NM_001128620.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:10707719 C>A maps to NM_017906.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr3:196530018 G>C maps to NM_002577.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr3:196545013 A>T maps to NM_002577.4 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:110385413 G>C did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr23:110435820 C>A did not map to a codon.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr23:110406905 G>A did not map to a codon.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr23:110385354 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:110385397 T>C did not map to a codon.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr23:110406176 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:39660312 G>A maps to NM_005884.3 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr15:40565663 C>G maps to NM_020168.4 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:40565874 G>T maps to NM_020168.4 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr20:9561115 G>T maps to NM_177990.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr20:9561502 C>T maps to NM_177990.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr20:9561424 G>A maps to NM_177990.2 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr20:9547018 G>A maps to NM_177990.2 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr20:9525045 C>T maps to NM_177990.2 E613E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr20:9546620 G>A maps to NM_177990.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr20:9561115 G>A maps to NM_177990.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr20:9546782 C>T maps to NM_177990.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:9560856 G>A maps to NM_177990.2 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr20:9525141 C>A did not map to a codon.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr20:9546590 C>T maps to NM_177990.2 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr16:23646936 A>G maps to NM_024675.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr16:23647269 A>C maps to NM_024675.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr16:23647098 G>A maps to NM_024675.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr4:169846388 C>T maps to NM_001166108.1 R1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr9:112705029 T>C maps to ENST00000413420 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr9:112705560 G>T maps to ENST00000413420 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:102343266 G>T maps to NM_000919.3 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:35513608 G>A maps to NM_015430.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr11:35454062 G>A maps to NM_015430.2 I685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr11:35496242 G>A maps to NM_015430.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr11:35454377 G>A maps to NM_015430.2 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr11:35515734 G>A maps to NM_015430.2 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr11:35454377 G>A maps to NM_015430.2 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr12:56718208 G>A maps to NM_001127460.2 D599D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr12:56721835 T>A maps to NM_001127460.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr12:56716929 G>A maps to NM_001127460.2 V807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr12:56712916 G>A maps to NM_001127460.2 R1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:28854570 A>C maps to NM_175854.7 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr13:28771371 A>T maps to NM_175854.7 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr13:28866541 A>G maps to NM_175854.7 K849K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:91353634 C>A maps to NM_148977.1 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:91404849 C>T maps to NM_148977.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr20:3897631 A>T maps to NM_153638.2 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr5:168006279 G>A maps to NM_024594.2 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:167991071 T>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:2445839 G>A maps to ENST00000425477 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr1:2451775 C>A maps to ENST00000425477 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:93911557 C>T maps to NM_015368.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr11:124487351 C>T maps to NM_052959.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr11:124489329 C>A maps to NM_052959.2 Y226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr10:135203151 G>A maps to NM_152911.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr10:135195044 C>A maps to NM_152911.2 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:135195062 C>T maps to NM_152911.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr5:6742600 A>T did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:6749697 C>T maps to NM_006999.4 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr19:39597657 C>T maps to NM_001004318.2 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:39591818 C>T maps to NM_001004318.2 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr14:73733289 C>T maps to ENST00000427855 F1115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr14:96998719 C>T maps to NM_032632.3 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr7:4900070 G>A maps to NM_020144.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr7:4899701 C>T maps to NM_020144.4 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr7:4901300 G>C maps to NM_020144.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr7:4900493 G>A maps to NM_020144.4 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr2:60998715 C>T maps to NM_022894.3 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr9:118973929 T>A maps to NM_002581.3 L546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:118950330 G>T maps to NM_002581.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr9:118997916 G>T did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr9:119065051 C>A maps to NM_002581.3 C990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr9:119093590 C>T maps to NM_002581.3 I1072I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:118949745 T>C maps to NM_002581.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:176668368 G>T maps to NM_020318.2 P960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:176668317 G>A maps to NM_020318.2 T943T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr1:176564032 C>T maps to NM_020318.2 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr1:176668474 C>T maps to NM_020318.2 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr1:176760545 C>T maps to NM_020318.2 Q1650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:176738745 G>T maps to NM_020318.2 E1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:176740226 C>T maps to NM_020318.2 L1542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:176668353 G>T maps to NM_020318.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:176526027 G>A maps to NM_020318.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:176679228 C>T maps to NM_020318.2 Q1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:176671755 G>T maps to NM_020318.2 G1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr1:176525772 C>T maps to NM_020318.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr1:176525490 G>T maps to NM_020318.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:108608318 T>C maps to NM_005443.4 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr15:69682092 C>T maps to NM_017705.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr6:52268766 C>A maps to ENST00000361841 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr6:52268775 C>T maps to ENST00000361841 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr6:52268775 C>T maps to ENST00000361841 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr6:52268169 C>T maps to ENST00000361841 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:142681167 G>C maps to NM_198504.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr10:34671825 G>A maps to NM_019619.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:34805968 G>C maps to NM_019619.3 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr10:34671813 G>A maps to NM_019619.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:34649065 G>C maps to NM_019619.3 S610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr10:34420468 C>G maps to NM_019619.3 L1157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr10:34408629 C>T maps to NM_019619.3 S1196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:34739280 G>A maps to NM_019619.3 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:205978292 G>A maps to ENST00000406610 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr2:206166296 C>G maps to ENST00000406610 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr18:77960665 G>A maps to NM_032510.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr18:77960805 C>A maps to NM_032510.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr18:77918382 G>A maps to NM_032510.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr6:162683676 C>A maps to NM_004562.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:8025463 C>T maps to NM_001123377.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:183547406 T>C maps to NM_018622.5 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:183585694 A>G maps to NM_018622.5 Y93Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr4:75938034 C>T maps to NM_015393.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr4:75938151 T>C maps to NM_015393.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:226549217 C>T maps to NM_001618.3 Q996Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr1:226567779 G>C maps to NM_001618.3 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr8:145059673 C>T maps to NM_032789.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:145058521 C>A maps to NM_032789.3 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:145060328 C>T maps to NM_032789.3 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:3935379 G>A maps to NM_020367.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr12:3921419 G>A maps to NM_020367.4 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:139724437 C>T maps to NM_022750.2 Q676Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:139756946 G>A maps to NM_022750.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr7:139741626 A>G maps to NM_022750.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr7:139727112 G>A maps to NM_022750.2 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:139727185 G>T maps to NM_022750.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:122432774 C>T maps to NM_017554.2 Q1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr3:122420436 A>T maps to NM_017554.2 G1012G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr3:122446756 C>G maps to NM_017554.2 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr3:122354764 C>T maps to NM_001113523.1 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr3:122354784 C>T maps to NM_001113523.1 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:122345842 A>G maps to NM_001113523.1 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr15:65555577 C>T maps to NM_017851.4 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr15:65555625 G>A maps to NM_017851.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr3:51979164 G>A maps to NM_001003931.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr3:51978491 C>A maps to NM_001003931.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:51982441 C>T maps to NM_001003931.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:25072324 G>A maps to NM_006437.3 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:25073510 A>G maps to NM_006437.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr15:72534498 T>C maps to NM_020214.2 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr15:72543223 C>T maps to NM_020214.2 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr5:50111355 C>T maps to ENST00000505697 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr5:50057653 G>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:50091251 G>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr5:50091025 G>A maps to ENST00000505697 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr5:50090899 G>A maps to ENST00000505697 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:122247276 T>C maps to NM_031458.2 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:44585009 C>T maps to NM_001137606.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr22:44583757 C>T maps to NM_001137606.1 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:150844492 G>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:150789406 G>C did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr23:150817137 A>C did not map to a codon.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr23:150832807 C>T did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr23:150828295 C>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:150780161 G>C did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:150791485 C>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:150840133 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:150840976 T>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:150773138 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:150832781 G>A did not map to a codon.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr23:150817167 C>G did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:150844504 G>T did not map to a codon.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr2:242054511 G>A maps to ENST00000358649 F1093F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:125647291 G>A maps to NM_212555.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr22:31731696 G>A maps to NM_014323.2 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr22:31731762 C>T maps to NM_014323.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr22:31740795 G>A maps to NM_014323.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr12:80014867 G>C maps to NM_002583.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr20:21687097 C>T maps to NM_006192.3 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr20:21687259 C>T maps to NM_006192.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr20:21689199 C>G maps to NM_006192.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr20:21687661 G>A maps to NM_006192.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr10:102584501 G>A maps to NM_003987.3 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr10:102510538 G>T maps to NM_003987.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:102566316 C>T maps to NM_003987.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:102568883 C>G maps to NM_003987.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr10:102586775 C>T maps to NM_003987.3 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:223158888 G>T maps to NM_181459.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:223066810 C>T maps to NM_181459.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:127253103 C>T maps to NM_006193.2 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:127255553 G>C maps to NM_006193.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr7:127253864 G>A maps to NM_006193.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:37014992 C>T did not map to a codon.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:31816280 G>A maps to NM_001604.4 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:19029672 C>T maps to NM_002584.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:18962743 G>A maps to NM_002584.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr2:114004386 G>T maps to NM_003466.3 C45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr14:37132576 C>A maps to NM_006194.3 Y160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:154738230 T>G maps to NM_007349.3 R1042R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr7:154767471 C>T maps to NM_007349.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr8:27668592 C>T maps to NM_018492.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr6:138539372 G>A maps to NM_021635.2 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr3:52675990 C>A maps to ENST00000296302 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr3:52623228 G>C maps to ENST00000296302 S941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:52637657 A>G maps to ENST00000296302 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:52637554 G>A maps to ENST00000296302 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr3:52597490 C>T maps to ENST00000296302 Q1298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:32154197 C>T maps to NM_002586.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr9:128723126 C>T maps to ENST00000373487 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr19:19675808 C>T maps to NM_025245.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr1:154919108 C>T maps to NM_020524.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:154924304 A>G maps to NM_020524.2 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr11:66617873 G>A maps to NM_022172.2 Y845Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr11:66620710 G>T maps to NM_022172.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr11:66617738 G>T maps to NM_022172.2 V890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr11:66617202 G>C maps to NM_022172.2 S1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr5:134296334 G>A maps to NM_032151.4 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:70315831 G>A maps to NM_006196.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:53849718 C>T maps to NM_005016.5 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr12:53854797 G>A did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr12:53849782 G>T maps to NM_005016.5 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:47360107 C>T maps to NM_020528.2 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:51993285 G>C maps to NM_033010.2 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr13:100992478 C>T maps to NM_000282.3 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr13:100982840 C>T maps to NM_000282.3 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr3:135969355 C>T maps to NM_001178014.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:136046021 C>T maps to NM_001178014.1 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr5:141244695 C>G maps to NM_032420.2 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:141248193 C>T maps to NM_032420.2 E281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr4:134071804 C>T maps to NM_032961.1 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr4:134084194 G>A maps to NM_032961.1 W954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:134084408 G>T maps to NM_032961.1 T1025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr4:134072872 C>T maps to NM_032961.1 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr4:134072701 C>T maps to NM_032961.1 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr4:134072410 G>A maps to NM_032961.1 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:134072305 C>A maps to NM_032961.1 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr4:134073850 C>G maps to NM_032961.1 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr4:134073257 G>T maps to NM_032961.1 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr4:134071801 G>A maps to NM_032961.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:91132610 G>C did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:91090604 G>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:91132396 G>C did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr23:91133548 G>T did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:91134063 C>A did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:91132914 G>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:91134248 C>T did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr23:91132757 C>A did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr23:91873418 C>T did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr23:91090569 G>A did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr23:91090649 G>T did not map to a codon.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr23:91873683 G>T did not map to a codon.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr23:91134232 G>A did not map to a codon.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr23:91873696 C>A did not map to a codon.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr23:91642835 C>G did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr23:91133769 C>A did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr23:91134269 C>G did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:91133290 G>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:91133291 G>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:91134301 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:91134148 C>A did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:91131787 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:91090897 T>C did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:91090648 T>C did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:91090729 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:91131889 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:91873699 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:91090942 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:91090550 C>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:91133257 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr23:91133663 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr23:91133552 G>A did not map to a codon.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr23:91133557 T>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:91132696 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:91642906 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:91642907 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr23:91132780 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr23:91131852 A>T did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr23:91090675 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:91090569 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:91133578 A>G did not map to a codon.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr23:91132436 A>G did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:91873366 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr23:91134208 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr23:91133748 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr23:91873877 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr23:91642805 C>A did not map to a codon.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr23:91133693 G>A did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:91133062 C>A did not map to a codon.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr23:91132769 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr23:91134143 G>C did not map to a codon.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr24:4968514 G>T did not map to a codon.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr24:5605923 C>T did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr24:5605717 C>T did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr24:4968224 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr24:4968436 C>T did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:141336332 G>A maps to NM_016580.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr5:141336462 G>A maps to NM_016580.2 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:141336083 G>A maps to NM_016580.2 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr5:141325323 C>T maps to NM_016580.2 A1059A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr5:141334956 C>T maps to NM_016580.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr5:141335105 G>A maps to NM_016580.2 Q771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:56106123 C>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:56106238 A>T maps to NM_001142763.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:56138616 C>A maps to NM_001142763.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr10:55581662 G>T maps to NM_001142763.1 V1948V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr10:55826621 T>A maps to NM_001142763.1 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:55566625 C>A maps to ENST00000373965 E1590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:55826606 G>C maps to NM_001142763.1 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr10:55626419 G>A maps to NM_001142763.1 S1238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:56106244 C>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:56077051 G>T maps to NM_001142763.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr10:56287614 T>C maps to NM_001142763.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:55568469 A>T maps to NM_001142769.1 G1785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr10:56077039 C>T maps to NM_001142763.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr10:55583102 G>C maps to NM_001142763.1 Y1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr10:56089400 G>A maps to NM_001142763.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:55587199 C>T maps to NM_001142763.1 P1445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:55663094 C>A maps to NM_001142763.1 E1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:56287637 C>G did not map to a codon.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr10:55780161 G>A maps to NM_001142763.1 D852D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr13:58208359 C>T maps to NM_001040429.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr13:58206751 C>G maps to NM_001040429.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr13:58208455 C>G maps to NM_001040429.2 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr13:58208416 C>T maps to NM_001040429.2 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr13:58207105 G>A maps to NM_001040429.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr13:58208416 C>T maps to NM_001040429.2 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr13:58208746 C>A maps to NM_001040429.2 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr13:58209107 C>A maps to NM_001040429.2 R810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr13:58208701 C>A maps to NM_001040429.2 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr13:58298780 C>T maps to NM_001040429.2 R945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr13:58207201 C>T maps to NM_001040429.2 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr13:58208986 G>T maps to NM_001040429.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr13:58208609 G>T maps to NM_001040429.2 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr13:58209158 C>T maps to NM_001040429.2 Q827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr23:99663450 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:99662472 C>A did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr23:99657784 C>G did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr23:99657582 G>C did not map to a codon.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr23:99662704 C>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:99551561 C>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:99662681 T>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:99662997 T>C did not map to a codon.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr23:99663056 G>A did not map to a codon.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr13:61985825 G>A maps to NM_022843.3 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr13:61986230 G>A maps to NM_022843.3 D667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:61986526 G>A maps to NM_022843.3 Q569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr13:61987982 G>T maps to NM_022843.3 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr13:61986155 A>G maps to NM_022843.3 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr13:61986442 G>A maps to NM_022843.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr4:30725116 G>A maps to NM_001173523.1 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr4:30723352 C>T maps to NM_001173523.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:30725161 C>T maps to NM_001173523.1 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr4:30723145 C>G maps to NM_001173523.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr4:30725737 A>G maps to NM_001173523.1 V898V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr13:53419749 C>T maps to NM_002590.2 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr13:53421569 G>A maps to NM_002590.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:53422220 C>T maps to NM_002590.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr13:53421548 G>A maps to NM_002590.2 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr13:67802499 C>A maps to NM_203487.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr13:67801806 G>A maps to NM_203487.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr13:67802485 A>T maps to NM_203487.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr13:67801351 G>A maps to NM_203487.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:67801102 A>T maps to NM_203487.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr13:67801134 C>A maps to NM_203487.2 E480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr13:67801522 A>G maps to NM_203487.2 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr5:140167197 G>T maps to NM_018900.2 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr5:140167278 C>T maps to NM_018900.2 N468N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:140167977 C>T maps to NM_018900.2 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr5:140165874 A>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140167950 G>A maps to NM_018900.2 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140166204 C>T maps to NM_018900.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr5:140167176 G>A maps to NM_018900.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr5:140167020 C>T maps to NM_018900.2 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr5:140237153 G>T maps to NM_018901.2 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140236299 G>T maps to NM_018901.2 G223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:140236322 G>C maps to NM_018901.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr5:140237237 C>T maps to NM_018901.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140236454 G>A maps to NM_018901.2 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr5:140236811 G>A maps to NM_018901.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr5:140248819 C>T maps to NM_018902.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr5:140250304 G>A maps to NM_018902.3 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:140250499 G>T maps to NM_018902.3 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140250826 G>T maps to NM_018902.3 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr5:140250226 C>T maps to NM_018902.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:140250370 G>A maps to NM_018902.3 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140249752 C>T maps to NM_018902.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr5:140250634 G>A maps to NM_018902.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140250598 C>T maps to NM_018902.3 D637D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:140256338 C>A maps to NM_018903.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr5:140255407 C>T maps to NM_018903.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140257258 G>T maps to NM_018903.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr5:140255326 C>A maps to NM_018903.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140255362 C>A maps to NM_018903.2 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140257123 C>T maps to NM_018903.2 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140255807 T>C maps to NM_018903.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr5:140257231 G>A maps to NM_018903.2 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr5:140256211 C>G maps to NM_018903.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr5:140256511 G>A maps to NM_018903.2 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr5:140263130 C>T maps to NM_018904.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr5:140263781 G>C maps to NM_018904.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr5:140264048 C>T maps to NM_018904.2 C732C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr5:140263295 C>T maps to NM_018904.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:140262395 C>T maps to NM_018904.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr5:140263295 C>T maps to NM_018904.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:140263364 G>A maps to NM_018904.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:140261864 C>T maps to NM_018904.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:140262128 C>T maps to NM_018904.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140263100 G>A maps to NM_018904.2 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140263334 G>A maps to NM_018904.2 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr5:140262179 C>T maps to NM_018904.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr5:140176609 G>T maps to NM_018905.2 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:140175844 G>A maps to NM_018905.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140176057 G>T maps to NM_018905.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr5:140175877 C>T maps to NM_018905.2 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:140175901 C>T maps to NM_018905.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:140176492 C>T maps to NM_018905.2 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:140176234 G>A maps to NM_018905.2 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr5:140176982 A>T maps to NM_031495.1 K812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr5:140181795 C>G maps to NM_018906.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr5:140182392 G>A maps to NM_018906.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140182401 G>T maps to NM_018906.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:140180928 G>T maps to NM_018906.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr5:140181873 A>T maps to NM_018906.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr5:140180883 C>A maps to NM_018906.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140182071 G>A maps to NM_018906.2 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr5:140182140 G>A maps to NM_018906.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:140188124 C>T maps to NM_018907.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr5:140188124 C>T maps to NM_018907.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr5:140189039 G>A maps to NM_018907.2 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr5:140188073 G>A maps to NM_018907.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr5:140188442 C>T maps to NM_018907.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140188562 G>A maps to NM_018907.2 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr5:140188817 G>A maps to NM_018907.2 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140186879 C>T maps to NM_018907.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140187185 G>A maps to NM_018907.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:140202874 T>C maps to NM_018908.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140201500 C>T maps to NM_018908.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140201579 C>T maps to NM_018908.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140203531 G>T maps to NM_018908.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr5:140201941 T>G maps to NM_018908.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:140202652 G>A maps to NM_018908.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr5:140202156 C>G maps to NM_018908.2 S266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:140209241 G>T maps to NM_018909.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr5:140209499 G>A maps to NM_018909.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:140207690 G>A maps to NM_018909.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140209499 G>A maps to NM_018909.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140209619 G>T maps to NM_018909.2 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:140209499 G>A maps to NM_018909.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr5:140207984 C>T maps to NM_018909.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr5:140209568 C>A maps to NM_018909.2 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr5:140209709 G>A maps to NM_018909.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:140215374 G>T maps to NM_018910.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:140214168 G>T maps to NM_018910.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:140216145 G>A maps to NM_018910.2 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:140215143 C>T maps to NM_018910.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr5:140215782 G>T maps to NM_018910.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:140215587 G>C maps to NM_018910.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr5:140215593 G>T maps to NM_018910.2 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr5:140215473 C>T maps to NM_018910.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:140214111 C>T maps to NM_018910.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140214060 C>T maps to NM_018910.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:140215184 C>A maps to NM_018910.2 S406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr5:140216299 C>T maps to NM_018910.2 Q778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:140223345 T>C maps to NM_031856.1 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140222261 T>C maps to NM_018911.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr5:140222762 C>A maps to NM_018911.2 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:140223206 G>C maps to NM_018911.2 T767T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:140221703 T>C maps to NM_018911.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr5:140222594 G>A maps to NM_018911.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr5:140222681 G>A maps to NM_018911.2 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr5:140222519 C>T maps to NM_018911.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:140230179 G>A maps to NM_031857.1 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140229948 C>T maps to NM_031857.1 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:140230191 C>T maps to NM_031857.1 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140229432 C>T maps to NM_031857.1 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:140228277 G>A maps to NM_031857.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr5:140229646 T>C maps to NM_031857.1 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140229612 C>T maps to NM_031857.1 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr5:140229462 G>A maps to NM_031857.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr5:140229354 T>G maps to NM_031857.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr5:140229381 A>G maps to NM_031857.1 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140308430 C>T maps to NM_018898.3 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr5:140307217 C>A maps to NM_018898.3 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:140348752 C>G maps to NM_018899.5 S801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr5:140348694 C>T maps to NM_018899.5 R782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:140346784 C>G maps to NM_018899.5 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr5:140346944 G>A maps to NM_018899.5 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140346539 C>T maps to NM_018899.5 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr5:140431658 C>T maps to NM_013340.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140433331 A>T maps to NM_013340.2 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:140433130 C>A maps to NM_013340.2 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:140431882 G>T maps to NM_013340.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:140574506 C>T maps to NM_018930.3 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140573627 C>A maps to NM_018930.3 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140573810 G>A maps to NM_018930.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr5:140574455 G>A maps to NM_018930.3 Q777Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:140580774 A>C maps to NM_018931.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:140579946 G>C maps to NM_018931.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr5:140580942 C>T maps to NM_018931.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140579469 C>T maps to NM_018931.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:140579438 G>A maps to NM_018931.2 W31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:140581329 C>G maps to NM_018931.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr5:140580972 C>T maps to NM_018931.2 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:140580819 C>A maps to NM_018931.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140580861 C>T maps to NM_018931.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:140579829 T>C maps to NM_018931.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr5:140580315 T>C maps to NM_018931.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr5:140580048 C>T maps to NM_018931.2 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:140588970 C>A maps to NM_018932.3 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr5:140590356 C>T maps to NM_018932.3 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:140589726 G>A maps to NM_018932.3 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140589606 G>A maps to NM_018932.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140590800 C>T maps to NM_018932.3 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:140590743 G>C maps to NM_018932.3 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr5:140589636 G>A maps to NM_018932.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr5:140589765 C>A maps to NM_018932.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr5:140590689 G>A maps to NM_018932.3 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr5:140594697 C>T maps to NM_018933.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140594900 C>T maps to NM_018933.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:140596038 G>T maps to NM_018933.2 E782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140595074 C>T maps to NM_018933.2 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr5:140595248 T>C maps to NM_018933.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:140604129 G>A maps to NM_018934.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr5:140604264 C>A maps to NM_018934.2 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr5:140626942 C>T maps to NM_018935.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:140626471 G>A maps to NM_018935.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr5:140627221 G>A maps to NM_018935.2 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr5:140626768 G>A maps to NM_018935.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr5:140563720 C>T maps to NM_020957.1 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:140562679 C>T maps to NM_020957.1 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr5:140564245 G>A maps to NM_020957.1 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140564269 G>A maps to NM_020957.1 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140563855 G>A maps to NM_020957.1 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr5:140563855 G>A maps to NM_020957.1 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr5:140562940 A>G maps to NM_020957.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:140476459 T>C maps to NM_018936.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr5:140476701 C>T maps to NM_018936.2 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:140476413 G>T maps to NM_018936.2 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140475885 C>T maps to NM_018936.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr5:140476000 T>C maps to NM_018936.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr5:140480301 G>A maps to NM_018937.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:140481672 A>G maps to NM_018937.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140481906 G>C maps to NM_018937.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:140482312 T>C maps to NM_018937.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr5:140480520 C>T maps to NM_018937.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr5:140482611 T>C maps to NM_018937.2 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr5:140481237 C>A maps to NM_018937.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:140502347 A>G maps to NM_018938.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:140503802 C>T maps to NM_018938.2 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr5:140503124 C>T maps to NM_018938.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr5:140501699 C>T maps to NM_018938.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:140502281 C>A maps to NM_018938.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140501984 G>A maps to NM_018938.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140502770 G>A maps to NM_018938.2 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr5:140502788 A>T maps to NM_018938.2 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr5:140503664 G>A maps to NM_018938.2 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr5:140515315 A>G maps to NM_015669.2 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:140516464 C>T maps to NM_015669.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr5:140516911 C>T maps to NM_015669.2 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140517376 C>T maps to NM_015669.2 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr5:140532030 A>G maps to NM_018939.2 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr5:140530096 G>T maps to NM_018939.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140532107 C>G maps to NM_018939.2 S757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:140530920 C>A maps to NM_018939.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr5:140531979 G>A maps to NM_018939.2 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr5:140531208 C>T maps to NM_018939.2 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:140554404 G>T maps to NM_018940.2 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:140553885 G>C maps to NM_018940.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:140554221 G>T maps to NM_018940.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr5:140553834 C>T maps to NM_018940.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:140553867 C>T maps to NM_018940.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:140554401 G>T maps to NM_018940.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140554212 C>T maps to NM_018940.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140554770 C>T maps to NM_018940.2 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr5:140558301 C>G maps to NM_019120.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:140558045 C>G maps to NM_019120.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr5:140559561 C>T maps to NM_019120.2 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr5:140558773 C>T maps to NM_019120.2 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr5:140559651 A>G maps to NM_019120.2 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr5:140558089 G>T maps to NM_019120.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr5:140559723 C>T maps to NM_019120.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr5:140559794 C>G maps to NM_019120.2 S727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr5:140559774 G>T maps to NM_019120.2 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:140711621 C>A maps to NM_018912.2 Y457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr5:140712458 C>T maps to NM_018912.2 P736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr5:140874378 C>A maps to NM_018915.2 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140712445 T>A maps to NM_018912.2 L732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:140712200 C>A maps to NM_018912.2 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140885037 G>A maps to NM_018915.2 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr5:140712044 G>A maps to NM_018912.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140794625 C>T maps to NM_018913.2 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr5:140794640 G>A maps to NM_018913.2 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:140795001 C>T maps to NM_018913.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140793083 G>A maps to NM_018913.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:140802482 C>T maps to NM_018914.2 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr5:140802776 C>T maps to NM_018914.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr5:140811288 A>G maps to NM_003735.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr5:140811312 G>A maps to NM_003735.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr5:140810886 C>T maps to NM_003735.2 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140811009 C>T maps to NM_003735.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140811954 C>T maps to NM_003735.2 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr5:140811312 G>A maps to NM_003735.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:140719965 C>A maps to NM_018915.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:140720877 C>T maps to NM_018915.2 I780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:140720646 C>T maps to NM_018915.2 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:140719023 A>T maps to NM_018915.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140720610 G>T maps to NM_018915.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:140719456 C>T maps to NM_018915.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:140720340 C>T maps to NM_018915.2 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr5:140720247 C>T maps to NM_018915.2 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr5:140719227 G>A maps to NM_018915.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr5:140719974 C>T maps to NM_018915.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr5:140718792 C>T maps to NM_018915.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr5:140725273 C>T maps to NM_018916.3 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:140735675 A>T maps to NM_018917.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:140735360 C>T maps to NM_018917.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr5:140734775 G>A maps to NM_018917.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr5:140736452 C>A maps to NM_018917.2 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr5:140745429 C>T maps to NM_018918.2 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr5:140745675 G>A maps to NM_018918.2 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:140744134 C>T maps to NM_018918.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140743968 C>A maps to NM_018918.2 C24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr5:140744163 G>A maps to NM_018918.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:140746179 G>A maps to NM_018918.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140745110 T>G maps to NM_018918.2 L405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr5:140745445 C>T maps to NM_018918.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:140755398 G>A maps to NM_018919.2 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:140754339 A>G maps to NM_018919.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr5:140755359 C>T maps to NM_018919.2 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:140754585 G>C maps to NM_018919.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:140755149 C>A maps to NM_018919.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:140755542 C>G maps to NM_018919.2 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr5:140762627 G>T maps to NM_018920.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr5:140764611 C>T maps to NM_018920.2 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:140764244 G>C maps to NM_018920.2 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr5:140763188 C>T maps to NM_018920.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:140763370 C>A maps to NM_018920.2 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:140764013 G>C maps to NM_018920.2 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr5:140762696 G>C maps to NM_018920.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr5:140774659 C>T maps to NM_032088.1 T760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140774686 C>T maps to NM_032088.1 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140773129 A>G maps to NM_032088.1 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr5:140784240 T>C maps to NM_018921.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140782699 G>T maps to NM_018921.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:140783493 G>A maps to NM_018921.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IH-01A-11D-A25Y-08 chr5:140732055 T>A maps to NM_018922.2 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr5:140731947 C>T maps to NM_018922.2 I707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140729973 C>A maps to NM_018922.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr5:140731530 C>T maps to NM_018922.2 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr5:140732208 C>A maps to NM_018922.2 I794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr5:140740502 C>T maps to NM_018923.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr5:140741081 C>T maps to NM_018923.2 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140740532 C>T maps to NM_018923.2 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr5:140742041 C>T maps to NM_018923.2 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:140751358 G>A maps to NM_018924.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:140751527 G>T maps to NM_018924.2 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:140751188 C>T maps to NM_018924.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:140751805 G>T maps to NM_018924.2 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr5:140751493 C>T maps to NM_018924.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr5:140768674 A>G maps to NM_003736.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:140768637 C>G maps to NM_003736.2 S396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr5:140769022 C>T maps to NM_003736.2 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr5:140768881 G>A maps to NM_003736.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:140788503 C>T maps to NM_018926.2 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140789265 G>T maps to NM_018926.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:140789448 G>A maps to NM_018926.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:140789784 G>A maps to NM_018926.2 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:140788983 G>T maps to NM_018926.2 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr5:140798772 G>A maps to NM_018927.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr5:140797509 G>T maps to NM_018927.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr5:140797443 G>T maps to NM_018927.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr5:140865759 G>T maps to NM_018928.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr5:140866932 T>C maps to NM_018928.2 C731C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr5:140865343 C>T maps to NM_018928.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr5:140866237 C>T maps to NM_018928.2 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:140868962 G>C maps to NM_018929.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr5:140868944 G>C maps to NM_018929.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:140869556 A>G maps to NM_018929.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr5:140871101 G>A maps to NM_018929.2 R765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:120388229 C>A maps to NM_001029996.3 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:120369264 C>T maps to NM_001029996.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:120362332 C>T maps to NM_001029996.3 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:120362332 C>A maps to NM_001029996.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:82878337 A>G maps to NM_015885.3 E663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:82880065 C>T maps to NM_015885.3 Q897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr2:74733101 C>T maps to NM_032673.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:74734012 T>C did not map to a codon.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr2:74733306 C>T did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr17:36896595 G>A maps to NM_007144.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr4:755158 G>A maps to NM_006315.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr10:93038048 T>G maps to NM_032373.3 Y249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:113852536 G>A maps to ENST00000246505 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr20:56139405 C>T maps to NM_002591.3 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr20:56137827 G>A maps to NM_002591.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:56139321 G>A maps to NM_002591.3 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr20:56139390 G>C maps to NM_002591.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr20:56137246 C>T maps to NM_002591.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:24566130 C>A maps to NM_004563.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr14:24569205 C>T maps to NM_004563.2 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:82583503 A>C maps to NM_033026.5 G2255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:82474616 T>A maps to NM_033026.5 S4672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:82474790 C>T maps to NM_033026.5 A4614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:82579580 C>A maps to NM_033026.5 V3441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:82582564 A>C maps to NM_033026.5 S2568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:82585440 G>A maps to NM_033026.5 R1610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:82784849 A>G maps to NM_033026.5 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:82584628 T>A maps to NM_033026.5 V1880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:82451862 C>A maps to NM_033026.5 G4913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:82763967 T>C maps to NM_033026.5 Q966Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:82584859 A>G maps to NM_033026.5 S1803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr7:82579178 T>A maps to NM_033026.5 T3575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:82545295 A>G maps to NM_033026.5 L4002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:82582944 T>A maps to NM_033026.5 K2442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:82763682 G>A maps to NM_033026.5 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:82545877 C>T maps to NM_033026.5 R3808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr7:82763691 G>A maps to NM_033026.5 T1058T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr7:82595454 C>A maps to NM_033026.5 E1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr8:52773447 T>C maps to NM_052937.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr20:62891515 G>A maps to NM_018257.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:5100330 C>T maps to NM_002592.2 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr21:47821490 G>A maps to NM_006031.5 Q1606Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr21:47851583 G>T maps to NM_006031.5 E2736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr21:47805844 C>T maps to NM_006031.5 G1137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr21:47775530 G>T maps to NM_006031.5 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr21:47776887 G>C did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr21:47831329 G>T maps to NM_006031.5 G1781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr21:47863721 G>C did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr21:47848406 G>A maps to NM_006031.5 T2531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr14:71485845 C>T maps to NM_014982.2 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr14:71444273 C>G maps to NM_014982.2 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr14:71493535 C>T maps to NM_014982.2 Q1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr14:71444808 T>A maps to NM_014982.2 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:71492877 C>T maps to NM_014982.2 C1076C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr1:233270851 C>T maps to NM_014801.3 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr1:233394938 G>A maps to NM_014801.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:233394515 G>A maps to NM_014801.3 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:233397850 A>G maps to NM_014801.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr11:65396094 C>T maps to NM_032223.2 F1244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr11:65393139 C>T maps to NM_032223.2 S1051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr11:65383850 C>T maps to NM_032223.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:65396296 C>A maps to NM_032223.2 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr11:65385112 C>T maps to NM_032223.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr7:100204122 C>A maps to NM_002593.3 Y270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr7:100205593 G>A maps to NM_002593.3 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr3:142561852 G>A maps to NM_013363.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:7697682 G>A maps to NM_174895.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr1:161254168 G>A maps to NM_001102566.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:95746663 G>A maps to NM_000439.4 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr5:95768695 G>A maps to NM_000439.4 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr5:95728767 A>T maps to NM_000439.4 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:17462558 G>A maps to NM_002594.2 W587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr20:17434529 C>T maps to NM_002594.2 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr20:17446183 C>T maps to NM_002594.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr20:17446186 G>A maps to NM_002594.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr20:17446003 G>A maps to NM_002594.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr20:17434460 C>T maps to NM_002594.2 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr9:78710972 G>T maps to NM_001190482.1 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr9:78774045 G>C maps to NM_001190482.1 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr15:101922382 G>A maps to NM_002570.3 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:117098988 C>T maps to NM_004716.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr11:117100338 C>T maps to NM_004716.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr2:70503971 G>A maps to NM_016297.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr5:148747931 G>A maps to NM_024028.3 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr5:148743767 C>T maps to NM_024028.3 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:195965714 C>T maps to NM_005017.2 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr17:79866788 G>A maps to NM_001184917.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr7:98995533 G>A maps to NM_014891.6 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr7:99002547 C>A maps to NM_014891.6 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr2:242793392 G>A maps to NM_005018.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:167437848 C>T did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr10:105172880 C>T maps to NM_014976.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr10:105176372 C>T maps to NM_014976.1 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr10:105172994 G>A maps to NM_014976.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:105174041 T>C maps to NM_014976.1 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr10:105205278 G>A maps to NM_014976.1 E1863E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr10:105174032 T>C maps to NM_014976.1 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr10:105201731 G>A maps to NM_014976.1 T1569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:34912526 C>T maps to NM_032346.1 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:34912555 C>G maps to NM_032346.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr19:34895681 G>T maps to NM_032346.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr10:112641195 C>T maps to NM_014456.4 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr9:125585306 C>T maps to NM_005388.4 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:125588972 G>A maps to NM_005388.4 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:125588916 G>T maps to NM_005388.4 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr2:101188228 G>A maps to NM_024065.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr11:773588 C>A maps to NM_182612.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:165792846 C>T maps to NM_001130690.1 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr6:165827150 G>T maps to NM_001130690.1 Y372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:165862442 T>A maps to NM_001130690.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:165809837 G>A maps to NM_001130690.1 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:178936873 G>T maps to NM_016953.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:178592822 G>A maps to NM_016953.3 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr2:178762844 G>A maps to NM_016953.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:178494257 C>T maps to NM_016953.3 P893P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr2:178936620 G>A maps to NM_016953.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr2:178681636 G>A maps to NM_016953.3 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr3:57542168 G>A maps to NM_177966.5 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:183104925 C>T maps to NM_005019.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:183104853 A>T maps to NM_005019.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:183129092 G>A maps to NM_005019.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr2:183070677 T>C maps to NM_005019.3 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:54969815 G>T maps to NM_000924.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:31890355 C>G did not map to a codon.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr7:31862846 G>A maps to NM_001191057.1 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:72290598 G>T maps to NM_002599.3 I745I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:72292992 T>C did not map to a codon.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr11:72299886 G>A maps to NM_002599.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:72292984 G>A maps to NM_002599.3 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr11:72296610 G>C maps to NM_002599.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr11:72290388 G>A maps to NM_002599.3 I765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr11:72296443 C>T maps to NM_002599.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr12:20833103 C>T maps to NM_000921.3 Q1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr12:20766438 C>A maps to NM_000921.3 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:20799469 T>C maps to NM_000921.3 Y766Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:20769240 T>C maps to NM_000921.3 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:20801788 G>A maps to NM_000921.3 K911K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr12:20833090 G>C maps to NM_000921.3 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:20806918 C>A maps to NM_000921.3 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr12:20833108 G>A maps to NM_000921.3 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr12:20792841 A>G maps to NM_000921.3 E734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:14853184 G>C did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr11:14853293 G>T maps to NM_000922.3 G689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:10574473 C>A maps to NM_001111307.1 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr1:66833699 T>C maps to NM_001037341.1 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr1:66379017 G>T maps to NM_001037341.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:66827445 C>G maps to NM_001037341.1 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr1:66384408 A>C maps to NM_001037341.1 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:18321949 G>C maps to NM_000923.3 S643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr19:18329001 G>A maps to NM_000923.3 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:18331311 C>T maps to NM_000923.3 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr5:59284493 G>A maps to ENST00000502484 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr5:58273017 G>A maps to NM_001104631.1 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:144882643 C>G maps to NM_014644.4 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:144882463 G>A maps to NM_014644.4 F1185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr1:144886197 C>T maps to NM_014644.4 E1012E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:145015937 C>T maps to NM_001198832.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:145075790 G>T maps to NM_022359.5 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:144879068 G>A maps to NM_014644.4 L1461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:144852490 G>A maps to NM_014644.4 S2336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:144922248 G>A maps to NM_014644.4 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:144931375 C>T maps to NM_001002811.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr1:144854604 G>A maps to NM_014644.4 Q2289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:144864166 C>T maps to NM_014644.4 E1976E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:145015894 G>A maps to NM_001198832.1 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr1:144994656 G>T maps to NM_014644.4 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr1:144879255 C>T maps to NM_014644.4 L1398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr1:144871747 G>T maps to NM_014644.4 S1738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:120481449 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:651153 C>T maps to NM_000283.3 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr4:619654 G>A maps to NM_000283.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:95372754 C>G maps to NM_006204.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:95415575 C>T maps to NM_006204.3 F665F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr10:95381780 G>A maps to NM_006204.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr12:15131062 A>G maps to NM_006205.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr6:136476803 C>T maps to NM_018945.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr15:85669604 G>A maps to NM_002605.2 Q751Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:76700609 C>T maps to NM_003719.3 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:76607879 T>A did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr5:76624876 G>T maps to NM_003719.3 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr5:76645308 C>T maps to NM_003719.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr5:76649231 G>C did not map to a codon.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr21:44153464 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr21:44152178 G>C did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:550595 G>T maps to NM_002607.5 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:552063 C>G maps to NM_002607.5 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr4:157771473 C>G maps to NM_016205.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:103870956 G>A maps to NM_025208.4 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:103866936 G>A maps to NM_025208.4 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr11:103780430 T>A maps to NM_025208.4 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr11:103780423 A>T maps to NM_025208.4 *371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:55136803 C>T maps to NM_006206.4 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:55131136 C>A maps to NM_006206.4 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:55161417 G>T maps to ENST00000507166 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr4:55138606 T>C maps to NM_006206.4 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:149516592 C>T maps to NM_002609.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:149500534 G>A maps to NM_002609.3 I834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:149514448 C>T maps to NM_002609.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr5:149506163 C>T maps to NM_002609.3 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:149506118 G>T maps to NM_002609.3 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr8:17491706 C>A maps to NM_006207.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr8:17434769 C>G maps to NM_006207.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr23:19373620 G>C did not map to a codon.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr23:19369426 G>A did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr23:19377654 G>A did not map to a codon.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr23:19373836 G>A did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr4:96762281 C>T maps to NM_005390.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr4:96761393 C>T maps to NM_005390.4 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:96761795 C>A maps to NM_005390.4 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr4:96761918 C>T maps to NM_005390.4 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr4:96762053 G>A maps to NM_005390.4 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr4:96762005 A>T maps to NM_005390.4 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr16:335008 C>T maps to NM_006849.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:44058970 C>G maps to NM_005313.4 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr15:44053673 C>G maps to NM_005313.4 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:148702239 G>A maps to NM_004911.4 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr7:148718077 G>A maps to NM_004911.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:122811250 G>T maps to NM_006810.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:122842956 C>T maps to NM_006810.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:122808106 C>T maps to NM_006810.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:122842923 G>A maps to NM_006810.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:10942635 G>A maps to ENST00000381611 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr16:20386257 C>T maps to NM_174924.1 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:20410586 G>T maps to NM_174924.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr16:20371930 G>A maps to NM_174924.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr16:20371928 C>T maps to NM_174924.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr16:20370763 G>A maps to NM_174924.1 Y544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:173429335 C>G maps to ENST00000392571 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr23:24521476 A>T did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:24546213 G>A did not map to a codon.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr23:24512954 C>G did not map to a codon.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr7:95224334 C>T maps to NM_002612.3 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:97050585 G>A maps to NM_020992.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:186425654 G>A maps to NM_014476.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:186423555 T>C maps to NM_014476.4 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:95496978 C>T maps to NM_006457.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr4:95496939 G>A maps to NM_006457.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr5:176910983 C>A did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr8:94934632 C>T maps to NM_001161778.1 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr16:2636823 G>T maps to NM_002613.3 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr1:13936916 C>A maps to NM_006474.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr4:39929691 G>A maps to NM_001100399.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr4:39978104 C>T maps to NM_001100399.1 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr4:39851151 G>A maps to NM_001100399.1 S1069S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr16:15122789 G>A maps to NM_015027.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr16:15127243 G>A maps to NM_015027.2 E600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr16:15130130 G>A maps to NM_015027.2 *789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr16:15128327 G>A maps to NM_015027.2 Q640Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr22:38061757 G>T maps to ENST00000442465 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr20:1961151 G>A maps to NM_024411.4 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr23:69507977 A>C did not map to a codon.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr23:69507126 G>A did not map to a codon.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr5:32058192 A>G maps to NM_178140.2 E728E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:31983278 C>T maps to NM_178140.2 C165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:32091008 G>C maps to NM_178140.2 L2485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr5:32088329 G>T maps to NM_178140.2 S1592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr5:31983413 G>A maps to NM_178140.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr5:32074068 C>T maps to NM_178140.2 R953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr5:32074068 C>T maps to NM_178140.2 R953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr5:32098723 C>T maps to NM_178140.2 P2734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:119059094 G>T maps to ENST00000392817 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:153070324 C>T did not map to a codon.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr10:102781635 G>A maps to NM_001195263.1 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr10:119134267 G>A maps to NM_173791.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:119042841 T>C maps to NM_173791.3 L1134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr16:21995734 C>A maps to ENST00000424898 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr16:21995691 C>A maps to ENST00000424898 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr3:73437117 C>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:73433787 G>A maps to NM_015009.1 C643C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr3:73433316 G>T maps to NM_015009.1 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr3:73432535 G>A maps to NM_015009.1 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr3:73440228 C>T maps to NM_015009.1 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr3:73434063 G>A maps to NM_015009.1 D551D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr12:41966827 G>T maps to NM_001164595.1 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr12:41961613 G>A maps to NM_001164595.1 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:41966993 G>T maps to NM_001164595.1 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:41966949 C>A maps to NM_001164595.1 S790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:41967304 C>T maps to NM_001164595.1 D908D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:160183266 G>A maps to ENST00000368075 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:160181450 C>T maps to ENST00000368075 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr1:156876576 T>A maps to NM_001080471.1 Y183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:156882414 G>T did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:156884445 C>T maps to NM_001080471.1 D990D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr1:156874632 C>T maps to NM_001080471.1 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156880482 G>A maps to NM_001080471.1 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr1:156873780 C>T maps to NM_001080471.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:118577300 C>A maps to NM_002567.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:22675245 G>T maps to NM_144962.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:4135746 C>G maps to NM_206836.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:216904000 G>C maps to NM_018441.5 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:57326338 G>T maps to NM_006210.2 Y1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr19:57328077 G>A maps to NM_006210.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:57327571 G>A maps to NM_006210.2 D746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr19:57328507 G>C maps to NM_006210.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr14:56755237 C>T maps to NM_021255.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr14:56755319 G>T maps to NM_021255.2 G159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr14:56763457 C>T maps to NM_021255.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr17:4575882 T>G maps to ENST00000301396 P945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:4576370 G>A maps to ENST00000301396 Q783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:17409125 G>A maps to NM_148172.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr17:8051405 C>A maps to NM_002616.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr17:8049768 G>A maps to NM_002616.2 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr17:8044496 G>A maps to NM_002616.2 A1254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr17:8047138 G>A maps to NM_002616.2 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr2:239186553 C>A maps to NM_022817.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:239170869 C>T maps to NM_022817.2 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr2:239162044 G>A maps to NM_022817.2 H873H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:7902813 G>C maps to ENST00000377532 *1211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:7870005 G>T maps to ENST00000377532 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:30977574 C>T maps to NM_014303.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr4:152593946 G>A maps to NM_004564.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:92134133 C>A maps to NM_000466.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr7:92136440 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:2337937 C>A maps to NM_153818.1 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr15:90229777 C>G did not map to a codon.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr15:90229713 C>T maps to NM_003847.1 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:145522726 C>A maps to NM_003846.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr1:145522768 C>T maps to NM_003846.2 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr2:61259090 C>T maps to NM_002618.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:10659376 A>C maps to NM_004565.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr1:10535034 G>C maps to NM_004565.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:160253343 C>T maps to NM_002857.3 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:160249958 G>A maps to NM_002857.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr8:77896368 T>A maps to NM_001172087.1 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr8:77896225 G>A maps to NM_001172087.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr22:18570816 C>G maps to NM_017929.5 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:143795985 T>C maps to NM_003630.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr12:7361163 G>A maps to NM_001131023.1 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr12:7343014 C>T maps to NM_001131023.1 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr3:179576921 G>C maps to NM_016559.1 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:179576912 G>A maps to NM_016559.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr3:179576863 T>A maps to NM_016559.1 K270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr3:179526209 C>A maps to NM_016559.1 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr3:179519702 G>C maps to NM_016559.1 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr6:42935144 G>A maps to NM_000287.3 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr6:42936616 G>A maps to NM_000287.3 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr6:42946177 C>T maps to NM_000287.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr4:74846998 C>T maps to NM_002619.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:8170876 C>T maps to NM_012393.2 D1092D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr17:8172073 C>T maps to NM_012393.2 Y1202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:8159847 C>A maps to NM_012393.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr17:8172073 C>T maps to NM_012393.2 Y1202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr17:8172142 C>T maps to NM_012393.2 A1225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:161072166 T>C did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:54971903 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr23:54971912 G>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:54978368 C>G did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:54985327 G>T did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:6257226 C>T maps to NM_004566.3 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr10:6261635 C>G maps to NM_004566.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:6263357 G>C maps to NM_004566.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr10:6255709 A>G maps to NM_004566.3 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr3:48560991 C>G maps to NM_004567.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr21:45730966 G>T did not map to a codon.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr21:45732960 C>T maps to NM_002626.4 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:45745854 A>G maps to NM_002626.4 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr21:45732996 C>T maps to NM_002626.4 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr21:45746600 C>T maps to NM_002626.4 H733H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:48535526 C>T maps to NM_001166686.1 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr12:48526695 C>T maps to NM_001166686.1 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr12:48524144 G>C did not map to a codon.
Alternatively spliced codon TCGA-CV-7095-01A-21D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr3:149684320 C>T maps to NM_053024.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:60971080 C>T maps to NM_001079807.1 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:77224508 G>A did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:77224531 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:77224940 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:77225021 C>T did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:197767386 T>A maps to NM_024989.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:197738420 C>G maps to NM_024989.3 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:197767326 G>T maps to NM_024989.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr2:197763048 G>A maps to NM_024989.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:197729785 C>A maps to NM_024989.3 G596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:3845336 C>T maps to NM_014489.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:3845189 C>T maps to NM_014489.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:37842183 G>A maps to NM_033419.3 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:28268866 C>G maps to NM_032507.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr6:28264675 C>G maps to NM_032507.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr6:28269232 C>G maps to NM_032507.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr6:28268866 C>G maps to NM_032507.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr6:28268548 G>A maps to NM_032507.3 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:249211311 C>T maps to NM_170725.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr10:50724314 G>A maps to ENST00000515869 C750C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr15:34395157 G>A maps to NM_152595.4 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr15:34395295 C>G maps to NM_152595.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:230473019 C>T maps to ENST00000321327 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:230492801 G>A maps to ENST00000321327 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr1:230492801 G>A maps to ENST00000321327 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:98155358 C>T maps to ENST00000325141 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr1:10477151 C>G maps to NM_002631.2 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr1:10479724 C>G maps to NM_002631.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:114573586 C>G maps to NM_005023.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:114588909 C>T maps to NM_005023.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr23:77365366 C>G did not map to a codon.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr23:77380863 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr23:77378329 A>C did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:77365393 C>G did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:49754393 T>C maps to NM_138733.4 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:49754449 G>A maps to NM_138733.4 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:49753699 C>A maps to NM_138733.4 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:49754867 T>C maps to NM_138733.4 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:17631871 G>A maps to NM_012088.2 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr19:15587144 C>T maps to NM_052890.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr19:15582726 C>T maps to NM_052890.3 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:64095638 A>T maps to NM_002633.2 K146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr4:37848659 G>A maps to NM_018290.3 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr11:74058231 G>A maps to NM_173582.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:74056564 G>C maps to NM_173582.3 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr11:74053583 T>C maps to NM_173582.3 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr6:83884176 C>T maps to ENST00000416472 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr19:18468194 G>C maps to NM_017712.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr15:99512850 G>A maps to NM_001102612.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:100933382 T>G maps to NM_000926.4 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr11:100999747 C>T maps to NM_000926.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr11:100909996 G>A maps to NM_000926.4 V884V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:118370575 G>A did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr23:118370415 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr23:118370342 T>C did not map to a codon.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr6:13206092 G>A maps to NM_030948.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:13053693 G>A maps to NM_030948.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr6:13230291 A>C maps to NM_030948.1 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:12749885 G>A maps to NM_030948.1 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:12719056 C>T maps to NM_030948.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr6:144093547 C>A maps to NM_001100164.1 Y462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr6:144086484 C>G maps to NM_001100164.1 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr6:144033315 G>A maps to NM_001100164.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr20:58349448 G>T maps to NM_080672.3 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:28817490 A>G maps to NM_023923.3 E625E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:28806961 G>A did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:28793130 C>T maps to NM_023923.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr12:9083497 G>T maps to ENST00000433083 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:33820074 C>T maps to ENST00000419414 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:33832908 G>A maps to ENST00000419414 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr1:33837994 C>T maps to ENST00000419414 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr3:169824652 G>T maps to NM_024947.3 S812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:22132679 C>G did not map to a codon.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr23:22117214 G>A did not map to a codon.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr23:22095597 G>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:22129608 G>C did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:33382809 G>T maps to NM_024165.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:27244464 C>G maps to NM_001033561.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr17:27239674 G>C maps to NM_001033561.1 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:6680239 C>T maps to NM_153812.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr7:11091406 G>A maps to ENST00000303905 T827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr5:133900185 C>T maps to ENST00000448712 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:46915516 G>C did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr23:46915503 G>C did not map to a codon.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr23:46887485 G>T did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr23:46884228 G>A did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr23:46887307 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:46857541 C>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:129770158 C>T maps to NM_199320.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:129776937 C>T maps to NM_199320.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:129778491 G>A did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:129770158 C>T maps to NM_199320.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr9:123632757 C>T maps to NM_015651.1 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr9:96418258 C>T maps to NM_005392.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr9:96418869 A>C maps to NM_005392.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:96437209 T>C maps to NM_005392.3 V876V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr20:34519276 G>A maps to NM_016436.4 K737K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr20:34505467 C>T maps to NM_016436.4 Q630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:34515746 C>T maps to NM_016436.4 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr20:34459692 G>A maps to NM_016436.4 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:133856459 A>G maps to ENST00000395386 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:133816971 T>G maps to ENST00000395386 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr8:133858164 A>G maps to ENST00000395386 V1018V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:45970964 G>A maps to ENST00000257821 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:45958120 C>G did not map to a codon.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr22:45309884 G>C maps to NM_138415.3 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr6:64416738 A>G maps to NM_015153.2 V1228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr6:64416675 C>T maps to NM_015153.2 F1207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr6:64394046 C>T maps to NM_015153.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr6:64422706 G>A maps to NM_015153.2 E1741E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr6:64408456 A>T maps to NM_015153.2 R982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr6:64422439 T>A maps to NM_015153.2 P1652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr23:133549099 G>A did not map to a codon.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr23:133527592 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr3:52457248 G>A maps to ENST00000454052 K355K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr23:54014373 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:120283057 G>A maps to NM_006623.3 W332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:120283058 G>A maps to NM_006623.3 W332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:120254773 G>A maps to NM_006623.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:79668288 G>A maps to NM_017934.5 R1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:71855024 G>T did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr23:71887230 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:71932656 C>T did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:71802360 C>A did not map to a codon.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr23:71800892 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:71800901 C>T did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:18972500 G>T did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr23:18924611 C>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:18911700 C>A did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:18956825 G>T did not map to a codon.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr23:18972424 G>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:18913305 G>A did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr23:18912410 G>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:18972376 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:18919704 G>T did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr23:18949758 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:18972464 G>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:18924673 G>C did not map to a codon.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr23:18959755 G>T did not map to a codon.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr16:47733261 G>A maps to NM_000293.2 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr16:47694702 C>G maps to NM_000293.2 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr16:47644776 G>A maps to NM_000293.2 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr16:47722982 C>T maps to NM_000293.2 Q888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:118513087 C>T maps to NM_015157.2 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:118499168 C>T maps to NM_015157.2 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr11:118516500 G>A maps to NM_015157.2 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr11:118498621 C>T maps to NM_015157.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr11:118498654 C>T maps to NM_015157.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:118516314 G>A maps to NM_015157.2 E1121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:111688637 A>G maps to NM_001134438.1 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr3:111688637 A>G maps to NM_001134438.1 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr3:111688670 C>T maps to NM_001134438.1 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:111603462 G>A maps to NM_001134438.1 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:111632431 C>T maps to NM_001134438.1 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:44008098 C>A maps to NM_198850.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr19:44008240 C>G maps to NM_198850.3 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr18:60642821 G>A maps to NM_194449.2 L1316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr18:60642650 G>A maps to NM_194449.2 Q1259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr16:71686698 G>A maps to NM_015020.2 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:71683623 G>A maps to NM_015020.2 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr4:41749527 G>A maps to NM_003924.3 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:41748273 G>A maps to NM_003924.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr4:41749389 G>A maps to NM_003924.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:605231 G>A maps to ENST00000264555 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr11:596952 C>G maps to ENST00000264555 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr11:607243 G>A maps to ENST00000264555 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr11:607618 G>A maps to ENST00000264555 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr1:114269128 G>A maps to NM_006608.2 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr7:77531082 T>C maps to ENST00000427986 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:131704016 C>T maps to NM_174933.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr9:131696335 C>T maps to NM_001100876.1 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr10:61005099 G>T maps to NM_032439.3 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:60936717 C>T maps to NM_032439.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:75761351 G>T did not map to a codon.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr20:43803614 C>T maps to NM_002638.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:25256887 G>A did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr4:25258232 G>A maps to NM_018323.3 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr4:25258217 A>G maps to NM_018323.3 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr22:21174108 A>G maps to NM_058004.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:21157490 G>A maps to NM_058004.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:21107309 C>T maps to NM_058004.2 K898K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr22:21156361 G>A maps to NM_058004.2 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr22:21083734 T>C maps to NM_058004.2 E1458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr18:44392404 T>G maps to NM_004671.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr18:44424057 C>A maps to NM_004671.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:145581456 G>T maps to NM_006099.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:145581457 C>T maps to NM_006099.3 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:4037461 G>A maps to NM_015897.2 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:73401256 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:85779726 G>A maps to ENST00000393343 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:85712202 T>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:85701437 A>G maps to ENST00000393343 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:229890386 G>A maps to NM_017933.4 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr15:65114582 C>T maps to ENST00000333425 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:15349560 C>G did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:15344162 C>T did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr23:15349713 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:15342944 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:15342945 G>A did not map to a codon.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr1:172411035 G>A maps to NM_153747.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:172410874 G>A maps to NM_153747.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:514998 G>A maps to NM_001127178.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:494215 A>G maps to NM_001127178.1 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr4:515514 C>T maps to NM_001127178.1 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:77558067 G>A maps to NM_005482.2 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:16203243 C>T maps to NM_004278.3 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr17:16120650 G>A maps to NM_004278.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:160001163 G>A maps to NM_145167.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:160001445 G>A maps to NM_145167.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr18:59777190 G>A maps to NM_176787.4 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr16:632904 G>T maps to NM_148920.1 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr16:624736 G>A maps to NM_148920.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr16:630910 C>T maps to NM_148920.1 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:207106356 C>A maps to NM_002644.3 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr1:207105857 G>A maps to NM_002644.3 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr1:207109002 C>T maps to NM_002644.3 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:207105831 C>A maps to NM_002644.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:26897882 C>T maps to NM_033198.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr17:26885584 C>A maps to NM_033198.3 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:26881399 G>A maps to NM_033198.3 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr20:44045291 C>A maps to NM_015937.4 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr20:33148762 G>C maps to NM_080476.4 Y405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr20:33176366 G>A maps to NM_080476.4 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr20:33173311 G>A maps to NM_080476.4 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr17:34893087 G>A maps to NM_178517.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr17:34893501 G>A maps to NM_178517.3 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:196674504 G>A maps to NM_025163.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr19:49952899 T>A maps to NM_017916.2 K57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr10:98386579 G>A maps to NM_152309.2 D518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr10:98469372 G>A maps to NM_152309.2 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr11:17140214 G>T maps to NM_002645.2 I1004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr11:17191185 C>A maps to NM_002645.2 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:17139067 T>C maps to NM_002645.2 K1062K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:204433258 A>G maps to NM_002646.3 C397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr1:204438849 G>A maps to NM_002646.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:18644452 T>G maps to NM_004570.4 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr12:18499617 C>A maps to NM_004570.4 Y491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr12:18524215 G>T maps to NM_004570.4 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:18435605 T>C maps to NM_004570.4 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:18715687 C>T maps to NM_004570.4 I1173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:178942527 C>T maps to NM_006218.2 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr3:138383966 A>C maps to NM_006219.1 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr3:138433522 G>A maps to NM_006219.1 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:9787004 G>A maps to ENST00000361110 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr1:9784116 C>T maps to ENST00000361110 H919H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:9775651 C>T maps to ENST00000361110 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:106509406 G>T maps to NM_002649.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr7:106508731 C>T maps to NM_002649.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:106509367 C>A maps to NM_002649.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:106508710 C>G maps to NM_002649.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr7:106545636 A>C maps to NM_002649.2 G1038G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:106508497 C>T maps to NM_002649.2 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr7:106509635 C>T maps to NM_002649.2 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr7:106524652 A>G maps to NM_002649.2 A938A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr7:106509635 C>T maps to NM_002649.2 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr22:31679216 T>A maps to NM_052880.4 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:67591278 A>T maps to ENST00000396611 K593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr5:67588980 C>T maps to ENST00000396611 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr1:46512293 C>T maps to NM_001114172.1 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:130463594 G>A maps to NM_014602.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:130442378 C>G maps to NM_014602.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr3:130452854 G>C maps to NM_014602.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:130452398 G>A maps to NM_014602.2 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:130405133 C>T maps to NM_014602.2 A1132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr3:130427222 C>T maps to NM_014602.2 Q815Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:8812416 C>A maps to NM_001142633.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr17:8793323 C>T maps to NM_001142633.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:8790442 G>C maps to NM_001142633.1 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:8791555 C>T maps to NM_001142633.1 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr17:8789597 G>T maps to NM_001142633.1 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr17:8732224 G>T maps to NM_001010855.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:8738682 T>C maps to NM_001010855.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr2:209138377 G>T maps to NM_015040.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:209180090 C>T maps to NM_015040.3 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr2:209136284 T>C maps to NM_015040.3 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr2:209191021 C>T maps to NM_015040.3 Q1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr2:209179973 A>T maps to NM_015040.3 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr6:37140829 G>A maps to ENST00000373507 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr6:37140899 G>T maps to ENST00000373507 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:71401626 G>A did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:77006224 C>G did not map to a codon.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr7:76984547 C>A maps to NM_017439.3 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr7:76984646 C>A maps to NM_017439.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr7:142836665 T>G maps to NM_002652.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr7:142836629 C>G maps to NM_002652.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr10:22898586 G>A maps to NM_005028.4 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr12:57992918 C>T maps to NM_024779.4 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr12:57988993 C>T maps to NM_024779.4 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:151210742 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:151205157 G>A maps to NM_001135638.1 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr1:151196742 C>G maps to NM_001135638.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr9:71606109 G>A maps to NM_003558.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr9:71503928 G>A maps to NM_003558.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr9:71532546 G>A maps to NM_003558.2 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:3664870 C>T maps to NM_012398.2 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:3641707 G>A maps to NM_012398.2 D594D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:130687444 G>A maps to NM_001135219.1 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:130687477 G>C maps to NM_001135219.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:130684359 C>G maps to NM_001135219.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:15497927 G>T did not map to a codon.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr22:32017675 G>A maps to ENST00000422296 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:1437392 T>C maps to ENST00000313486 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr17:65688859 C>T maps to NM_012417.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:65628288 A>T maps to NM_012417.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr11:67263727 C>T maps to NM_004910.2 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr11:67261027 G>A maps to NM_004910.2 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:67262397 C>T maps to NM_004910.2 A887A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:67262616 G>A maps to NM_004910.2 V854V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:67271645 G>T maps to NM_004910.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr11:67262421 G>A maps to NM_004910.2 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr12:123481121 G>A maps to NM_020845.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr12:123475221 T>C maps to NM_020845.2 Q813Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:123485363 G>A maps to NM_020845.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:123482023 C>T maps to NM_020845.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr12:123489928 G>A maps to NM_020845.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:6373603 G>A maps to NM_031220.3 D583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr17:6373654 G>T maps to NM_031220.3 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:3190186 T>A maps to ENST00000380989 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr10:3180434 C>T maps to ENST00000380989 V1005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr10:3197894 C>T maps to ENST00000380989 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr5:134364687 G>T maps to NM_002653.4 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:134364546 G>A maps to NM_002653.4 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr5:134364504 C>T maps to NM_002653.4 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr4:111539442 G>C maps to NM_153426.1 Y264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:130847536 G>A maps to NM_004764.4 A681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:130827638 G>A maps to NM_004764.4 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:130851758 A>G maps to NM_004764.4 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:130827177 C>T maps to NM_004764.4 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr12:130841545 G>A maps to NM_004764.4 W496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr8:22145046 T>C maps to NM_001135721.1 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:22210624 C>T maps to NM_001135721.1 Q853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr8:22212930 G>A maps to NM_001135721.1 K945K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:25150054 T>G maps to NM_001008496.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr22:25131808 G>A maps to NM_001008496.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:94340738 C>T maps to NM_152431.2 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:68381790 C>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:68382106 T>A did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr23:68381830 A>C did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:68381192 C>T did not map to a codon.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr16:2166553 G>A maps to NM_001009944.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr16:2154547 C>T maps to NM_001009944.2 A2704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr16:2150559 C>T maps to NM_001009944.2 T3135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:2159506 G>A maps to NM_001009944.2 I1887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:2167055 T>C did not map to a codon.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:2164257 G>C maps to NM_001009944.2 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr16:2159542 G>C maps to NM_001009944.2 V1875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr16:2158546 G>A maps to NM_001009944.2 P2207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2158531 G>A maps to NM_001009944.2 S2212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2158552 G>A maps to NM_001009944.2 A2205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:2143019 G>A maps to NM_001009944.2 H3697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr16:2160310 G>A maps to NM_001009944.2 S1619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr16:2143661 G>A maps to NM_001009944.2 S3633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:47870816 G>C maps to NM_138295.3 Y2157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr7:47915767 G>A maps to NM_138295.3 H1237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr7:47944860 A>T maps to NM_138295.3 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:47913504 G>A maps to NM_138295.3 G1296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr7:47882700 G>T maps to NM_138295.3 V1768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:47913531 G>A maps to NM_138295.3 P1287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:47842807 C>T maps to NM_138295.3 G2654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:47947812 G>A maps to NM_138295.3 N421N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:81145965 G>A maps to NM_052892.3 F2261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr16:81219115 C>A maps to NM_052892.3 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr16:81236233 G>A maps to NM_052892.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr16:81181077 C>T maps to NM_052892.3 K1671K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr16:81181079 T>A maps to NM_052892.3 K1671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:81134880 C>T maps to NM_052892.3 E2408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:81193336 G>A maps to NM_052892.3 D1262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr16:81208414 G>T maps to NM_052892.3 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr16:81236229 G>A maps to NM_052892.3 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr4:88973182 C>G maps to NM_000297.2 S530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr4:88986916 G>A maps to NM_000297.2 K748K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:102054859 G>A maps to NM_016112.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:102050188 C>A maps to NM_016112.2 G699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr10:102056007 G>C maps to NM_016112.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr10:102089668 G>T maps to NM_016112.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr5:137228187 C>T maps to ENST00000230643 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr22:46653800 G>A maps to NM_006071.1 L1807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr22:46657866 G>C maps to NM_006071.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr22:46655439 G>A maps to NM_006071.1 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr22:46658433 G>A maps to NM_006071.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr22:46652484 C>T maps to NM_006071.1 G2245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr22:46654044 C>T maps to NM_006071.1 L1725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr22:46654119 C>T maps to NM_006071.1 K1700K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:51947242 G>A maps to NM_138694.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:51890863 C>T maps to NM_138694.3 W1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:51890827 C>G maps to NM_138694.3 A1260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:51893045 C>G maps to NM_138694.3 S1156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr6:51889465 G>A maps to NM_138694.3 Y1714Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:51890957 G>C maps to NM_138694.3 S1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:51890329 C>T maps to NM_138694.3 S1426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:51484070 C>T maps to NM_138694.3 L4011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr6:51524465 C>T maps to NM_138694.3 L3486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr6:51920456 G>A maps to NM_138694.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:51921547 G>A maps to NM_138694.3 C547C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:51524372 G>A maps to NM_138694.3 P3517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:51924786 C>T maps to NM_138694.3 W391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr6:51944775 C>A maps to NM_138694.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr6:51949722 G>T maps to NM_138694.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:51768498 T>A maps to NM_138694.3 R2298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:51892672 G>A maps to NM_138694.3 Y1194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:51613355 G>A maps to NM_138694.3 L3020L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:51768525 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr6:51612981 G>A maps to NM_138694.3 I3144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr6:51897825 A>C did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:110402679 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:110425732 C>T maps to ENST00000426474 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:110416785 C>G maps to ENST00000426474 Y459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr8:110478834 C>T maps to ENST00000426474 H2814H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr8:110466950 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:110397820 T>A maps to ENST00000426474 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:110535589 C>T maps to ENST00000426474 Y4154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr8:110520438 C>A maps to ENST00000426474 R3782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr8:110447467 C>T maps to ENST00000426474 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:110497289 G>C maps to ENST00000426474 V3198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:110510776 T>C maps to ENST00000426474 A3562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr8:110477208 G>T maps to ENST00000426474 L2716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:110420424 C>G maps to ENST00000426474 S654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:110431466 A>T maps to ENST00000426474 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr8:110401305 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:110509196 T>A maps to ENST00000426474 G3459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr8:110448631 G>T maps to ENST00000426474 E1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr8:110441661 C>T maps to ENST00000426474 L1032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:110437462 T>C did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:110412467 T>C maps to ENST00000426474 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:110535535 C>T maps to ENST00000426474 V4136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr8:110393596 A>G did not map to a codon.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr8:110422189 G>T maps to ENST00000426474 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr8:110530663 G>A maps to ENST00000426474 K3987K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr8:110516712 T>C maps to ENST00000426474 P3663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr8:110477429 G>A maps to ENST00000426474 W2790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr20:43243304 G>A maps to NM_181805.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr20:43246998 G>A maps to NM_181805.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr15:72502753 G>A maps to ENST00000419739 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:3024068 A>T maps to NM_004203.4 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr19:14568885 G>T maps to NM_213560.1 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr19:14581478 C>T maps to NM_213560.1 I849I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:89271324 A>T maps to NM_006256.2 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr21:44450049 C>T maps to NM_004571.3 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:125301234 C>T maps to NM_022062.2 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:125299946 C>T maps to NM_022062.2 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:125267804 G>T maps to NM_022062.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr1:201286834 C>T maps to NM_000299.3 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr12:33031090 G>A maps to NM_004572.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:399092 C>G maps to NM_007183.2 Y390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:159530187 G>A did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr2:159530274 T>G did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr3:119325793 G>T maps to NM_015900.2 G83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr12:120759995 T>G maps to NM_000928.2 *149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:20246800 C>T maps to NM_014589.1 *143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:20474785 C>T maps to NM_022819.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:31536190 C>T maps to NM_015715.3 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:186948480 C>T maps to NM_024420.2 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:186909194 C>T maps to NM_024420.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr19:48608634 A>C maps to NM_003706.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:42363025 G>A maps to NM_178034.3 C644C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:42278075 G>A maps to NM_001080490.1 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr15:42437771 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:42436232 A>G maps to ENST00000397272 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:20417103 G>T maps to NM_000929.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:20417130 C>T maps to NM_000929.2 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:20417131 C>T maps to NM_000929.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:20416374 C>T maps to NM_000929.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr22:38565424 G>A maps to NM_003560.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr6:46678284 C>A maps to NM_001168357.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr2:160832578 C>T maps to NM_007366.4 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:160807910 G>A maps to NM_007366.4 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:160833231 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr2:160806212 G>C maps to NM_007366.4 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:26905640 A>G maps to NM_001031689.2 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr9:26905733 C>G maps to NM_001031689.2 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr23:133700418 T>C did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:133700081 A>T did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr11:59807994 T>C maps to NM_173801.3 H21H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:59814416 G>A maps to NM_173801.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:57079616 G>A maps to NM_002655.2 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:57080774 G>A maps to NM_002655.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:144263313 T>C maps to NM_001080951.1 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr6:144263778 G>A maps to NM_001080951.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:30785253 G>A maps to NM_002657.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:42038170 G>A maps to NM_000930.3 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:42046584 G>A maps to NM_000930.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:42038040 C>T maps to NM_000930.3 W351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:75672796 G>A maps to NM_002658.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr10:75671330 G>T maps to NM_002658.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:44160640 T>C maps to NM_002659.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr2:28812420 G>A maps to NM_153021.4 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr2:28766124 G>A maps to NM_153021.4 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr12:14659875 G>A maps to NM_024829.5 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr20:8737793 C>T maps to NM_015192.2 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr20:8741078 A>G maps to NM_015192.2 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr20:8722153 G>A maps to NM_015192.2 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7100-01A-11D-2012-08 chr20:8678322 C>T maps to NM_015192.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr20:8745841 C>T maps to NM_015192.2 Q923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr20:8113333 A>G maps to NM_015192.2 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr15:40591134 C>T maps to NM_004573.2 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr15:40581115 G>A maps to NM_004573.2 Q1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr15:40584264 C>T maps to NM_004573.2 E842E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr15:40591369 G>A maps to NM_004573.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:64033384 G>A maps to NM_000932.2 T1021T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr11:64022743 C>T maps to NM_000932.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:64022703 A>T did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:64027600 C>T maps to NM_000932.2 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr20:9434013 G>A maps to NM_001172646.1 K967K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr20:9388619 T>C maps to NM_001172646.1 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr20:9391724 G>T maps to NM_001172646.1 G681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr20:9453969 C>T maps to NM_001172646.1 V1151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:9364866 G>A maps to NM_001172646.1 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr20:9459634 G>C maps to NM_001172646.1 *1188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr3:38049774 G>A maps to NM_001130964.1 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:43190028 C>T maps to NM_133373.3 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr2:219500993 A>G maps to ENST00000432688 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr2:219492878 C>T maps to ENST00000432688 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr10:95790918 C>G maps to ENST00000371380 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:95995800 G>T maps to ENST00000371380 E782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr10:95995856 G>A maps to ENST00000371380 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr10:95791309 G>A maps to ENST00000371380 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:95791540 T>C maps to ENST00000371380 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr10:95791985 C>T maps to ENST00000371380 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr10:96006282 G>T maps to ENST00000371380 G1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:96064339 C>T maps to ENST00000371380 Q1854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:95892094 C>G maps to ENST00000371380 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr10:95791018 T>C maps to ENST00000371380 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr10:96014689 C>A maps to ENST00000371380 S1146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr10:95791948 G>A maps to ENST00000371380 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr20:39788393 G>T maps to NM_002660.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr20:39794929 C>G maps to NM_002660.2 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr16:81971421 C>T maps to NM_002661.2 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:81929466 G>A maps to NM_002661.2 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr16:81927340 C>T maps to NM_002661.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:81971421 C>T maps to NM_002661.2 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr3:155301386 C>T maps to ENST00000340059 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr3:155203373 G>A maps to ENST00000340059 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:155199668 G>C maps to ENST00000340059 L1390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:155200324 G>A maps to ENST00000340059 L1172L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-6935-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:155200496 C>T maps to ENST00000340059 E1114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr3:155200526 A>G maps to ENST00000340059 G1104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr3:155267707 G>A maps to ENST00000340059 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:155199304 G>A maps to ENST00000340059 Q1512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:155199305 G>A maps to ENST00000340059 Y1511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr3:155303874 T>C maps to ENST00000340059 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr3:155215155 A>T maps to ENST00000340059 L604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:2428298 G>T maps to NM_014638.2 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr1:2411335 C>A maps to NM_014638.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr2:198949734 G>A maps to NM_006226.3 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:198949572 C>G maps to NM_006226.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:198953647 T>C maps to NM_006226.3 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr2:198949558 C>T maps to NM_006226.3 R440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr2:198950712 G>A maps to NM_006226.3 R824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:17056234 C>T maps to NM_001144382.1 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:17051330 C>T maps to NM_001144382.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr3:17056294 C>T maps to NM_001144382.1 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:209701 G>T did not map to a codon.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr23:208210 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:41382319 C>T maps to NM_001005473.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr5:41382583 A>G maps to NM_001005473.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:18872483 A>G maps to ENST00000266505 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:171431714 C>G maps to NM_002662.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:171394567 T>G maps to NM_002662.3 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr3:171431701 G>A maps to NM_002662.3 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:171451287 T>C maps to NM_002662.3 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:171395395 G>A maps to NM_002662.3 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:171338242 G>A maps to NM_002662.3 N887N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr3:171338282 G>T maps to NM_002662.3 S874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr19:40872531 G>T maps to NM_012268.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr1:242277313 G>C maps to NM_152666.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:242277262 T>A maps to NM_152666.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr8:144996017 C>T maps to NM_201380.2 R2794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:144994358 C>G maps to NM_201380.2 L3347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144993497 C>T maps to NM_201380.2 E3634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144995837 C>T maps to NM_201380.2 Q2854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144997460 C>T maps to NM_201380.2 L2349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144997544 C>T maps to NM_201380.2 V2321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144997568 C>T maps to NM_201380.2 Q2313Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144998345 C>G maps to NM_201380.2 L2054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144998528 G>A maps to NM_201380.2 L1993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:144996153 G>C maps to NM_201380.2 S2749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr8:145001011 T>C maps to NM_201380.2 T1465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr8:144993269 G>A maps to NM_201380.2 D3710D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr8:144992792 G>A maps to NM_201380.2 F3869F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr8:144992203 G>A maps to NM_201380.2 L4066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr8:144995408 C>T maps to NM_201380.2 E2997E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr8:144996218 C>T maps to NM_201380.2 E2727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:145012831 G>T maps to NM_201380.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:144995519 G>A maps to NM_201380.2 R2960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:144993791 C>T maps to NM_201380.2 V3536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:144991748 C>T maps to NM_201380.2 L4217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:145007121 G>A maps to NM_201380.2 Q663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr8:144998291 C>T maps to NM_201380.2 E2072E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:144990623 C>T maps to NM_201380.2 V4592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:144995081 C>T maps to NM_201380.2 K3106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr8:144997784 C>T maps to NM_201380.2 A2241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr8:144992234 G>A maps to NM_201380.2 I4055I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:144991526 C>G maps to NM_201380.2 V4291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:145001817 C>T maps to NM_201380.2 V1309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:145001739 C>A maps to NM_201380.2 R1335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:145001840 G>A maps to NM_201380.2 Q1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:145024805 G>A maps to NM_201380.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:144991067 C>T maps to NM_201380.2 T4444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr8:144996308 A>G maps to NM_201380.2 H2697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:144991625 C>T maps to NM_201380.2 L4258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:145024687 C>A maps to NM_201380.2 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr8:144994472 C>T maps to NM_201380.2 S3309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr8:144992777 C>A maps to NM_201380.2 V3874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr8:144991436 G>A maps to NM_201380.2 S4321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr8:145001195 G>A maps to NM_201380.2 S1435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:68609700 T>A maps to NM_002664.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:68613640 C>T maps to NM_002664.2 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:68607874 G>A maps to NM_002664.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr14:67864497 G>A maps to NM_016445.1 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr14:67859512 C>A maps to NM_016445.1 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:67859924 G>A maps to NM_016445.1 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:179365827 C>T maps to NM_019091.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr19:49341310 C>T maps to NM_020904.2 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr12:19427862 T>A maps to ENST00000429027 L420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr12:19413941 C>G maps to ENST00000429027 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:19475472 C>T maps to ENST00000429027 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr12:19501414 C>A maps to ENST00000429027 S989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr1:204226791 G>A maps to ENST00000367191 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr1:204236636 G>A maps to ENST00000367191 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:16834668 C>A maps to ENST00000448080 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr11:16816212 G>C maps to ENST00000448080 S856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr11:16812674 C>T maps to ENST00000448080 P940P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr11:16812447 C>T maps to ENST00000448080 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:16847839 C>T maps to ENST00000448080 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:30094364 G>A maps to ENST00000440706 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr7:30084776 T>C maps to ENST00000440706 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:73366909 G>A maps to NM_021200.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr2:131904247 C>T maps to ENST00000409158 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:30164826 G>A maps to ENST00000436066 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr8:96166673 C>T maps to NM_024613.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr8:96166875 C>A maps to NM_024613.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:151055104 C>T maps to NM_001029884.1 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:151161324 C>T maps to NM_001029884.1 Q1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr6:151121854 G>A maps to NM_001029884.1 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr6:151152586 C>T maps to NM_001029884.1 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:39905660 C>T maps to NM_022835.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr14:65198092 C>G maps to ENST00000394691 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr14:65208841 C>T maps to ENST00000394691 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr14:65198158 C>T maps to ENST00000394691 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr16:67315486 C>T maps to NM_001129729.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr5:171219 C>G maps to NM_052909.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr5:181767 C>T maps to NM_052909.3 P1158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:6528528 G>C maps to NM_198681.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:6534541 G>A maps to NM_198681.2 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr12:6435719 C>T maps to NM_001144856.1 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr12:93162804 T>G maps to NM_001004330.2 Y327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr14:68008607 G>A maps to NM_020715.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:68043189 G>T maps to NM_020715.2 G811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr14:68050594 G>A maps to NM_020715.2 Q1188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr14:68050595 C>T maps to NM_020715.2 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr2:43927381 C>T maps to NM_172069.3 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr2:43927242 C>T maps to NM_172069.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:43980806 C>T maps to NM_172069.3 L1235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr17:40823066 C>A maps to NM_024927.4 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:40823109 C>G maps to NM_024927.4 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr17:40825795 G>A maps to NM_024927.4 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:2234192 G>A maps to NM_018049.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:43517534 G>A maps to NM_014798.2 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:43522843 G>A maps to NM_014798.2 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr17:43545613 T>A maps to NM_014798.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr17:43531384 G>A maps to NM_014798.2 D611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr17:43522834 C>A did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:16046257 C>T maps to ENST00000420314 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:16059014 C>G maps to ENST00000420314 Y1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr1:16046239 C>T maps to ENST00000420314 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:208795810 G>A maps to NM_001080475.2 Y575Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:909867 C>T maps to ENST00000379409 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:907525 T>C maps to ENST00000379409 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr1:906557 G>A maps to ENST00000379409 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr1:150128297 G>C maps to ENST00000443480 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:150131447 G>A maps to ENST00000443480 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:150131288 C>A maps to ENST00000443480 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:150128283 G>T maps to ENST00000443480 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:161157958 G>A maps to NM_000301.3 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr6:161139389 C>T maps to NM_000301.3 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:161160162 G>A maps to NM_000301.3 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:161159605 C>T maps to NM_000301.3 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:161173291 G>A maps to NM_000301.3 Q757Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:161134059 C>T maps to NM_000301.3 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr15:90210856 C>T maps to NM_002666.4 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:90210982 C>T maps to NM_002666.4 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr9:19126393 C>G did not map to a codon.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr9:19126392 A>G did not map to a codon.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr19:4847852 C>T maps to NM_005817.4 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr19:4512222 G>T maps to NM_001080400.1 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:4504668 C>T maps to NM_001080400.1 R1292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:4510824 G>C maps to NM_001080400.1 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:4511814 C>T maps to NM_001080400.1 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr19:4511709 A>G maps to NM_001080400.1 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr19:4529175 C>T maps to NM_001013706.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr16:23700658 C>T maps to NM_005030.3 D457D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr16:23700834 C>T maps to NM_005030.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr20:21143677 C>A maps to NM_018474.4 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:45269013 G>A maps to NM_004073.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:128806872 C>T maps to NM_014264.4 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr16:57290896 G>A maps to NM_015993.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:12017007 G>A maps to ENST00000376369 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr1:12030857 C>T maps to ENST00000376369 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:12024726 C>G maps to ENST00000376369 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:145789108 G>A maps to NM_182943.2 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr3:145809655 G>T maps to NM_182943.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:100859191 C>G maps to NM_001084.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr7:100859996 C>T maps to NM_001084.4 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:103041592 C>G did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:103041525 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr23:103041640 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr23:49029527 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr23:49029610 A>T did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr3:142388319 C>T maps to NM_001172312.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:142394997 G>C did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:114869294 G>A did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:114856587 A>G did not map to a codon.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr23:114874791 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:114877686 A>G did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:114869217 C>G did not map to a codon.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:146171941 G>A maps to ENST00000497985 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:7297015 G>A maps to NM_020360.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:145917673 G>A maps to NM_020353.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:145913024 C>T maps to NM_020353.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:145917611 A>G maps to NM_020353.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:146309587 G>T maps to NM_001085420.1 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:146307602 T>A did not map to a codon.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr20:44533676 C>A maps to NM_006227.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:31829251 C>T maps to NM_130852.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr20:31830291 G>C did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:17476502 G>C maps to NM_031310.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:17487788 C>G maps to NM_031310.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr19:17476148 G>T maps to NM_031310.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr19:17476277 C>T maps to NM_031310.1 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:37264406 G>A maps to NM_020405.4 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr10:20290915 G>T did not map to a codon.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:126708595 G>A maps to NM_032242.3 W387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr3:126710285 A>G maps to NM_032242.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr3:126747876 G>T maps to NM_032242.3 E1571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr3:126735799 C>T maps to NM_032242.3 L1066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:126748858 C>T maps to NM_032242.3 G1671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:126740944 G>A maps to NM_032242.3 E1352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr3:126707990 C>G maps to NM_032242.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:208218432 G>A maps to NM_025179.3 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:208257733 C>T maps to NM_025179.3 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:208202359 C>A maps to NM_025179.3 V1751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr1:208218410 C>A did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:153689683 C>T did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:153689090 G>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:153693210 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr23:153688919 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:153696269 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:153693805 G>A did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:153698456 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr23:153696764 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr23:153694585 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:153696340 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:153696644 G>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:153695706 C>T did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr23:153689701 C>T did not map to a codon.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr23:153694348 G>T did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:153698125 C>T did not map to a codon.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr23:153689950 G>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:153694153 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr23:153688924 G>A did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:153695620 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr23:153697013 C>T did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:153690646 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr23:153696261 T>A did not map to a codon.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr23:153694098 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:131853235 C>A maps to NM_020911.1 T1371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr7:132192726 G>T maps to NM_020911.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:132193308 G>T maps to NM_020911.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:131815312 G>A maps to NM_020911.1 H1870H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr7:132192786 G>A maps to NM_020911.1 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:131848900 C>A maps to NM_020911.1 L1500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr7:131925847 A>G maps to NM_020911.1 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr7:131817921 G>A maps to NM_020911.1 S1825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr7:131883334 G>A maps to NM_020911.1 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr7:132193416 G>C maps to NM_020911.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr3:48465366 G>A maps to NM_001130082.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr3:48451944 C>A maps to NM_001130082.1 G1813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr3:48456411 G>A maps to NM_001130082.1 I1335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:48447184 C>T maps to NM_001130082.1 G2083G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:48453894 C>T maps to NM_001130082.1 L1663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr3:48454537 G>A maps to NM_001130082.1 Q1526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:50718103 G>C maps to NM_012401.2 L1448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr22:50716548 G>A maps to NM_012401.2 V1628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr22:50720045 C>T maps to NM_012401.2 P1157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:50724680 G>A maps to NM_012401.2 R600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr22:50717425 G>A maps to NM_012401.2 I1468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:50728134 T>C maps to NM_012401.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:153035336 C>G did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:153032531 G>C did not map to a codon.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr23:153036774 C>T did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr23:153043514 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:153042339 A>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:153039010 A>T did not map to a codon.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr23:153036809 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:94694715 G>A maps to NM_005761.1 L1423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr12:94654552 G>A maps to NM_005761.1 T1129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr3:129290405 G>A maps to NM_015103.2 F1094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr3:129290644 G>T maps to NM_015103.2 A1040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr3:129324753 C>T maps to NM_015103.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:129303020 G>A maps to NM_015103.2 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:129286539 C>A did not map to a codon.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:129293181 G>A maps to NM_015103.2 H894H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:129291682 A>G did not map to a codon.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr3:129292447 C>T maps to NM_015103.2 T942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:205801747 C>T maps to NM_152491.4 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr6:89862894 A>T maps to NM_001010853.1 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr18:57569916 G>A maps to ENST00000269518 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr20:56234685 C>A maps to NM_020182.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:156206090 G>T maps to NM_007221.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr1:156209337 G>T did not map to a codon.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr16:72159280 T>G maps to NM_031293.2 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:72158691 C>A maps to NM_031293.2 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr16:72184545 C>T maps to NM_031293.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr15:74290541 C>T maps to NM_033238.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr22:41980049 G>A maps to NM_002676.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:102952104 A>T maps to NM_004279.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr7:102937968 C>T maps to NM_004279.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:190719575 T>C maps to NM_000534.4 C526C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:190718962 A>G did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:6043689 C>G did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:6042082 C>T did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr7:6045546 G>A maps to NM_000535.5 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:6027039 A>G maps to NM_000535.5 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr7:6048643 G>A maps to NM_000535.5 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:154898893 C>T maps to NM_006556.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:154898881 G>A maps to NM_006556.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr1:154901616 G>A maps to NM_006556.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr23:152936780 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:152938045 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:152938046 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:152938471 C>T did not map to a codon.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr23:152938023 C>T did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:50368398 C>T maps to NM_007254.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:50364537 C>A maps to NM_007254.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:50368398 C>T maps to NM_007254.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr10:118313297 C>T maps to NM_000936.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:118355781 C>G maps to NM_006229.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr10:118231355 G>C maps to NM_001011709.2 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:152225665 A>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr23:152226118 T>A did not map to a codon.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr23:152226305 A>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:152226133 G>A did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:152159411 G>T did not map to a codon.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr23:152159373 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:152159806 A>G did not map to a codon.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr23:152159176 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:152159280 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr23:152159046 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:152159712 A>T did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:46973548 C>T maps to NM_018215.3 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr19:46973191 C>T maps to NM_018215.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr19:46973755 G>A maps to NM_018215.3 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:46997420 G>A maps to NM_020709.1 L434L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-A468-01A-11D-A25Y-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DQ-7592-01A-11D-2078-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr19:46998416 G>A maps to ENST00000377652 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:46997420 G>T maps to NM_020709.1 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr17:37826488 G>A maps to NM_002686.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr14:39650862 G>T maps to NM_002687.3 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr14:39648652 G>A maps to NM_002687.3 Q260Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-7071-01A-12D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:28196681 C>T maps to NM_006228.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:28196630 G>A maps to NM_006228.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr6:36270065 C>T maps to ENST00000457797 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr6:36262088 C>T maps to ENST00000457797 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr22:44340663 C>T maps to NM_025225.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr22:44340651 G>A maps to NM_025225.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:7889800 C>A did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:7870154 C>A did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr23:7868776 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr23:7870134 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr23:7890080 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:44286941 C>T maps to ENST00000216177 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:7605583 G>A maps to NM_001166111.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr19:7619912 C>T maps to NM_001166111.1 H933H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr9:140356756 C>T maps to NM_001098537.1 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr9:140437129 C>T maps to NM_001098537.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr9:140400146 C>A maps to NM_001098537.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr9:140438231 A>C maps to NM_001098537.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr9:140361906 G>A maps to NM_001098537.1 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:140358626 G>A maps to NM_001098537.1 F1059F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:140389514 G>A maps to NM_001098537.1 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr9:140356439 G>T maps to NM_001098537.1 G1233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:108155014 A>G maps to NM_015723.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr2:55900086 G>C maps to NM_033109.3 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr2:55900073 G>A maps to NM_033109.3 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr2:55874496 C>T maps to NM_033109.3 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:89793536 T>C maps to NM_006813.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:52109923 G>T maps to NM_015426.4 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:52185029 A>G did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr3:52183326 G>A maps to NM_015426.4 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr12:89819072 T>C maps to NM_172240.2 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:53543412 C>T maps to NM_153703.4 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:14043637 G>T maps to NM_024825.3 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:131191356 G>A maps to NM_001018111.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:84634341 G>T did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr23:84585989 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:30797913 G>T maps to NM_015352.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr20:30797940 C>T maps to NM_015352.1 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr21:46685543 A>G maps to NM_133635.4 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:166819357 G>C maps to NM_017542.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:166818448 T>C maps to NM_017542.3 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:166818316 G>A maps to NM_017542.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:151377601 G>C maps to NM_015100.3 V1303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr1:151377433 C>G maps to NM_015100.3 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:24742494 C>T did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr23:24745917 C>G did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:24757588 A>G did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:24844669 T>A did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:24844701 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:24741351 G>A did not map to a codon.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr11:65064727 C>T maps to NM_002689.2 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr8:42196203 G>T did not map to a codon.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr8:42229168 C>T maps to NM_002690.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:50906793 C>G maps to ENST00000391817 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr19:50905483 C>T maps to ENST00000391817 H204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:74347276 C>A maps to NM_006591.1 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:67120196 C>T maps to NM_021173.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:133241049 T>A did not map to a codon.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr12:133215739 G>A maps to ENST00000455752 L1844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:133225972 C>A maps to ENST00000455752 R1311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:133257866 T>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:133212600 T>C maps to ENST00000455752 S1899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr12:133225537 C>A maps to ENST00000455752 E1379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:50117105 G>C maps to NM_002692.3 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr15:89871965 G>A maps to NM_002693.2 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:89862532 G>A maps to NM_002693.2 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:89873427 G>A maps to NM_002693.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr15:89864133 G>A maps to NM_002693.2 I948I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr15:89876484 C>T maps to NM_002693.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr15:89873461 C>T maps to NM_002693.2 W235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr15:89867077 G>A maps to NM_002693.2 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr17:62493002 C>T maps to NM_007215.3 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:62479089 G>A maps to NM_007215.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:74865316 G>T maps to NM_016218.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr5:74892235 C>G maps to NM_016218.2 S573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr5:74872758 G>A did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:103344391 G>A maps to NM_013274.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:103344515 G>C maps to NM_013274.3 S245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr10:103339235 G>A maps to NM_013274.3 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr10:103343336 G>A maps to NM_013274.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr4:2209863 C>T maps to NM_181808.2 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr3:121206857 T>A maps to ENST00000393672 P1776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr3:121186389 G>A maps to ENST00000393672 R2451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr3:121206398 G>A maps to ENST00000393672 F1929F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr3:121208234 A>G maps to ENST00000393672 N1317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:121217351 G>A maps to ENST00000393672 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr3:121207696 G>A maps to ENST00000393672 Q1497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:121207526 G>A maps to ENST00000393672 F1553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:121260260 G>T maps to ENST00000393672 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:86276327 G>C maps to NM_015425.3 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:86302278 G>A maps to NM_015425.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr2:86279994 G>A maps to NM_015425.3 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:86276113 G>A maps to NM_015425.3 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:113331324 C>T maps to NM_019014.4 Q820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:113316882 A>G maps to NM_019014.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr2:113322051 C>T maps to NM_019014.4 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:37503069 G>A maps to NM_022490.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr17:7399625 C>T maps to NM_000937.4 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:7415499 C>T maps to NM_000937.4 A1443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr17:7414792 G>A maps to NM_000937.4 K1329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:7417450 C>T maps to NM_000937.4 L1956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:7417465 C>T maps to NM_000937.4 I1961I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:7416661 G>A maps to NM_000937.4 S1693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr4:57896546 C>T maps to NM_000938.1 G1139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr19:1091819 G>A maps to NM_002695.3 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:38349815 T>C did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:62533148 G>T maps to NM_002696.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:62529265 G>T did not map to a codon.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr8:101163636 C>A maps to NM_005034.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr10:79737375 C>A maps to NM_007055.3 E1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr10:79760813 C>A maps to NM_007055.3 G800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:79784810 G>A maps to NM_007055.3 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr10:79764512 C>T maps to NM_007055.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:79764569 C>T maps to NM_007055.3 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr10:79781929 G>A maps to NM_007055.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:106760310 A>G maps to NM_018082.5 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:106895151 G>A maps to NM_018082.5 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr8:22106635 C>T maps to NM_001722.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr16:22344978 C>T maps to NM_018119.2 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:22320754 G>A maps to NM_018119.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:22343421 G>A maps to NM_018119.2 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr1:145457070 C>A maps to NM_032305.1 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr22:41925316 C>T maps to NM_138338.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:621365 C>A maps to NM_005035.3 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr19:623566 A>G maps to NM_005035.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr7:72413759 C>T maps to ENST00000434423 T1076T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr7:72413672 C>T maps to ENST00000434423 F1047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr7:72413726 C>T maps to ENST00000434423 F1065F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:72413633 G>A maps to ENST00000434423 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:72413273 C>T maps to ENST00000434423 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:72413416 C>G maps to ENST00000434423 S962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr7:72413744 C>T maps to ENST00000434423 S1071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr7:75051092 G>A maps to ENST00000257665 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr7:53103444 C>T maps to NM_182595.3 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr7:53103796 G>T maps to NM_182595.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:53103939 C>T maps to NM_182595.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr7:53103480 G>A maps to NM_182595.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr7:53103831 G>A maps to NM_182595.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr7:53103954 G>A maps to NM_182595.3 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:25384195 C>T maps to NM_001035256.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:25384060 C>T maps to NM_001035256.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:46655572 G>A maps to ENST00000371986 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr1:46656423 C>T maps to ENST00000371986 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr1:46656405 G>C maps to ENST00000371986 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr13:29252223 A>G maps to NM_015932.5 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:134394276 G>A maps to NM_007171.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr14:77745120 G>C maps to NM_013382.5 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr14:77786985 C>T maps to NM_013382.5 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr7:76254990 C>T maps to NM_012230.3 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr7:94953715 G>T maps to NM_000446.5 Y24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:94944745 A>G maps to NM_000446.5 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:94937342 G>A maps to NM_000446.5 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:95034734 C>T maps to NM_000305.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr7:95039307 G>A maps to NM_000305.2 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:94996774 C>T maps to NM_000940.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:95019513 G>C maps to NM_000940.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr7:94989367 G>A maps to NM_000940.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr8:99170477 G>A maps to NM_015029.2 A1018A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:99158844 T>C maps to NM_015029.2 C548C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr19:30101536 G>A maps to NM_006627.2 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr6:105606551 C>T maps to NM_022361.4 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr6:105606560 G>A maps to NM_022361.4 L220L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-F7-A620-01A-11D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr6:105606598 G>A maps to NM_022361.4 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr7:75608782 C>T maps to NM_000941.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:48370282 G>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:48374169 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr23:48370790 T>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:38153455 C>T maps to NM_006475.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr13:38138654 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr13:38160372 G>A maps to NM_006475.2 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:38143520 C>T did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:38160348 G>T maps to NM_006475.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:124499082 G>A maps to NM_015450.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr8:43173711 C>T maps to NM_001005365.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:43157154 T>C maps to NM_001005365.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:43173690 A>T maps to NM_001005365.2 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr18:14542629 T>C maps to ENST00000444806 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr18:14537868 G>T maps to ENST00000444806 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr18:14542736 G>A maps to ENST00000444806 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:14534952 C>T maps to ENST00000444806 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr18:14542998 G>A maps to ENST00000444806 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr18:14542641 C>T maps to ENST00000444806 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr21:15011856 G>T maps to NM_174981.3 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr2:131976076 C>T maps to NM_001083538.1 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:132021424 G>A maps to NM_001083538.1 E799E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr2:132021793 C>T maps to NM_001083538.1 D922D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:130832365 G>A maps to NM_001099771.2 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:130832650 G>A maps to NM_001099771.2 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr2:130832563 G>A maps to NM_001099771.2 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:19566009 A>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr14:19553511 C>T maps to NM_001005356.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr14:19553697 C>T maps to NM_001005356.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr22:16267040 G>A maps to NM_001136213.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr22:16267044 T>C maps to NM_001136213.1 E468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr22:16287549 G>A maps to NM_001136213.1 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr14:20020022 G>C maps to ENST00000439503 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:87322644 G>C maps to NM_001122757.1 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:87325509 G>A maps to NM_001122757.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr1:167353160 G>A maps to NM_002697.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:167384806 G>A maps to NM_002697.3 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:42600012 G>A maps to ENST00000342301 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr11:120180295 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:120180220 C>A maps to NM_014352.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:99282854 G>T maps to NM_005604.2 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr6:99283870 C>G maps to NM_005604.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr6:99283615 G>A maps to NM_005604.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr23:82763827 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:82763400 G>A did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr23:82764274 C>T did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr23:82763807 C>T did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr4:147561056 C>A maps to NM_004575.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr4:147561488 C>A maps to NM_004575.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr4:147561254 C>T maps to NM_004575.2 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr5:145719961 C>T maps to NM_002700.2 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr5:145719520 C>T maps to NM_002700.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:31132542 T>C maps to NM_002701.4 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:93076444 C>T maps to NM_153216.1 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr5:93076291 G>A maps to NM_153216.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:51584172 T>A maps to NM_002702.3 K255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:51584077 G>A maps to NM_002702.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:51585437 C>T maps to NM_002702.3 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr7:39247046 C>A maps to NM_007252.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr7:39500155 G>A maps to NM_007252.3 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr7:39472770 G>A maps to NM_007252.3 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr7:39500195 C>T maps to NM_007252.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr7:39504008 C>T maps to NM_007252.3 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:71974335 C>A maps to NM_021129.3 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:10221510 C>T maps to NM_001040664.2 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr19:288130 C>T maps to NM_177543.1 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr10:122348921 C>T maps to NM_001030059.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:134165520 C>G maps to NM_032728.3 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr9:134165695 G>A maps to NM_032728.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:35378950 C>G maps to NM_006238.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:23886406 G>A maps to NM_013261.3 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr4:23815563 G>A maps to NM_013261.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IH-01A-11D-A25Y-08 chr5:149212835 C>G maps to NM_133263.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr5:149213162 G>T maps to NM_133263.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr5:149216429 C>T maps to NM_133263.3 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr4:57301514 C>A did not map to a codon.
Alternatively spliced codon TCGA-CR-5248-01A-01D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:18836238 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:18842186 G>A did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr23:18748391 C>G did not map to a codon.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr23:18748379 C>T did not map to a codon.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr23:18748408 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr4:76797790 C>T maps to NM_006239.2 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr4:76805745 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:76812834 G>T maps to NM_006239.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:70170533 C>T maps to NM_003626.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr11:70200477 C>T maps to NM_003626.2 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:70218612 G>C maps to NM_003626.2 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr11:70224266 C>T maps to NM_003626.2 S1172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr11:70176373 C>G maps to NM_003626.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:70224302 T>C maps to NM_177423.1 G1184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr11:70222702 T>C maps to NM_003626.2 D1127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr12:81693144 C>A maps to NM_003625.2 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:81768457 A>T maps to NM_003625.2 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:81839427 C>T maps to NM_003625.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:82147792 G>T maps to NM_003625.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr12:81661804 T>C maps to NM_003625.2 E1124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr12:81719650 T>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr12:81741329 C>T maps to NM_003625.2 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr12:82147850 C>G maps to NM_003625.2 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:81747118 C>T did not map to a codon.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr12:81732998 A>G maps to NM_003625.2 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr12:81746959 G>C maps to NM_003625.2 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr19:49631303 G>A maps to NM_003660.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr19:49631640 G>A maps to NM_003660.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:49652885 C>G maps to NM_003660.2 S1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:203024700 C>T maps to ENST00000367238 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:27841991 G>A maps to NM_003622.3 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr12:27824449 T>G maps to NM_003622.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr11:7670884 G>A maps to NM_003621.2 E707E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr12:42778763 C>A maps to NM_016488.6 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:81113531 T>A maps to NM_005729.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:170492732 G>T maps to NM_004792.2 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:43130565 G>A maps to NM_006347.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr6:36824425 T>C maps to NM_016059.4 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr22:22035600 C>T maps to NM_148175.2 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr22:22035639 C>T maps to NM_148175.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:201750419 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:109740402 A>C maps to NM_001111298.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:43827591 G>A maps to NM_001130858.2 F1194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr5:102487034 A>T maps to ENST00000451606 K329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:102472490 C>T maps to ENST00000451606 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:102493940 T>C maps to ENST00000451606 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr16:4947768 C>T maps to NM_002705.4 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:4934902 G>C maps to NM_002705.4 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr16:4941823 C>G maps to NM_002705.4 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:4944532 C>T maps to NM_002705.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:60756618 G>T maps to NM_177952.2 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H8-01A-21D-A34J-08 chr14:60752347 C>T maps to NM_177952.2 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:44428820 A>G maps to NM_002706.4 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:58740466 C>T maps to NM_003620.3 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr17:58740835 C>T maps to NM_003620.3 R581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:57058233 C>T maps to NM_014906.3 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr17:57050197 A>G maps to NM_014906.3 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:22277593 G>A maps to NM_014634.3 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr22:22277782 C>T maps to NM_014634.3 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:27609063 C>T maps to NM_177983.1 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr2:27605046 G>A maps to NM_177983.1 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:63225905 C>T maps to NM_020700.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:160474320 T>C maps to NM_139245.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr3:52283690 C>G maps to NM_144641.2 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:73962724 G>A maps to NM_016147.1 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:161140305 G>A maps to NM_001122764.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr2:29006791 A>G maps to NM_002709.2 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:111168433 G>A maps to NM_002710.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr6:30571951 C>T maps to NM_002714.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr6:30571942 C>T maps to NM_002714.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr6:30576879 C>T maps to NM_002714.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr12:80203691 A>G maps to NM_001143885.1 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:202464746 C>T maps to ENST00000367270 I795I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:202406977 A>G maps to ENST00000367270 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr1:202464470 G>C maps to ENST00000367270 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr1:202394712 A>G maps to ENST00000367270 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr19:55623922 G>A maps to NM_017607.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr19:55623898 C>A maps to NM_017607.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr14:104206646 G>C maps to NM_015316.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:104209071 C>T maps to NM_015316.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:104206421 G>A maps to NM_015316.2 P777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:104205237 C>T maps to NM_015316.2 Q905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr19:45889215 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:45885895 G>A maps to NM_001142502.1 F779F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:45900259 G>A maps to NM_001142502.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:45899944 C>T maps to NM_001142502.1 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:64012226 C>T maps to NM_138689.2 *148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr6:150464597 G>A maps to NM_030949.2 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr6:150535944 G>A maps to NM_030949.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr15:41120650 C>G maps to NM_001130143.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:49379228 G>A maps to NM_014330.3 *675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:49379061 C>G maps to NM_014330.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:49377371 C>A maps to NM_014330.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr19:49379130 C>T maps to NM_014330.3 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:37464724 C>A maps to NM_015568.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr20:37534655 C>T maps to NM_015568.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr20:37536545 G>A maps to NM_015568.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:182852606 C>G maps to ENST00000280295 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:195256616 C>A maps to NM_006241.4 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:113519931 T>C maps to NM_002711.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:113518192 G>T maps to NM_002711.3 S985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:113519997 G>A maps to NM_002711.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:113558352 C>T maps to NM_002711.3 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:8998839 C>A maps to NM_024607.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr10:93390208 G>A maps to NM_005398.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr10:93389932 G>T maps to NM_005398.4 C235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr20:58514188 G>C maps to NM_006242.3 Y266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:49142666 G>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:49142666 G>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:49142812 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:49127084 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:49142331 G>A did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:49127006 T>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:242105760 C>T maps to NM_002712.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr1:28176680 C>T maps to NM_014110.4 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:94879403 G>T maps to NM_001166160.1 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr7:94879415 G>T maps to NM_001166160.1 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:94740689 G>T maps to NM_001166160.1 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:94540363 C>A maps to NM_001166160.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr7:94897988 C>A maps to NM_001166160.1 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr7:94539550 A>G maps to NM_001166160.1 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:94919527 G>A maps to NM_001166160.1 R1346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr8:30657105 C>A maps to NM_001009552.1 G90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:52709300 C>T maps to NM_014225.5 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:52724382 C>A maps to NM_014225.5 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:52722987 G>A maps to NM_014225.5 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr5:145979964 C>A maps to ENST00000394414 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:6374334 G>A maps to NM_181876.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr10:133761151 G>A maps to ENST00000455566 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr3:135722253 A>T maps to NM_002718.4 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:135721836 T>C maps to NM_002718.4 D499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:135721086 C>T maps to NM_002718.4 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:135720852 C>T maps to NM_002718.4 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr3:135721722 C>T maps to NM_002718.4 C461C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr23:299608 C>G did not map to a codon.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr23:322204 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr23:295162 G>A did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr23:306381 G>A did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:299393 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:131899913 C>T maps to NM_178001.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr1:212530320 C>T maps to NM_006243.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr11:64695278 A>T maps to NM_006244.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr11:64698015 G>A maps to NM_006244.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr6:42975719 C>G maps to NM_006245.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr14:63860549 G>C maps to ENST00000422769 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr4:101947114 G>A maps to NM_000944.4 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:75230955 G>A maps to NM_001142353.1 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr9:104357131 G>T maps to NM_147180.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr18:9563519 T>A maps to NM_001042388.1 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr18:9570205 C>A maps to NM_001042388.1 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:9570372 A>T maps to NM_001042388.1 L452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr18:9559476 G>A maps to NM_001042388.1 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr18:9584723 G>A maps to NM_001042388.1 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr14:94711995 C>T maps to NM_058237.1 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:94722875 G>T maps to NM_058237.1 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr14:94700897 G>T did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr14:94700934 C>G maps to NM_058237.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr19:46879818 A>G maps to NM_006247.2 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr10:103900409 C>T maps to NM_015062.3 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:32122554 G>T did not map to a codon.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr10:47086821 A>G maps to NM_005972.4 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:47087742 C>T maps to NM_005972.4 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr10:47087601 C>A maps to NM_005972.4 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:47087814 C>G maps to NM_005972.4 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr10:47087865 C>A maps to NM_005972.4 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:47087637 C>T maps to NM_005972.4 N285N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr1:19653875 C>T maps to NM_017765.2 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:19651168 G>A maps to NM_017765.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr17:46799745 G>A maps to NM_032391.2 C3C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr23:48931478 G>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:8555791 C>T maps to NM_032152.4 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr19:8563896 G>A maps to NM_032152.4 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr22:22892734 C>G maps to NM_206954.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr22:22890815 G>A maps to NM_206954.1 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:12854234 C>T maps to NM_023013.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:12854333 C>G maps to NM_023013.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:12855676 C>G maps to NM_023013.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:12854111 C>T maps to NM_023013.2 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:12855706 C>T maps to NM_023013.2 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:12855676 C>T maps to NM_023013.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr1:12854240 C>T maps to NM_023013.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:12955429 C>T maps to NM_001039361.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:12884918 G>A maps to NM_001146344.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr1:12884892 C>T maps to NM_001146344.1 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:12835019 C>T maps to NM_001080830.1 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:12837315 G>A maps to NM_001080830.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:12837642 C>T maps to NM_001080830.1 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr1:12837450 C>T maps to NM_001080830.1 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr1:12837498 G>A maps to NM_001080830.1 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:13495994 C>A maps to NM_001045480.1 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr1:12918968 C>G maps to NM_023014.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr1:12920036 C>T maps to NM_023014.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:12919595 C>T maps to NM_023014.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr1:12919922 A>T maps to NM_023014.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:12943023 G>A maps to NM_001009611.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:12939532 A>G maps to ENST00000376192 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:12979809 C>T maps to NM_001012277.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr10:135165853 C>T maps to ENST00000423766 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr12:11506283 A>C maps to NM_005039.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:11506793 G>T maps to NM_005039.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr12:11545925 A>G maps to NM_006248.3 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:11546119 G>A maps to NM_006248.3 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr12:11421067 G>A maps to NM_006249.4 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr12:11421067 G>A maps to NM_006249.4 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr12:11421067 G>A maps to NM_006249.4 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:11422582 C>T maps to NM_006249.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr12:11422596 G>A maps to NM_006249.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:11461214 G>C maps to NM_002723.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr12:11461742 T>C maps to NM_002723.3 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:91512854 T>C did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:156756530 G>A maps to NM_005973.4 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:156770248 C>T maps to NM_005973.4 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr17:74538649 G>A maps to NM_001077620.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr6:106552716 C>T maps to NM_001198.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr6:106553063 C>T maps to NM_001198.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr11:129794872 G>A maps to NM_020228.2 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:129772279 C>T maps to NM_020228.2 Q1137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr11:129827742 G>A maps to NM_020228.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:129802047 G>A maps to NM_020228.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr11:45246017 C>T maps to NM_020229.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr9:133540114 C>T maps to NM_021619.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr6:100057103 G>A maps to ENST00000359773 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr8:70980725 G>A maps to NM_024504.2 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr21:43258050 C>T maps to NM_022115.3 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr21:43221623 C>A maps to NM_022115.3 E1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr21:43287418 C>T maps to NM_022115.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr21:43279699 C>A did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:3342264 G>A maps to NM_022114.3 Q1020Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:3334403 G>T maps to NM_022114.3 E902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:3328623 G>A maps to NM_022114.3 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:3313152 G>A maps to NM_022114.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr1:3102851 G>A maps to NM_022114.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr1:14075947 C>A maps to NM_012231.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:14106923 A>G maps to NM_012231.4 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:14108592 C>T maps to NM_012231.4 Q1435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:14105420 T>C maps to NM_012231.4 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:14105906 A>G maps to NM_012231.4 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:108134780 G>A maps to NM_012406.3 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr12:108128116 G>T maps to NM_012406.3 S759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:121828687 C>A maps to NM_018699.2 G40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr4:121631547 T>A maps to NM_018699.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr4:121616406 C>T maps to NM_018699.2 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:90141416 G>A maps to NM_001098173.1 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr4:81123530 C>T maps to NM_001099403.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr4:81122460 A>C maps to NM_001099403.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr4:81123446 C>T maps to NM_001099403.1 C277C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr4:81123491 C>A maps to NM_001099403.1 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr5:23522480 G>T maps to NM_020227.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:23527818 C>T maps to NM_020227.2 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:23510089 G>T maps to NM_020227.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:23526849 C>T maps to NM_020227.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr5:23510042 C>A maps to NM_020227.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr5:23524473 C>T maps to NM_020227.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr5:23526666 A>T maps to NM_020227.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:23527461 G>T maps to NM_020227.2 R755R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr5:23522936 T>C maps to NM_020227.2 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:23526576 C>A maps to NM_020227.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr5:23526948 G>A maps to NM_020227.2 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:23526912 G>A maps to NM_020227.2 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr5:23509592 C>T maps to NM_020227.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr23:23700511 G>A did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:23700514 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr6:105845799 T>C maps to NM_002726.4 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:105824003 G>C maps to NM_002726.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:44549939 C>G maps to NM_001171603.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:44586818 C>T maps to NM_001171603.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr20:47309257 G>A maps to NM_020820.3 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr20:47266744 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr20:47266016 G>A maps to NM_020820.3 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr20:47296245 G>A maps to NM_020820.3 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr8:69028101 T>C maps to NM_024870.2 F1087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr8:68992763 C>T maps to NM_024870.2 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr8:69005940 T>C maps to NM_024870.2 F784F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:69046471 T>G maps to NM_024870.2 G1315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr8:69136816 G>A maps to NM_024870.2 A1577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr8:68999985 T>C maps to NM_024870.2 D685D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:57155326 T>C maps to NM_002728.4 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:186276563 C>T maps to NM_005807.3 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:186275735 G>A maps to NM_005807.3 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:186276563 C>T maps to NM_005807.3 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:186275988 G>T maps to NM_005807.3 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:186276401 C>T maps to NM_005807.3 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:186277352 T>C maps to NM_005807.3 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr1:186276380 C>T maps to NM_005807.3 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:11035683 C>A maps to NM_006250.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:11034875 C>A maps to NM_006250.2 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:11034866 T>A maps to NM_006250.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:11082883 C>T maps to NM_001110213.1 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr20:62197117 C>T maps to NM_001037335.2 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr20:62192985 G>A maps to NM_001037335.2 S2268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:62196772 G>A maps to NM_001037335.2 F1134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:62191954 G>A maps to NM_001037335.2 H2459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:62200814 G>C maps to NM_001037335.2 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr3:64133295 T>C maps to NM_198859.3 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr3:64085133 G>T maps to NM_198859.3 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr23:49032202 G>T did not map to a codon.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr23:49032431 G>T did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:41753184 G>C maps to NM_013397.5 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:57135603 G>A maps to NM_000946.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr12:57145980 T>A maps to NM_000946.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:57398274 C>T maps to NM_000947.2 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:94187822 G>A maps to NM_178013.3 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:94245528 G>A maps to NM_178013.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr14:94245528 G>C maps to NM_178013.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr5:40777688 C>G did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr5:40798207 A>G maps to NM_206907.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr5:40765030 G>A maps to NM_206907.3 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr5:40765108 G>A maps to NM_206907.3 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:40765237 A>G maps to NM_206907.3 C323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:57140141 A>C maps to NM_006252.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:57161833 T>C did not map to a codon.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr1:57161754 C>G maps to NM_006252.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:120114376 G>T maps to NM_006253.4 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:120112224 A>G maps to NM_006253.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:14213714 C>T maps to NM_002730.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr19:14217607 C>T maps to NM_002730.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr1:84668367 C>A maps to NM_182948.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:84649755 G>T maps to NM_182948.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:71628519 G>A maps to NM_002732.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr9:71628057 C>T maps to NM_002732.3 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:71628432 C>T maps to NM_002732.3 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr9:71628162 G>A maps to NM_002732.3 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr12:49399266 A>G maps to NM_002733.3 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr7:151261268 C>T maps to NM_016203.3 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:151262821 A>T maps to NM_016203.3 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:66518979 C>A maps to NM_212472.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:48789026 G>A maps to NM_004157.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr17:64785039 G>A maps to NM_002737.2 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:64299052 G>A maps to NM_002737.2 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr17:64684444 C>T maps to NM_002737.2 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr16:24192239 C>A maps to NM_002738.6 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:24196443 C>T maps to NM_002738.6 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:53221364 C>T maps to NM_212539.1 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr2:46070194 G>A maps to NM_005400.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:54409998 G>A maps to NM_002739.3 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:54396286 G>A maps to NM_002739.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:54401340 T>C maps to NM_002739.3 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr19:54401791 G>C maps to NM_002739.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr19:54401268 C>T maps to NM_002739.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr19:54395867 G>A maps to NM_002739.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr14:61857998 C>T maps to NM_006255.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:61917603 C>T maps to NM_006255.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr14:61997129 C>A maps to NM_006255.3 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr3:169940504 C>T maps to NM_002740.5 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr10:6506273 C>T did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr10:6525467 C>T maps to NM_006257.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr19:11559734 C>G maps to ENST00000436195 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:2077509 C>T maps to NM_002744.4 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:2103807 C>T maps to NM_002744.4 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr14:30100143 G>A maps to NM_002742.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr14:30046467 G>A maps to NM_002742.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:30046527 G>T maps to NM_002742.2 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:30066889 G>A maps to NM_002742.2 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr14:30107996 C>T maps to NM_002742.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr14:30135409 G>A maps to NM_002742.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr14:30046530 C>A maps to NM_002742.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:30107746 A>G maps to NM_002742.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:30108089 C>T maps to NM_002742.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:37520322 G>C maps to NM_005813.3 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:48777318 G>T maps to NM_006904.6 S1789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:48697812 G>A maps to NM_006904.6 L3655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:48801648 C>A maps to NM_006904.6 L1401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr8:48839754 T>A maps to NM_006904.6 S806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:48842537 C>A maps to NM_006904.6 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:48697803 G>A maps to NM_006904.6 F3658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:48697682 C>A maps to NM_006904.6 E3699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:48715930 G>A maps to NM_006904.6 C3285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr8:48798672 C>T maps to NM_006904.6 A1535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr8:48733338 G>A maps to NM_006904.6 Q3092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr8:48761983 C>T maps to NM_006904.6 V2361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:48815310 A>G maps to NM_006904.6 C1029C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:48842448 A>G maps to NM_006904.6 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr10:54031234 C>T maps to NM_001098512.1 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr4:82056395 T>A maps to NM_006259.1 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:179309172 C>T maps to NM_003690.4 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:76062411 G>A maps to NM_004705.2 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:76063226 C>A maps to NM_004705.2 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:76062453 G>A maps to NM_004705.2 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr23:3573308 G>A did not map to a codon.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr23:3573221 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:3592652 C>T did not map to a codon.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr23:3592788 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr6:22294766 G>A maps to ENST00000397199 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr5:35066070 G>C maps to NM_000949.4 S330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr5:35065730 A>T maps to NM_000949.4 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr19:50188181 G>A maps to NM_001536.3 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:50185210 C>T maps to NM_001536.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:20483562 G>T maps to NM_005788.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr11:20486033 C>G maps to NM_005788.3 S430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr11:20424502 C>A maps to NM_005788.3 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:4705247 C>G maps to NM_012409.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr20:4680246 C>A maps to NM_001080123.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:128186311 G>A maps to ENST00000409048 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:128186315 C>A maps to ENST00000409048 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:128180492 C>T maps to ENST00000409048 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:27031230 C>T did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr20:33764085 G>A maps to NM_006404.3 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:33764534 C>T maps to NM_006404.3 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr22:18909860 C>T maps to NM_016335.4 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr3:71830629 T>A maps to NM_001126128.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:68882428 C>T maps to NM_138964.2 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr20:5294736 G>T maps to NM_144773.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:5283102 G>T maps to NM_144773.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:5294625 G>A maps to NM_144773.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:5294895 A>G maps to NM_144773.2 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:71275726 C>T maps to NM_021225.4 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr4:71275590 C>T maps to NM_021225.4 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr4:15995642 G>A maps to NM_006017.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr2:95947716 G>A maps to NM_144707.2 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:95953209 G>T maps to NM_144707.2 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:95952297 C>A maps to NM_144707.2 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr2:95941258 G>T did not map to a codon.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr5:177420033 G>A maps to NM_006261.4 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:93615488 A>T maps to NM_000313.3 L299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr3:93624661 A>T maps to NM_000313.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr3:93646164 C>A maps to NM_000313.3 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:37623866 T>C maps to NM_007198.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:37623260 C>A maps to NM_007198.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:214170735 C>T maps to NM_002763.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:214184943 C>G maps to NM_002763.3 Y638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:214171245 C>A maps to NM_002763.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:214171293 C>A maps to NM_002763.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr14:75323590 G>A maps to ENST00000445876 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:113826403 A>G maps to ENST00000342783 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr10:13642273 T>C maps to NM_003675.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr10:13658405 T>C maps to NM_003675.3 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:150316707 C>T maps to NM_004698.2 H499H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:150300843 C>T maps to NM_004698.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr1:52882356 G>T maps to NM_032864.3 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr2:153532917 C>G did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr12:50027755 C>T maps to NM_001031698.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:50035773 G>A maps to NM_001031698.1 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:50035743 C>T maps to NM_001031698.1 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:50027426 C>G maps to NM_001031698.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr12:50026873 G>A maps to NM_001031698.1 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr17:1563821 G>A maps to NM_006445.3 H1563H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr17:1561561 C>T maps to NM_006445.3 Q1830Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr17:1582625 C>T maps to NM_006445.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr17:1582625 C>G maps to NM_006445.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr17:1582343 G>A maps to NM_006445.3 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:1584902 G>A maps to NM_006445.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:1554576 C>A maps to NM_006445.3 T2226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:49690817 G>A maps to ENST00000451891 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:49689165 T>C maps to ENST00000451891 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr12:49691345 G>A maps to ENST00000451891 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr6:42689519 G>A maps to NM_000322.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr6:42666176 A>G maps to NM_000322.4 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr6:42689523 G>A maps to NM_000322.4 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:106885675 G>T did not map to a codon.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr23:106882552 G>C did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr23:106888429 T>C did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:106882527 G>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr7:18067267 C>T maps to NM_175886.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:12837667 G>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:12809654 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr23:12837735 G>T did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:18775923 G>T maps to NM_002767.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:18833956 C>T maps to NM_002767.2 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:18814457 G>A maps to NM_002767.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr17:57270974 C>A maps to NM_018304.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:57270938 G>C maps to NM_018304.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:50098458 C>T maps to NM_020719.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr19:50098371 G>A maps to NM_020719.1 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr19:50098965 G>T maps to NM_020719.1 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr19:50102548 G>A maps to NM_020719.1 K1233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:50099934 C>T maps to NM_020719.1 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr16:30666034 G>A maps to NM_024031.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr17:46030324 G>C maps to NM_024320.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:120021839 G>A maps to NM_016644.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr19:42813748 G>T maps to NM_199285.2 G5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr19:42814890 G>A maps to NM_199285.2 *357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr2:240982231 G>T maps to NM_001080835.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr19:5783177 C>G maps to NM_001134316.1 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:5783813 C>A maps to NM_001134316.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr3:138739167 T>C maps to NM_001013650.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr3:138738768 G>A maps to NM_001013650.2 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:138738792 C>A maps to NM_001013650.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr3:138739188 C>T maps to NM_001013650.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:138763108 C>T maps to NM_001134657.1 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:863383 C>T maps to NM_001013638.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr6:30530164 G>T did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr11:36472864 C>G maps to NM_001160167.1 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:37285131 G>A did not map to a codon.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr23:37285148 G>C did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr23:37285196 G>A did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:150869333 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:150869340 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:150869491 G>T did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:150868556 G>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:32117025 C>T maps to NM_030651.3 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:9990497 G>C maps to NM_207351.3 S372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:170633412 C>A maps to NM_022716.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:170695425 C>T maps to NM_022716.2 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:170688865 G>C did not map to a codon.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr1:170705311 G>A maps to NM_022716.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr7:142460801 G>A maps to ENST00000486171 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:142459767 C>G maps to ENST00000486171 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr7:142458442 G>T maps to ENST00000486171 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:119256646 G>C maps to NM_003619.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr4:119252893 C>G maps to NM_003619.3 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr7:142481345 T>C maps to ENST00000311757 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr16:2871025 C>G maps to NM_006799.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr16:2905797 C>T maps to NM_022119.3 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr16:2905602 G>T maps to NM_022119.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr11:86519136 C>G maps to NM_007173.4 S151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr16:2762621 C>G maps to NM_031948.3 *291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:2765774 G>A maps to NM_031948.3 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:33799063 C>G maps to NM_007343.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr9:33796722 G>A maps to NM_007343.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr16:2834669 C>T maps to NM_152891.2 W273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr16:31151713 G>A maps to NM_173502.3 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr16:31155035 G>C maps to NM_173502.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr7:141536335 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:141537831 G>A maps to NM_001008270.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:46759218 C>G maps to NM_013270.4 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr3:46754405 C>T maps to NM_013270.4 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:46755990 C>T maps to NM_013270.4 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr16:31098883 G>A maps to NM_001039503.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr16:58324918 G>A maps to NM_001080492.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr16:31143905 C>T maps to NM_002773.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr15:55972791 A>T maps to NM_173814.4 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr15:55933314 G>A maps to NM_173814.4 C711C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr15:55931940 G>A maps to NM_173814.4 H741H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr15:55919292 G>C maps to NM_173814.4 S947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:151001308 C>T maps to NM_021222.1 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:151006631 C>G maps to NM_021222.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr1:150997140 C>T maps to NM_021222.1 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr9:79324741 C>T maps to NM_015225.2 W816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:79320153 C>A maps to NM_015225.2 E2346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr9:79321540 A>G maps to NM_015225.2 Y1883Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr9:79318746 G>A maps to NM_015225.2 F2594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr9:79325764 C>A maps to NM_015225.2 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr9:79461548 C>T maps to NM_015225.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr9:79465380 C>T maps to NM_015225.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr9:79319817 G>A maps to NM_015225.2 L2458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr9:79465560 C>G maps to NM_015225.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr9:79323208 C>T maps to NM_015225.2 E1327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr19:40900808 G>A maps to NM_181882.2 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:40900136 G>A maps to NM_181882.2 V1374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr19:40900808 G>A maps to NM_181882.2 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr9:80921299 G>A maps to ENST00000421149 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:104172142 G>A maps to NM_002779.3 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr10:104164345 G>C maps to NM_002779.3 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr10:104164417 G>A maps to NM_002779.3 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr10:104173809 G>A maps to NM_002779.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:139193007 C>T maps to NM_032289.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr5:139201498 G>A maps to NM_032289.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:139192995 C>T maps to NM_032289.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr5:139189168 C>T maps to NM_032289.2 H48H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr5:139216518 C>A maps to NM_032289.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:18729697 G>A maps to ENST00000440756 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr8:18729566 C>T maps to ENST00000440756 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:113940968 C>T maps to NM_012455.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr2:113951500 G>A maps to NM_012455.2 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:227069673 G>A maps to ENST00000391872 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr1:227079501 C>G maps to ENST00000391872 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:36237738 C>T maps to NM_172341.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr19:43376171 G>T maps to NM_006905.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:43530464 G>C maps to ENST00000306308 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:43529017 G>A maps to ENST00000306308 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr19:43523105 G>A maps to ENST00000449000 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:43585207 G>A maps to ENST00000449000 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:43579506 G>A maps to NM_031246.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr19:43237074 A>T maps to NM_021016.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:43233293 G>A maps to NM_021016.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr19:43242948 G>T maps to NM_021016.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:43414912 T>C maps to NM_002782.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr19:43414864 C>T maps to NM_002782.3 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:43439856 T>C maps to NM_002783.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr19:43430084 C>T maps to NM_002783.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:43430804 G>C maps to NM_002783.2 S258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr19:43268170 G>T maps to NM_182707.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:43268173 C>T maps to NM_182707.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:43269719 G>C maps to NM_182707.2 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:43763285 C>T maps to NM_002784.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr19:43766195 G>A maps to NM_002784.3 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr9:15469057 T>C did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr9:15468727 C>T maps to NM_001128217.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr9:15468960 C>T maps to NM_001128217.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr8:87076415 G>A maps to ENST00000276616 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr8:87076790 G>T maps to ENST00000276616 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr11:14632513 T>A maps to NM_148976.2 K7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr7:42957397 A>G maps to NM_002787.4 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr14:35778160 G>A maps to NM_002791.1 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr18:23714009 G>T maps to NM_144662.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:36068885 G>A maps to NM_002794.4 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:151373788 C>A maps to NM_002796.2 C217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr1:151372585 C>T maps to NM_002796.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr14:90734635 G>T maps to NM_002802.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr14:90730031 G>C maps to NM_002802.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:102996210 C>G maps to NM_002803.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr17:40725340 C>T maps to NM_016556.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr17:61907803 C>T maps to NM_002805.5 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:61908486 G>A maps to NM_002805.5 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:231944261 A>G maps to NM_002807.3 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr23:107331313 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr17:30796050 C>T maps to NM_002815.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr17:30801832 A>G maps to NM_002815.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:30806360 G>A maps to NM_002815.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:65346398 G>A maps to NM_002816.3 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr2:162242000 C>A maps to NM_005805.4 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:184026288 G>A maps to NM_002808.3 Q826Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:184023707 C>G maps to NM_002808.3 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr3:184025483 G>A maps to NM_002808.3 V762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:184022097 C>T maps to NM_002808.3 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr3:184023941 A>C maps to NM_002808.3 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr17:38142871 A>G maps to NM_002809.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:38145045 C>T maps to NM_002809.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:151234660 G>A maps to ENST00000368881 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:151237664 C>G maps to ENST00000368881 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:151237330 C>T maps to ENST00000368881 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr3:64005072 C>T maps to ENST00000492933 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:38871606 C>T maps to NM_002812.4 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr14:24607451 C>G maps to NM_176783.1 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr14:24606930 C>T maps to NM_176783.1 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr2:54120867 T>C maps to NM_014614.2 S1327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:54112829 G>A maps to NM_014614.2 F1604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr2:54155436 T>C maps to NM_014614.2 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:54137241 C>A maps to NM_014614.2 E848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr2:54133993 T>C maps to NM_014614.2 K932K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr21:40547563 T>A maps to NM_003720.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr13:20304416 G>A maps to NM_001042414.1 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr15:77324640 C>G maps to NM_003978.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:806555 G>A maps to NM_002819.4 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr19:810547 C>G maps to NM_002819.4 S490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr1:97272477 C>T maps to ENST00000370197 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:97235415 G>C maps to ENST00000370197 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:71654229 C>G maps to NM_024754.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr5:71654181 G>A maps to NM_024754.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:86350829 G>T maps to NM_017952.5 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr9:98238314 C>A did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:98268845 C>G maps to NM_000264.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr9:98220447 C>A maps to NM_000264.3 G1005G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr9:98218641 G>A maps to NM_000264.3 I1074I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr9:98239881 C>A maps to NM_000264.3 G484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr9:98242783 C>T maps to NM_000264.3 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr9:98232132 G>A maps to NM_000264.3 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr9:98238419 T>A maps to NM_000264.3 K542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr1:45293265 G>A maps to NM_003738.4 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr1:45292685 G>T maps to NM_003738.4 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:45295678 C>G maps to NM_003738.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:45292234 G>C maps to NM_003738.4 A967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr23:23398141 G>T did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr23:23412248 G>A did not map to a codon.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr23:23411519 G>A did not map to a codon.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr23:23353313 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:23353007 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr23:23411377 G>A did not map to a codon.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr23:23411903 T>G did not map to a codon.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr1:11561828 C>T maps to NM_020780.1 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr1:11562934 C>T maps to NM_020780.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:11579444 G>T maps to NM_020780.1 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:11596424 G>T maps to NM_020780.1 R1287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr1:11561057 G>T maps to NM_020780.1 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:11562014 C>G maps to NM_020780.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr10:27700798 C>T maps to NM_001034842.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr10:27702585 G>A maps to NM_001034842.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:27687276 G>A maps to NM_001034842.3 F750F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:27687957 C>A maps to NM_001034842.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:27702470 G>A maps to NM_001034842.3 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr10:27702648 C>T maps to NM_001034842.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr10:27703079 G>A maps to NM_001034842.3 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr10:27702453 C>T maps to NM_001034842.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr10:27702333 G>A maps to NM_001034842.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr8:97311962 G>A maps to NM_014754.1 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr8:97311986 C>A maps to NM_014754.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:479109 G>C maps to NM_030783.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr10:89711892 C>T maps to NM_000314.4 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr10:89692804 C>T maps to NM_000314.4 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr10:89653780 G>C did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr10:89717660 C>A maps to NM_000314.4 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr10:16528556 C>T maps to NM_030664.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr10:16553182 G>A maps to NM_030664.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr10:16526538 C>T maps to NM_030664.3 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr14:52734573 G>A maps to NM_000953.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H8-01A-21D-A34J-08 chr14:52735008 C>T maps to NM_000953.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr14:52781580 G>A maps to NM_000956.3 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr14:52794008 C>G maps to NM_000956.3 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:40681094 C>A did not map to a codon.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:40681847 C>G maps to NM_000958.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr9:130884673 G>A maps to NM_025072.5 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr12:57058263 T>G maps to NM_006601.5 *161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:117487466 C>T maps to NM_020440.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:117492009 G>A maps to NM_020440.2 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:117484583 C>T maps to NM_020440.2 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:117527431 C>T maps to NM_020440.2 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr1:117484383 C>T maps to NM_020440.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr1:117503895 C>G maps to NM_020440.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:48166641 G>A maps to NM_000961.3 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr20:48124480 G>C maps to NM_000961.3 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr14:74327273 C>T maps to NM_152444.2 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:74345929 C>A maps to NM_152444.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr9:125154465 A>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:125154750 C>A maps to NM_000962.2 Y576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr9:125154627 G>A maps to NM_000962.2 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr9:125149012 T>C did not map to a codon.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr1:186648487 G>A maps to NM_000963.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:186645173 A>C maps to NM_000963.2 Y371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:186648238 C>T maps to NM_000963.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr1:186645076 C>A maps to NM_000963.2 G404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr3:46939345 G>A maps to NM_000316.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:209308081 T>C maps to NM_005048.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:209308193 G>T maps to NM_005048.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:209302278 G>T maps to NM_005048.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr12:28122337 G>A maps to ENST00000354417 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr8:141678370 C>T maps to NM_005607.4 V976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr8:141856356 A>G did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr8:141900644 G>C maps to NM_005607.4 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr8:141874415 G>A maps to NM_005607.4 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr8:141669597 T>C maps to NM_005607.4 R1064R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr8:141754815 C>T maps to NM_005607.4 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:27310643 G>A maps to NM_004103.3 G854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:27289832 G>A maps to NM_004103.3 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:27278227 G>A maps to NM_004103.3 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:27312076 C>T maps to NM_004103.3 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr6:43113016 G>A maps to NM_002821.3 V829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:43109978 C>T maps to NM_002821.3 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr6:43096997 C>T maps to NM_002821.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:43098330 C>T maps to NM_002821.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:43096754 C>T maps to NM_002821.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr6:43111248 C>G maps to NM_002821.3 A714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:232576620 G>T maps to ENST00000409321 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:136938250 C>T maps to NM_002825.5 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr19:50357787 C>T maps to NM_017432.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:50361358 G>A maps to NM_017432.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr19:50357787 C>T maps to NM_017432.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:50360311 C>T maps to NM_017432.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr8:142441134 C>T maps to NM_032611.1 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:49197816 T>C maps to NM_002827.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr12:112940024 T>C maps to ENST00000392596 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr7:77256105 C>G maps to NM_002835.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:77256780 C>T maps to NM_002835.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:77240342 C>T maps to NM_002835.3 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr7:77230123 G>T did not map to a codon.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr4:87692490 G>A maps to NM_080685.2 G1662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr4:87671738 C>T maps to NM_080685.2 R923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:214549656 G>A maps to NM_005401.4 R938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:214542899 C>T maps to NM_005401.4 K1057K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr1:214557390 G>A maps to NM_005401.4 Q603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr1:214625280 G>A maps to NM_005401.4 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:214585061 G>A maps to NM_005401.4 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr1:214543024 G>A maps to NM_005401.4 R1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr1:214557223 G>C maps to NM_005401.4 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:131117185 C>T maps to NM_014369.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr14:88945293 C>T maps to NM_007039.3 K827K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr14:88940130 G>A maps to NM_007039.3 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr14:88935897 G>T maps to NM_007039.3 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr14:88936011 G>T maps to NM_007039.3 T1022T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr14:88963634 C>T did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:114397602 G>A maps to NM_015967.5 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:114376997 G>T maps to NM_015967.5 S653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr3:47450917 G>A maps to NM_015466.2 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:47448092 C>G maps to NM_015466.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:47450662 C>T maps to NM_015466.2 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr9:112172685 G>A maps to NM_002829.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:112172684 C>A maps to NM_002829.3 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7596-01A-11D-2229-08 chr9:112166751 G>A maps to NM_002829.3 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr2:120620220 T>G did not map to a codon.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr12:7065323 C>T maps to ENST00000416215 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr20:2944949 G>T maps to NM_002836.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr12:70946774 C>T maps to NM_001109754.1 Q1723Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr12:71016373 G>C maps to NM_001109754.1 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr12:70956846 G>A maps to NM_001109754.1 S1315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:70954685 C>A maps to NM_001109754.1 G1399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:70963580 G>A maps to NM_001109754.1 Q1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr12:70974930 A>G maps to NM_001109754.1 S821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:70918332 G>A maps to NM_001109754.1 V2181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr12:70946776 G>A maps to NM_001109754.1 Q1723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:71016364 G>T maps to NM_001109754.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:198721487 G>A maps to ENST00000271610 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:198701642 C>T maps to ENST00000271610 N700N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:198703457 T>C maps to ENST00000271610 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr1:198719712 C>G maps to ENST00000271610 V1055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr1:198723446 G>T maps to ENST00000271610 E1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:198682088 A>G maps to ENST00000271610 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:198665839 G>A did not map to a codon.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:198719737 C>T maps to ENST00000271610 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:198671528 G>A maps to ENST00000271610 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:198713185 C>T maps to ENST00000271610 Q901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:198671621 A>G maps to ENST00000271610 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:198718659 C>A maps to ENST00000271610 I1018I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr9:8485930 G>A maps to NM_002839.3 N962N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:8340363 G>T maps to NM_002839.3 T1744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr9:8499727 A>G maps to NM_002839.3 Y747Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr9:8465606 A>G maps to NM_002839.3 Y1191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:8331711 G>A maps to NM_002839.3 Q1802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr10:129877892 A>C maps to NM_006504.4 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr10:129877949 G>A maps to NM_006504.4 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr10:129839246 G>A maps to NM_006504.4 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr10:129839234 C>T maps to NM_006504.4 N30N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:129866424 A>G maps to NM_006504.4 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:44044586 G>A maps to NM_002840.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:44069438 G>A maps to NM_002840.3 K872K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr1:44084957 G>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:44058189 C>G maps to NM_002840.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:44069507 G>A maps to NM_002840.3 K895K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:44019308 G>A did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr3:62153670 C>T maps to NM_002841.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:62063841 G>A maps to NM_002841.3 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr19:55718093 T>A maps to NM_002842.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr19:55718096 G>A maps to NM_002842.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:48166646 C>G maps to NM_002843.3 S961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr11:48149383 G>A maps to NM_002843.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr11:48166389 C>G maps to NM_002843.3 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr6:128563724 G>C maps to ENST00000368210 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:128411003 G>A maps to ENST00000368210 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:128411045 C>T maps to ENST00000368210 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr18:7926656 G>A maps to NM_001105244.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr18:8113616 G>T maps to NM_001105244.1 E664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr18:7949202 C>T maps to NM_001105244.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:7888243 T>C maps to NM_001105244.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr18:8394530 C>A maps to NM_001105244.1 L1422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr18:8394531 C>A maps to NM_001105244.1 R1423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr18:7955362 T>A maps to NM_001105244.1 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr18:7955230 G>A maps to NM_001105244.1 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr18:7906564 G>T maps to NM_001105244.1 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr2:220164843 G>A maps to NM_002846.3 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:220172279 C>A did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr7:157959788 G>A maps to NM_002847.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr7:157414144 C>T maps to NM_002847.3 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:15654947 C>G maps to NM_030667.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:15475701 C>A maps to NM_030667.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:15669883 A>T maps to NM_030667.1 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr12:15742397 G>A maps to NM_030667.1 V1140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr12:15636951 C>T maps to NM_030667.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr12:15669841 G>A maps to NM_030667.1 W577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr12:15673220 C>T maps to NM_030667.1 D622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:71158498 T>G maps to NM_002849.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:71078045 T>A did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:71155304 G>T maps to NM_002849.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:5207950 C>T maps to NM_002850.3 P1920P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:5208366 G>A maps to NM_002850.3 F1841F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr20:40979289 G>A maps to ENST00000373198 Q615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr20:41101055 G>A maps to ENST00000373198 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr20:40980907 G>T maps to ENST00000373198 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr20:41306785 G>T maps to ENST00000373198 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr20:41385105 C>T maps to ENST00000373198 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr20:40710551 A>G maps to ENST00000373198 R1436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:29587161 T>C maps to NM_005704.4 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:29644357 G>C maps to NM_005704.4 P1214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:29631879 G>A maps to NM_005704.4 V930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr1:29587212 C>T maps to NM_005704.4 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:29638031 C>T maps to NM_005704.4 I984I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:121699857 C>T maps to NM_002851.2 H2241H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr7:121701228 A>C maps to NM_002851.2 A2301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr7:121691547 A>T maps to NM_002851.2 K2051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:121671534 C>T maps to NM_002851.2 V1696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr7:121608116 A>G maps to NM_002851.2 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr7:121623769 C>G maps to NM_002851.2 S224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr17:40557363 G>A maps to NM_012232.5 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:40557193 G>A maps to NM_012232.5 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:40574758 G>A maps to NM_012232.5 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:40556779 G>A maps to NM_012232.5 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:130476447 C>T maps to NM_001002913.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr17:57775024 G>C maps to ENST00000409433 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:157160248 C>T maps to NM_002852.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:1538462 C>T maps to NM_001013658.1 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:1537431 C>T maps to NM_001013658.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:144902848 G>C maps to NM_078480.1 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:144900182 T>G maps to NM_078480.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:144899259 C>T maps to NM_078480.1 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:31423054 G>A maps to ENST00000373741 V961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr2:20451387 C>A maps to ENST00000361078 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:20463021 G>A maps to ENST00000361078 F719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:20497356 A>G maps to ENST00000361078 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:44924865 C>A maps to NM_033224.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:30889547 G>A maps to NM_013357.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:30889785 C>G maps to NM_013357.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr8:30889926 C>T maps to NM_013357.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr8:30890026 C>T maps to NM_013357.2 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr2:61180203 C>T maps to NM_144709.2 K412K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:105146707 G>A maps to NM_019042.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:105111199 C>A maps to NM_019042.3 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr7:105099647 G>A maps to NM_019042.3 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr12:44148514 G>A maps to NM_031292.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr12:44148847 A>G maps to NM_031292.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:44148205 C>T maps to NM_031292.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr11:119536007 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:119535588 G>A maps to NM_002855.4 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:45381750 G>A maps to NM_002856.2 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:45391564 C>T maps to NM_001042724.1 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr1:161043539 C>T maps to NM_030916.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr1:161043041 G>A maps to NM_030916.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr1:161047417 C>A maps to NM_030916.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:108082472 C>T maps to NM_007062.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:108102725 A>G maps to NM_007062.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr21:45535280 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:45540616 T>C maps to NM_005049.2 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr5:159520156 G>C maps to NM_001130864.1 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr10:134219518 G>A maps to NM_138499.3 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr2:1652572 G>A maps to NM_012293.1 R993R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:1677463 G>A maps to NM_012293.1 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr2:1652026 G>C maps to NM_012293.1 V1175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:1658259 C>A maps to NM_012293.1 G620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:1680769 C>T maps to NM_012293.1 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr2:1648499 G>A maps to NM_012293.1 I1211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:1653340 G>A maps to NM_012293.1 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:1664728 T>C maps to NM_012293.1 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr2:1651987 C>T maps to NM_012293.1 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr2:1677574 C>T maps to NM_012293.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr2:1652647 G>A maps to NM_012293.1 I968I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr2:1652398 G>A maps to NM_012293.1 H1051H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:52284540 G>A maps to NM_144651.4 Q1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:52287227 A>G maps to NM_144651.4 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:52336291 C>G did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr8:52284568 C>A maps to NM_144651.4 R1255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:52384808 G>T maps to NM_144651.4 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr8:52336258 G>A maps to NM_144651.4 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr8:52321225 G>A maps to NM_144651.4 S986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr8:52321747 G>A maps to NM_144651.4 H812H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr8:52387661 C>A maps to NM_144651.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:58395288 C>T maps to NM_017771.3 Q447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:133266847 G>A did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:133266863 A>T maps to NM_018663.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr12:120651734 T>C maps to NM_001080855.1 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:120650197 G>C maps to NM_001080855.1 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:120652756 G>T maps to NM_001080855.1 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:31213942 G>A maps to NM_013258.4 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr17:79892828 C>T maps to ENST00000432920 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:79892537 C>T maps to ENST00000432920 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:226108947 G>A maps to NM_013328.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:226109590 G>A maps to NM_013328.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr8:144687914 G>C maps to NM_023078.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr16:31228220 C>T maps to NM_152901.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:191179205 T>G maps to NM_001083308.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr20:25255256 C>T maps to NM_002862.3 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr20:25262776 C>A maps to NM_002862.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr20:25262743 G>T maps to NM_002862.3 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:51411034 C>T maps to NM_002863.4 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:51375032 C>A maps to NM_002863.4 E779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:51381451 G>C maps to NM_002863.4 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr14:51382668 C>T maps to NM_002863.4 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr11:64519901 G>A maps to NM_005609.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:64521494 C>T maps to NM_005609.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr11:64521022 C>T maps to NM_005609.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr11:64521766 C>G maps to NM_005609.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:64521440 C>T maps to NM_005609.2 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:64521784 G>T maps to NM_005609.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr11:64521043 C>T maps to NM_005609.2 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:55838570 G>A maps to NM_015617.1 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr15:55838316 T>A maps to NM_015617.1 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:154931793 G>A maps to NM_138300.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:158911996 T>C maps to NM_152501.3 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr12:21613999 G>A maps to NM_024854.3 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:100167371 C>T maps to NM_032709.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:100144782 G>A maps to NM_032709.2 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr12:9318712 C>A maps to NM_002864.2 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr12:9303305 G>A maps to NM_002864.2 L1440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:9349218 C>T maps to NM_002864.2 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr12:9353587 G>C maps to NM_002864.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr12:9313712 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr12:9318715 T>C maps to NM_002864.2 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr12:9334672 G>A maps to NM_002864.2 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr20:3147716 C>T maps to NM_014731.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:49137813 T>G maps to NM_005051.1 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:49142160 C>G maps to NM_005051.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr6:163991739 T>C maps to ENST00000361752 *348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:46206183 C>T maps to NM_017659.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr19:46198709 C>T maps to NM_017659.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr17:74287584 G>A maps to NM_032134.1 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr17:74287999 G>T maps to NM_032134.1 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr17:74274101 G>A maps to NM_032134.1 H1529H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr11:32953740 C>T maps to NM_001076786.1 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:180165520 C>G maps to NM_002826.4 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:180151442 C>A maps to NM_002826.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:180155268 A>G maps to NM_002826.4 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:180163462 G>A maps to NM_002826.4 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:139100648 G>A maps to NM_181701.3 F674F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr9:139115872 G>A maps to NM_181701.3 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr9:139100936 G>A maps to NM_181701.3 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr19:10823849 C>T maps to NM_031209.2 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr2:136418926 C>T maps to ENST00000409606 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:136467632 A>G maps to ENST00000409606 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:136399346 C>T maps to ENST00000409606 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:136396633 C>T maps to ENST00000409606 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:136396634 C>T maps to ENST00000409606 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:136379095 T>C maps to ENST00000409606 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr12:57662213 A>G maps to ENST00000438036 N686N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr8:37756683 C>T maps to NM_001002814.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr8:37730675 C>T maps to NM_001002814.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr8:37730228 A>C maps to NM_001002814.2 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr10:119768712 A>T maps to ENST00000369199 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr10:119799784 A>G maps to ENST00000369199 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:119799985 G>A maps to ENST00000369199 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr16:532706 C>T maps to NM_014700.3 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:570490 G>A maps to NM_014700.3 E683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:73303222 C>T maps to NM_015470.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:73315800 C>G maps to NM_015470.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr18:8638166 G>A maps to NM_001025300.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr1:153955284 C>T did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:238483688 C>T maps to NM_022449.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:140125808 C>T maps to ENST00000275874 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr7:140111744 C>T maps to ENST00000275874 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr11:66043604 G>T maps to NM_030981.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:72176379 T>G maps to NM_014999.2 Y159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr1:156035756 G>A maps to NM_020387.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:156039462 A>G maps to NM_020387.2 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr16:2201694 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:2201700 G>A maps to NM_014353.4 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr18:9708422 C>G maps to NM_006868.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:146865141 C>G maps to NM_006834.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr17:27041919 T>A did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr17:27042863 C>A maps to NM_001144943.1 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr17:27042130 G>A maps to NM_001144943.1 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr11:87908417 G>A maps to NM_022337.2 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:154493402 G>C did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:154490408 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:58147123 G>A maps to NM_138453.2 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr19:11446171 G>A maps to NM_004283.3 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:135893465 G>A maps to NM_001172435.1 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:61672058 C>A maps to NM_013401.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:61672225 C>T maps to NM_013401.2 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:70149379 T>A maps to NM_175623.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:102755662 C>A did not map to a codon.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr23:102192946 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:102192823 A>G did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:80615804 C>A maps to NM_006822.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:69502177 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:69502096 G>A did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:69502410 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr19:41292771 G>A maps to ENST00000419646 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr3:20017550 A>T maps to NM_004162.4 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr12:56380869 A>G maps to NM_002868.2 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr17:40282495 G>A maps to NM_201434.1 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr11:73429682 C>T maps to NM_198896.1 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:133553478 G>A maps to NM_016577.3 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:130738095 G>C maps to NM_032144.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr3:128532229 C>A maps to NM_004637.5 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:63481933 C>T maps to NM_016530.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:103080373 G>T did not map to a codon.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr23:103080241 T>C did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr17:5276626 C>A maps to NM_004703.4 R635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr17:5235281 C>T maps to NM_004703.4 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr16:28917493 G>A maps to NM_024816.2 C423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr9:127990195 G>T maps to NM_005833.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr9:127996096 G>A maps to NM_005833.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:125865490 G>A maps to NM_012197.3 *1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:125861041 A>T maps to NM_012197.3 K928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr1:174188382 C>T maps to NM_014857.3 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:66264399 A>T maps to ENST00000451741 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr14:24737594 C>T maps to NM_182836.1 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr22:37637673 G>A maps to NM_002872.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:79991360 C>T maps to NM_005052.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:79991598 C>G maps to NM_005052.2 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:50388082 G>A maps to NM_013277.3 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:50400384 G>A maps to NM_013277.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr5:68680679 C>T maps to NM_133339.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:8940659 C>A maps to NM_020165.3 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:8990249 G>A maps to NM_020165.3 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:117874119 C>A maps to NM_006265.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:117861265 A>G maps to NM_006265.2 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:13063835 C>A maps to NM_005053.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr9:110091855 G>C maps to NM_002874.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:110073971 T>C maps to NM_002874.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:131953938 A>T maps to NM_005732.3 T1114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr5:131915146 A>G maps to NM_005732.3 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr5:131911504 C>T maps to NM_005732.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:131931410 C>T maps to NM_005732.3 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr2:17697543 A>G maps to NM_001099218.2 C713C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr2:17696514 A>G maps to NM_001099218.2 N1056N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr17:56770069 G>A maps to NM_058216.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr17:56787302 T>C maps to NM_058216.1 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr14:68352615 C>T maps to NM_133509.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr14:69061263 C>T maps to NM_133509.3 Q367*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-6491-01A-11D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:33433485 C>T maps to NM_002878.3 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr17:33430518 C>A maps to NM_002878.3 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr12:1023246 G>C maps to NM_134424.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr12:1036312 G>T maps to NM_134424.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:95470493 A>G did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:46739821 C>T maps to NM_003579.3 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:46726409 C>T maps to NM_003579.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr3:51679076 C>T maps to NM_015106.2 R830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr3:51696556 C>T maps to NM_015106.2 I1175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:67161082 T>C did not map to a codon.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr12:110968352 A>G maps to NM_152442.3 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr7:4856926 C>T maps to NM_018059.4 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr7:4917506 G>A maps to NM_018059.4 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:4862112 C>T maps to NM_018059.4 W509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:4917455 C>T maps to NM_018059.4 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr7:4862157 G>A maps to NM_018059.4 C494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:4874564 G>A maps to NM_018059.4 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr7:4874237 C>T maps to NM_018059.4 W472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr7:4839062 C>T maps to NM_018059.4 A1058A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr7:4917482 C>T maps to NM_018059.4 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:150210517 G>A maps to NM_139165.1 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:150210685 G>A maps to NM_139165.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr6:150240359 G>C maps to NM_001001788.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr3:12660012 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:12626378 C>T maps to ENST00000415519 K610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr1:155108443 C>G maps to NM_018845.3 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr11:36614686 A>G maps to NM_000536.3 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr14:102717261 C>G maps to NM_014226.1 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr14:102732226 G>T maps to NM_014226.1 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr14:102698091 C>T maps to NM_014226.1 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr17:17701460 G>A maps to ENST00000395776 S1733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:17699918 C>T maps to ENST00000395776 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:17701184 C>T maps to ENST00000395776 S1641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:17699906 T>C maps to ENST00000395776 S1215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr17:17697665 C>T maps to ENST00000395776 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr17:17698484 C>T maps to ENST00000395776 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr5:34824124 C>T maps to NM_001145521.1 N726N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:17819470 G>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:17819547 G>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:17819548 G>T did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:17819887 C>G did not map to a codon.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr23:17818620 T>G did not map to a codon.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr18:9535826 G>A maps to NM_006788.3 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr14:36103864 A>G maps to NM_194301.2 F1464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr14:36128344 G>A maps to NM_194301.2 R1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IF-01A-11D-A31L-08 chr14:36190921 C>A maps to NM_194301.2 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr14:36143915 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr14:36074809 T>A maps to NM_194301.2 V1839V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr20:20453483 G>C maps to NM_020343.3 L1828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr20:20453516 G>A maps to NM_020343.3 N1817N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr20:20601266 A>T maps to NM_020343.3 L414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr20:37144952 C>T maps to NM_020336.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:37146166 C>G maps to NM_020336.2 S357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr20:37182547 C>G maps to NM_020336.2 A1067A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:135975665 G>C maps to NM_006266.2 S853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:135984210 C>T maps to NM_006266.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:129975311 G>A maps to NM_014636.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr9:129958791 G>A maps to NM_014636.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr9:129974475 G>A maps to NM_014636.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:129931021 C>T maps to NM_014636.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr9:129958827 C>T maps to NM_014636.2 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr1:178854322 G>A maps to NM_152663.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr8:85799857 G>A maps to NM_001100391.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:238785962 C>A maps to NM_005855.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:40914627 C>T maps to ENST00000456272 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr17:40914815 C>T maps to ENST00000456272 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:131359089 G>A did not map to a codon.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr16:67778206 C>T maps to NM_020850.1 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr16:67778257 G>A maps to NM_020850.1 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:67763682 T>G maps to NM_020850.1 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr16:67768909 A>C maps to NM_020850.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:170720912 T>A maps to NM_022897.3 I990I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr5:170668103 T>G maps to NM_022897.3 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr5:170725846 C>T maps to NM_022897.3 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr5:170720930 G>A maps to NM_022897.3 R996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr2:109382595 A>G maps to NM_006267.4 E1867E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IH-01A-11D-A25Y-08 chr2:109357022 A>T maps to NM_006267.4 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:109382139 C>T maps to NM_006267.4 S1715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr2:109370369 G>A maps to NM_006267.4 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr2:109399177 C>T maps to NM_006267.4 L3077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7391-01A-11D-2012-08 chr2:109352600 T>C maps to NM_006267.4 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:109367718 G>T did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:109398720 G>A maps to NM_006267.4 K2966K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr2:109382703 G>A maps to NM_006267.4 S1903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:36251469 G>A maps to NM_001161429.1 C458C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:36265594 G>C maps to NM_001161429.1 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr9:6012685 G>A maps to NM_012416.2 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr6:13642753 G>A maps to NM_005493.2 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:41652029 G>A maps to NM_002883.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:8192665 G>C maps to NM_016492.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr1:21928277 C>T maps to NM_001145658.1 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr1:21943974 G>A maps to NM_001145658.1 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:21936073 G>A maps to NM_001145658.1 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr17:2867169 G>A maps to NM_015085.4 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr17:2867250 G>C maps to NM_015085.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr17:2923847 G>T maps to NM_015085.4 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:99342514 G>C maps to NM_001100426.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:98086810 C>T maps to NM_021033.6 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr13:98086795 G>C maps to NM_021033.6 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:131351187 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:134501393 G>A maps to NM_198679.1 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:134473642 G>A maps to NM_198679.1 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr9:134503938 C>T maps to NM_198679.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr4:160273852 C>T maps to NM_014247.2 P1133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr4:160251523 G>A maps to NM_014247.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr4:160274812 G>A maps to NM_014247.2 Q1261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:48141545 G>T maps to NM_001098531.2 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr12:48143716 G>A maps to NM_001098531.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr12:48142707 C>A maps to NM_001098531.2 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr7:22190075 G>C maps to ENST00000344041 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr7:22190087 G>A maps to ENST00000344041 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:130815437 C>A maps to ENST00000514667 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr5:130764619 C>G maps to ENST00000514667 V1635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr5:130797623 C>A maps to ENST00000514667 E930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr17:38340837 A>G maps to ENST00000456989 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:204305155 G>T maps to ENST00000374493 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr2:204305713 A>G maps to ENST00000374493 C785C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:204354462 T>A maps to ENST00000374493 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr2:204326585 C>T maps to ENST00000374493 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr11:47464318 G>C maps to NM_005055.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr17:38508321 G>A maps to NM_001145301.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr17:38512357 G>A maps to NM_001145301.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr3:25611300 C>T maps to NM_000965.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr7:150037212 G>C maps to NM_002889.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr7:150037233 C>T maps to NM_002889.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr5:167921570 C>T maps to NM_002887.3 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr5:86667933 G>A did not map to a codon.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr5:86676365 C>T maps to NM_002890.1 Q882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr5:86659188 T>A maps to NM_002890.1 L493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr5:86675621 C>G maps to NM_002890.1 S853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr5:86659244 C>T maps to NM_002890.1 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr5:86681170 C>T maps to NM_002890.1 Q938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr5:86675667 G>T did not map to a codon.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr3:141231005 T>A maps to ENST00000452898 C45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr3:141292834 C>G maps to ENST00000452898 S470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr3:141328365 G>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:141290311 T>A maps to ENST00000452898 L362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:141205978 G>C maps to ENST00000452898 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr13:114781702 C>T maps to ENST00000389544 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr13:114780793 C>T maps to ENST00000389544 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:113543581 G>A maps to NM_001193520.1 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr12:113559375 C>A maps to NM_001193520.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:113543659 C>A maps to NM_001193520.1 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:113541857 G>T maps to NM_001193520.1 S667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:113553840 G>A maps to NM_001193520.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr12:113553482 C>T maps to NM_001193520.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:178414789 C>T maps to ENST00000263528 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:178433453 G>A maps to ENST00000263528 E1087E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:17399348 G>A maps to NM_016084.3 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:17398762 G>A maps to NM_016084.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr17:17399375 G>A maps to NM_016084.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr22:35947785 G>T maps to NM_014310.3 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr9:85616026 A>T maps to NM_152573.2 Y407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr9:85615350 G>A maps to NM_152573.2 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr4:82366943 C>A maps to NM_152545.1 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr4:82369371 G>A maps to NM_152545.1 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:79294084 G>A maps to NM_002891.4 Q848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:79292108 G>T maps to NM_002891.4 R924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr15:79294031 G>T maps to NM_002891.4 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr15:79382663 G>A maps to NM_002891.4 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr15:79291062 G>A maps to NM_002891.4 Q967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr5:80408575 C>G maps to NM_006909.1 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:80363997 G>A maps to NM_006909.1 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr5:80256688 C>T maps to NM_006909.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr5:80256601 G>C maps to NM_006909.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:80382758 G>A maps to NM_006909.1 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:80419548 C>A maps to NM_006909.1 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:64510266 G>A maps to ENST00000320253 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:64507520 G>T maps to ENST00000320253 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr11:64508538 G>A maps to ENST00000320253 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:64502699 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:33752313 G>A maps to NM_170672.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr2:33784036 C>T maps to NM_170672.2 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:33741636 T>C maps to NM_170672.2 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr2:33774784 C>G maps to NM_170672.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr2:33774796 C>T maps to NM_170672.2 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr2:33774799 C>T maps to NM_170672.2 C508C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr19:49238476 C>T maps to NM_017805.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:49224213 G>A maps to NM_017805.2 I911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:34068185 C>T maps to NM_033315.3 C158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:34068215 G>A maps to NM_033315.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr13:27845675 A>G maps to NM_206827.1 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr13:27847629 G>A maps to NM_206827.1 *243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:65350895 G>A maps to NM_016563.2 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr20:4768914 C>G did not map to a codon.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr10:45480279 G>A maps to NM_032023.3 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr10:45479529 G>T maps to NM_032023.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr10:45484753 G>A maps to NM_032023.3 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr1:206681309 C>T maps to NM_182663.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:26217551 C>G maps to NM_001164747.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:10428228 C>T maps to NM_133452.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr18:56939840 G>A maps to NM_013435.2 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr13:49033969 G>T did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr13:48951100 T>C maps to NM_000321.2 D421D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr13:48941647 C>T maps to NM_000321.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr13:48954378 T>G did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr13:48955579 G>A did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr13:49027133 A>T maps to NM_000321.2 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr13:48881511 G>A maps to NM_000321.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr13:48947539 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr13:48951140 G>T maps to NM_000321.2 G435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr13:48936982 C>T maps to NM_000321.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr13:49027167 C>T maps to NM_000321.2 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr8:53570372 T>A maps to NM_014781.4 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:53570559 T>A maps to NM_014781.4 K640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr7:5104737 T>C maps to NM_021163.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr7:5097369 G>A maps to NM_021163.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr7:5103362 A>G maps to NM_021163.3 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:5104850 A>G maps to NM_021163.3 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:205069074 G>A maps to NM_005057.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:24580863 A>T maps to NM_006910.4 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:24580071 A>G maps to NM_006910.4 K687K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:24580554 A>G maps to NM_006910.4 G848G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr23:16887262 G>C did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:16881167 C>G did not map to a codon.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr23:16871870 T>A did not map to a codon.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr23:16870183 T>G did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:16863979 C>G did not map to a codon.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr23:16887231 C>A did not map to a codon.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr23:16887236 C>G did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:16887241 G>A did not map to a codon.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr18:20516825 G>A maps to ENST00000360790 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr18:20581636 C>T maps to ENST00000360790 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr20:398253 C>G maps to NM_031229.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr20:408137 T>C did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr20:402810 G>T maps to NM_031229.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr20:398398 A>G maps to NM_031229.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr20:35717459 C>T maps to NM_002895.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr20:35661154 C>T maps to NM_002895.2 Q765Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr20:35695459 A>G maps to NM_002895.2 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr20:35668561 G>A maps to NM_002895.2 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:53513067 C>T maps to NM_005611.3 V902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr16:53496503 C>G maps to NM_005611.3 Y499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr23:47045132 C>T did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:47034419 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:47034442 C>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr21:15599566 G>T maps to NM_144770.3 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr21:15599598 G>A maps to NM_144770.3 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:94746325 G>A maps to NM_203390.2 F771F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr8:94746868 A>G maps to NM_203390.2 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr8:94747090 T>C maps to NM_203390.2 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:66392978 A>T maps to NM_006328.3 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:66391952 C>T maps to NM_006328.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr1:110882128 C>T maps to NM_022768.4 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr1:110882110 G>A maps to NM_022768.4 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:110883455 C>T maps to NM_022768.4 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr3:51430467 G>A maps to NM_013286.4 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:51430951 C>T maps to NM_013286.4 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr3:51429756 G>T maps to NM_013286.4 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:155131213 C>G maps to NM_014892.3 S431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr6:155143452 C>T maps to NM_014892.3 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr6:155145425 C>A maps to NM_014892.3 S662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr6:155145426 G>A maps to NM_014892.3 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr10:6139142 C>T maps to NM_001145547.1 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:6148124 A>G maps to NM_001145547.1 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:114358414 C>A did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr12:114261055 G>A maps to NM_016196.3 D952D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr12:114395755 G>T maps to NM_016196.3 S224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr14:23374208 G>A maps to NM_001077351.1 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr14:23374206 T>A maps to NM_001077351.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr14:73566392 G>T maps to NM_021239.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr14:73563708 T>G maps to NM_021239.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr14:73538408 G>T maps to NM_021239.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr13:79911234 A>G did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr13:79945212 G>A maps to ENST00000438737 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:145610480 G>A did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr5:145641353 C>T maps to NM_018989.1 H725H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr5:145651233 C>T maps to NM_018989.1 F995F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:145665538 T>C maps to NM_018989.1 P1043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr7:127953233 G>A maps to NM_018077.2 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr7:127957755 G>A maps to NM_018077.2 R582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:155503973 G>A maps to NM_053043.2 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr7:155534529 T>C maps to NM_053043.2 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr1:235324258 G>C maps to NM_015014.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr1:235295102 T>C maps to NM_015014.2 K406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr20:34292656 A>G maps to NM_184234.1 Y475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:66411035 G>A maps to NM_001198845.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:66407346 G>A maps to NM_002896.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr23:106312632 C>G did not map to a codon.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr23:106358743 G>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:36125267 G>A maps to NM_024321.3 W376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:36128162 C>T maps to NM_024321.3 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr2:238726674 C>G maps to NM_001080504.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:238728940 C>T maps to NM_001080504.2 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:178977395 G>C maps to ENST00000456670 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr2:178988611 G>A maps to ENST00000456670 W349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr4:40440250 C>T maps to NM_001098634.1 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr4:40440733 C>T maps to NM_001098634.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7593-01A-11D-2229-08 chr4:40439976 C>A maps to NM_001098634.1 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:40439926 C>T maps to NM_001098634.1 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:50127885 T>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:50145725 C>G maps to NM_005778.2 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr3:50142979 A>G did not map to a codon.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr3:50142522 A>G maps to NM_005778.2 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:50091778 C>T maps to NM_005777.2 N548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:50095329 A>G maps to NM_005777.2 E621E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr1:145508276 A>T maps to NM_005105.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr22:36140241 T>G maps to ENST00000338644 *389C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:161223857 G>A maps to NM_016836.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:161223851 G>T maps to NM_016836.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr12:56975651 T>C maps to NM_002898.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:29938881 A>C maps to NM_001003793.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr3:30032697 T>C maps to NM_001003793.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:135961277 G>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:129546422 A>T did not map to a codon.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr23:129545369 C>T did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:7110533 C>T maps to NM_014469.4 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr11:7111301 T>C maps to NM_014469.4 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:7111241 G>A maps to NM_014469.4 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr3:139173604 C>T maps to NM_004164.2 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:48388396 G>T maps to NM_002900.2 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:48387901 G>T maps to NM_002900.2 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:48390445 C>G maps to NM_002900.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr10:48388537 G>A maps to NM_002900.2 I780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:48388750 C>T maps to NM_002900.2 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr10:48388213 G>T maps to NM_002900.2 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:48389614 G>A maps to NM_002900.2 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr10:48388264 G>T maps to NM_002900.2 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:48385881 C>T maps to NM_002900.2 K1070K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:7280931 C>T maps to NM_031491.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr4:26422342 T>C maps to NM_005349.2 A177A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-7263-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr20:43945403 C>A maps to NM_014276.2 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr20:43944844 G>T maps to NM_014276.2 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr20:43936861 C>T maps to NM_014276.2 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr8:30332299 G>C maps to NM_001008712.1 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr22:41347431 G>T maps to NM_014248.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr22:41360102 C>T maps to NM_014248.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:173952660 C>A maps to NM_172071.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:125643073 C>A did not map to a codon.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr9:125627746 C>T maps to NM_001100588.1 Q505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:46190880 G>A maps to ENST00000405162 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:46191012 C>T maps to ENST00000405162 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr13:50108310 G>A maps to NM_018191.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr13:50123785 T>C did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr1:28862413 G>A maps to NM_001048194.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr1:28858315 C>T maps to NM_001048194.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:17743044 C>T maps to NM_018715.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr11:66611084 C>G maps to NM_005133.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:76415817 T>C maps to NM_015436.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr4:76439451 T>G maps to NM_015436.2 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:4826915 T>C maps to NM_005772.3 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:32124995 G>A maps to NM_002901.2 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr15:77241520 C>A maps to ENST00000320963 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr19:50042434 C>T maps to NM_020650.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:50046457 C>T maps to NM_020650.2 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:103148295 A>G maps to NM_015156.2 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr17:9808173 G>C maps to NM_002903.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr1:211654484 G>A maps to NM_183059.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr1:211652473 G>A maps to NM_183059.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:211652548 C>T maps to NM_183059.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr6:31922530 G>A maps to ENST00000375425 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr8:74231359 G>C maps to NM_172037.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr14:68193773 G>A maps to NM_152443.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:55559838 G>C maps to NM_001145971.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:18736912 G>A maps to ENST00000444297 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:57348691 G>A maps to NM_003708.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr12:57351083 G>T maps to NM_003708.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:57348844 C>T maps to NM_003708.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:10132364 C>G maps to NM_015725.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:10127886 G>A maps to NM_015725.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:10129434 G>T maps to NM_015725.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:10132277 G>A maps to NM_015725.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:10124178 C>T maps to NM_015725.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr11:110102758 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr11:110104000 G>C maps to ENST00000405097 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:24641796 C>T maps to NM_005132.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr14:24642505 C>T maps to NM_005132.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr14:24641963 C>T maps to NM_005132.2 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:24647313 C>T maps to NM_005132.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr14:24648887 G>A maps to NM_005132.2 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:36083380 T>C maps to NM_021111.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:21629872 G>C maps to NM_032941.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr12:21628611 G>A maps to NM_032941.2 Q366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr8:145742568 T>A maps to ENST00000428558 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr8:145738092 C>T maps to ENST00000428558 A939A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:145742148 C>G did not map to a codon.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr8:145738639 G>A maps to ENST00000428558 D808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr8:145739864 C>A maps to ENST00000428558 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr8:145737552 C>T maps to ENST00000428558 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:73658603 C>T maps to NM_004259.5 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr17:73624384 G>A maps to NM_004259.5 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr17:73625552 G>C maps to NM_004259.5 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr17:73661145 G>C maps to NM_004259.5 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:86444186 G>C maps to NM_001164732.1 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr5:137780951 C>T maps to ENST00000378339 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr10:65354572 C>T maps to NM_001001330.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:112256897 G>C maps to NM_005669.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:79349244 C>A maps to NM_002909.4 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr2:79350328 G>A maps to NM_002909.4 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr2:79385862 G>T maps to NM_138937.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:79254985 T>C maps to NM_001008387.1 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:79255020 T>A maps to NM_001008387.1 L141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr2:79255000 G>A maps to NM_001008387.1 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:65425830 G>A maps to NM_021975.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:65421989 T>A maps to NM_021975.3 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:45528912 C>T maps to ENST00000221452 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:45540981 C>T maps to ENST00000221452 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr19:45515200 C>T maps to ENST00000221452 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr19:45515404 G>A maps to ENST00000221452 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr4:37633099 C>T maps to NM_001085399.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr5:141019627 G>C maps to NM_173828.4 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:141019744 G>A maps to NM_173828.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:141018522 C>T maps to NM_173828.4 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:103234158 G>T maps to ENST00000428762 T1294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr7:103417016 C>T maps to ENST00000428762 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:103126771 G>T maps to ENST00000428762 T3285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:103155674 G>A maps to ENST00000428762 V2692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:103243843 C>T maps to ENST00000428762 E1080E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:103143678 T>A did not map to a codon.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr7:103270589 C>T maps to ENST00000428762 K833K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:103202351 C>T maps to ENST00000428762 G1753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr7:103270582 C>A maps to ENST00000428762 G836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:103216152 C>A did not map to a codon.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr7:103243885 C>T maps to ENST00000428762 P1066P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:103243846 C>T maps to ENST00000428762 W1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:103301847 C>T maps to ENST00000428762 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr7:103180642 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr7:103234329 C>G did not map to a codon.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr7:103341354 A>G did not map to a codon.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr7:103175929 C>T maps to ENST00000428762 A2394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:103155698 G>A maps to ENST00000428762 R2684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr7:103130246 G>A maps to ENST00000428762 C3235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr7:103137150 G>A maps to ENST00000428762 Y3005Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:73101848 C>G maps to NM_152222.1 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr11:73106302 G>A maps to NM_152222.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr11:73101945 C>G maps to NM_152222.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:204130516 G>A maps to NM_000537.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:204131244 G>T maps to NM_000537.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:204124946 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:204124206 G>A maps to NM_000537.3 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr23:153209358 C>T did not map to a codon.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr23:153207480 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153205607 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:153208458 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:153205599 C>T did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:153207039 C>G did not map to a codon.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr23:17047657 A>G did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:17072946 G>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:17040362 C>T did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:8425905 G>A maps to NM_012102.3 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:8418745 G>A maps to NM_012102.3 P1283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:8716263 C>T maps to NM_012102.3 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:8420635 T>C maps to NM_012102.3 T977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr12:15262343 G>A maps to NM_032918.2 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr12:15262052 G>A maps to NM_032918.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:18234235 G>A maps to NM_024730.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr4:57796371 C>T maps to NM_005612.4 Q450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr4:57785988 C>G maps to NM_005612.4 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:57777136 G>C maps to NM_005612.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr4:57797435 C>G maps to NM_005612.4 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr10:43606743 G>A maps to NM_020975.4 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:43612120 G>A maps to NM_020975.4 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr10:43617452 G>A maps to NM_020975.4 T930T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr3:108475981 C>T maps to NM_032579.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:85581596 G>A maps to NM_017750.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr2:100055564 C>T maps to NM_016316.2 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:100038069 T>C maps to NM_016316.2 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:111697183 G>A maps to NM_002912.3 Q792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr6:111678328 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr6:111680070 G>A maps to NM_002912.3 L2342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:111693796 A>G did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:111695450 T>C maps to NM_002912.3 A1369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr6:111695501 C>T maps to NM_002912.3 T1352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:111631163 C>G maps to NM_002912.3 L2978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:1818553 G>A maps to NM_020695.3 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:1828052 G>A maps to NM_020695.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr19:1818780 G>A maps to NM_020695.3 N942N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr19:1821532 G>A maps to NM_020695.3 H793H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:114314648 C>T maps to NM_015523.3 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr4:39290413 G>A maps to ENST00000381897 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr3:186507996 G>C maps to NM_181573.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:33348691 G>A maps to NM_001017368.1 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:33343398 G>C maps to NM_001017368.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr22:29835040 G>A maps to NM_021026.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:29837927 C>T maps to NM_021026.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr22:29837558 C>G maps to NM_021026.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:32587229 C>T maps to NM_001098527.2 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:32586941 G>A maps to NM_001098527.2 S318S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-A6JE-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:32756464 T>C maps to NM_001098535.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr22:32754309 C>G maps to NM_001098535.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr22:32754255 G>A maps to NM_001098535.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr6:112671338 C>T maps to NM_001013734.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:112671179 C>G maps to NM_001013734.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr6:112671569 T>C maps to NM_001013734.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr3:53133434 A>G maps to NM_052859.3 C390C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:53157825 G>A maps to NM_052859.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:53153914 A>G maps to NM_052859.3 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr3:16411643 G>A maps to NM_015150.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:176012349 G>C maps to NM_022457.5 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr1:176132983 C>T maps to NM_022457.5 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:14090330 T>A maps to NM_002918.4 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr19:14076338 G>A maps to NM_002918.4 I711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr19:6004276 T>A maps to NM_000635.3 K479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr19:6040053 G>T maps to NM_000635.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr9:3263050 G>A maps to NM_134428.1 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:3330438 C>T maps to NM_134428.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:107126786 C>G maps to ENST00000357881 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:107109318 C>T maps to ENST00000357881 Q388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr12:107113759 C>G maps to ENST00000357881 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:151317304 C>A maps to NM_000449.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:151315025 G>C maps to NM_000449.3 S496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr1:151315104 G>T maps to NM_000449.3 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:117232166 C>T maps to NM_173560.3 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr6:117246697 C>T maps to NM_173560.3 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:117198534 C>T maps to NM_173560.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr15:56387890 G>A maps to NM_022841.5 Q679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr15:56387729 C>T maps to NM_022841.5 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:56386607 A>C maps to NM_022841.5 S1106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr15:56387308 C>A maps to NM_022841.5 E873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr15:56387816 C>A maps to NM_022841.5 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr15:56388212 C>T maps to NM_022841.5 Q571Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr15:56388407 C>T maps to NM_022841.5 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr13:37401781 G>A maps to NM_000538.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:100479318 G>A maps to NM_001134666.1 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr23:109694272 T>C did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:109695338 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr23:109694159 G>A did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr23:109696313 G>A did not map to a codon.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr23:109694738 C>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:109695143 C>G did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:109696196 C>T did not map to a codon.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr23:109696371 G>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:109695754 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr23:109695357 C>G did not map to a codon.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr23:71350463 T>G did not map to a codon.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr23:71350447 T>C did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:71351043 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr23:71350364 C>G did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr1:183895365 G>A maps to NM_015149.3 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:183775567 C>T maps to NM_015149.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:183816704 A>G maps to NM_015149.3 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:33262942 C>T maps to NM_004761.3 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr6:33261400 C>T maps to NM_004761.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr6:33263455 G>C maps to NM_004761.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:11510942 T>C maps to NM_001161616.1 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:11517469 G>A maps to NM_001161616.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:11526778 C>T maps to NM_001161616.1 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:24034854 G>A did not map to a codon.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr15:93588296 C>T maps to NM_020211.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr15:93595603 C>T maps to NM_020211.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:98129141 G>C maps to NM_001012761.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr23:46951162 G>C did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr23:46949305 C>A did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr5:73091191 G>T maps to NM_001080479.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr2:87141031 G>T maps to NM_001078170.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:107042507 G>T maps to ENST00000304514 S881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr2:107032305 C>T maps to ENST00000304514 K1688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr2:107049684 G>C maps to ENST00000304514 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:108487256 C>T maps to NM_182588.2 Q933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr2:108488224 G>A maps to NM_182588.2 R1255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:108488440 A>G maps to NM_182588.2 E1327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr2:108488114 G>T maps to NM_182588.2 E1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:113147641 C>G maps to NM_005054.2 V960V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr2:113146876 G>A maps to NM_005054.2 V1215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr10:86012691 C>A maps to ENST00000358110 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr10:86014099 C>G maps to ENST00000358110 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:192544927 C>A maps to NM_002922.3 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr16:321022 C>A maps to NM_183337.1 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:320992 C>T maps to NM_183337.1 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:3419260 C>T maps to NM_198229.2 H918H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr4:3432593 G>A maps to NM_198229.2 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr4:3424167 C>T maps to NM_198229.2 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr4:3318625 G>A maps to NM_198229.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr4:3429889 G>A maps to NM_198229.2 S1135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr5:176794746 G>A maps to ENST00000398128 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr5:176794767 G>T maps to ENST00000398128 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr6:153347671 A>T maps to NM_012419.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr1:192153554 G>A maps to NM_130782.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr1:192778227 T>C maps to NM_002923.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr8:54764581 C>T maps to NM_170587.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr8:54859257 C>T maps to NM_170587.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr8:54791897 C>G maps to NM_170587.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:192321322 G>T maps to NM_001039152.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:192335208 T>C maps to NM_001039152.3 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:192321330 T>C maps to NM_001039152.3 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr9:116356435 G>A maps to NM_144489.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr9:116267801 C>T maps to NM_144488.4 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr9:116356333 G>C maps to NM_144489.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:116353611 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:116224446 G>A maps to NM_144488.4 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr9:116356597 G>A maps to NM_144489.2 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr1:163131766 C>G did not map to a codon.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:240966239 G>A maps to ENST00000407727 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:240964754 C>G maps to ENST00000407727 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:241094031 C>A maps to ENST00000407727 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:241099908 G>T maps to ENST00000407727 Y108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:240990450 C>A maps to ENST00000407727 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:241032089 T>A maps to ENST00000407727 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr1:240975266 C>A maps to ENST00000407727 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:240979622 T>C maps to ENST00000407727 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr1:240990400 C>T maps to ENST00000407727 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:63871634 C>A maps to NM_001029875.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr5:63871703 C>T maps to NM_001029875.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:182640844 G>A maps to NM_033345.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr6:49580133 A>T maps to NM_000324.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr6:49585873 C>G maps to NM_000324.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr7:75517438 G>A maps to NM_001040456.1 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:75513014 G>A did not map to a codon.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr7:75511237 C>T maps to NM_001040456.1 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:111983 G>A maps to NM_022450.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:74475232 C>T maps to NM_024599.5 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr16:727017 G>A maps to NM_003961.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156348149 C>T maps to NM_020407.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr1:25717248 C>T maps to NM_020485.4 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:90020343 C>T maps to NM_016321.1 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr15:90021121 G>T maps to NM_016321.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:25611199 C>T maps to ENST00000357542 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr7:151167696 C>T maps to NM_005614.3 W141*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-6484-01A-11D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:49462887 C>T maps to NM_144593.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr3:129247884 C>T maps to NM_000539.3 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr3:129251467 C>T maps to NM_000539.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr3:49405977 C>A maps to NM_001664.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr3:49412947 G>A maps to NM_001664.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:20647663 C>A maps to NM_004040.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr10:62648291 G>A maps to NM_014836.4 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr10:62648570 G>A maps to NM_014836.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr10:62648783 C>T maps to NM_014836.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr10:62648687 T>A maps to NM_014836.4 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr10:62637690 G>A maps to NM_014836.4 C567C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr10:62647976 C>T maps to NM_014836.4 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr10:62647982 C>T maps to NM_014836.4 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr10:62648789 C>T maps to NM_014836.4 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr8:22863631 C>T maps to NM_001160036.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr8:22864370 C>T maps to NM_001160036.1 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:95087995 G>A maps to NM_014899.3 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr5:95072636 G>C maps to NM_014899.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:66838946 C>T maps to NM_014578.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr4:40245287 G>A maps to NM_004310.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:63749900 C>T maps to NM_020663.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr14:63671682 G>C maps to NM_020663.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:46770214 C>T maps to NM_012249.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr16:723124 C>T maps to NM_138769.1 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:722104 C>T maps to NM_138769.1 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr16:721933 C>G maps to NM_138769.1 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr15:41165519 G>A maps to NM_133639.3 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:119249461 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:119249484 C>T did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:119211022 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:119293315 C>T did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:144463845 G>A maps to ENST00000422773 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr8:144459585 G>T maps to ENST00000422773 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:33482783 A>T maps to NM_033103.4 L530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr19:33482767 G>A maps to NM_033103.4 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:33535240 C>T maps to NM_033103.4 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:33493155 G>A maps to NM_033103.4 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:53455529 C>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:53455482 C>G did not map to a codon.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr23:53455325 C>T did not map to a codon.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr11:8132424 G>A maps to ENST00000309737 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr11:209867 G>A maps to NM_021932.4 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr11:212414 G>A did not map to a codon.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr12:107236417 C>T maps to ENST00000392837 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:107208847 C>T maps to ENST00000392837 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr17:12812248 G>C maps to NM_014859.4 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:12823100 G>A maps to NM_014859.4 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:12819312 G>T maps to NM_014859.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr17:12862202 C>A maps to NM_014859.4 Y504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr5:38944563 C>A maps to ENST00000296782 E1657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr2:152289597 A>G maps to NM_018151.4 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:152321319 A>G maps to NM_018151.4 T1762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr2:152276865 A>G maps to NM_018151.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr2:152320476 A>G maps to NM_018151.4 K1481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:152319684 G>A maps to NM_018151.4 R1217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr2:152298456 A>G maps to NM_018151.4 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr2:152325271 T>C did not map to a codon.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr2:152276854 C>T maps to NM_018151.4 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr2:152322481 G>T maps to NM_018151.4 E2150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr2:152321640 G>A maps to NM_018151.4 S1869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr12:124008156 C>T maps to NM_178314.3 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr12:123984018 G>A maps to NM_178314.3 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr12:123915095 C>T maps to NM_145058.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr12:130927170 G>A maps to NM_015347.4 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr12:130921645 G>C maps to NM_015347.4 S599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr12:130926552 G>A maps to NM_015347.4 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr12:130912861 G>A maps to NM_015347.4 D741D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:130926459 C>A maps to NM_015347.4 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:130912809 C>A maps to NM_015347.4 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr12:130926627 G>A maps to NM_015347.4 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr12:130927080 G>A maps to NM_015347.4 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr12:130963554 G>T maps to NM_015347.4 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr22:20458537 G>A maps to NM_015672.1 Q922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:20457161 C>T maps to NM_015672.1 K1380K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:42880191 C>T maps to NM_173642.3 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:8906663 G>C maps to NM_020734.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:8866470 T>C maps to NM_020734.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:72889448 C>T maps to NM_014989.4 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr6:72970464 T>C maps to NM_014989.4 T1037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:72984051 G>A maps to NM_014989.4 R1133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr6:72984117 G>A maps to NM_014989.4 A1155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr6:72975744 C>T maps to NM_014989.4 R1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr8:104897723 A>G maps to NM_001100117.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:104898350 C>T maps to NM_001100117.2 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr8:104898191 G>T maps to NM_001100117.2 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr8:105026751 G>A maps to NM_001100117.2 G1081G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr8:104709389 C>T maps to NM_001100117.2 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:104940077 C>T maps to NM_001100117.2 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:41101586 C>A did not map to a codon.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr1:41107555 G>A maps to NM_014747.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr20:43385613 G>A maps to NM_182970.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr14:93118017 C>G maps to NM_024832.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr14:93043784 C>T maps to NM_024832.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr14:93118911 T>A maps to NM_024832.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr14:93151467 G>A maps to NM_024832.3 K868K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr14:93151410 G>A maps to NM_024832.3 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr6:33176604 G>A maps to NM_002931.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr19:39361609 G>A maps to NM_001195833.1 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:39361465 C>T maps to NM_001195833.1 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:39361378 G>A maps to NM_001195833.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr7:105182868 A>T maps to NM_021930.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:105190712 A>G maps to NM_021930.4 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:105205727 T>C maps to NM_021930.4 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr6:7403091 G>A maps to NM_031480.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr6:7405509 C>T maps to NM_031480.2 V375V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BA-A6DJ-01A-11D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr5:96503520 C>G maps to NM_018343.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:96498920 C>T maps to NM_018343.2 V501V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HL-7533-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr6:3085631 G>T maps to NM_003804.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr6:3113557 C>T maps to NM_003804.3 Y667Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:90777690 G>A maps to NM_003821.5 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr14:24808259 C>T maps to NM_006871.3 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr14:24806947 C>A maps to NM_006871.3 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr21:43161650 T>A maps to ENST00000352483 K616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr21:43161807 C>T maps to ENST00000352483 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr21:43187144 C>A maps to ENST00000352483 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr21:43164072 C>T maps to ENST00000352483 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:43165916 A>G did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr23:106144712 T>A did not map to a codon.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr23:106144026 G>A did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:84567049 C>G maps to NM_001009994.1 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr18:40503581 G>T maps to NM_002930.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr18:40323625 G>T maps to NM_002930.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr15:89760506 G>A maps to NM_000326.4 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr1:40703346 A>G maps to NM_012421.3 K991K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:40627250 G>A maps to NM_012421.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:40703618 C>G maps to NM_012421.3 S1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr1:40703343 G>A maps to NM_012421.3 T990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:40661332 G>A maps to NM_012421.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:73811416 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:73812473 C>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:73811495 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:73811507 G>C did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr23:73811531 C>T did not map to a codon.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr23:73812878 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr23:73811444 T>G did not map to a codon.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr23:73811694 A>G did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr16:67685182 G>T maps to NM_001013838.1 E760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr16:67683843 G>A maps to NM_001013838.1 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:67682064 C>A maps to NM_001013838.1 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr16:67683163 C>T maps to NM_001013838.1 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:67680669 C>T maps to NM_001013838.1 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:67683450 C>T maps to NM_001013838.1 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:86616878 C>T maps to NM_024945.2 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:86616413 A>G maps to NM_024945.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:151766519 G>A maps to NM_017909.2 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr5:177574773 C>T maps to NM_022762.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr5:177569713 C>A maps to NM_022762.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr14:21052159 G>T maps to NM_145250.3 C158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr14:21058543 G>A maps to NM_001024822.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:21058669 C>T maps to NM_001024822.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr14:21502042 G>C maps to NM_001012264.3 Y135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr14:21167748 C>T maps to NM_194431.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:21167682 C>T maps to NM_194431.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:3598054 G>A maps to NM_002936.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr11:65487841 C>T maps to NM_032193.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:182555530 C>T maps to NM_021133.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:182554926 G>A maps to NM_021133.3 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:182555478 G>A maps to NM_021133.3 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:182555617 C>T maps to NM_021133.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:182555659 C>T maps to NM_021133.3 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr5:31511214 C>T maps to NM_013235.4 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr6:167344564 C>A maps to ENST00000428859 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr12:121009001 C>T maps to ENST00000458409 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:121000764 G>T maps to ENST00000458409 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr12:121013685 C>T maps to ENST00000458409 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr15:59368278 C>T maps to ENST00000434298 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:59373349 C>T maps to ENST00000434298 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr15:59350643 C>T maps to ENST00000434298 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:59359173 C>T maps to ENST00000434298 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:59383307 C>T maps to ENST00000434298 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:59323314 G>A maps to ENST00000434298 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr23:119005205 G>A did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:119005173 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:119005249 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:119005302 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr23:119005407 C>T did not map to a codon.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr13:98828824 G>A maps to NM_178861.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr13:98828833 A>G maps to NM_178861.4 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr13:98829283 G>T maps to NM_178861.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr11:71705772 C>T maps to NM_018320.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:49738098 C>T maps to NM_022064.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr3:49736207 C>T maps to NM_022064.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr3:49735361 C>T maps to NM_022064.2 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr3:49742511 C>T maps to NM_022064.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr23:105937341 A>G did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:105937452 A>T did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:149589831 C>G maps to NM_007282.4 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:122338456 G>A maps to NM_139175.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr8:125498930 G>A maps to NM_007218.3 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr8:125498990 C>T maps to NM_007218.3 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:141358229 T>C maps to NM_183399.1 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr5:141358011 C>T maps to NM_183399.1 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:7164498 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:158630510 G>A maps to NM_144726.2 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:127607814 G>A maps to ENST00000368314 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr7:122342731 G>A maps to NM_198085.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:142053644 G>T maps to NM_020724.1 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:141868812 G>T maps to NM_020724.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:141888962 C>A maps to NM_020724.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr21:30315990 G>C maps to NM_015565.2 Y1452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr21:30318478 G>A maps to NM_015565.2 F1252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr21:30318478 G>A maps to NM_015565.2 F1252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr21:30308974 C>T maps to NM_015565.2 L1555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:4847868 C>T maps to NM_015528.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:196198800 C>T maps to NM_152617.3 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr11:74546711 C>A maps to NM_001098638.1 S355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:25448362 C>A maps to ENST00000381927 S1569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr13:25451308 C>G maps to ENST00000381927 L1635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:25348971 A>C maps to ENST00000381927 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr13:25453368 G>A maps to ENST00000381927 Q1655Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:25376517 G>C did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:63509382 A>T did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr9:116060062 C>A maps to NM_145051.3 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr22:31597554 G>A maps to NM_152267.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr8:101300144 G>A maps to NM_183419.1 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr8:101300160 G>C maps to NM_183419.1 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr8:101299799 G>A maps to NM_183419.1 Y201Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr1:33402523 G>A maps to NM_153341.2 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr9:104319793 G>A maps to NM_019592.5 E766E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:104319875 C>T maps to NM_019592.5 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr1:6266753 G>A maps to NM_207396.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:6267453 G>A maps to NM_207396.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr9:140114908 C>T maps to NM_031297.3 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr9:140115190 G>A maps to NM_031297.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr17:78338337 C>T maps to NM_020914.4 V4001V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr17:78293222 A>T maps to NM_020954.2 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr17:78321812 C>T maps to NM_020914.4 C3275C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr17:78313927 C>A maps to NM_020914.4 R1970R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr17:78319550 C>T maps to NM_020914.4 F2521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr17:78363061 C>G maps to NM_020914.4 V5079V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:78320512 C>G maps to NM_020914.4 S2842*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-7374-01A-11D-2012-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CV-5979-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:78358942 C>T maps to NM_020914.4 I4858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:78321974 G>A maps to NM_020914.4 A3329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr17:78263579 G>A maps to NM_020914.4 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:78321902 G>A maps to NM_020914.4 S3305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr17:78355363 T>A maps to NM_020914.4 I4654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:78286924 C>T maps to NM_020914.4 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:78293249 C>T maps to NM_020954.2 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:78319832 C>T maps to NM_020914.4 Y2615Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:78332093 C>T maps to NM_020914.4 T3672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr17:78319808 C>G maps to NM_020914.4 S2607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr17:78286918 C>T maps to NM_020914.4 N970N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:78357724 G>A maps to NM_020914.4 Q4822Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr17:78321213 C>T maps to NM_020914.4 Q3076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr17:78321707 C>A maps to NM_020914.4 L3240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:117110555 C>T maps to NM_207343.2 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr11:117152362 G>A maps to NM_207343.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr11:117117601 G>A maps to NM_207343.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:5662574 G>A maps to NM_207111.2 V896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr6:125379203 C>T maps to NM_152553.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr13:79213139 G>A maps to NM_024546.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:45091997 G>A maps to ENST00000453887 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr20:3944598 G>A maps to NM_001134338.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:219529907 C>G maps to NM_022453.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:219536675 A>G maps to NM_022453.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr14:24617532 G>T maps to NM_017999.4 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr14:24624490 C>G maps to NM_017999.4 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:156450871 C>T maps to NM_001184997.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:36375983 G>A maps to NM_022781.4 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:30779632 G>A maps to NM_014771.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr16:30779807 C>A maps to NM_014771.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr16:30780712 G>A maps to NM_014771.2 K818K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:56440746 C>T maps to NM_017763.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr17:56492887 C>T maps to NM_017763.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr13:26789039 G>A maps to NM_005977.3 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr13:26788499 G>A maps to NM_005977.3 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr6:37344796 A>G maps to NM_003958.3 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr17:58040502 A>G maps to NM_016125.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr12:117217095 C>T maps to NM_001109903.1 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr12:117217149 C>T maps to NM_001109903.1 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:89650811 G>C maps to NM_003800.3 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr6:89388086 G>A maps to NM_003800.3 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:89554216 A>G maps to NM_003800.3 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:90122453 C>T maps to NM_001031709.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr10:90122396 C>T maps to NM_001031709.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr18:13737129 T>A maps to NM_003799.1 C225*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-A63Y-01A-11D-A30E-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CR-6472-01A-11D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr17:691247 G>A maps to NM_018146.2 K201K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-A463-01A-11D-A25Y-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D6-6516-01A-11D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:695068 T>C maps to NM_018146.2 S341S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HL-7533-01A-11D-2229-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CX-A4AQ-01A-11D-A25D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:2313198 G>C maps to NM_080594.2 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr1:156024745 C>T maps to NM_014017.3 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:78766928 G>A maps to NM_002941.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:78701046 G>A maps to NM_002941.3 Q883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr3:77614131 C>G maps to ENST00000332191 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:124750347 C>T maps to NM_022370.3 F1331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr11:124743755 C>T maps to NM_022370.3 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr11:124747166 C>T maps to NM_022370.3 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr11:124740595 T>A maps to NM_022370.3 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:124761402 A>G maps to NM_019055.5 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:124765698 C>G maps to NM_019055.5 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:124765071 G>A maps to NM_019055.5 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr11:124756426 G>T maps to NM_019055.5 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:18548730 A>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:18608855 A>G maps to NM_005406.2 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr18:18547727 C>T maps to NM_005406.2 L1059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr18:18588118 G>A maps to NM_005406.2 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr2:11347877 C>T maps to NM_004850.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr2:11332359 G>A maps to NM_004850.3 A1359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:11354482 C>T maps to NM_004850.3 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr2:11341163 C>T maps to NM_004850.3 K943K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:11354566 T>C maps to NM_004850.3 E653E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr2:11338712 T>A did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:114986136 T>C maps to NM_001163790.1 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr3:123695770 T>C maps to NM_017578.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr5:10448389 G>A maps to NM_031916.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:64515513 C>T maps to NM_005012.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:64643981 C>G maps to NM_005012.2 S753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr9:94488897 G>T maps to NM_004560.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr9:94486330 C>T maps to NM_004560.2 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr9:94486930 G>A maps to NM_004560.2 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr15:60907183 T>C maps to NM_002943.3 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr9:77257705 A>G maps to ENST00000396204 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:77286706 C>A maps to ENST00000396204 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:117710680 C>A maps to NM_002944.2 G531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr6:117724425 C>T maps to NM_002944.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr6:117724425 C>T maps to NM_002944.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:117710591 G>A maps to NM_002944.2 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr6:117677900 G>A maps to NM_002944.2 T1344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:117650565 C>T maps to NM_002944.2 G1764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr6:117642485 C>A maps to NM_002944.2 E1905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr6:117647565 G>C maps to NM_002944.2 S1793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr8:55534065 C>T maps to NM_006269.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr8:55539399 A>G maps to NM_006269.1 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr8:55539812 C>A maps to NM_006269.1 S1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr8:55540809 A>G maps to NM_006269.1 T1456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr8:55542591 T>C maps to NM_006269.1 N2050N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr8:55533930 G>A maps to NM_006269.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:55537479 C>T maps to NM_006269.1 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr8:55534742 A>T maps to NM_006269.1 K228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:55533786 G>A maps to NM_006269.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr8:55539429 C>T maps to NM_006269.1 A996A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:55534122 C>T maps to NM_006269.1 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr8:55538910 T>C maps to NM_006269.1 F823F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr8:10467545 C>T maps to NM_178857.5 A1354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:10469744 C>T maps to NM_178857.5 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr8:10466396 C>A maps to NM_178857.5 G1737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr8:10465187 C>T maps to NM_178857.5 E2140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr7:33134956 G>A maps to NM_203288.1 H185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:33134977 G>A maps to NM_203288.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:1787117 A>G maps to NM_002945.3 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr17:1782579 G>A maps to NM_002945.3 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr17:1792039 G>A maps to NM_002945.3 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr23:96139779 T>A did not map to a codon.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr23:96139794 C>A did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:5323529 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:5323604 C>T maps to NM_001033002.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr17:5329381 C>T maps to NM_001033002.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr15:41819776 C>T maps to NM_015540.2 W485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr12:48060841 G>A maps to NM_024604.2 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:48090186 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:68897199 C>T maps to NM_000329.2 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr1:68896859 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:84946694 G>A maps to NM_025065.6 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr23:38145067 C>G did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr23:38156555 G>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:38145137 T>C did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr23:38135928 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:38129022 C>T did not map to a codon.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:53639438 G>A maps to NM_015272.2 A1263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:53708988 C>T maps to NM_015272.2 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr16:53708962 G>T maps to NM_015272.2 S283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr12:113328748 A>T maps to NM_001143854.1 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:88991473 C>T maps to NM_144563.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr23:153628937 G>A did not map to a codon.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr23:153628945 C>G did not map to a codon.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr23:153627857 G>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:35438520 A>G maps to NM_007104.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:35436735 G>T maps to NM_007104.4 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr6:35436774 G>A maps to NM_007104.4 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:47120417 C>T maps to NM_080746.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr1:24019118 G>A maps to NM_000975.3 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr16:89627381 G>C maps to NM_033251.1 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:23959349 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr3:23960060 T>A maps to NM_002948.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr18:47017914 C>T maps to NM_001035006.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:37008938 C>T maps to NM_000978.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:41154915 C>T maps to NM_000988.3 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:39711392 G>A maps to NM_000967.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr22:39713610 C>A maps to NM_000967.3 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr3:12881679 C>T maps to ENST00000273223 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:40834691 G>T maps to NM_000997.4 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:118920695 C>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr16:1996718 G>C maps to NM_005061.2 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr16:1995859 C>T maps to NM_005061.2 K341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr15:66791762 C>T maps to NM_000968.2 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr15:66793303 G>A maps to NM_000968.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr1:93301775 C>T maps to NM_000969.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr8:74204132 C>T maps to ENST00000396470 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:42851352 G>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:146017245 C>A maps to NM_000973.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr12:120634605 G>A maps to NM_053275.3 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:120636692 G>A maps to NM_053275.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:120635241 G>C maps to NM_053275.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr12:120636944 G>A maps to NM_053275.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:812801 C>G maps to NM_001004.3 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr20:35827571 C>T maps to NM_002951.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr20:35827604 C>T maps to NM_002951.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:35827507 C>A maps to NM_002951.3 S120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr20:35857005 C>T maps to NM_002951.3 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr10:92634656 C>A maps to ENST00000458617 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr6:4998959 C>T maps to NM_006638.2 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:5002434 C>G maps to NM_006638.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr18:33613771 G>C maps to NM_018170.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr1:150416839 C>G maps to NM_015203.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr1:150445605 C>T maps to NM_015203.3 S1394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr1:150432680 G>A maps to NM_015203.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:45056163 G>T maps to NM_203400.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr19:50002789 C>T maps to NM_001015.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr16:18796109 G>C maps to NM_001030009.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr5:81571951 G>A maps to NM_001025.4 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:81571972 A>G maps to NM_001025.4 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr10:79797022 C>T maps to NM_001142285.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr11:118888676 G>A maps to NM_001028.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr11:118888250 C>T maps to NM_001028.2 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr12:56436378 C>G maps to NM_001029.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:153964114 C>G maps to NM_001030.4 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:55462058 G>A maps to NM_001177413.1 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr24:22930713 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr1:26887588 G>T maps to NM_001006665.1 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr1:26883511 G>A maps to NM_001006665.1 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:166918076 G>A maps to ENST00000510118 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr6:166831721 G>A maps to ENST00000510118 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:166944771 G>A maps to ENST00000510118 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr6:166952260 G>A maps to ENST00000510118 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:166873036 C>G maps to ENST00000510118 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr6:166902390 C>G maps to ENST00000510118 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:20211696 T>A did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr23:20190889 C>T did not map to a codon.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr23:20190988 G>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr11:64138161 G>A maps to NM_003942.2 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:83371244 C>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:83351276 C>T did not map to a codon.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr23:83357103 G>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:83361413 G>A did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr23:83411199 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:83374961 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:83402051 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:83352784 C>A did not map to a codon.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr23:83390118 G>A did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr17:58009057 G>A maps to NM_003161.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr17:57970559 G>A maps to NM_003161.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:67200086 G>A maps to NM_003952.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr1:213436153 C>T maps to NM_012424.3 Q1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:213414695 C>A maps to NM_012424.3 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:213414330 A>C maps to NM_012424.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:213277817 C>A maps to NM_012424.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:213414909 T>G maps to NM_012424.3 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr1:213405593 G>A maps to NM_012424.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr14:75376270 G>A maps to NM_031464.3 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:45243772 G>A maps to NM_001012.1 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:152128884 C>T maps to NM_001122965.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr1:152128692 G>A maps to NM_001122965.1 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr1:152128185 A>G maps to NM_001122965.1 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr17:78899183 G>A maps to NM_020761.2 A941A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr17:78938108 G>A maps to NM_020761.2 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:78882728 G>A maps to NM_020761.2 K840K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr17:78681789 C>G maps to NM_020761.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:836893 G>A maps to NM_058192.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr16:836036 T>A maps to NM_058192.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:55757889 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:55784704 C>A did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr1:39317430 T>C did not map to a codon.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr1:39305257 C>T maps to NM_022157.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:39322559 A>G maps to NM_022157.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr6:90097154 G>T maps to NM_021244.4 C101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr20:17600949 C>T maps to ENST00000377813 S1191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr20:17599306 T>C maps to ENST00000377813 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr20:17610501 G>A maps to ENST00000377813 A905A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr20:17610537 G>A maps to ENST00000377813 H893H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr6:7230731 G>A maps to NM_001003699.3 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:7229783 C>T maps to NM_001003699.3 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr6:7229768 G>A maps to NM_001003699.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr6:7231220 G>A maps to NM_001003699.3 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:7232111 C>T maps to NM_001003699.3 S1260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:7232112 C>T maps to NM_001003699.3 L1261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr6:7230563 G>T maps to NM_001003699.3 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr6:7230236 G>A maps to NM_001003699.3 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr8:103236306 A>G maps to NM_015713.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr16:15157136 T>G maps to NM_018427.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr16:15170450 A>G maps to NM_018427.3 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr21:45217865 C>T maps to NM_003683.5 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr21:45219457 C>T maps to NM_003683.5 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:99130757 G>C maps to NM_015179.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:99123619 G>A maps to NM_015179.3 I1186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:45107739 G>A maps to NM_015056.2 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr21:45107524 G>T maps to NM_015056.2 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:6621415 G>C maps to NM_015324.2 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:67341836 G>A maps to NM_015169.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr23:18660165 G>A did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:18662614 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:18660201 G>T did not map to a codon.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr23:18662589 A>C did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr23:18660204 G>A did not map to a codon.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr23:18674849 T>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:18660261 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr17:48562220 G>A maps to NM_018346.1 *443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr17:48559616 G>T maps to NM_018346.1 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr17:48559726 G>A maps to NM_018346.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr2:7027108 C>T maps to NM_080657.4 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:114354935 C>T maps to NM_018364.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr1:114308736 T>A maps to NM_018364.3 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr7:77379047 C>G maps to NM_198467.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:77379266 T>A maps to NM_198467.2 Y410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:15987994 T>C maps to NM_006511.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr1:15986467 T>G maps to NM_006511.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr11:77377982 G>C maps to NM_016578.3 V1435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:77378292 G>C maps to NM_016578.3 S1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:77413133 G>A maps to NM_016578.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr11:77412476 G>A maps to NM_016578.3 D599D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:77412959 C>T maps to NM_016578.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr11:77402210 C>A maps to NM_016578.3 E965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr11:77378519 C>T maps to NM_016578.3 K1256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr11:77386243 C>T maps to NM_016578.3 P1133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:11935670 C>A maps to NM_015659.2 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:6820508 C>A maps to NM_173565.3 C533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:116938127 G>C maps to NM_001010892.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr6:116938022 A>G maps to NM_001010892.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:116938342 C>G maps to NM_001010892.2 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:43638529 C>A maps to NM_152732.4 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr6:43638683 T>C maps to NM_152732.4 *277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:127471640 A>G maps to ENST00000368317 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr6:127476477 C>T maps to ENST00000368317 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr6:127471622 T>A maps to ENST00000368317 C114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr6:127476452 C>T maps to ENST00000368317 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr20:947817 C>T maps to NM_001029871.3 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr3:157841761 C>G maps to NM_016625.2 S101*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-KU-A66S-01A-21D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:122991392 C>T maps to NM_023012.5 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr10:16794652 C>A did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:100736124 C>T maps to NM_001130841.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr22:23406114 G>A maps to NM_014433.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr22:23401714 G>A maps to NM_014433.2 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr20:62321523 C>T maps to ENST00000482936 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:62298845 G>C maps to ENST00000482936 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr20:62326477 C>T maps to ENST00000482936 L1135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr15:41767763 C>G maps to NM_015138.4 S443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr2:74654584 C>T maps to NM_001015055.1 W407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:63957981 G>A maps to NM_145307.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:63959549 G>A maps to NM_145307.2 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr14:101347318 G>T maps to NM_001134888.2 P1269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr14:101349301 G>T maps to NM_001134888.2 Y608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr14:60072192 G>A maps to NM_021136.2 Q669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr14:60212701 C>A maps to NM_021136.2 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:45997426 G>A maps to NM_005619.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:63487850 C>A maps to ENST00000377819 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr11:63517598 C>T maps to ENST00000377819 V889V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:55209755 C>T maps to NM_020532.4 E1085E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr6:107019899 G>A maps to NM_032730.4 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:107069362 C>T maps to NM_032730.4 W144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:107040175 C>A did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr22:20229736 G>A maps to ENST00000425986 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:1840776 C>T maps to NM_178568.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr17:1840239 G>A maps to NM_178568.2 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:186917659 C>T maps to NM_153708.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr3:186917821 C>T maps to NM_153708.2 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr3:187416477 G>T maps to NM_001004312.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr3:187089109 C>A maps to NM_022147.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr18:67801777 C>T did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:67801734 G>A maps to NM_173630.3 F976F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr18:67843964 G>A maps to NM_173630.3 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:67812916 A>G maps to NM_173630.3 V804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr18:67727259 G>T maps to NM_173630.3 S1589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr10:70156606 G>A maps to NM_017987.4 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr10:70156541 G>A maps to NM_017987.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:41141509 G>C maps to NM_173079.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr16:12145725 G>C maps to NM_032167.2 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:12136910 C>T maps to NM_032167.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr16:12121227 G>A maps to NM_032167.2 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:42390844 G>T maps to NM_001144825.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:87459341 C>T maps to NM_138290.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr21:36206845 G>A maps to NM_001754.4 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr8:93017495 G>A maps to NM_175634.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:92982909 G>T maps to NM_175634.2 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr8:93026817 G>A maps to NM_175634.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr8:92988160 G>A maps to NM_175634.2 Y440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:93027016 G>A maps to NM_175634.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:92972553 C>T maps to NM_175634.2 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr8:92972687 G>A maps to NM_175634.2 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:93003885 C>T maps to NM_175634.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:93017468 C>T maps to NM_175634.2 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:92998474 G>T maps to NM_175634.2 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr8:93003945 A>G maps to NM_175634.2 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr6:45459774 C>A maps to ENST00000359524 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:45390426 G>A maps to ENST00000359524 Q120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:45390429 A>G maps to ENST00000359524 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:25254160 C>A maps to NM_001031680.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:25245772 G>A maps to NM_001031680.2 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:155295460 C>T maps to NM_001105203.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:155292475 C>T maps to NM_001105203.1 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:35556329 G>A maps to NM_001135999.1 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr9:35546715 A>G maps to NM_001135999.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:35557971 G>T maps to NM_001135999.1 R1015R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:35548375 C>T maps to NM_001135999.1 Q620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr19:49513115 G>C maps to NM_006666.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:49514283 C>T maps to NM_006666.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr21:30391544 C>T maps to NM_016940.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr1:95709956 G>A maps to NM_015485.4 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:95710025 C>A maps to NM_015485.4 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr4:159568072 C>A maps to ENST00000440678 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr13:32313844 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:32367007 C>T maps to NM_130806.3 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:33937765 G>A maps to NM_016568.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:33937867 C>A maps to NM_016568.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr5:33937333 C>A maps to NM_016568.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr5:33937015 G>A maps to NM_016568.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr1:155912003 G>A maps to NM_181885.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:33165571 G>A maps to ENST00000374685 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:33163690 C>T maps to ENST00000374685 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:165380003 C>T maps to NM_006917.4 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:165377462 C>A did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr3:72495695 C>A maps to ENST00000477973 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:72428558 G>A maps to ENST00000477973 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr19:38960131 C>T maps to NM_000540.2 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr19:39071026 C>T maps to NM_000540.2 G4843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr19:38976679 G>A maps to NM_000540.2 P1795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:38976616 G>A maps to NM_000540.2 P1774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr19:38973677 C>T maps to NM_000540.2 N1544N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr19:39023128 G>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:38956796 G>C maps to NM_000540.2 A979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:39013682 G>A maps to NM_000540.2 T3425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:38980888 C>T maps to NM_000540.2 R1996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:38948882 C>T maps to NM_000540.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:38956790 G>A maps to NM_000540.2 T977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:39075701 C>T maps to NM_000540.2 F4922F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr19:38951141 C>A maps to NM_000540.2 R830R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:38997013 G>T maps to NM_000540.2 L2871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:38942466 G>T maps to NM_000540.2 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr19:38958445 G>A maps to NM_000540.2 G1125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:237670114 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:237711877 T>A maps to NM_001035.2 Y1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:237540621 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:237870369 C>G maps to NM_001035.2 V3234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr1:237729888 C>T maps to NM_001035.2 S1079S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:237617717 G>T maps to NM_001035.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:237829846 G>T maps to NM_001035.2 R2824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:237935318 G>A maps to NM_001035.2 Q3855Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:237758917 A>T maps to NM_001035.2 T1519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:237868593 A>G maps to NM_001035.2 K3177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:237947095 G>A maps to NM_001035.2 S4028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr1:237850781 C>T maps to NM_001035.2 V3015V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr1:237947221 G>A maps to NM_001035.2 A4070A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:237780710 C>A maps to NM_001035.2 V1947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:237951286 G>A did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:237659855 G>A maps to NM_001035.2 Q669Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:237817704 G>T maps to NM_001035.2 L2652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr1:237961366 C>T maps to NM_001035.2 R4663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:237777905 T>C maps to NM_001035.2 Y1826Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:237942009 G>T maps to NM_001035.2 L3940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:237608771 C>A maps to NM_001035.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:237813232 C>T maps to NM_001035.2 A2523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:237796939 A>T maps to NM_001035.2 I2206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:237664038 A>G maps to NM_001035.2 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:237798219 G>A maps to NM_001035.2 L2240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:237895413 C>T maps to NM_001035.2 I3668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:237777747 G>T maps to NM_001035.2 E1774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:237777848 G>C maps to NM_001035.2 R1807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:237540663 C>T maps to NM_001035.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:237754052 G>A maps to NM_001035.2 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:237947404 C>G maps to NM_001035.2 P4131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:237656291 G>C maps to NM_001035.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:237580387 A>T maps to NM_001035.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:237921018 A>G maps to NM_001035.2 A3756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr1:237972269 C>T maps to NM_001035.2 R4790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr1:237829885 G>A maps to NM_001035.2 L2837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr1:237791329 G>C maps to NM_001035.2 L2130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr1:237580423 G>A did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:33926902 G>A maps to NM_001036.3 G1048G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr15:33954656 C>T maps to NM_001036.3 L1642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr15:33905501 C>T maps to NM_001036.3 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr15:33955092 G>T maps to NM_001036.3 E1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr15:34115204 A>G maps to NM_001036.3 L3668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr15:34040340 G>T maps to NM_001036.3 A2672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr15:33878307 G>T maps to NM_001036.3 R593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr15:33765660 G>A maps to NM_001036.3 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:34072525 C>T maps to NM_001036.3 T3084T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr15:34105781 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:33878259 G>A maps to NM_001036.3 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr15:33962689 T>G maps to NM_001036.3 V1931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr15:33954827 G>C maps to NM_001036.3 L1699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr15:33990139 C>G maps to NM_001036.3 G2064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr15:34080542 C>T maps to NM_001036.3 A3238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr15:34072456 C>T maps to NM_001036.3 A3061A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr1:153598849 G>A maps to NM_001024210.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:153580540 G>C maps to NM_080388.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:153533965 G>A maps to ENST00000368707 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:153533986 C>T maps to ENST00000368707 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:153520179 G>C maps to NM_002960.1 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:153520230 G>C maps to NM_002960.1 S78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:153516399 C>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:153430419 G>T maps to NM_002963.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr1:153431378 C>T maps to NM_002963.3 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:153390677 C>T maps to NM_176823.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr1:153391772 G>A maps to NM_176823.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr23:16669150 G>A did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:33292422 C>A maps to NM_022753.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:101704650 C>T maps to NM_001400.4 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:101704695 C>T maps to NM_001400.4 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:101705598 C>T maps to NM_001400.4 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr1:101705577 C>T maps to NM_001400.4 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:91617110 C>T maps to NM_005226.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:3179317 G>A maps to NM_003775.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:3179236 G>A maps to NM_003775.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr19:3179689 G>A maps to NM_003775.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:10625609 G>A maps to NM_001166215.1 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr11:18257395 C>T maps to NM_006512.3 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:18103050 C>G did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:18105279 T>A did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:45744941 T>C maps to NM_014016.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:45776774 C>T maps to NM_014016.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr13:23942585 G>C maps to NM_014363.4 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr13:23906533 C>T maps to NM_014363.4 K3827K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr13:23905801 T>C maps to NM_014363.4 E4071E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr13:23915743 G>C maps to NM_014363.4 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr13:23908831 G>C maps to NM_014363.4 L3061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:23913991 G>C maps to NM_014363.4 L1341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:23913424 G>A maps to NM_014363.4 F1530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:23930132 G>A maps to NM_014363.4 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr13:23915281 G>A maps to NM_014363.4 T911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr13:23907283 T>C maps to NM_014363.4 T3577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr13:23912106 C>A maps to NM_014363.4 G1970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:23932594 G>A maps to NM_014363.4 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr13:23929019 G>A maps to NM_014363.4 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr13:23906233 C>T maps to NM_014363.4 A3927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr19:47656162 G>C maps to NM_005500.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:47712511 C>G maps to NM_001145713.1 S277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr19:5664424 C>G maps to ENST00000433404 S770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr19:5641945 C>T maps to ENST00000433404 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr19:5664418 C>G maps to ENST00000433404 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:5598875 C>G maps to NM_014649.2 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:5593975 C>T maps to NM_014649.2 E711E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:5595457 G>A maps to NM_014649.2 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:234229348 G>A maps to NM_000541.4 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H8-01A-21D-A34J-08 chr2:234243613 A>G maps to NM_000541.4 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr23:134994508 G>C did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr23:134994089 A>G did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:134989481 C>T did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:134991056 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr23:134988620 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr23:134993809 C>G did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr16:51173270 G>A maps to ENST00000251020 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:51171061 G>C maps to ENST00000251020 T1312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr16:51174767 C>T maps to ENST00000251020 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr16:51175391 G>A maps to ENST00000251020 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr16:51172805 C>T maps to ENST00000251020 P1109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:51175025 C>G maps to ENST00000251020 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr16:51174002 G>A maps to ENST00000251020 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:51174818 C>T maps to ENST00000251020 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:51171358 G>A maps to ENST00000251020 F1213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr16:51172805 C>T maps to ENST00000251020 P1109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr16:51173849 C>T maps to ENST00000251020 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr14:21991047 C>T maps to NM_005407.1 P938P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr18:76754480 G>A maps to NM_171999.2 P830P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr18:76753934 G>A maps to NM_171999.2 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr18:76754126 C>T maps to NM_171999.2 C712C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:76752296 C>T maps to NM_171999.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:76753295 C>T maps to NM_171999.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr18:76753496 G>T maps to NM_171999.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr18:76755392 G>A maps to NM_171999.2 T1134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr18:76753376 C>T maps to NM_171999.2 N462N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr18:76753743 C>T maps to NM_171999.2 Q585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr20:50418836 C>T maps to NM_020436.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:50407412 G>A maps to NM_020436.3 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr20:50407710 T>C maps to NM_020436.3 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:866466 C>T maps to ENST00000443100 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr17:48195665 C>T maps to NM_174920.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr6:130505271 G>A maps to ENST00000457563 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:130535480 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr6:130497045 G>T maps to ENST00000457563 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr14:55168921 T>C maps to NM_015589.4 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr14:55218239 G>C maps to NM_015589.4 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr14:55169179 C>T maps to NM_015589.4 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:169639091 T>C maps to NM_182610.2 N59N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr3:169644928 G>A maps to NM_182610.2 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:76928340 A>G maps to ENST00000372690 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:92731897 T>C maps to NM_017654.3 E1171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr7:92732103 G>A maps to NM_017654.3 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr7:92733304 A>G maps to NM_017654.3 S702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr7:92761231 G>T maps to NM_152703.2 Y1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:92761450 C>T maps to NM_152703.2 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:92761381 C>T maps to NM_152703.2 R1301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:92762800 T>C maps to NM_152703.2 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:92761645 G>A maps to NM_152703.2 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr20:35532576 C>A maps to NM_015474.3 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:44385099 C>T maps to NM_015380.4 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr22:44386274 G>A maps to NM_015380.4 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr21:15889299 G>A maps to ENST00000285670 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr21:15872960 C>G maps to ENST00000285670 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr2:128712713 C>T maps to NM_001145928.1 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:128712890 C>A maps to NM_001145928.1 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:128775457 G>A maps to NM_001145928.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:128757381 A>G maps to NM_001145928.1 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:73698630 G>A maps to NM_013260.6 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr5:153826343 C>A maps to NM_024632.5 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:153832993 A>G maps to NM_024632.5 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:55756737 G>A maps to ENST00000443936 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:55758260 C>A maps to ENST00000443936 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr19:55748069 G>A maps to ENST00000443936 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr22:50854546 G>A maps to ENST00000216061 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr22:50862015 C>T maps to ENST00000216061 C366C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr22:50860745 C>T maps to ENST00000216061 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr22:50854549 G>A maps to ENST00000216061 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr22:50845168 C>T maps to ENST00000216061 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr11:68318641 G>T maps to NM_001164160.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr11:68312324 G>T maps to NM_001164160.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr11:68326136 C>T maps to NM_001164160.1 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:71912252 C>T maps to NM_020150.4 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr9:136536696 G>A maps to NM_007101.3 N762N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr9:136573441 G>A maps to NM_007101.3 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr9:136578217 C>G maps to NM_007101.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr11:65732030 C>T maps to NM_005146.4 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:108939001 G>C maps to NM_014706.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:108930561 C>A did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr12:108920070 G>A maps to NM_014706.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr12:108942936 G>A maps to NM_014706.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr6:148865296 C>T maps to NM_015278.3 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:148864927 A>G maps to NM_015278.3 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr6:148869663 C>T maps to NM_015278.3 F1238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr6:148840731 C>T maps to NM_015278.3 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:128926744 G>C did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:128926785 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:128926346 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:128927037 T>C did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr23:128927004 T>G did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:100572485 G>A maps to NM_194292.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:100550934 C>T maps to NM_194292.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:100551110 C>T maps to NM_194292.1 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr23:23803927 C>A did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr23:23801826 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr23:23803920 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr2:200298059 C>A did not map to a codon.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr2:200193462 G>A maps to NM_001172509.1 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:200137184 G>A maps to NM_001172509.1 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:200193506 G>A maps to NM_001172509.1 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr2:200245203 T>A maps to NM_001172509.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:200173602 G>A maps to NM_001172509.1 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr2:200137014 G>A maps to NM_001172509.1 S707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr2:200188669 C>T maps to NM_001172509.1 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr2:200137347 G>T maps to NM_001172509.1 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr2:200137050 C>A maps to NM_001172509.1 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:84363827 C>G did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:84363897 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:84362471 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr23:84363319 T>A did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr14:51102086 C>T maps to NM_021818.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:51111688 G>A maps to NM_021818.2 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr7:66453483 T>C maps to NM_016038.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr7:66456168 C>T maps to NM_016038.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr7:66456189 C>T maps to NM_016038.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:50898406 G>C maps to ENST00000337034 V1165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr22:50903691 G>T maps to ENST00000337034 C395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:50885810 C>T maps to ENST00000337034 V1851V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:50899027 G>A maps to ENST00000337034 T1037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:50903742 G>A maps to ENST00000337034 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr22:50903083 G>A maps to ENST00000337034 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr11:10064471 A>G maps to NM_030962.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:9917510 A>T maps to NM_030962.3 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr11:10064501 C>A maps to NM_030962.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr11:10064485 G>A maps to NM_030962.3 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr16:28328855 C>T maps to NM_001024401.2 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:56042590 A>G maps to NM_001101401.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:56047457 C>T maps to NM_001101401.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr19:56041198 G>A maps to NM_001101401.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:123810856 G>A maps to NM_001167856.1 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr19:1122253 C>A maps to NM_014963.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:1109707 G>A maps to NM_014963.2 Q1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7596-01A-11D-2229-08 chr19:1123581 C>T maps to NM_014963.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:36018687 C>A maps to NM_001166034.1 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:36018829 C>T maps to NM_001166034.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr11:121174254 C>G maps to NM_001024956.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr11:121178028 T>C maps to NM_001024956.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr19:50157645 G>A maps to NM_021228.2 A1119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr19:50154614 C>T maps to NM_021228.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:155227140 G>A maps to NM_005698.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:34542149 C>T maps to NM_033630.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr6:28540655 C>A maps to NM_052923.1 E1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr6:28543104 A>G maps to NM_052923.1 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:28541502 A>C maps to NM_052923.1 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:28543799 T>A maps to NM_052923.1 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:28543893 G>A maps to NM_052923.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:28542878 G>A maps to NM_052923.1 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr3:47484396 G>T maps to NM_012235.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:47462226 G>T maps to NM_012235.2 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:47484420 G>A maps to NM_012235.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr3:47456102 G>A maps to NM_012235.2 Q1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr3:47455798 A>G maps to NM_012235.2 H1155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr3:47456603 G>A maps to NM_012235.2 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr8:27516475 C>T maps to NM_016240.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr8:27779352 G>A maps to NM_173833.5 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr8:27779709 C>T maps to NM_173833.5 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr17:1538597 C>T maps to NM_003693.2 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr17:1542220 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:20784020 G>A maps to NM_153334.4 H434H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr10:102116450 C>G maps to NM_005063.4 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr13:78171682 A>G maps to NM_144777.2 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr13:78167686 C>A maps to NM_144777.2 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr13:78192193 C>T maps to NM_144777.2 R543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr14:31142516 A>T maps to ENST00000311943 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr14:31122763 G>A maps to ENST00000311943 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:31185182 C>T maps to ENST00000311943 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr4:54231625 G>T maps to NM_152540.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:224462506 G>A maps to NM_003469.4 N498N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr15:51975581 G>T maps to NM_013243.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr15:51981444 A>G maps to NM_013243.3 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr15:32972060 T>C maps to NM_001144757.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:147261108 T>C maps to NM_054023.4 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr6:25701544 G>T maps to NM_006998.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr3:159605681 C>T maps to NM_001197113.1 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr3:159604001 G>A maps to NM_001197113.1 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr3:158991673 T>G did not map to a codon.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr4:129864210 C>T maps to NM_144643.2 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr4:129873943 C>A maps to NM_144643.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr4:129886440 C>T maps to NM_144643.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:239003068 C>T maps to NM_016510.4 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr2:238990768 G>A maps to NM_016510.4 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:41540980 C>T maps to NM_001031694.2 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:17762332 C>G did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr23:17768105 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:17771377 G>A did not map to a codon.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr23:17771492 G>A did not map to a codon.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr23:17768242 C>G did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr23:18338539 C>G did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr23:18283828 A>G did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:18283735 G>T did not map to a codon.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr23:18323202 C>T did not map to a codon.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr6:108068061 C>T maps to NM_198081.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr3:38805035 G>A maps to NM_006514.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:38763807 C>A maps to NM_006514.2 E1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:38793847 C>G maps to NM_006514.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:38743590 G>A maps to NM_006514.2 Q1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:38748835 C>T maps to NM_006514.2 K1440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:38888754 C>A maps to ENST00000302328 V1602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:38921581 G>T maps to ENST00000302328 P1084P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr3:38888754 C>A maps to ENST00000302328 V1602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:38951679 A>T maps to ENST00000302328 Y326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr3:38888793 G>T maps to ENST00000302328 I1589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr3:38950664 G>A maps to ENST00000302328 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H8-01A-21D-A34J-08 chr3:38938440 G>A maps to ENST00000302328 C766C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr2:166848066 G>A maps to NM_001165963.1 I1906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:166848384 C>T maps to NM_001165963.1 L1800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:166901606 G>A maps to NM_001165963.1 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:166894585 G>A maps to NM_001165963.1 I882I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr2:166929996 G>A maps to NM_001165963.1 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr2:166848804 G>C maps to NM_001165963.1 L1660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:166900255 C>A maps to NM_001165963.1 G656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:166872123 G>A maps to NM_001165963.1 F1181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr2:166905424 T>C maps to NM_001165963.1 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr2:166897881 T>C maps to NM_001165963.1 K758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr2:166848050 G>A maps to NM_001165963.1 R1912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:35524698 G>A maps to NM_199037.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr2:166172117 A>G maps to NM_001040142.1 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:166210925 A>G maps to NM_001040142.1 K1048K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:166020402 C>G maps to ENST00000360093 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr2:165986509 G>T maps to NM_006922.3 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:166003415 G>A maps to NM_006922.3 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:166020351 G>A maps to ENST00000360093 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr2:166003407 C>T maps to NM_006922.3 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:165947361 G>A maps to NM_006922.3 I1767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr2:166019312 C>G maps to NM_006922.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr2:165953012 C>T maps to NM_006922.3 W1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr11:123513319 C>T maps to NM_018400.3 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr11:123516408 G>A maps to NM_018400.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr17:62022764 G>C maps to NM_000334.4 V1225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:62049719 G>A maps to NM_000334.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:62049988 G>T maps to NM_000334.4 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:62034548 G>A maps to NM_000334.4 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:62036777 T>C maps to NM_000334.4 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr17:62018475 G>C maps to NM_000334.4 L1722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:118007834 C>T maps to NM_174934.3 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:38622703 A>G maps to NM_001099404.1 C982C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr3:38597250 A>G maps to NM_001099404.1 L1480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr3:38622502 G>A maps to NM_001099404.1 I1049I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr3:38648249 G>A maps to NM_001099404.1 H350H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:167330397 G>C maps to NM_002976.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:167273408 G>T maps to NM_002976.2 I1074I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:167262118 C>A maps to NM_002976.2 E1674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:167301367 G>A maps to NM_002976.2 F510F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:167298178 T>C maps to NM_002976.2 K628K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr2:167313565 C>T maps to NM_002976.2 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr2:167262274 G>A maps to NM_002976.2 R1622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr2:167273360 T>A maps to NM_002976.2 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:52159507 G>A maps to NM_014191.2 K866K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:52201176 C>T maps to NM_014191.2 A1969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr12:52145364 T>A maps to NM_014191.2 A786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr12:52201212 G>C maps to NM_014191.2 *1981Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:52200795 C>A maps to NM_014191.2 I1842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:52115637 G>T maps to NM_014191.2 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:52200861 C>T maps to NM_014191.2 I1864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr12:52163650 G>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:167056252 C>G maps to ENST00000303354 T1633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:167141151 C>T maps to ENST00000303354 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:167056096 A>G maps to ENST00000303354 F1685F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr2:167163021 G>A maps to ENST00000303354 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr2:167168038 C>T maps to ENST00000303354 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr12:6457161 T>C maps to NM_001159576.1 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:6457039 C>G maps to NM_001159576.1 *729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr12:6471398 C>T maps to NM_001159576.1 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr16:23382770 C>T maps to ENST00000307331 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr16:23383140 G>A maps to ENST00000307331 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:23391743 C>T maps to ENST00000307331 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr16:23364283 C>T maps to ENST00000307331 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:1226641 G>A maps to NM_001130413.2 Q589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr16:23208745 C>T maps to NM_001039.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr17:10584495 C>T maps to NM_004589.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr22:50962504 C>G maps to NM_001169111.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr22:50962768 C>T maps to NM_001169111.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr22:50962300 G>A maps to NM_001169111.1 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr22:50962126 C>T maps to NM_001169111.1 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:55075840 G>T maps to NM_021626.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:174309512 C>T maps to NM_007281.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:144877206 C>A did not map to a codon.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr8:144893220 C>T maps to NM_182706.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:144887383 G>A maps to NM_182706.3 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr8:144895847 C>T maps to NM_182706.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr8:144893097 G>A maps to NM_182706.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr8:144885675 C>T maps to NM_182706.3 V1160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr8:144893329 G>A maps to NM_182706.3 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr7:29983662 C>G maps to NM_001145514.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr8:145559792 G>A maps to NM_031309.4 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:120204415 G>T maps to NM_002980.2 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:9090929 C>T maps to ENST00000457346 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:9068951 G>A maps to ENST00000457346 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:35213721 A>G maps to ENST00000394681 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr6:35196407 C>A maps to ENST00000394681 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr11:65298218 C>T maps to NM_020680.3 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:65293809 C>T maps to NM_020680.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:65294569 C>T maps to NM_020680.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr12:100728041 G>A maps to NM_017988.4 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr4:76879031 G>A maps to NM_018115.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr4:76879074 A>G maps to NM_018115.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:76891489 T>C maps to NM_018115.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:43964467 G>A maps to NM_002999.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr14:50312959 C>T maps to NM_004713.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr14:50262629 G>C maps to NM_004713.3 S833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:50295331 A>G did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr9:139301869 G>A maps to NM_001039707.1 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:243456391 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:243504339 G>A did not map to a codon.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:1152945 G>A maps to NM_016176.3 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:1153118 C>T maps to NM_016547.2 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:251132 C>T maps to NM_004168.2 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:161326610 G>A maps to NM_003001.3 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:4169595 G>A maps to NM_152744.3 G1332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr7:4249657 C>T maps to NM_152744.3 A1801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:4089028 C>A maps to NM_152744.3 T884T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:4247912 G>A maps to NM_152744.3 Q1799Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:4091358 G>C maps to NM_152744.3 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr7:4272923 G>A maps to NM_152744.3 P1955P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr7:4185402 C>A maps to NM_152744.3 T1426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:4188975 C>T maps to NM_152744.3 G1502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr7:4153691 C>T maps to NM_152744.3 N1203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr7:3658736 G>T maps to NM_152744.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr7:4259831 C>T maps to NM_152744.3 F1877F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:4152953 G>A maps to NM_152744.3 P1156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr7:3991529 G>A maps to NM_152744.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:4089059 C>T maps to NM_152744.3 Q895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr7:4169590 C>T maps to NM_152744.3 R1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr7:4026874 C>T maps to NM_152744.3 H684H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr7:4008964 G>T maps to NM_152744.3 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:71390386 G>A maps to NM_001144952.1 V1223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr17:71375665 G>A maps to NM_001144952.1 Y1595Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr17:71418541 C>T maps to NM_001144952.1 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:192700957 C>T maps to NM_004657.5 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:192711276 C>T maps to NM_004657.5 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:57323206 G>T maps to NM_148897.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:57317739 A>G maps to NM_148897.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:57324257 G>A maps to NM_148897.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57324257 G>A maps to NM_148897.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:113872018 C>A maps to NM_138432.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr12:113873328 C>T maps to NM_138432.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:26691846 C>T maps to NM_001080837.2 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr18:56816785 T>C maps to NM_033280.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr17:75187291 C>T maps to NM_001039573.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:75212634 C>T maps to NM_001039573.2 R717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:75205425 C>T maps to NM_001039573.2 C493C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr17:75199694 C>G maps to NM_001039573.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr22:30812007 C>T maps to NM_012429.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr22:30803468 C>T maps to NM_012429.2 Y100Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr22:30857318 G>C maps to NM_174975.4 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr22:30887557 A>G did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr22:30887572 G>A maps to NM_174977.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:5055946 G>A maps to NM_014692.1 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:5058636 G>A maps to NM_014692.1 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr9:139339533 T>C maps to NM_014866.1 L2299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr9:139366548 G>T maps to NM_014866.1 L1194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:139371757 G>A maps to NM_014866.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:139371344 C>T maps to NM_014866.1 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr9:139369941 G>C maps to NM_014866.1 S709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr9:139350101 A>C maps to NM_014866.1 P1936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:177909816 C>T maps to NM_033127.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:177930829 C>A maps to NM_033127.2 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:177909765 C>T maps to NM_033127.2 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:177909753 C>T maps to NM_033127.2 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr1:177901894 G>T maps to NM_033127.2 S957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr3:122964833 C>T maps to NM_012430.4 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr3:122928126 T>C maps to NM_012430.4 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr3:42594850 G>A maps to NM_032970.2 H267H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr14:39517934 T>A did not map to a codon.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr14:39565169 T>C maps to NM_006364.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr14:39508283 G>C maps to NM_006364.2 S720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr20:18506491 G>A maps to NM_001172745.1 Q250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr10:121662312 T>G maps to NM_007190.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr10:121693240 C>T maps to NM_007190.2 R989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:134029559 C>A maps to NM_021982.1 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:133997208 T>C maps to NM_021982.1 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:110433144 G>A maps to NM_006323.2 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr4:110394258 C>G maps to NM_006323.2 S326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:75525643 G>T maps to NM_198597.1 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr10:75526246 C>T maps to NM_198597.1 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr4:119649745 A>T maps to ENST00000379735 I977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr4:119754818 C>G maps to ENST00000379735 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr4:83785612 G>A maps to ENST00000505472 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr10:102247815 C>A maps to NM_015490.3 E1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:102267288 T>A maps to NM_015490.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:102249489 T>A maps to NM_015490.3 P998P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:127783718 G>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:127783840 C>T maps to ENST00000464451 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr10:12197793 G>A maps to NM_018144.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:12197791 T>C maps to NM_018144.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr6:108197818 C>T maps to NM_007214.4 Q661Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr9:91963070 C>T maps to NM_024077.3 D560D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr9:91972916 C>T maps to NM_024077.3 Q758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr15:49320676 C>T maps to NM_001193489.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr15:49320739 A>G maps to NM_001193489.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr20:13856746 C>A maps to NM_025229.1 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr20:13839997 T>C maps to NM_025229.1 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr20:13839916 G>A maps to NM_025229.1 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:25780750 G>A maps to NM_015187.3 Y844Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr4:25783862 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr4:25849150 G>T maps to NM_015187.3 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr4:25760610 G>C maps to NM_015187.3 S1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr1:169702092 C>T maps to NM_000450.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:169696637 C>A maps to NM_000450.2 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:169696912 C>A maps to NM_000450.2 G479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:169701063 G>A maps to NM_000450.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:169697063 C>T maps to NM_000450.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:151341920 G>A maps to ENST00000435071 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:169672450 C>T maps to NM_000655.4 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr22:50647024 C>T maps to NM_031454.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:50654233 G>A maps to NM_031454.1 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:169562915 C>A maps to NM_003005.3 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:169578748 G>A maps to NM_003005.3 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:169572297 C>A maps to NM_003005.3 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:169565301 G>T maps to NM_003005.3 Y654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:109017612 C>T maps to ENST00000228463 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr12:109016913 C>A maps to ENST00000228463 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr7:83590839 G>A maps to NM_006080.2 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr7:83640335 A>G did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:83610668 A>T maps to NM_006080.2 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr7:83758444 G>A maps to NM_006080.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr7:83675759 C>G did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr3:50313226 G>A maps to NM_004636.2 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr7:80439969 G>A maps to NM_006379.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:80418763 A>G maps to NM_006379.2 H404H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:80394476 G>C maps to NM_006379.2 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:80546040 C>T maps to NM_006379.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr7:80378273 G>A maps to NM_006379.2 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr7:80430071 C>A did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr7:80418628 G>A maps to NM_006379.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr7:84651710 T>G maps to NM_152754.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:84649547 C>A did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr7:84651773 C>T maps to NM_152754.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:83014749 C>T did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr7:82996903 A>G maps to NM_012431.2 *776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr7:82996928 G>A maps to NM_012431.2 R767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr7:83014671 G>A maps to NM_012431.2 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr7:83014714 A>T maps to NM_012431.2 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:83029527 G>T maps to NM_012431.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr7:83119452 T>A maps to NM_012431.2 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:83021871 T>G maps to NM_012431.2 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr3:52469792 G>T maps to NM_020163.1 Y725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156145016 C>T maps to NM_022367.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr1:156130750 C>T maps to NM_022367.3 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:156132737 G>A maps to NM_022367.3 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr2:97526458 G>A maps to NM_017789.4 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr2:97527622 G>A maps to NM_017789.4 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr2:97531480 G>A maps to NM_017789.4 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:92003800 G>A maps to NM_006378.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:92017920 C>T maps to NM_006378.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr9:92014250 C>G maps to NM_006378.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr9:91993761 C>A maps to NM_006378.3 E816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr9:92003562 C>T maps to NM_006378.3 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr9:91994242 G>T maps to NM_006378.3 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:74902407 C>T maps to NM_004263.3 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:102743434 C>T maps to NM_017893.2 C693C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:102743389 G>C maps to NM_017893.2 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:9052124 C>T maps to NM_003966.2 W902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:9044560 G>T maps to NM_003966.2 S1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:9108254 A>G maps to NM_003966.2 N690N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:9154807 C>G did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:9136621 C>A maps to NM_003966.2 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr5:9063170 C>T maps to NM_003966.2 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr5:9063073 C>A maps to NM_003966.2 E815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:122662293 G>T maps to NM_001031702.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr3:122634456 C>T maps to NM_001031702.2 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr3:122629103 G>A maps to NM_001031702.2 F1114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr3:122645414 G>A maps to NM_001031702.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr3:122642481 G>A maps to NM_001031702.2 N418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:122629073 C>A maps to NM_001031702.2 T1124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr5:115783451 G>A maps to ENST00000257414 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr5:115783097 C>G maps to ENST00000257414 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr5:115782988 G>A maps to ENST00000257414 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr5:115783319 C>T maps to ENST00000257414 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:4552582 C>T maps to NM_032108.3 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr15:48056382 T>C maps to NM_153618.1 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr15:48056144 G>C maps to NM_153618.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:48055234 A>T maps to NM_153618.1 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr15:48056927 C>T maps to NM_153618.1 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:48058128 C>T maps to NM_153618.1 H497H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr15:74707065 C>T maps to NM_003612.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:43837050 A>G maps to NM_003007.3 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr20:43836060 C>T maps to NM_003007.3 H41H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr20:43851823 A>G maps to NM_003008.2 Q517Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr20:43851451 T>G maps to NM_003008.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:48477536 G>C maps to ENST00000004980 S130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:48458912 G>A maps to ENST00000004980 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr3:185347617 C>T maps to ENST00000427465 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:196656541 C>G maps to NM_152699.4 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr3:196650378 C>G maps to NM_152699.4 S660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:76344432 C>T maps to NM_015571.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr6:76372992 A>G maps to NM_015571.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr6:76333614 G>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:13378323 G>A maps to NM_012247.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:30456869 C>T maps to ENST00000478753 *60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr16:30456190 C>T maps to ENST00000478753 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:26138255 C>T maps to NM_020451.2 H389H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:26136266 C>T maps to NM_020451.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr1:26135117 C>T maps to NM_020451.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr5:42801321 G>A maps to NM_001093726.1 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr16:30389948 G>A maps to NM_052838.3 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr4:77940385 C>A maps to ENST00000510515 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:4835883 C>A maps to NM_144605.3 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:55874868 G>A maps to NM_207366.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr7:55863611 C>T maps to NM_207366.2 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:242277150 C>T maps to ENST00000391972 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr22:42390636 G>A maps to NM_145733.2 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr22:42390723 C>T maps to NM_019106.5 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr22:42383670 C>T maps to NM_145733.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr22:42383246 C>T maps to NM_145733.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr23:118797578 C>T did not map to a codon.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr23:118797473 G>A did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:118763372 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:118771103 A>G did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:118787003 C>T did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:35930337 C>T maps to NM_001788.4 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:75398525 C>T maps to NM_001113491.1 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:158569895 C>G did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr6:158540195 G>A maps to NM_032861.3 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:158538838 T>C maps to NM_032861.3 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:67889985 G>A maps to NM_001018067.1 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:18010156 C>G maps to NM_012139.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr6:122777666 T>C maps to NM_020755.2 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr6:122779663 C>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:79498803 G>C maps to NM_001174072.1 S32S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-UF-A7JA-01A-12D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:94849226 G>A maps to NM_001127707.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr14:94754645 T>A maps to NM_001100607.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:94756785 C>A maps to NM_001100607.1 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr14:94750478 T>G maps to NM_001100607.1 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr14:94756657 G>C maps to NM_001100607.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:94914814 G>T maps to NM_001080451.1 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:94964422 G>A maps to NM_173850.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr14:94956064 G>T maps to NM_173850.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:95080960 C>A maps to ENST00000393080 Y86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr14:95090072 C>A maps to ENST00000393080 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr14:95088734 C>T maps to ENST00000393080 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr14:95034591 C>T maps to NM_006215.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr14:95033333 C>G maps to NM_006215.2 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr14:95033316 G>A maps to NM_006215.2 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:95035799 G>A maps to NM_006215.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:95030211 C>T maps to NM_006215.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr14:95058470 C>T maps to NM_000624.4 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:105280473 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:105279275 C>T did not map to a codon.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr23:105280604 C>T did not map to a codon.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr23:105280479 T>A did not map to a codon.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr23:105277536 C>A did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr23:105280647 G>A did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:105280662 C>G did not map to a codon.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr14:94929633 C>A did not map to a codon.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr18:61602475 A>T maps to NM_005024.1 *398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr18:61264494 C>A maps to NM_012397.3 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr18:61328438 G>C maps to NM_006919.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr18:61309122 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:61154285 C>T maps to NM_002639.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr6:2948609 G>A maps to ENST00000316782 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:173878795 C>A maps to NM_000488.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr22:21138320 G>A maps to NM_000185.3 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr22:21133857 C>T maps to NM_000185.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:21134214 G>A maps to NM_000185.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134278 C>T maps to NM_000185.3 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134358 C>T maps to NM_000185.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134378 C>G maps to NM_000185.3 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134469 C>T maps to NM_000185.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134478 C>T maps to NM_000185.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr22:21133695 G>A maps to NM_000185.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr7:100778861 C>T maps to NM_000602.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:100775222 C>T maps to NM_000602.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr2:224856625 C>T maps to NM_001136530.1 W205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:1648677 T>C maps to NM_000934.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:57379318 G>T maps to ENST00000403558 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:57379389 C>A maps to ENST00000403558 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:57381960 C>T maps to ENST00000403558 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:75282866 G>A maps to NM_001235.2 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr11:75277798 C>T maps to NM_001235.2 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:75277819 C>T maps to NM_001235.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr11:75277939 C>T maps to NM_001235.2 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr11:75277978 G>A maps to NM_001235.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr3:167512408 G>T maps to NM_005025.4 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr3:167543054 C>T maps to NM_005025.4 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:167167166 G>A maps to NM_006217.3 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr3:167183381 T>C maps to NM_006217.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:40928871 G>C maps to NM_013376.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:40929339 C>T maps to NM_013376.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr19:40929408 C>T maps to NM_013376.3 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:64863927 G>A maps to NM_014755.2 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:210415651 A>G maps to NM_019605.3 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr6:109323524 G>T maps to NM_014454.1 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:28599969 G>A maps to NM_031459.3 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr2:179979881 C>A maps to NM_178123.4 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:180008415 A>T maps to NM_178123.4 L251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr2:179997066 T>C maps to NM_178123.4 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:180008405 G>A maps to NM_178123.4 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr18:42530339 G>A maps to NM_015559.2 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr18:42531992 C>T maps to NM_015559.2 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr18:42529989 G>T maps to NM_015559.2 G229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr18:42530734 C>A maps to NM_015559.2 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr18:42281445 G>C maps to NM_015559.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr16:30990626 G>T maps to NM_014712.1 E1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:30974856 G>A maps to NM_014712.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:30980948 G>A maps to NM_014712.1 E985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr16:30982756 C>T maps to NM_014712.1 G1025G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:30977520 C>T maps to NM_014712.1 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr16:30978856 C>A maps to NM_014712.1 A906A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr3:47163753 G>C maps to NM_014159.6 S791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:47163557 G>A maps to NM_014159.6 I856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr3:47079268 T>A did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:99932039 T>A maps to NM_032233.2 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr21:37429428 G>A maps to NM_017438.3 N49N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr3:9514921 A>T maps to ENST00000407969 V1085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:9517532 C>T maps to ENST00000407969 Q1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:9512327 G>A maps to ENST00000407969 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr3:9512474 T>A maps to ENST00000407969 C1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr16:58550235 C>T maps to NM_001160305.1 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr4:140441447 G>A maps to NM_030648.2 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr1:150923167 A>G maps to NM_001145415.1 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:150900252 G>A maps to NM_001145415.1 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr13:50054402 C>T maps to NM_031915.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:50035240 C>T maps to NM_031915.2 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:135204920 G>A maps to ENST00000372169 C688C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr9:135205409 G>A maps to ENST00000372169 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr9:135163670 A>G maps to ENST00000372169 D2092D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr9:135173681 C>A maps to ENST00000372169 E1856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr9:135204701 C>T maps to ENST00000372169 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr9:135205856 T>C maps to ENST00000372169 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:27284447 C>A maps to NM_178860.4 V804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr17:27308503 G>A maps to NM_178860.4 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:26688597 C>T maps to NM_021115.4 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr22:26695085 C>T maps to NM_021115.4 C433C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr16:29884919 G>A maps to NM_201575.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr16:29891362 G>A maps to NM_201575.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr16:29888271 C>T did not map to a codon.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr16:29884952 C>A maps to NM_201575.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:64536791 G>A maps to NM_201995.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:64534667 T>C maps to NM_201995.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr11:64536773 C>A maps to NM_201995.2 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr11:64533418 A>C maps to NM_004630.3 Y597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:64536577 G>C maps to NM_201995.2 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr22:30736774 C>T maps to NM_005877.4 Q366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:38449852 C>T maps to NM_006802.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr1:38455600 C>A maps to NM_006802.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:198299714 C>T maps to NM_012433.2 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:198285203 C>T maps to NM_012433.2 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:198272766 T>C maps to NM_012433.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:198263270 C>G maps to NM_012433.2 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr2:198260868 C>A maps to NM_012433.2 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:65826341 C>T maps to NM_006842.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr11:65826721 C>T maps to NM_006842.2 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr16:70575706 G>A maps to NM_012426.4 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr16:70597895 G>A maps to NM_012426.4 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:70575646 A>G maps to NM_012426.4 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr16:70602959 T>C maps to NM_012426.4 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr6:144416374 C>G maps to NM_031287.2 *87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr19:19414162 G>A maps to NM_172231.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:19431287 G>A maps to NM_172231.2 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr22:31979943 C>G maps to NM_001007467.1 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr22:32009446 G>T maps to NM_001007467.1 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr22:32003954 G>C maps to NM_001007467.1 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr22:32011158 C>G maps to NM_001007467.1 S1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:52977587 C>A maps to NM_016329.3 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:52947575 G>C maps to NM_016329.3 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:7239524 C>G maps to NM_001018039.1 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr10:7214494 T>G maps to NM_001018039.1 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:7217982 C>T maps to NM_001018039.1 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr10:7214102 G>A maps to NM_001018039.1 D723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:27190330 G>T maps to NM_006142.3 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr1:27190209 C>T maps to NM_006142.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:27190365 G>A maps to NM_006142.3 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:27190296 C>T maps to NM_006142.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr8:41122967 G>A maps to NM_003012.4 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr7:37955851 C>T maps to ENST00000223214 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:37955824 G>T maps to ENST00000223214 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:37951857 C>G maps to ENST00000223214 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr7:37956079 G>A maps to ENST00000223214 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr7:37955806 G>A maps to ENST00000223214 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr10:99527327 G>A maps to NM_003015.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:70716155 A>G maps to NM_004768.3 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:65466623 C>T maps to NM_001077199.1 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr19:19120693 G>A maps to NM_001017392.3 Q770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr21:33044290 C>T maps to NM_020706.2 A955A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr21:33065708 G>A maps to NM_020706.2 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr21:33068511 G>A maps to NM_020706.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr21:33067130 G>A maps to NM_020706.2 Q411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr21:33057368 T>A maps to NM_020706.2 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr21:33076109 G>A maps to NM_020706.2 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:33044428 G>A maps to NM_020706.2 F909F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr21:33044515 G>A maps to NM_020706.2 P880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:45561106 G>A maps to NM_007056.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:45567446 G>A maps to NM_007056.2 Q361Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:1720158 G>A did not map to a codon.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr23:1719885 C>G did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr23:1720073 G>T did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:1712552 G>T did not map to a codon.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr23:1712435 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr23:1712668 G>C did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:99850545 C>T maps to NM_032870.2 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:74732509 C>T maps to NM_003016.4 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr12:46316326 T>C maps to NM_004719.2 K1388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:46321866 T>C maps to NM_004719.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:46328279 A>G maps to NM_004719.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr12:46320062 C>A maps to NM_004719.2 G1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr1:29475407 C>T maps to NM_005626.4 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr1:29475098 G>T maps to NM_005626.4 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr1:29508252 C>T maps to NM_005626.4 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IF-01A-11D-A31L-08 chr14:70235547 A>G maps to NM_006925.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr20:42089354 G>C maps to NM_006275.5 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:132238981 C>T maps to NM_004592.2 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:168200756 T>C maps to NM_199344.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:81372066 G>T did not map to a codon.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr10:81371616 G>A maps to NM_001093770.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr10:81371739 C>T maps to NM_001093770.2 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr10:81319203 C>T maps to NM_001098668.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:85892749 C>T maps to NM_198843.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr10:81701731 G>T maps to NM_003019.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr10:120917409 G>A maps to NM_213649.1 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:48243420 G>A maps to NM_000023.2 W7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr17:48245849 C>T maps to NM_000023.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:48252743 G>A maps to NM_000023.2 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:52895088 T>A did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:94230020 G>T maps to NM_001099401.1 S325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr13:23777922 C>T maps to NM_000231.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:23853607 C>T maps to NM_000231.2 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr8:13947987 A>T maps to NM_139167.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:13959908 G>T maps to NM_139167.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr8:14095173 G>T maps to NM_139167.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr1:67195003 A>G maps to ENST00000237247 R631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:67205085 C>T maps to ENST00000237247 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr1:67185025 C>G maps to ENST00000237247 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr6:134495870 G>A maps to NM_005627.3 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:42199696 C>A maps to NM_016276.3 C229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr20:42195736 G>A maps to NM_016276.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr20:42198104 C>T maps to NM_016276.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:8235564 G>C maps to NM_001080826.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr8:8185977 C>G did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr8:8234393 C>A maps to NM_001080826.1 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr8:8233962 C>T maps to NM_001080826.1 W652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:77473952 G>A maps to NM_024776.2 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr15:77472680 G>A maps to NM_024776.2 R530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr15:77406605 C>G maps to NM_024776.2 L1711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:67759504 G>C maps to NM_013257.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr8:67740901 C>G maps to NM_013257.3 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:52103622 G>A maps to ENST00000361543 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr10:52103820 C>T maps to ENST00000361543 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr10:52067885 C>T maps to ENST00000361543 W312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:201437984 T>C maps to NM_152524.5 S972S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr10:72636949 A>G did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:223423615 G>C maps to NM_152386.2 *400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr2:223423241 G>A maps to NM_152386.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:78184559 C>T maps to NM_000199.3 Q400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr17:78184574 G>T maps to NM_000199.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr17:78184601 G>A maps to NM_000199.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr22:25264736 C>T maps to NM_001039948.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr22:25294144 G>C maps to NM_001039948.2 R798R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr22:25294003 C>T maps to NM_001039948.2 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr22:40800431 C>T maps to NM_015705.4 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:40804824 C>T maps to NM_015705.4 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr22:40802506 G>A maps to NM_015705.4 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:2759261 G>A maps to NM_003021.3 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr19:2767676 G>A maps to NM_003021.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr5:64976528 G>C maps to NM_019072.2 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr16:28883682 T>G maps to NM_001145795.1 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr16:28883643 C>T maps to NM_001145795.1 H549H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr23:123480504 G>A did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:123480564 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:123504073 A>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr23:123504070 C>A did not map to a codon.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr23:123499671 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:156777035 G>A maps to NM_001161441.1 H378H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:156779021 G>A maps to NM_001161441.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr9:130536746 C>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:130506940 G>T maps to NM_170600.2 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:19231061 A>G maps to NM_022071.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr10:82330000 C>T maps to NM_207372.2 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr10:82403806 A>C maps to NM_207372.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:82363434 G>A maps to NM_207372.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:21050666 G>A maps to ENST00000444387 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr15:78390832 G>A maps to NM_001101404.1 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:80532533 G>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr22:38040920 G>A maps to NM_018957.3 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr4:2831400 G>A maps to NM_001145856.1 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:235950501 G>A maps to NM_014521.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr2:235951773 C>A maps to NM_014521.2 C787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr2:235950834 C>G maps to NM_014521.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr2:235951473 C>T maps to NM_014521.2 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:15300344 G>A maps to NM_004844.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:249107241 G>A maps to NM_030645.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:249106317 G>A maps to NM_030645.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr4:152058966 G>A maps to NM_001009555.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr19:4366920 A>G did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:4365607 G>A maps to NM_003025.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr19:4363715 C>A did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:17793363 G>A did not map to a codon.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr9:17793389 A>T maps to NM_003026.2 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr15:84286873 C>G maps to ENST00000434347 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:87208082 A>C maps to ENST00000482504 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7593-01A-11D-2229-08 chr9:131783492 G>A maps to ENST00000372554 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr23:19555887 T>G did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:19764534 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:19702000 C>A did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:19725000 C>G did not map to a codon.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr23:19587304 C>T did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr23:19568090 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:19854367 G>T did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:19702075 G>A did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr23:19702121 T>A did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:19560227 C>T did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr10:105362899 G>C maps to ENST00000369774 S692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr10:105363417 C>T maps to ENST00000369774 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:105362409 C>T maps to ENST00000369774 Q855Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:105363402 C>T maps to ENST00000369774 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr5:171809083 C>A maps to NM_001017995.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr5:171774316 C>T maps to NM_001017995.2 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr4:170042097 T>C maps to NM_020870.3 E463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr5:145379751 C>T maps to NM_152550.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr5:145442147 C>T maps to NM_152550.3 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:145439600 C>T maps to NM_152550.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr5:145379826 C>G maps to NM_152550.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:145439427 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:109988085 G>T maps to NM_001099289.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr2:109964266 C>T maps to NM_001099289.1 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr4:8239291 C>T maps to NM_018986.3 L1216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr4:8229850 G>T maps to NM_018986.3 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr4:8229892 C>T maps to NM_018986.3 I824I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr4:8218735 C>T maps to NM_018986.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:8229621 C>G maps to NM_018986.3 S734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:148427535 G>A maps to NM_024577.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:148407062 C>A maps to NM_024577.3 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr5:148407521 C>A maps to NM_024577.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:148406771 G>A maps to NM_024577.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr5:148418027 C>T maps to NM_024577.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr5:148388504 G>A maps to NM_024577.3 F1129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr19:51218988 T>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:51192463 C>T maps to ENST00000391814 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr19:51217437 C>T did not map to a codon.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr19:51201114 G>A maps to ENST00000391814 Q616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:70333069 C>A maps to ENST00000338508 E1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:70333673 G>A maps to ENST00000338508 C902C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:70348919 G>A maps to ENST00000338508 D727D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr11:70332419 G>A maps to ENST00000338508 N1320N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr11:70331426 G>A maps to ENST00000338508 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr11:70319249 C>T maps to ENST00000338508 A1752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr22:51137178 C>T maps to NM_001080420.1 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr22:51137136 C>T maps to NM_001080420.1 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr22:51117038 C>T maps to NM_001080420.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr8:145154028 G>A maps to NM_030974.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr8:145154327 G>A maps to NM_030974.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr8:145154649 C>G maps to NM_030974.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr9:38016077 G>C maps to NM_003028.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr9:37948720 G>A maps to NM_003028.2 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:37955887 C>T maps to NM_003028.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:38016098 G>T maps to NM_003028.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr17:7534048 T>C maps to NM_001040.3 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr9:91653162 G>T maps to NM_016848.5 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:91652994 C>T maps to NM_016848.5 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr15:49176471 G>T maps to NM_203349.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:49254846 G>A maps to NM_203349.3 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr15:49127201 G>A maps to NM_203349.3 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:4280257 C>A maps to NM_020209.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr19:4282868 G>A maps to NM_020209.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:154459000 A>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:45460273 C>G maps to ENST00000437903 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr7:155599119 G>A maps to NM_000193.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:42403209 C>G maps to NM_001080505.1 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:42403266 C>G maps to NM_001080505.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr4:42403038 C>T maps to NM_001080505.1 Y96Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:41089338 G>T maps to NM_138392.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr19:41086388 C>G maps to NM_138392.3 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:18238930 A>C maps to NM_004169.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr12:57626557 G>A maps to NM_005412.5 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:57626333 C>G maps to NM_005412.5 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:112724337 G>T maps to NM_007373.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr10:112745398 C>T maps to NM_007373.3 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:112724465 C>G maps to NM_007373.3 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr10:112724420 C>G maps to NM_007373.3 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr10:112724465 C>A maps to NM_007373.3 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr10:112764470 C>G maps to NM_007373.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:601733 G>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:601762 G>A did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr23:591897 G>C did not map to a codon.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr3:157815866 G>A maps to NM_003030.4 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr3:157820502 C>T maps to NM_003030.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr3:157815816 C>T maps to NM_003030.4 *356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr3:157820513 G>A maps to NM_003030.4 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr3:157820661 C>G maps to NM_003030.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:146267450 C>T maps to ENST00000367503 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:146271502 C>T maps to ENST00000367503 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:146247399 C>T maps to ENST00000367503 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr6:146276245 C>T maps to ENST00000367503 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:72799728 G>A maps to NM_018130.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr3:72890270 T>C maps to NM_018130.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr5:132158992 G>A maps to NM_001172700.1 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:9900878 C>G did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:9862690 G>T did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr23:9863268 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:9900521 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr23:9862971 G>C did not map to a codon.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:77675898 G>A maps to NM_020859.3 S1421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr4:77675520 C>T maps to NM_020859.3 L1295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr4:77662553 C>T maps to NM_020859.3 P1076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr4:77660199 C>T maps to NM_020859.3 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr4:77662322 G>A maps to NM_020859.3 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:50350536 G>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:50556994 G>T did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr23:50377068 G>A did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr23:50377081 G>A did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr23:50377855 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:50376524 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:50377847 G>C did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:50376869 G>C did not map to a codon.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr23:50377684 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr23:50377685 G>T did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:50350943 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr23:50376609 C>A did not map to a codon.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr23:50350982 C>A did not map to a codon.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr23:50350952 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:50377157 G>C did not map to a codon.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr23:50376687 A>G did not map to a codon.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr23:50350963 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr23:50378315 G>C did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr3:164772992 C>A maps to NM_001041.3 G501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:164737395 G>T maps to NM_001041.3 P1139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr3:164737434 C>T maps to NM_001041.3 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr3:164758882 C>T did not map to a codon.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr3:164758750 T>G maps to NM_001041.3 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:164704992 G>A maps to NM_001041.3 L1710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:164741484 G>T maps to NM_001041.3 S991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr3:164735777 A>T maps to NM_001041.3 L1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:164758777 A>G maps to NM_001041.3 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr3:164727147 G>A maps to NM_001041.3 F1366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr3:164741543 T>A maps to NM_001041.3 A971A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr3:164773032 T>G maps to NM_001041.3 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:164733861 G>A maps to NM_001041.3 Q1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr3:164704924 C>A did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:164764694 A>T maps to NM_001041.3 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr3:164725726 G>A maps to NM_001041.3 D1413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:164697200 C>T maps to NM_001041.3 L1811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr3:164754248 C>A maps to NM_001041.3 G815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr3:164714391 G>C maps to NM_001041.3 L1541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr3:164758726 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr3:164716393 G>A maps to NM_001041.3 R1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:124524554 G>C maps to NM_170601.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr11:124519603 G>T maps to NM_170601.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:124524632 G>A maps to NM_170601.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:48399303 T>A maps to NM_001006610.1 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr16:48396173 G>A maps to NM_001006610.1 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr3:150460338 G>C maps to NM_005067.5 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr13:46357978 C>A maps to NM_198849.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr13:46357625 G>A maps to NM_198849.2 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:113323755 G>A did not map to a codon.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr3:113327030 G>A maps to ENST00000393830 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr3:113327357 C>T maps to ENST00000393830 C565C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr11:407458 G>T maps to NM_021805.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:407114 G>A maps to NM_021805.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr20:3675352 T>A maps to NM_023068.3 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr20:3677789 G>A maps to NM_023068.3 C774C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:3679948 G>A maps to NM_023068.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:51919977 A>G maps to NM_033130.4 H216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:51917031 C>T maps to NM_033130.4 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr19:51914353 C>T maps to NM_033130.4 *698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:51914598 T>C maps to NM_033130.4 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr19:51918187 C>T maps to NM_033130.4 W502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr19:50463938 G>A maps to NM_052884.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:50461906 G>A maps to NM_052884.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr19:52001377 C>A maps to NM_053003.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:51994963 C>T maps to NM_053003.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr19:52000214 C>T maps to NM_053003.2 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:52034537 C>T maps to NM_001245.5 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr19:52033053 T>G maps to NM_001245.5 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:51958027 G>C maps to NM_014442.2 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:51955700 G>A maps to NM_014442.2 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:51955671 C>T maps to NM_014442.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:51633176 C>T maps to NM_014441.2 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:51633326 C>A maps to NM_014441.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr19:51633225 G>T maps to NM_014441.2 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:51631688 G>A maps to NM_014441.2 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr9:34635730 G>C maps to NM_005866.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:34635730 G>T maps to NM_005866.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:44841566 G>C maps to NM_173354.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr21:44837481 G>A maps to NM_173354.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:111571712 A>G maps to NM_015191.1 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:111593424 C>T maps to NM_015191.1 Q698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:111592631 C>T maps to NM_015191.1 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:111594825 A>G maps to NM_015191.1 Q918Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr11:111594273 T>C maps to NM_015191.1 F734F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:116730263 G>A maps to ENST00000445177 Q821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr11:116746968 C>T maps to ENST00000445177 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr1:115323141 C>T maps to NM_001102396.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr5:138283162 C>G did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr5:138362570 C>T maps to ENST00000509534 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr12:56351770 G>A maps to NM_006928.3 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr6:100838257 A>T maps to ENST00000262901 V760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:100901695 G>C maps to ENST00000262901 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:100901655 C>T maps to ENST00000262901 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:100868713 G>A maps to ENST00000262901 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr6:100841582 C>A maps to ENST00000262901 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr6:100841663 G>A maps to ENST00000262901 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr6:100838938 C>T maps to ENST00000262901 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr6:100841612 C>G maps to ENST00000262901 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr21:38072051 G>A maps to NM_005069.3 K2K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr21:38115849 C>T maps to NM_005069.3 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr21:38084918 C>G maps to NM_005069.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr21:38117418 C>T maps to NM_005069.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:75668137 C>T maps to NM_001145357.1 K1153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:75702242 C>T maps to NM_001145357.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:75702497 G>A maps to NM_001145357.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:16977363 C>T maps to NM_015260.1 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr11:65417891 C>G maps to NM_153253.29 S975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr11:65417518 G>T maps to NM_153253.29 E949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:65413732 C>T maps to NM_153253.29 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr11:65410028 G>A maps to NM_153253.29 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:72200506 A>G maps to NM_015556.1 V1683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr14:72138363 T>C maps to NM_015556.1 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr14:72054660 C>T maps to NM_015556.1 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr14:72191393 C>T maps to NM_015556.1 Q1507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr14:72152219 G>A maps to NM_015556.1 P1082P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:232601013 G>T maps to NM_020808.3 R798R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:232600687 T>C maps to NM_020808.3 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:232601074 C>A maps to NM_020808.3 R777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr1:232649840 C>T maps to NM_020808.3 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:38692544 G>C maps to NM_015073.1 L1676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr19:38600874 G>A maps to NM_015073.1 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:38655372 C>G maps to NM_015073.1 G1345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr19:38573488 G>A maps to NM_015073.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr20:1903190 C>T maps to ENST00000400068 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr20:1918051 G>T maps to ENST00000400068 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr20:1559071 G>C maps to NM_006065.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr20:1558984 G>A maps to NM_006065.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr20:1592330 C>G maps to NM_001135844.1 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr20:1456847 G>T maps to NM_001122962.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr20:1629896 G>A maps to NM_018556.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr20:1629752 C>T maps to NM_018556.3 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:39390155 T>C maps to NM_012237.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:39369800 G>A maps to NM_012237.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:4180807 G>A maps to NM_016539.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr17:79872319 G>A maps to NM_016538.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr17:79872536 C>T maps to NM_016538.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:105225820 G>A maps to NM_006427.3 *176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:45233599 A>G maps to NM_016932.4 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr2:45233323 C>T maps to NM_016932.4 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:45169452 C>T maps to NM_005413.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:45169509 G>A maps to NM_005413.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:45169575 C>T maps to NM_005413.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:45169458 C>T maps to NM_005413.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr14:61180763 C>T maps to NM_017420.4 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:46268860 C>A maps to NM_175875.4 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr19:46271376 G>A maps to NM_175875.4 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr14:60976680 A>T maps to ENST00000381716 K248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr17:57196838 G>C maps to NM_182620.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:21729930 G>C maps to NM_145061.5 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr13:21742368 G>A maps to NM_145061.5 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr17:46239900 C>T maps to NM_003726.3 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr7:26779554 T>C maps to NM_003930.3 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:2160774 C>T maps to NM_003036.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:2235417 C>T maps to NM_003036.3 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr1:2234791 G>A maps to NM_003036.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:2160688 A>T maps to NM_003036.3 K162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:2160912 C>T maps to NM_003036.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:2160702 C>T maps to NM_003036.3 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:2160946 C>T maps to NM_003036.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:2234517 G>A maps to NM_003036.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:2160627 G>C maps to NM_003036.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr1:2235347 G>A maps to NM_003036.3 Q427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr3:170078547 A>G maps to NM_005414.3 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr6:31928455 A>G maps to NM_006929.4 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr6:31931704 C>T maps to NM_006929.4 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:31934520 C>T maps to NM_006929.4 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:31934893 G>C maps to NM_006929.4 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr6:31931237 C>T maps to NM_006929.4 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr6:31930805 C>T maps to NM_006929.4 H447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr6:31927108 C>A maps to NM_006929.4 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:133494133 T>C maps to NM_006930.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:36184010 T>G maps to ENST00000308927 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:36181998 G>T maps to NM_005983.2 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr5:36152986 G>C maps to NM_005983.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr5:36181967 C>T maps to NM_005983.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr8:134072439 C>T maps to NM_006748.3 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:134050882 C>A maps to NM_006748.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr8:134072414 T>C maps to NM_006748.3 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr8:134050924 G>A maps to NM_006748.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:78335134 G>A maps to ENST00000389459 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr4:48380074 C>G maps to NM_020846.1 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:160466126 C>A maps to NM_001184714.1 E36*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-P3-A6T7-01A-11D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr1:160720094 T>C maps to NM_021181.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr23:153716764 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153716488 G>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:48490598 T>A maps to NM_152679.3 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:82606589 A>G maps to NM_001010893.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr8:82606634 G>A maps to NM_001010893.2 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:219249961 C>T maps to NM_000578.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:51404505 C>T maps to NM_001174125.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr12:51382164 C>T maps to NM_001174125.1 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr15:48500095 C>T maps to NM_000338.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:48500014 T>C maps to NM_000338.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr15:48500248 G>A maps to NM_000338.2 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:48577393 C>T maps to NM_000338.2 G859G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:48500320 C>T maps to NM_000338.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr5:127507428 C>T maps to NM_001046.2 Q932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr5:127507385 A>T maps to NM_001046.2 V917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr16:56904068 C>T maps to NM_000339.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:56899254 C>T maps to NM_000339.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:56917997 G>T maps to NM_000339.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr16:56904620 C>T maps to NM_000339.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr16:56916368 C>T maps to NM_000339.2 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr16:67981322 C>T maps to NM_005072.4 W661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:67985729 G>C maps to NM_005072.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr16:67979116 T>C maps to NM_005072.4 Q1013Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr20:44675030 G>T maps to NM_001134771.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr20:44686241 T>A maps to NM_001134771.1 *1140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:44673610 C>T maps to NM_001134771.1 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:44664080 C>G maps to NM_001134771.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:34542829 A>C did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr15:34610822 C>A maps to NM_005135.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:1089144 C>T maps to NM_006598.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr5:1075523 G>A maps to NM_006598.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr3:124906104 G>A maps to NM_001195483.1 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:124837684 G>A maps to NM_001195483.1 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:100463639 C>T maps to NM_020246.2 Q720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr7:100457854 G>A did not map to a codon.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr7:100463758 C>A maps to NM_020246.2 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:100452245 C>T maps to NM_020246.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr7:100459109 C>T maps to NM_020246.2 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:100459151 G>T maps to NM_020246.2 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:122787211 C>T did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr7:122787223 C>T maps to NM_022444.3 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:122759278 C>T maps to NM_022444.3 K456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr7:122774492 G>T maps to NM_022444.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr17:26822749 C>T maps to NM_001145975.1 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr20:45217894 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr20:45224896 C>T maps to NM_022829.5 W231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr7:135378966 G>A maps to NM_012450.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr17:6606427 G>A maps to NM_177550.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr17:6599180 G>T maps to NM_177550.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr17:6610394 G>C maps to NM_177550.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr18:43316444 T>C maps to NM_001146037.1 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:43329783 G>A maps to NM_001146037.1 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr18:43207084 T>A maps to NM_007163.3 L165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr13:99364805 A>G maps to NM_005073.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr13:99340611 T>C did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr13:99376167 G>A maps to NM_005073.3 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr13:99378414 G>A maps to NM_005073.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr3:121641669 C>T maps to NM_021082.3 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr3:121649689 T>C maps to NM_021082.3 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr3:121643790 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:60718767 G>A maps to NM_016582.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:60714104 G>A maps to NM_016582.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:129294619 T>C maps to ENST00000376744 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:113460415 C>T maps to NM_003051.3 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:6940070 G>A maps to NM_201566.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr23:73740905 G>A did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr17:73096606 C>T maps to ENST00000450736 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:73096564 C>T maps to ENST00000450736 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr17:73096474 C>T maps to ENST00000450736 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:66267355 G>A maps to NM_004694.4 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:66268876 A>G maps to NM_004694.4 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr12:60169149 C>G maps to NM_004731.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:60168918 G>T maps to NM_004731.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:60173399 T>C maps to NM_004731.3 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:60169128 T>C maps to NM_004731.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr12:60169146 T>G maps to NM_004731.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr10:61412621 G>A maps to NM_194298.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr10:61414209 G>A maps to NM_194298.2 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:25830750 C>T did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr6:25826724 G>A maps to NM_005074.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:25850330 G>A maps to NM_001098486.1 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:25851035 C>T maps to NM_001098486.1 W261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr6:74331547 G>A maps to NM_012434.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:22396419 C>A maps to NM_020346.2 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr11:22363085 G>A maps to NM_020346.2 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:22364833 C>T maps to NM_020346.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr19:49933916 G>A maps to NM_020309.3 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:49934295 G>A maps to NM_020309.3 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr12:100784776 A>G did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:100797817 G>T maps to NM_139319.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr12:100774586 C>T maps to NM_139319.2 C70C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:61594628 C>T maps to NM_022082.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr20:61594047 C>T maps to NM_022082.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr20:61597909 G>A maps to NM_022082.3 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr20:61598791 C>A maps to NM_022082.3 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr8:20005171 C>T maps to NM_001135691.2 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:50819670 C>T maps to NM_003055.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:50820090 G>A maps to NM_003055.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr10:50819628 C>A maps to NM_003055.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:50819199 G>C maps to NM_003055.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr10:50820225 C>T maps to NM_003055.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:50820231 C>T maps to NM_003055.2 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr10:50819259 C>A maps to NM_003055.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr10:50819553 G>A maps to NM_003055.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr10:50820312 C>T maps to NM_003055.2 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr21:46945760 C>A maps to NM_194255.1 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr21:46951983 G>A maps to NM_194255.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr21:46957702 C>T maps to NM_194255.1 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:46950871 G>A maps to NM_194255.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:228564091 A>G maps to NM_025243.3 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr2:228563677 G>A maps to NM_025243.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr5:36686247 G>A maps to NM_004172.4 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:36686316 G>A maps to NM_004172.4 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr2:65245372 C>G maps to NM_003038.4 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr19:47278811 G>A maps to NM_005628.2 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr19:15072887 G>A maps to NM_005071.1 H287H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr19:15061150 G>T maps to NM_005071.1 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr19:15072830 C>A maps to NM_005071.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr19:15072947 G>A maps to NM_005071.1 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr19:15061027 T>A maps to NM_005071.1 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:53555530 G>A maps to NM_006671.4 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:53580587 G>A maps to NM_006671.4 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:53558359 G>A maps to NM_006671.4 T299T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-A6K1-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr1:53600101 C>T did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:113410355 C>T maps to NM_005415.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr2:113404461 G>A maps to NM_005415.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:42294988 C>A maps to NM_006749.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:160557344 G>A maps to NM_003057.2 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr6:160557619 A>T maps to NM_003057.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr11:64329823 C>T maps to NM_018484.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr11:64335154 C>T maps to NM_018484.2 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:64368359 C>A maps to NM_144585.2 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:64361158 T>C maps to NM_144585.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr11:64368957 A>T did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr3:38357067 C>G maps to NM_004803.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:116577933 G>A maps to NM_018420.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr1:116605437 G>A maps to NM_018420.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:116579932 G>T maps to NM_018420.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:160645780 C>A maps to NM_003058.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:160670389 G>T maps to NM_003058.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:160864769 C>T maps to ENST00000392145 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:160828084 C>T maps to ENST00000392145 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:160858094 T>C maps to ENST00000392145 Y380Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:131630516 C>A maps to NM_003059.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:131714116 C>T maps to ENST00000435065 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:62751492 G>A maps to NM_004790.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr11:62744280 C>T maps to NM_004790.3 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr6:43269337 C>T maps to ENST00000372585 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr5:138715752 C>T maps to NM_152685.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:4843460 C>T maps to NM_203327.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr20:4855260 T>A maps to NM_203327.1 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr20:4865410 G>A maps to NM_203327.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr9:19786495 G>A maps to NM_020344.2 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr9:19576920 C>T did not map to a codon.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr9:19619580 C>T did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr9:19516219 G>C maps to NM_020344.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr20:19673992 G>A maps to NM_020689.3 W472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr20:19679320 C>A maps to NM_020689.3 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:19665796 C>T maps to NM_020689.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr20:19560690 C>T maps to NM_020689.3 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:92949144 C>T maps to NM_153646.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:92949033 G>A maps to NM_153646.3 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr14:92922824 C>T maps to NM_153646.3 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:48428996 C>A maps to NM_205850.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr15:48434436 C>T maps to NM_205850.2 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:48434323 G>T maps to NM_205850.2 G427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr15:48414189 C>G maps to NM_205850.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr12:113758154 G>A maps to NM_024959.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr12:113770536 G>A maps to NM_024959.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:113754408 C>A maps to NM_024959.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr12:113744330 C>G maps to NM_024959.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:4843163 C>A maps to NM_003562.4 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr7:95761097 C>G maps to NM_001160210.1 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:129483263 C>A did not map to a codon.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr23:129479182 G>T did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:129484679 T>C did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:129480562 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr23:129499633 T>C did not map to a codon.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr22:41173339 C>T maps to NM_006358.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:73282737 G>A maps to NM_021734.4 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr5:140683342 G>A maps to NM_031947.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr5:140683195 C>T maps to NM_031947.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr3:48921542 T>C maps to NM_000387.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:37153063 G>A maps to NM_030631.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr11:792391 C>T maps to NM_001191061.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:6442072 G>T maps to NM_024103.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr9:130830798 C>T maps to ENST00000373069 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr6:46644142 G>A maps to NM_004277.3 W308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:128688368 A>G maps to NM_031291.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr8:104417025 G>A maps to NM_030780.3 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr8:104419869 G>T maps to NM_030780.3 Y99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr17:8197903 G>A maps to NM_201520.1 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr3:140695130 G>T maps to NM_001104647.1 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr3:140692717 C>T maps to NM_001104647.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:23429112 C>T maps to NM_016612.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:42399066 C>A did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr7:87476267 G>A maps to NM_018843.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:6427440 G>A maps to NM_173637.3 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr19:19218753 G>A maps to NM_178526.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:19221655 C>T maps to NM_178526.3 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr19:19217185 G>A maps to NM_178526.3 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:118586007 G>C did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:118586985 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:118585996 G>A did not map to a codon.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr23:118586105 G>A did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:65144111 T>A maps to NM_182556.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr23:118604390 G>A did not map to a codon.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr23:1506192 T>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:1508131 A>G did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr23:1508294 C>G did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr23:1508617 G>C did not map to a codon.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr23:1505587 C>T did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr4:982692 G>A maps to NM_213613.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:985326 G>A maps to NM_213613.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr12:58018674 C>A maps to NM_133489.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:58018659 C>T maps to NM_133489.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:78197054 C>T maps to NM_173626.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr17:78196509 C>G maps to NM_173626.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:149360190 A>G maps to NM_000112.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:107408303 C>T maps to NM_000111.2 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:107340589 C>T maps to NM_000441.1 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr7:107314735 A>G maps to NM_000441.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr3:48665935 C>T maps to NM_022911.2 K577K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr8:92406044 C>G maps to NM_134266.1 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:92365164 G>T maps to NM_134266.1 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr8:92352727 T>C maps to NM_134266.1 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr8:92407323 G>C maps to NM_052832.2 *657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr8:92346548 C>A maps to NM_134266.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr6:35919264 G>A maps to NM_052961.3 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:205888027 G>A maps to NM_134325.2 D732D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:205904873 C>T maps to NM_134325.2 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr19:17599704 G>A maps to NM_198580.1 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:17615339 C>T maps to NM_198580.1 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:17615339 C>T maps to NM_198580.1 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr15:50519204 C>T maps to NM_003645.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:131117374 C>T maps to NM_005094.3 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr9:131107580 C>T maps to NM_005094.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:59010013 C>T maps to NM_012254.2 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:59010863 G>A maps to NM_012254.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:59022656 G>T maps to NM_012254.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:128364097 C>T maps to NM_001017372.1 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:128302162 G>A maps to NM_001017372.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr5:128324311 G>A maps to NM_001017372.1 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr5:128302063 C>T maps to NM_001017372.1 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr15:85447465 C>T maps to NM_004213.3 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr15:85478709 G>C maps to NM_004213.3 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr15:85487996 C>T maps to NM_004213.3 Y591Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr15:85486698 G>A maps to NM_004213.3 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr15:85447423 C>T maps to NM_004213.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr15:85486740 C>T maps to NM_004213.3 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:45560573 C>T maps to NM_004212.3 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr15:45555358 G>A maps to NM_004212.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr9:86905134 G>A maps to NM_022127.2 H361H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr9:86903087 T>C maps to NM_022127.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:44197180 G>A maps to ENST00000313248 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:66133979 G>A maps to NM_001532.2 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:5340093 G>C maps to NM_153247.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:5342476 C>T maps to NM_153247.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr20:45353863 G>T maps to NM_030777.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr20:45354421 C>T maps to NM_030777.3 N249N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:45354664 G>C maps to NM_030777.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr22:24224829 C>T maps to NM_030807.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr22:24219247 G>A maps to NM_030807.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr6:134323169 G>T maps to NM_145176.2 C555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr6:134312436 C>T maps to NM_145176.2 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:40422129 C>A maps to NM_052885.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:40345096 T>C maps to NM_052885.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr12:40158309 G>A maps to NM_052885.3 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr12:40441949 G>A maps to NM_052885.3 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:7973849 C>T maps to NM_153449.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr3:170732403 G>A maps to NM_000340.1 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr3:170716164 A>G maps to NM_000340.1 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr12:8077032 C>G maps to NM_006931.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr12:8083915 G>A maps to NM_006931.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:8074140 G>A maps to NM_006931.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:8083211 C>A maps to NM_006931.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr17:7189831 C>T maps to NM_001042.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:9101784 G>T maps to NM_001135585.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:9097692 C>T maps to NM_003039.2 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr1:9097782 G>T maps to NM_003039.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:9100041 T>A maps to NM_003039.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr9:136338605 G>A maps to NM_017585.3 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr9:136338606 C>T maps to NM_017585.3 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:136343498 G>C maps to NM_017585.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:9067372 C>T maps to NM_207420.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr4:9828062 G>A maps to NM_020041.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr4:10022969 C>T maps to NM_020041.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:211751729 G>A maps to NM_021194.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:220091720 G>T maps to NM_018713.2 Y278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:220089060 T>C maps to NM_018713.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:220101746 G>C maps to NM_018713.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:220088799 C>T maps to NM_018713.2 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:26366379 G>A maps to NM_001004434.1 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:26370858 G>A maps to NM_001004434.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:27480192 C>G maps to NM_003459.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr2:27480852 G>T maps to NM_003459.4 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:27479725 G>A maps to NM_003459.4 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:27481074 G>A maps to NM_003459.4 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr15:45778866 A>G maps to NM_013309.4 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:68412344 C>T maps to NM_022902.2 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr9:116022566 C>T maps to NM_001859.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr20:37356987 G>A maps to NM_080552.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr20:37356387 C>T maps to NM_080552.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr20:37357218 G>A maps to NM_080552.2 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr20:37356975 C>T maps to NM_080552.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr20:37356753 C>A maps to NM_080552.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr20:37356201 C>T maps to NM_080552.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr3:155551698 T>C maps to NM_004733.3 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr5:176812988 C>T maps to NM_003052.4 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr4:25671433 C>T maps to NM_006424.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr4:25677926 G>T maps to NM_006424.2 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr4:25664202 T>G maps to NM_006424.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:25676181 C>T maps to NM_006424.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:25665875 G>A maps to NM_006424.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr9:140128316 C>A maps to NM_080877.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr9:140127072 C>G maps to NM_080877.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:48762558 G>A did not map to a codon.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr23:48762650 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:44224577 G>A maps to NM_178148.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:44224578 G>A maps to NM_178148.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr6:8421005 C>T maps to NM_001142540.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr7:133979788 G>A maps to NM_032826.4 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr11:45827444 G>A maps to NM_018389.4 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr11:45827726 C>T maps to NM_018389.4 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:44983790 G>A maps to NM_173179.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:67516167 G>A maps to NM_015139.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:67507984 A>G maps to NM_015139.2 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:67507962 G>A maps to NM_015139.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr6:137243652 C>G maps to NM_001008783.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:137245832 G>C maps to NM_001008783.1 *417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:137245832 G>C maps to NM_001008783.1 *417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:137243565 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:1663929 G>A maps to NM_182838.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:1606914 C>A maps to NM_001110781.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr12:69140552 C>T maps to NM_018656.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr6:118475754 C>G maps to NM_001029858.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr6:118596757 A>G maps to NM_001029858.3 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:118635270 C>A maps to NM_001029858.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr6:118228942 G>A maps to NM_001029858.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:118475783 G>A did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr11:107676146 C>T maps to NM_017515.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:234041451 C>A maps to NM_173508.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:234452394 C>T maps to NM_173508.2 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:58048117 C>A maps to NM_001080455.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:114503856 A>T maps to NM_025181.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:114500439 A>G maps to NM_025181.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr2:114482972 G>C maps to NM_025181.2 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:150723126 G>A maps to NM_181776.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:150712871 G>A maps to NM_181776.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr5:150723749 G>A maps to NM_181776.2 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:150696551 C>T maps to NM_181776.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:150664218 C>T maps to NM_001145017.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr11:92918981 T>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr21:43979138 C>T maps to NM_018964.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr11:118895757 G>A maps to NM_001164278.1 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:46592497 T>C maps to NM_030674.3 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr12:46594951 G>C maps to NM_030674.3 S311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:79226903 C>T maps to NM_001037984.1 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:79234187 G>A maps to NM_001037984.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:46760702 C>T maps to NM_018976.4 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:46761091 G>A maps to NM_018976.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:46764401 A>G maps to NM_018976.4 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr12:47182394 A>G maps to NM_018018.4 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr12:47170741 C>T maps to NM_018018.4 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:47181733 G>A maps to NM_018018.4 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:48319087 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:48320413 C>G did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr23:48325428 G>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:48320449 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:48318231 G>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr14:61519119 C>G maps to NM_153811.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:58704060 G>A maps to NM_018231.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr16:84065569 G>A maps to NM_001080442.1 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:54945035 T>C maps to NM_173514.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr5:54929598 G>A maps to NM_173514.2 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr5:54960617 C>T maps to NM_173514.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:196544870 G>A maps to NM_001127257.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:196578253 G>A maps to NM_001127257.1 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr17:70645093 C>T maps to NM_001159770.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr10:18289627 C>T maps to NM_001145195.1 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr10:18276457 C>T maps to NM_001145195.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr10:18276462 G>T maps to NM_001145195.1 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:22262321 G>A maps to NM_001135153.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr8:22267519 C>T maps to NM_015359.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:2732883 G>A maps to NM_144564.4 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:2737026 G>A maps to NM_213568.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr8:145642056 C>A maps to NM_130849.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:56625235 C>A maps to NM_001135195.1 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr18:33706964 C>T maps to NM_012319.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:33704510 G>A maps to NM_012319.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr18:33706694 T>A maps to NM_012319.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr18:33706799 T>C maps to NM_012319.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:33170439 G>C maps to NM_006979.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:33170385 A>G maps to NM_006979.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:69866166 T>A maps to NM_018375.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr11:62655846 G>T maps to NM_001012661.1 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:62649515 C>T maps to NM_001012661.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:62655840 C>T maps to NM_001012661.1 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr11:62656014 C>T maps to NM_001012661.1 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:190430078 C>A did not map to a codon.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr2:190430212 C>T maps to NM_014585.5 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:205779302 G>A maps to NM_173854.4 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:205779419 C>G maps to NM_173854.4 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr12:105280119 T>A maps to NM_032148.3 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:125741707 C>T maps to NM_001008485.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:57261526 G>A maps to NM_003627.5 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:57256843 G>A maps to NM_003627.5 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:57254630 G>A maps to NM_003627.5 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:57256750 G>T maps to NM_003627.5 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr17:1479908 G>A maps to ENST00000382147 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:1519989 C>T maps to ENST00000382147 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:1519990 C>T maps to ENST00000382147 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:1519989 C>T maps to ENST00000382147 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:1518309 G>A maps to ENST00000382147 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:1478936 G>C maps to ENST00000382147 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr11:57176683 G>A maps to ENST00000428603 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:57175324 G>A maps to ENST00000428603 H485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr11:57176767 G>A maps to ENST00000428603 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr9:108151335 G>C maps to NM_080546.3 *658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr9:108110641 C>G maps to NM_080546.3 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:10747141 C>T maps to NM_020428.3 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr19:10742816 C>T maps to NM_020428.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:10753953 G>A did not map to a codon.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr19:10745692 C>T maps to NM_020428.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr19:10747141 C>T maps to NM_020428.3 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:95293065 C>T maps to NM_001114106.1 H94H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:31833470 G>A maps to NM_025257.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr6:31832498 C>A maps to NM_025257.2 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:75805304 C>T maps to NM_152697.4 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:75716975 G>A maps to NM_152697.4 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:75685019 C>T maps to NM_152697.4 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:8390836 C>T maps to ENST00000377479 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr1:8399556 C>T maps to ENST00000377479 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K0-01B-21D-A31L-08 chr5:33947384 G>A maps to NM_016180.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr5:33963898 G>C maps to NM_016180.3 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr1:205633660 G>A maps to NM_033102.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr1:205632624 C>T maps to NM_033102.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:205631060 G>A maps to NM_033102.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr1:205632309 G>C maps to NM_033102.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr1:205628433 C>A maps to NM_033102.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr8:142228640 G>A maps to NM_001080431.1 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:142238342 G>C maps to NM_001080431.1 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr17:26731994 G>A maps to ENST00000440501 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr17:26731757 C>A maps to ENST00000440501 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr17:26726701 G>C maps to ENST00000440501 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr9:115648855 G>T maps to NM_033051.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:19470500 C>T maps to ENST00000395585 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr17:19445704 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:19470407 G>A did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr17:19605987 C>G did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:19610063 G>A maps to NM_152908.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr17:19583337 T>G maps to NM_152908.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:42338012 G>C maps to NM_000342.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:42335513 C>T maps to NM_000342.3 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:162711548 T>C maps to NM_001178015.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr2:162735687 G>A maps to NM_001178015.1 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:162761308 A>G maps to NM_001178015.1 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr20:3209784 G>A maps to NM_001174090.1 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr20:3211606 G>A maps to NM_001174090.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr20:3210333 G>A maps to NM_001174090.1 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr20:3211198 G>A maps to NM_001174090.1 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:3212164 C>T maps to NM_001174090.1 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr20:3212125 G>A maps to NM_001174090.1 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr7:150767611 G>T maps to NM_003040.3 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr7:150767612 C>T maps to NM_003040.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr7:150773104 G>A maps to NM_003040.3 R1159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr7:150772825 G>A maps to NM_003040.3 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr7:150771301 G>A maps to NM_003040.3 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr2:220501430 C>G maps to NM_201574.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr2:220501535 G>A maps to NM_201574.2 E852E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr2:220501090 C>G maps to NM_201574.2 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:220501487 C>T maps to NM_201574.2 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:220500449 G>A maps to NM_201574.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr2:220505518 G>A maps to NM_201574.2 T1179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr2:220502431 C>T maps to NM_201574.2 Q916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr4:72363396 T>C maps to NM_001098484.2 Y718Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr4:72316994 T>C maps to NM_001098484.2 C433C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr4:72363342 C>T maps to NM_001098484.2 F700F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr4:72316104 G>T did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr4:72423470 C>T maps to NM_001098484.2 Q936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr4:72215742 A>T maps to NM_001098484.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr4:72397810 C>T maps to NM_001098484.2 I733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:72412179 C>T maps to NM_001098484.2 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:72397868 C>T maps to NM_001098484.2 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:72425847 C>T maps to NM_001098484.2 Y992Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr4:72352673 C>G maps to NM_001098484.2 S638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr4:72102334 C>G maps to NM_001098484.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr4:72412191 G>A maps to NM_001098484.2 K856K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr2:74454960 G>A maps to NM_021196.3 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr2:74531625 G>A maps to NM_021196.3 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:74466494 C>T maps to NM_021196.3 K762K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:27490192 T>A maps to ENST00000454389 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:51834518 C>T maps to NM_001039960.1 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr12:51883735 G>A did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr12:51851324 T>C did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:51853841 G>T maps to NM_001039960.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr12:51857495 G>C maps to NM_001039960.1 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr12:51845918 C>T maps to NM_001039960.1 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr5:139747330 C>G maps to ENST00000507527 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr5:139743447 T>C maps to ENST00000507527 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr5:139743691 G>A maps to ENST00000507527 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr22:32479070 G>A maps to NM_000343.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr22:32477866 G>A maps to NM_000343.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr17:18923024 G>A did not map to a codon.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr11:26734240 G>A maps to NM_178498.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:26742937 G>A maps to NM_178498.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:26725199 G>A maps to NM_178498.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr11:26714149 T>C did not map to a codon.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr11:26743120 T>C maps to NM_178498.3 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr16:31501730 G>T maps to ENST00000431354 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr21:35467895 C>G maps to NM_006933.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr22:32650128 C>T maps to NM_014227.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:18004622 T>A maps to NM_000453.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr19:17999158 C>T maps to NM_000453.2 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:17994512 C>T maps to NM_000453.2 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr19:17983382 C>G maps to NM_000453.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:108626896 T>A maps to NM_021815.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:108626800 T>C maps to NM_021815.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:101603500 G>A maps to NM_145913.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:101603613 G>T maps to NM_145913.3 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:101576604 G>A maps to NM_145913.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:101560441 A>G maps to NM_145913.3 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:48697259 G>A maps to NM_001135181.1 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:48703349 G>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:48708176 G>T maps to NM_001135181.1 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:48705106 G>A maps to NM_001135181.1 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:48694627 T>C did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:11059595 C>T maps to NM_003042.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:11072888 T>C maps to NM_003042.3 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr3:10971009 C>T maps to NM_014229.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr3:10861255 T>C maps to NM_014229.1 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr12:301769 G>A maps to NM_003044.3 Y525Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:309925 G>T maps to NM_003044.3 S201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr12:313742 G>A maps to NM_003044.3 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr12:302466 G>A maps to NM_003044.3 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:351876 G>C maps to NM_016615.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr12:333172 C>G maps to NM_016615.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr12:330577 G>A maps to NM_016615.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:336789 G>A maps to NM_016615.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:115585605 C>T did not map to a codon.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr23:115582640 C>T did not map to a codon.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr23:115582731 G>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:85255710 G>T maps to NM_182767.4 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:49813423 C>A did not map to a codon.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr19:49813000 G>A maps to NM_014037.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr1:110709556 G>A maps to NM_001010898.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr1:110737358 C>T maps to NM_001010898.2 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr1:110734820 G>A maps to NM_001010898.2 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:1246006 G>A maps to NM_182632.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:1239638 C>T maps to NM_182632.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr5:1232406 C>T maps to NM_182632.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr5:1219623 C>T maps to NM_001003841.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:1214087 G>A maps to NM_001003841.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr5:1212484 C>T maps to NM_001003841.2 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr5:1219196 G>A maps to NM_001003841.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr5:1219653 C>T maps to NM_001003841.2 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr16:55730199 G>A maps to NM_001043.3 W404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:55690665 T>G maps to NM_001043.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr3:45804559 C>G maps to NM_020208.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:1432742 C>A maps to NM_001044.4 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:1409144 G>A maps to NM_001044.4 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr5:1422041 G>C maps to NM_001044.4 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:1416214 G>T maps to NM_001044.4 Y343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr17:28548856 G>A maps to ENST00000394821 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:28530256 G>T maps to ENST00000394821 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:28537589 C>T maps to ENST00000394821 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr17:28544278 G>A maps to ENST00000394821 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr11:20648344 G>A maps to NM_004211.3 W451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:20673941 C>T maps to NM_004211.3 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr11:20648339 G>C maps to NM_004211.3 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr3:14499523 C>T maps to NM_001134367.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:14508062 C>T maps to NM_001134367.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr5:149582168 C>T maps to NM_014228.3 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:149576345 C>G maps to NM_014228.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:149589168 G>C maps to NM_014228.3 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr23:152956768 C>T did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr23:152960238 G>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:152960178 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:152957557 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr23:152959012 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:44467253 A>G maps to NM_201649.2 Y409Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr1:44475694 G>A maps to NM_201649.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:30104748 C>T maps to NM_003045.4 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr13:30110112 C>A maps to NM_003045.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:30098368 G>A maps to NM_003045.4 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:33699841 T>G maps to NM_019849.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:87242047 C>G maps to NM_138817.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr8:87242428 G>A maps to NM_138817.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:87242275 A>G maps to NM_138817.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr3:170216563 G>C maps to NM_020949.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr3:170201149 C>T maps to NM_020949.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr3:170198807 C>T maps to NM_020949.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr3:170198782 G>A maps to NM_020949.2 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:17419528 C>T maps to NM_001164771.1 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:17412170 A>G maps to NM_001164771.1 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr23:70149726 C>T did not map to a codon.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr23:70149727 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:70147852 G>A did not map to a codon.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr23:70146400 C>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:70146773 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:70148006 T>C did not map to a codon.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr23:70145792 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:68330579 G>A maps to NM_003983.4 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:68336299 T>C maps to NM_032178.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:68344296 A>G maps to NM_032178.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr14:23243253 A>G maps to NM_001126106.1 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr14:23243307 C>T maps to NM_001126106.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr14:23609753 G>A maps to NM_012244.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr14:23609699 C>T maps to NM_012244.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:23635669 G>A maps to NM_012244.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr19:33355053 C>T maps to NM_014270.4 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:33333130 C>A maps to NM_014270.4 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr19:33353088 G>A maps to NM_014270.4 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr2:40366548 G>C maps to NM_021097.2 S846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr2:40397430 G>A maps to NM_021097.2 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:40656664 C>G maps to NM_021097.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr2:40366586 A>G maps to NM_021097.2 D833D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:40657171 C>G maps to NM_021097.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr2:40656193 G>T maps to NM_021097.2 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:47969075 C>T maps to NM_015063.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:47969129 G>A maps to NM_015063.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr19:47969075 C>T maps to NM_015063.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:70633618 G>T maps to NM_183002.1 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr14:70518745 G>T maps to NM_183002.1 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr14:70633783 C>A maps to NM_183002.1 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:70634139 G>A maps to NM_183002.1 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:70634794 C>T maps to NM_183002.1 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:27427042 C>A maps to NM_003047.3 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr1:27427082 C>T maps to NM_003047.3 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:111918275 C>T maps to NM_183061.1 V805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:173545822 C>T maps to NM_178527.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr1:173545816 G>A maps to NM_178527.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr2:103324902 G>A maps to NM_003048.3 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr2:103274383 C>A maps to NM_003048.3 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:103324785 G>C maps to NM_003048.3 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr2:103322354 T>C maps to NM_003048.3 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr5:477499 G>A maps to NM_004174.2 N569N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr17:72759609 C>T maps to NM_004252.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:103125362 G>T maps to NM_001011552.3 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:67292322 C>T maps to NM_004594.2 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:67305079 G>A maps to NM_004594.2 W886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr16:67293508 C>T maps to NM_004594.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:135098864 T>A did not map to a codon.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr23:135106626 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr23:135095107 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr23:135106524 G>A did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:46466623 C>A did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:46472744 C>G did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr20:48491308 C>A maps to ENST00000417961 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr20:48503377 C>T maps to ENST00000417961 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr3:142985668 G>A maps to NM_173653.3 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr3:143082404 C>A maps to NM_173653.3 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:143371182 G>A maps to NM_173653.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr12:21422496 C>T maps to NM_134431.3 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:21457427 G>T maps to NM_134431.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr12:21450357 G>T maps to NM_134431.3 S352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:21375294 C>T maps to NM_006446.4 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:21350087 C>A maps to NM_006446.4 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr12:21377743 A>T maps to NM_006446.4 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr12:21325612 T>C maps to NM_006446.4 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:21349913 G>A maps to NM_006446.4 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:21358888 C>G maps to NM_006446.4 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr12:21355449 A>T maps to NM_006446.4 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr12:21327509 G>C did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr12:21377689 G>C maps to NM_006446.4 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:21030850 T>A maps to NM_019844.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr12:21028328 G>A maps to NM_019844.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr12:20968718 C>G maps to NM_019844.2 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr12:21032550 C>T maps to NM_019844.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr12:21015379 C>A maps to NM_019844.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:20876189 T>G did not map to a codon.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr12:20885954 C>G maps to NM_017435.4 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:20876183 G>A maps to NM_017435.4 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:20876120 G>A maps to NM_017435.4 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr12:20893266 C>T maps to NM_017435.4 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr12:20893143 A>G maps to NM_017435.4 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:20854394 T>C did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr3:133661522 C>T maps to NM_005630.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:133667437 G>C maps to NM_005630.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr11:74904299 C>T maps to NM_007256.4 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr15:92459365 G>T maps to NM_013272.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr15:92647587 C>T maps to NM_013272.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr15:92647731 G>T maps to NM_013272.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr15:92459323 C>T maps to NM_013272.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr20:61288357 G>A maps to NM_016354.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr20:61296315 G>T maps to NM_016354.3 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr20:61299844 C>T maps to NM_016354.3 Q610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr5:101606379 T>A maps to NM_180991.4 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:101597727 G>T maps to NM_180991.4 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr5:101627080 G>A maps to NM_180991.4 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:101606490 C>T maps to NM_180991.4 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr5:101599461 G>T maps to NM_180991.4 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr8:70744482 C>T maps to NM_030958.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr8:70585256 G>A maps to NM_030958.2 F798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr8:70674021 A>G maps to NM_030958.2 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:70594433 A>G maps to NM_030958.2 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr8:70594469 G>A maps to NM_030958.2 Y577Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr5:101795456 T>C maps to NM_173488.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr5:101834542 G>A maps to NM_173488.3 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr5:101834431 C>T maps to NM_173488.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr17:33680114 T>A maps to NM_152270.3 R656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:33679467 C>T maps to NM_152270.3 R871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:33738500 C>T maps to NM_018042.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:33768372 G>A maps to NM_144682.5 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr17:33768386 T>A did not map to a codon.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr17:33771679 G>A maps to NM_144682.5 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:41481843 C>T maps to NM_144990.3 E386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:41481852 C>T maps to NM_144990.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:41483464 G>A maps to NM_144990.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:41486212 G>A maps to NM_144990.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:98770784 G>C maps to NM_003061.2 V1102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr10:98762696 G>A maps to NM_003061.2 N1306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr4:20597337 G>T maps to ENST00000273739 G1080G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:20597442 C>T maps to ENST00000273739 C1115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr4:20619088 C>T maps to ENST00000273739 I1401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr4:20619060 G>C did not map to a codon.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr4:20512712 T>C maps to ENST00000273739 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr4:20530584 T>C maps to ENST00000273739 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:20568975 C>T maps to ENST00000273739 D943D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr4:20493432 C>T maps to ENST00000273739 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr4:20599919 G>C maps to ENST00000273739 L1211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr4:20618683 T>C maps to ENST00000273739 C1346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:168127612 C>G maps to NM_003062.2 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr5:168112760 G>A maps to NM_003062.2 F1162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:168123339 G>A maps to NM_003062.2 D1013D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:168135106 T>G did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr5:168620508 G>A maps to NM_003062.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:168671712 G>T maps to NM_003062.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:168180951 G>A maps to NM_003062.2 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr13:84453668 C>T maps to NM_052910.1 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr13:84453688 G>A maps to NM_052910.1 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr13:84453706 G>A maps to NM_052910.1 R646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr13:84453962 C>T maps to NM_052910.1 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr13:84454739 T>A maps to NM_052910.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:84453775 C>A maps to NM_052910.1 G623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:144905947 T>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:144904342 G>C did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr23:144905687 C>G did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:144905020 C>G did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr23:144906199 G>C did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:144904199 C>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:144906313 C>T did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr23:144904538 C>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:144906245 G>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:144904577 A>G did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr23:144904555 A>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:144905933 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:144903948 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:144904772 A>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:144906316 C>A did not map to a codon.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr23:144904871 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr23:144904512 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr23:144906250 G>C did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr23:144904885 G>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:144905888 G>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:144906108 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr23:144906468 C>T did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr3:164905936 G>T maps to NM_014926.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:164905717 G>A maps to NM_014926.2 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr3:164907435 G>A maps to NM_014926.2 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:164907250 G>T maps to NM_014926.2 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:164906544 G>T maps to NM_014926.2 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr3:164906824 C>T maps to NM_014926.2 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr3:164905726 C>A maps to NM_014926.2 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr3:164906485 A>G maps to NM_014926.2 D711D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:164907541 G>C maps to NM_014926.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:164906953 G>C maps to NM_014926.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:164905756 G>A maps to NM_014926.2 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:164908114 T>A maps to NM_014926.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr3:164908104 G>A maps to NM_014926.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr3:164907640 G>T maps to NM_014926.2 Y326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:142717686 A>G did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:142717001 A>C did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:142717054 T>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:142718334 C>A did not map to a codon.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr23:142716899 G>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:142717165 G>T did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:142717806 A>G did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:142716465 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:142717844 G>T did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr23:142718313 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:142717765 T>A did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:142718515 G>C did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:142717000 C>A did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr23:142716822 C>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:142718806 A>G did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr23:142718784 G>A did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:142717243 C>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr23:142716918 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:142716802 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:142718347 G>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:142718629 C>T did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr23:142716542 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr23:142717514 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:142718732 G>C did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:88327783 C>A maps to NM_015567.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr13:88329622 G>A maps to NM_015567.1 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr13:88330087 G>A maps to NM_015567.1 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr13:88329466 G>A maps to NM_015567.1 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr13:88329445 C>T maps to NM_015567.1 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr13:88329805 C>T maps to NM_015567.1 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr13:88327891 C>T maps to NM_015567.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr13:88329859 C>A maps to NM_015567.1 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr13:88330021 G>A maps to NM_015567.1 Q793Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr13:88327744 C>A maps to NM_015567.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr13:88328917 C>T maps to NM_015567.1 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:88329394 C>T maps to NM_015567.1 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr13:88329718 G>A maps to NM_015567.1 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr13:88328728 C>A maps to NM_015567.1 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr13:88328032 T>C maps to NM_015567.1 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr13:86369374 C>A maps to NM_032229.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:86369100 C>A maps to NM_032229.2 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr13:86369425 C>T maps to NM_032229.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:86368629 T>A maps to NM_032229.2 R672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:86370631 C>T maps to NM_032229.2 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr13:86368993 C>T maps to NM_032229.2 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr10:105781403 G>A maps to NM_014720.2 E1158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:57743443 C>T maps to ENST00000428312 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr3:57898144 C>T maps to ENST00000428312 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr3:57875801 G>A maps to ENST00000428312 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr20:43882276 C>T maps to NM_003064.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr15:59172278 T>C maps to NM_024755.2 V1008V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr4:146467853 G>A did not map to a codon.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:146435851 G>A maps to NM_001003688.1 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr4:146460986 C>T maps to NM_001003688.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr18:45368238 G>A maps to NM_001003652.2 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr18:45394804 G>A maps to NM_001003652.2 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr18:45422947 C>T maps to NM_001003652.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr15:67477137 C>G maps to NM_005902.3 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:67459159 T>C maps to NM_005902.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr18:48584568 C>T maps to NM_005359.5 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr18:48581280 C>G maps to NM_005359.5 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr18:48584551 C>G maps to NM_005359.5 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr18:48573553 G>A maps to NM_005359.5 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr18:48603079 C>T maps to NM_005359.5 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr18:48603046 C>T maps to NM_005359.5 Q450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr5:135508249 T>C maps to NM_001001419.1 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:67073770 C>T maps to NM_005585.4 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr15:67073335 C>T maps to NM_005585.4 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr13:37439826 G>A maps to NM_001127217.2 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr13:37453793 G>A maps to NM_001127217.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:71442123 C>T maps to NM_001044305.1 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:71570015 C>G maps to NM_001044305.1 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr6:71501415 C>T maps to NM_001044305.1 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr23:128640092 G>A did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr23:128599868 T>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:128602774 G>A did not map to a codon.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr23:128615128 G>A did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:128642065 A>C did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr9:2039805 G>A maps to NM_003070.3 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr9:2101567 A>G did not map to a codon.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr9:2058445 G>A maps to NM_003070.3 E501E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:11145804 C>G maps to NM_001128849.1 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:11144852 G>T maps to NM_001128849.1 E1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:11098480 C>T maps to NM_001128849.1 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:11107213 T>C maps to NM_001128849.1 D602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr19:11144111 C>T maps to NM_001128849.1 A1231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr4:144460009 T>C maps to NM_003601.2 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr2:217279567 C>T maps to NM_014140.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr22:24135758 G>T maps to NM_003073.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr22:24145544 C>T maps to NM_003073.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:47712146 C>A did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:56566446 T>C maps to NM_003075.3 K564K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr12:56575489 C>A maps to NM_003075.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:56572246 C>T maps to NM_003075.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr12:56575363 T>C maps to NM_003075.3 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:50488228 G>A maps to NM_003076.4 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:50483705 C>T maps to NM_003076.4 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:61910723 G>C maps to NM_001098426.1 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:150945606 C>T maps to NM_001003801.1 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr7:150936505 G>A maps to NM_003078.3 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr7:150939641 C>T maps to NM_003078.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:38793755 C>T maps to NM_003079.4 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr23:53421730 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr23:53439160 G>C did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr23:53426516 G>A did not map to a codon.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr23:53432539 C>T did not map to a codon.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr23:53423263 A>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:45802678 T>C maps to NM_148674.3 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr9:106864324 C>T maps to NM_001042550.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr9:106891993 T>C maps to NM_001042550.1 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:106891978 T>C maps to NM_001042550.1 F948F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:106876293 T>C maps to NM_001042550.1 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr10:112361902 G>T maps to NM_005445.3 R1024R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr10:112356207 G>A maps to NM_005445.3 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:160120483 G>A maps to NM_005496.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:160120572 C>A maps to NM_005496.3 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr3:160149429 G>A did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr18:2751279 T>C maps to NM_015295.2 F1390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr18:2738441 G>T maps to NM_015295.2 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr18:2673309 C>G maps to NM_015295.2 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr18:2732450 A>G maps to NM_015295.2 R1079R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr18:2718394 A>G maps to NM_015295.2 R807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:152856942 C>T maps to NM_030663.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr17:18166072 C>T maps to NM_148886.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr17:18167696 C>T maps to NM_148886.1 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr22:39910114 C>T maps to NM_019008.4 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr22:39907349 C>A maps to NM_019008.4 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:18220059 G>A maps to NM_144775.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:91948114 T>A maps to ENST00000417249 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr2:55804492 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:18841659 G>A maps to ENST00000389467 Q2942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr16:18849512 C>A maps to ENST00000389467 T2412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:18823384 C>T maps to ENST00000389467 L3563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr16:18882802 T>A maps to ENST00000389467 K729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr16:18866197 G>T maps to ENST00000389467 L1421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:156243194 G>A maps to NM_015327.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:156222722 G>A maps to NM_015327.2 I883I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:156233277 G>A maps to NM_015327.2 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr1:156233236 G>C maps to NM_015327.2 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr1:156235605 G>A maps to NM_015327.2 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156246879 G>A maps to NM_015327.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:156235590 T>C maps to NM_015327.2 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr1:156236413 G>A maps to NM_015327.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr17:2202459 C>T maps to NM_017575.4 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:2090119 G>A maps to NM_017575.4 L998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr17:2203589 G>A maps to NM_017575.4 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:183511285 C>T maps to ENST00000367537 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr1:183513601 G>T maps to ENST00000367537 G650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr14:70418919 C>A maps to NM_001034852.1 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr14:70418889 C>G maps to NM_001034852.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr14:70418878 C>T maps to NM_001034852.1 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:169053672 G>A maps to NM_022138.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr11:6414490 C>T maps to NM_000543.4 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:6412942 G>A maps to NM_000543.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:6412669 G>A maps to NM_000543.4 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr11:6412780 C>G maps to NM_000543.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr16:68405205 G>A maps to NM_018667.3 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:68405850 C>T maps to NM_018667.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr16:68405622 G>A maps to NM_018667.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr1:28282328 C>T maps to NM_014474.2 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr4:71227861 T>G maps to NM_012390.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:71232380 C>T maps to NM_012390.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:71232542 C>A maps to NM_012390.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:21995232 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:22010721 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:21985362 G>T did not map to a codon.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr22:31484060 C>T maps to ENST00000454496 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:57310640 C>T maps to ENST00000457912 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr11:57317566 G>A maps to ENST00000457912 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr11:57313476 G>A maps to ENST00000457912 Q365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:4510764 C>T maps to NM_001114974.1 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr9:33056955 T>A maps to NM_018225.2 K292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr12:54576248 G>A maps to NM_014311.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr12:54576028 G>A maps to NM_014311.1 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr7:98636132 C>A maps to NM_020429.2 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr7:98645384 G>A maps to NM_020429.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr17:62582255 C>A maps to NM_022739.3 G145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr17:62552005 C>G maps to NM_022739.3 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr17:62582205 G>A maps to NM_022739.3 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:88405917 G>C maps to NM_198274.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr2:88405914 G>A maps to NM_198274.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr1:214478568 A>C maps to NM_020197.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:214488114 G>A maps to NM_020197.2 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr17:1704288 C>T maps to NM_052928.2 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:1704087 T>C maps to NM_052928.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:73447179 C>T maps to NM_006062.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:49832559 G>A maps to NM_003068.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr16:88747559 G>A maps to NM_178310.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:227935682 C>T maps to NM_053052.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr1:227968340 C>T maps to NM_053052.3 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:84350841 T>C maps to NM_014841.2 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:84311157 C>G did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr6:84375258 G>A maps to NM_014841.2 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:7987008 G>C maps to NM_003083.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr9:15457956 G>C did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr9:139272615 C>A maps to NM_003086.2 T1221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr9:139273677 C>A maps to NM_003086.2 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:139275782 C>T maps to NM_003086.2 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr9:139282280 C>T maps to NM_003086.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr5:121786359 G>T maps to ENST00000379533 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:127569371 C>T maps to NM_014390.2 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:241987825 C>T maps to NM_001080437.1 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:38019680 A>G maps to NM_024700.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr20:1286352 C>A maps to ENST00000381876 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr3:43344764 C>T maps to NM_017719.4 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr3:43381992 T>C did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:43388881 C>G maps to NM_017719.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr2:96953192 C>T maps to NM_014014.3 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr2:96950194 C>T maps to NM_014014.3 K1431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr2:96970570 G>A maps to NM_014014.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr2:96956102 G>C maps to NM_014014.3 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr2:96951034 C>T maps to NM_014014.3 G1349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:123950296 C>G maps to NM_180699.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:31740719 G>A maps to ENST00000446633 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:7609063 G>A maps to NM_152551.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr20:2443870 C>T maps to ENST00000339610 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr20:16717970 A>G maps to NM_198220.2 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr20:16721613 G>A maps to NM_198220.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr20:16712385 T>C maps to NM_198220.2 N13N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr6:34741319 G>A maps to ENST00000374017 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr19:46190834 C>G maps to NM_004597.5 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr22:24953662 T>A maps to NM_004175.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr15:25222050 G>T maps to NM_022805.2 G99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr20:32026797 G>A maps to NM_003098.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:32026758 G>A maps to NM_003098.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr20:32005703 C>G maps to NM_003098.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:121823956 C>A maps to NM_021021.3 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr8:121705981 G>C maps to NM_021021.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr16:69333547 C>T maps to NM_006750.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:51571219 C>A maps to NM_018967.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:51449263 G>T maps to NM_018967.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:51617305 G>A maps to NM_018967.2 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr8:51621456 T>C maps to NM_018967.2 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr8:51503437 G>C did not map to a codon.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr2:1271276 C>A maps to NM_018968.3 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr2:1271318 G>A maps to NM_018968.3 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr15:25213156 C>T maps to NM_022804.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr14:78202300 G>A maps to NM_012245.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr7:26404669 A>G maps to ENST00000446848 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:46196401 G>A maps to NM_152244.1 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:70282791 A>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:70281696 T>C did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:70281737 G>C did not map to a codon.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr7:17833689 C>T maps to ENST00000417048 A999A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr7:17843203 C>G did not map to a codon.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr6:86259571 T>C maps to NM_153816.3 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr11:64802350 C>T maps to NM_013306.4 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:27596750 G>A maps to NM_014748.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:27599206 C>T maps to NM_014748.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:53814495 C>T maps to NM_052870.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr5:53815203 C>T maps to NM_052870.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:130785039 C>G maps to NM_014758.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:130773226 T>C maps to NM_014758.2 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr16:50707786 G>A maps to NM_182854.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:50707481 G>A maps to NM_182854.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr16:50707317 C>G maps to NM_182854.2 *317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr20:44463730 C>T maps to NM_033421.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:44463688 A>G maps to NM_033421.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:186253746 A>C did not map to a codon.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr4:186272621 G>C maps to NM_031953.2 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:151611498 G>T maps to ENST00000458013 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:151640991 C>T maps to ENST00000458013 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr16:12162923 C>T maps to NM_001080530.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr16:12223507 C>T maps to NM_001080530.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:12662374 G>A maps to NM_001080530.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:115567234 G>A maps to NM_001012994.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr9:115598544 G>T maps to NM_001012994.1 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:115626606 G>A maps to NM_001012994.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr8:101589288 C>G maps to NM_152628.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr8:101629872 G>C maps to NM_152628.3 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr8:101608995 T>C maps to NM_152628.3 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:65617934 G>A maps to NM_152760.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr3:125176124 C>T maps to NM_003794.2 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr3:125172709 T>C maps to NM_003794.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr20:17937597 G>C maps to NM_152227.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr7:2317746 C>T maps to NM_013321.2 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr7:2296547 G>A maps to NM_013321.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:2302891 C>A maps to NM_013321.2 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr6:158359774 G>A maps to NM_016224.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:179271878 T>C maps to NM_003101.4 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr12:53509200 C>T maps to NM_003578.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr12:53516947 C>T maps to NM_003578.3 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr12:53514637 C>T maps to NM_003578.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:107955073 C>T maps to NM_018013.3 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr6:107854756 C>T maps to NM_018013.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr6:107955646 A>T maps to NM_018013.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:107827578 T>C maps to NM_018013.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr12:93968822 G>A maps to NM_003877.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:76354903 C>T maps to NM_003955.3 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:76354696 G>A maps to NM_003955.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr14:55510853 G>A maps to NM_199421.1 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr18:67993163 G>A maps to NM_004232.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:36552193 G>A maps to NM_014598.2 Q573Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr6:160113792 G>A maps to NM_000636.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr4:24801553 G>C maps to NM_003102.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:36744766 T>G maps to ENST00000511166 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr13:36776119 C>T maps to ENST00000511166 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:599377 C>T maps to NM_005632.2 Y583Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr16:603476 G>A maps to NM_005632.2 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr16:603389 C>T maps to NM_005632.2 I1045I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr21:34923210 G>T maps to NM_138927.1 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:34932434 T>C maps to NM_032195.1 *2304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr21:34931546 G>A maps to NM_138927.1 Q2111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr21:34923612 T>A maps to NM_138927.1 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:34921998 C>T maps to NM_138927.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr21:34922187 A>G maps to NM_138927.1 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:97194427 G>A maps to NM_001034954.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr10:97098979 C>A maps to NM_001034954.1 V925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr4:186544293 G>T maps to ENST00000355634 R859R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr4:186545292 G>A maps to ENST00000355634 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:186536270 C>T maps to ENST00000355634 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:186545478 G>A maps to ENST00000355634 N464N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:186536297 C>T maps to ENST00000355634 K985K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr8:22429317 C>T maps to NM_005775.4 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:108427559 G>T maps to NM_001013031.1 C730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr10:108489806 C>T did not map to a codon.
Alternatively spliced codon TCGA-BB-7862-01A-21D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr10:108923960 C>T maps to NM_001013031.1 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr10:108371725 C>T maps to NM_001013031.1 P992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:108589382 A>G maps to NM_001013031.1 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr10:108339185 C>T maps to NM_001013031.1 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr10:108924005 C>A maps to NM_001013031.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr4:7533274 G>A maps to NM_020777.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr4:7735047 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr4:7728556 C>T maps to NM_020777.2 G932G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr10:106907397 C>T maps to NM_014978.1 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr10:107012615 C>A maps to NM_014978.1 P1063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:106960921 T>A maps to NM_014978.1 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr10:106737172 G>T maps to NM_014978.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr10:106960975 A>C maps to NM_014978.1 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:106970960 C>T maps to NM_014978.1 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr10:106960934 C>T maps to NM_014978.1 Q729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:121478811 G>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:121476227 C>G maps to NM_003105.5 L1632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr11:121444947 A>T did not map to a codon.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr11:121384940 C>T maps to NM_003105.5 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:121476201 C>T maps to NM_003105.5 Q1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr11:121367577 G>A maps to NM_003105.5 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr11:121474983 C>T maps to NM_003105.5 C1534C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr1:109870184 C>T maps to NM_002959.4 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:109869744 A>G maps to NM_002959.4 D504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr1:109893591 T>C maps to NM_002959.4 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr2:39237831 T>C maps to NM_005633.3 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:50616838 T>A maps to NM_006939.2 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr14:50626719 G>A maps to NM_006939.2 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr14:50600866 G>A maps to NM_006939.2 R1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr13:112722211 G>A maps to NM_005986.2 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:5832930 C>T maps to NM_003108.3 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr2:5833120 C>T maps to NM_003108.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:5833254 C>A maps to NM_003108.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:5833794 C>T maps to NM_003108.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr2:5833020 C>T maps to NM_003108.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:137483940 C>G maps to NM_004189.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr8:55372476 C>T maps to NM_022454.3 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr8:55372371 C>A maps to NM_022454.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr8:55372416 C>T maps to NM_022454.3 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr3:181430498 G>A maps to NM_003106.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr23:139586793 G>A did not map to a codon.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr23:139586673 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:139586787 G>T did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:139586096 C>G did not map to a codon.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr23:139586658 G>A did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:21595658 G>T maps to NM_003107.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr12:23696175 G>A maps to NM_006940.4 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:23696241 A>G maps to NM_006940.4 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:16077303 T>C maps to NM_001145819.1 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:16071442 G>C maps to NM_001145819.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:15994654 T>C maps to NM_001145819.1 Q742Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr11:16208373 C>T maps to NM_001145819.1 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:10583448 T>C maps to ENST00000354846 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr16:1035130 C>T maps to NM_014587.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr16:1035025 G>A maps to NM_014587.3 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:70120398 C>A maps to NM_000346.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr17:70120526 G>A maps to NM_000346.3 *510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:70120497 A>G maps to NM_000346.3 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr12:53776192 C>T maps to NM_138473.2 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr12:53777155 G>A maps to NM_138473.2 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:53804894 T>C maps to NM_138473.2 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:231380099 C>T maps to NM_003113.3 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:231380267 G>A maps to NM_003113.3 K851K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr2:231380189 G>C maps to NM_003113.3 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr2:231067412 C>T maps to NM_080424.2 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr2:231042313 G>A maps to NM_080424.2 N510N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:231112643 C>T maps to NM_007237.4 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr2:231162143 G>T maps to NM_007237.4 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:231249969 G>A maps to NM_138402.4 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:46000472 C>G maps to NM_003110.5 S402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr2:174820351 C>T maps to NM_003111.4 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr2:174820723 C>T maps to NM_003111.4 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:21469032 C>T maps to NM_003112.3 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:21550739 G>A maps to NM_003112.3 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:171573746 C>T maps to NM_001003845.2 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr17:45924943 G>A maps to NM_199262.2 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr7:20825288 G>A maps to NM_182700.4 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr7:20824319 G>A maps to NM_182700.4 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr17:31322640 C>T maps to NM_173847.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr19:49110399 G>T maps to NM_133498.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr8:101245761 C>G maps to NM_003114.3 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:101174570 C>T maps to NM_003114.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr8:101252863 G>A maps to NM_003114.3 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:215275037 G>C maps to NM_024532.3 *632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr2:215274871 T>C maps to NM_024532.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:215013943 C>T maps to NM_024532.3 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:118583437 T>A maps to NM_206996.2 I1027I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr1:118527385 G>A maps to NM_206996.2 Q1897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:118623781 A>G maps to NM_206996.2 N717N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr1:118629568 G>A maps to NM_206996.2 D474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr1:118534049 G>C maps to NM_206996.2 L1821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr1:118512702 C>T maps to NM_206996.2 L2121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:26906473 C>A maps to NM_006461.3 E972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:22680656 G>A did not map to a codon.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr10:22680761 C>T maps to ENST00000376603 H446H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr10:22653827 A>T maps to ENST00000376603 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:4863613 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:35809451 C>A maps to NM_172312.1 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr17:49074036 G>T maps to ENST00000376407 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr17:49074018 C>T maps to ENST00000376407 K625K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:49057212 G>C maps to ENST00000376407 G1102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:140335791 A>T did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr23:140786552 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:140785675 G>T did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr23:140785696 T>C did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:140785836 C>A did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:140785837 C>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:144337332 G>T did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr23:144329144 G>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:144337279 C>A did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:144337189 G>A did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr23:144329126 C>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:142803751 G>T did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr23:142795412 G>T did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:142795393 G>A did not map to a codon.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr23:142795517 C>A did not map to a codon.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr23:142795497 A>G did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr23:142795430 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:142795315 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:142795354 G>T did not map to a codon.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr23:142795487 T>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:142795188 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr23:142795402 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr23:142795237 G>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:142596991 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:142605180 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr23:142596801 C>A did not map to a codon.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr23:142605188 C>A did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:142605192 A>G did not map to a codon.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr23:52825612 G>C did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:151052774 T>C maps to NM_003118.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:32289082 C>T maps to NM_014946.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr1:84982060 C>T maps to ENST00000263717 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr13:24868930 G>A maps to ENST00000424834 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:172835422 G>C maps to NM_031955.5 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr1:217856682 A>G maps to NM_138796.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr1:217955574 G>A maps to NM_138796.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr4:52943088 C>A maps to NM_145263.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr4:52946082 C>T maps to NM_145263.2 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:52938152 C>A maps to NM_145263.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:133712444 G>A maps to NM_174927.1 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:133714493 G>A maps to NM_174927.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr11:133714532 T>A maps to NM_174927.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr17:48631732 C>T maps to NM_022827.2 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:48628247 C>G maps to NM_022827.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr1:16725271 A>T maps to NM_198546.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:89764656 G>A maps to NM_152339.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr4:177113892 G>A maps to NM_144644.2 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr4:177113862 G>T maps to NM_144644.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:123844434 G>A maps to NM_145207.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr4:123949450 A>G maps to NM_145207.2 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr1:48764385 C>T maps to NM_019073.2 *489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:48764464 C>A maps to NM_019073.2 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr14:88899481 A>G maps to NM_018418.4 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:97327403 A>G maps to NM_173499.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr15:97327424 C>T maps to NM_173499.3 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr5:94994440 C>T maps to NM_031952.3 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr8:145094864 G>A maps to NM_198572.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:145096193 G>A maps to NM_198572.2 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:44320586 C>G maps to NM_145026.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A622-01A-11D-A28R-08 chr6:44337829 G>A maps to NM_145026.3 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr12:49883255 G>C maps to NM_023071.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:49888750 C>T maps to NM_023071.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr2:201305465 C>A maps to ENST00000409151 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr3:52740831 C>A maps to NM_014041.3 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:52740852 G>A maps to NM_014041.3 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr6:34506203 G>A maps to NM_012391.1 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:34512013 C>T maps to NM_012391.1 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:29063066 C>T maps to NM_182756.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr11:64939778 C>T maps to NM_001008778.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:99917322 G>A maps to NM_001004351.4 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr20:3759998 C>T maps to NM_015417.4 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr5:35705875 T>C maps to NM_024867.3 I877I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:35641631 A>C maps to NM_024867.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr5:35806815 C>G maps to NM_024867.3 S1673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:35654801 C>T maps to NM_024867.3 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:35727887 C>A maps to NM_024867.3 S1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:35641596 C>T maps to NM_024867.3 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr5:35763639 C>T maps to NM_024867.3 R1213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:35806927 C>T maps to NM_024867.3 I1710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:35740239 C>T maps to NM_024867.3 F1067F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr5:35659167 C>T maps to NM_024867.3 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr5:35727787 G>T maps to NM_024867.3 G976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:220354644 C>T maps to NM_005876.4 L2969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr2:220338271 C>T maps to NM_005876.4 I1398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:220312734 C>T maps to NM_005876.4 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr2:220333617 G>T maps to NM_005876.4 R1113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:220355163 G>A maps to NM_005876.4 E2985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr2:220334042 C>T maps to NM_005876.4 I1219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr2:220336979 G>A maps to NM_005876.4 P1289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:220348595 G>A maps to NM_005876.4 E2137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr2:220347552 C>T maps to NM_005876.4 F1871F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr2:220309637 C>T maps to NM_005876.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:16203018 C>A maps to NM_015001.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr1:16258888 A>T maps to NM_015001.2 K2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr1:16258245 G>A maps to NM_015001.2 E1837E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:16257102 A>G maps to NM_015001.2 S1456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:16256526 C>T maps to NM_015001.2 V1264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr1:16254888 G>A maps to NM_015001.2 E718E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr1:16255477 C>T maps to NM_015001.2 Q915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:16260135 C>T maps to NM_015001.2 I2467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr13:46287816 G>A maps to NM_152719.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr15:69238802 C>G maps to NM_145658.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:69238371 G>T maps to NM_145658.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr15:44856770 G>T maps to NM_025137.3 S2375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr15:44941066 T>A maps to NM_025137.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:44890997 C>A maps to NM_025137.3 G1241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr15:44862785 G>A maps to NM_025137.3 V2138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:44921517 G>A maps to NM_025137.3 Q602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:44881480 G>A maps to NM_025137.3 L1625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr15:44951325 C>T maps to NM_025137.3 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr15:44944451 T>C maps to NM_025137.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:89597146 C>T maps to NM_003119.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:89603248 C>G maps to NM_199367.1 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr16:89619493 C>T maps to NM_003119.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:89603314 C>T maps to NM_199367.1 H489H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr16:89590510 C>T maps to NM_003119.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr19:49132291 G>A maps to NM_020126.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:49132516 A>G maps to NM_020126.3 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:228881384 G>A maps to NM_001142644.1 N1395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:228973574 T>A maps to NM_001142644.1 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr2:228882640 G>A maps to NM_001142644.1 R977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:228884716 G>A maps to NM_001142644.1 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:228881798 G>T maps to NM_001142644.1 A1257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr2:228884678 C>T maps to NM_001142644.1 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:228883696 G>A maps to NM_001142644.1 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr2:228890245 T>A did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr2:228884144 G>T maps to NM_001142644.1 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:228855880 A>T maps to NM_001142644.1 P1598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr2:228886586 C>T maps to NM_001142644.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr2:228882731 C>T maps to NM_001142644.1 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:228855742 C>T maps to NM_001142644.1 K1644K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr11:47399865 G>T maps to NM_001080547.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:50925755 G>A maps to NM_003121.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr19:50926134 C>A maps to NM_003121.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:101873414 C>T maps to ENST00000299272 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr9:91041468 C>T maps to NM_006717.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr23:57020779 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr23:62570368 G>C did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr23:62570268 G>C did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:62570190 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:62570070 C>G did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr5:147207655 C>T maps to NM_003122.3 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr5:147553846 C>G maps to NM_001001325.1 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr5:147470776 C>A maps to NM_001127698.1 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:147715229 C>T maps to NM_001040433.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr15:41145415 C>A maps to NM_181642.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr18:12452291 G>A maps to NM_001128626.1 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr18:12493137 T>C maps to NM_001128626.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr18:12454452 G>A maps to NM_001128626.1 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:89930014 G>T maps to NM_032451.1 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr16:89922591 C>A maps to NM_032451.1 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:29675975 C>T maps to NM_003123.3 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr16:28995108 C>T maps to NM_032038.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr16:28992918 G>A maps to NM_032038.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr16:28992820 C>T maps to NM_032038.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:4439592 C>T maps to NM_001124758.1 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:32267262 A>G did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:32257954 C>T maps to NM_144569.4 Q941Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:136403476 G>A maps to NM_004598.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr5:136834060 C>T did not map to a codon.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr5:136448237 C>T maps to NM_004598.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr5:136324222 G>A maps to NM_004598.3 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr10:73822655 G>A maps to NM_014767.2 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr4:167983652 G>T maps to NM_016950.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:167675843 G>C maps to NM_016950.2 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr11:14282158 A>T maps to NM_006108.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:14280916 G>A maps to NM_006108.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:14277227 C>A maps to NM_006108.2 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:14276214 G>A maps to NM_006108.2 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr4:1164229 G>T maps to NM_012445.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:47699429 C>G did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr17:47696728 G>C maps to NM_003563.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:139316620 A>C maps to NM_001001664.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K0-01B-21D-A31L-08 chr2:139326634 G>A maps to NM_001001664.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr4:88903946 G>T maps to NM_001040058.1 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr2:234975871 C>T maps to NM_006944.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr15:51031994 A>G maps to NM_032802.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:2344592 C>T maps to NM_152988.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:2340961 C>G maps to NM_152988.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:121206201 C>T maps to NM_139015.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr12:121206806 G>C maps to NM_139015.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:73115470 C>T maps to NM_003124.4 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr15:38643247 C>T maps to NM_152594.2 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:38591586 C>T maps to NM_152594.2 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr15:38632025 C>G maps to NM_152594.2 S171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr2:65571948 G>A maps to NM_181784.2 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:65541018 C>T maps to NM_181784.2 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:65540892 C>G maps to NM_181784.2 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:153004976 A>G maps to NM_003125.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:153004997 C>A maps to NM_003125.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:153043108 C>T maps to NM_001017418.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:153043108 C>T maps to NM_001017418.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr13:80911636 C>T maps to NM_005842.2 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr13:80911078 T>C maps to NM_005842.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:155004338 T>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:155004161 C>T did not map to a codon.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr23:155004049 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr23:155003584 C>T did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:141694649 G>A maps to NM_030964.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:55659077 C>T maps to NM_032681.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:55653179 A>T maps to NM_032681.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:55658942 G>T maps to NM_032681.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:55652951 C>T maps to NM_032681.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:55653011 G>A maps to NM_032681.3 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:9427561 G>C maps to NM_025106.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr12:6981423 G>A maps to NM_032641.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr16:1828031 C>T maps to NM_080861.3 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr16:1827826 G>A maps to NM_080861.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr3:140785392 C>T maps to NM_080862.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr3:140785629 C>T maps to NM_080862.1 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:158582744 G>T maps to NM_003126.2 G2332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:158650471 G>A maps to NM_003126.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:158585169 C>T maps to NM_003126.2 A2208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr1:158618301 A>G maps to NM_003126.2 D1237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:158587332 T>G maps to NM_003126.2 A2198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:158582606 C>T maps to NM_003126.2 Q2378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr1:158639215 T>C maps to NM_003126.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:158641850 C>A maps to NM_003126.2 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:158615001 G>A maps to NM_003126.2 I1390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:158595953 G>T maps to NM_003126.2 L1964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:158583632 C>G maps to NM_003126.2 G2289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr1:158646058 C>T maps to NM_003126.2 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:158641185 G>A maps to NM_003126.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:158614051 G>A maps to NM_003126.2 I1443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:158627452 C>T maps to NM_003126.2 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr1:158639534 A>G maps to NM_003126.2 H547H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:158650414 C>A maps to NM_003126.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:158641986 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:158651379 C>T maps to NM_003126.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:158641150 G>A maps to NM_003126.2 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:158641243 C>A did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:158637773 C>A maps to NM_003126.2 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr1:158650471 G>A maps to NM_003126.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:158637732 A>G maps to NM_003126.2 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:158637816 C>T maps to NM_003126.2 Q623Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr1:158619720 C>T maps to NM_003126.2 W1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr1:158637690 A>T maps to NM_003126.2 V665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr1:158585172 C>T maps to NM_003126.2 Q2207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:131365868 G>A maps to NM_001130438.2 K1209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:131362395 T>G did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr9:131343202 G>T maps to NM_001130438.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:131371247 C>T maps to NM_001130438.2 V1529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr9:131339678 C>T maps to NM_001130438.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr9:131339446 G>A maps to NM_001130438.2 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr14:65239588 G>A maps to ENST00000389723 I1758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr14:65260352 C>T maps to ENST00000389723 Q680Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:54852071 G>A maps to NM_003128.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:54856883 G>A maps to NM_003128.2 W871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr2:54856155 G>T maps to NM_003128.2 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:54856683 G>T maps to NM_003128.2 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr2:54858009 A>G maps to NM_003128.2 E942E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:66473194 G>A maps to NM_006946.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:66466926 G>T maps to NM_006946.2 G1242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr11:66468475 G>A maps to NM_006946.2 Q1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:66460039 G>A maps to NM_006946.2 S1719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr11:66456267 G>A maps to NM_006946.2 L2029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr11:66466932 A>T maps to NM_006946.2 S1240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:66461786 G>A maps to NM_006946.2 I1442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:41009735 G>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:41066347 G>A maps to NM_025213.2 W661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:41026012 C>T maps to NM_020971.2 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr19:41061989 C>T maps to NM_020971.2 S1695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr19:41025958 C>G maps to NM_020971.2 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr15:42169092 C>A maps to ENST00000320955 R1255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:42168380 T>A maps to ENST00000320955 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr15:42174865 G>A maps to ENST00000320955 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr15:42166141 G>T maps to ENST00000320955 I1597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr15:42149830 G>C maps to ENST00000320955 L2768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr15:42153687 G>A maps to ENST00000320955 L2582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:42149209 C>T maps to ENST00000320955 Q2883Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr15:42173393 C>T maps to ENST00000320955 R832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr15:42169044 G>A maps to ENST00000320955 G1271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr9:94794749 G>C maps to NM_006415.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr9:94794748 A>G maps to NM_006415.2 *474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr9:94830313 G>C maps to NM_006415.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr14:78063665 C>A maps to NM_004863.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr14:78028817 C>G maps to NM_004863.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:18633880 G>A maps to NM_194285.2 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:18637343 G>A maps to NM_194285.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:126011788 C>T maps to NM_003129.3 H48H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:126011729 C>T maps to NM_003129.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr15:45981252 C>G maps to NM_021199.2 S378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr15:45968408 C>T maps to NM_021199.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr15:45962151 T>G maps to NM_021199.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr15:45954316 C>T maps to NM_021199.2 D133D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr5:179260065 G>A maps to NM_003900.4 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:142742815 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr3:142740398 T>C did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr3:142740366 T>C maps to NM_001080415.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr3:142735172 G>C maps to NM_001080415.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr20:36012654 C>T maps to ENST00000373558 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:36012651 C>T maps to ENST00000373558 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:30727496 C>G maps to NM_006662.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr16:30736321 C>T maps to NM_006662.2 S1859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr16:30748953 A>C maps to NM_006662.2 P2531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:30712175 C>T maps to NM_006662.2 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:30723671 G>A maps to NM_006662.2 K635K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr16:30749356 G>T maps to NM_006662.2 E2666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr16:30750151 C>T maps to NM_006662.2 L2931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:30747678 C>T maps to NM_006662.2 S2296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr16:30735403 G>A maps to NM_006662.2 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr16:30750522 C>G maps to NM_006662.2 S3054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:36704825 C>T maps to NM_025248.2 E1079E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:76019432 C>T maps to NM_080744.1 W557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:76019438 G>A maps to NM_080744.1 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:31805846 G>A maps to NM_000348.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr2:31805804 G>T maps to NM_000348.3 C55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:56225582 C>T maps to NM_024592.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:56212586 G>A maps to NM_024592.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr17:17716990 C>T maps to NM_001005291.2 Q1028Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:43144379 C>T maps to NM_003131.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr6:43143451 G>A maps to NM_003131.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:121309962 C>T maps to NM_152546.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:64472739 T>C maps to NM_020762.2 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:64437225 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr12:64505655 T>C maps to NM_020762.2 H678H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr1:206628235 C>T maps to ENST00000414359 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr1:206592729 C>A maps to ENST00000414359 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr1:206619612 C>G maps to ENST00000414359 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr3:9027553 C>A maps to NM_014850.2 T983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:9055173 C>T maps to NM_014850.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:70847957 T>C maps to NM_002727.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:87840217 C>T maps to NM_003130.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr16:4242492 G>A maps to ENST00000330063 F799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:11119844 G>T maps to NM_003132.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr20:62178519 G>A maps to NM_080823.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr20:62172622 G>C maps to NM_080823.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IH-01A-11D-A25Y-08 chr15:40330521 C>A maps to NM_003134.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr17:74035885 G>A maps to NM_014230.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:35888246 C>T maps to ENST00000361690 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr7:104801042 C>A maps to ENST00000336613 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:153046725 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:153049746 A>T did not map to a codon.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr23:38024063 T>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:38009041 G>A did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr23:38009016 T>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:38033499 G>A did not map to a codon.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr23:38013774 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:99917254 C>T did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:99917201 C>T did not map to a codon.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr23:99925826 C>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:99920266 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr16:2815911 C>T maps to NM_016333.3 Q1795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:2811882 G>T maps to NM_016333.3 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr16:2816181 C>T maps to NM_016333.3 R1885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr16:2819132 C>T maps to NM_016333.3 S2623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr16:2819144 T>C maps to NM_016333.3 S2627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:75889304 G>T maps to ENST00000388802 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:119592087 C>A maps to NM_194286.2 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:119568509 G>A maps to NM_194286.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr12:119583251 G>T maps to NM_194286.2 G280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr12:119568488 C>T maps to NM_194286.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr12:119583315 C>A maps to NM_194286.2 S301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:100485055 G>A maps to NM_015908.5 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr7:100482942 C>G maps to NM_015908.5 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr7:100482978 C>T maps to NM_015908.5 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr18:23612434 C>T maps to ENST00000415083 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr20:60738655 G>A maps to NM_198935.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:170667534 A>G maps to NM_003142.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr5:80809448 G>A maps to ENST00000380182 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:18543508 G>C did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:182783379 C>G maps to NM_001130445.1 S948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:182763788 G>A maps to NM_001130445.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:182781035 C>G maps to NM_001130445.1 S890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr12:109201542 G>A maps to NM_018984.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr12:109201542 G>A maps to NM_018984.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr12:109194620 G>A maps to NM_018984.3 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr12:109182987 C>T maps to NM_018984.3 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr12:109186364 G>T maps to NM_018984.3 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:109182303 G>A maps to NM_018984.3 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:27963639 T>C maps to NM_033389.2 E509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr17:27999101 C>T maps to NM_033389.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr17:27963168 G>A maps to NM_033389.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr17:27958125 C>T maps to NM_033389.2 Q1335Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr11:67077771 G>T maps to NM_017857.3 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr7:149510809 C>T maps to NM_198455.2 C3368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:149508764 C>A maps to NM_198455.2 S3171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr7:149515819 C>A maps to NM_198455.2 R3911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr7:149474827 C>T maps to NM_198455.2 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr7:149486776 C>T maps to NM_198455.2 C1518C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:149482235 T>A maps to NM_198455.2 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:149481148 C>G maps to NM_198455.2 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:149482280 C>G maps to NM_198455.2 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr7:149493813 G>A maps to NM_198455.2 L2271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:149477971 C>T maps to NM_198455.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:149494380 C>T maps to NM_198455.2 T2285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr7:149489169 C>T maps to NM_198455.2 D1806D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:149492407 C>A maps to NM_198455.2 T2100T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-MT-A67A-01A-11D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr7:149515759 C>T maps to NM_198455.2 S3891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr7:149484607 C>T maps to NM_198455.2 L1178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr7:149529909 G>A maps to NM_198455.2 E5114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr7:149514779 C>G maps to NM_198455.2 L3777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:155989898 T>A maps to ENST00000368312 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr1:155989933 A>G maps to ENST00000368312 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr3:156272785 G>C maps to ENST00000467789 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr23:153063239 G>A did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr11:57100269 G>A maps to NM_003146.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:57095836 C>T maps to NM_003146.2 K515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:65338883 C>G maps to NM_006396.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr11:65338156 C>T maps to NM_006396.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:38679679 C>A maps to NM_001049.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:38678914 C>T maps to NM_001049.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:38678891 C>T maps to NM_001049.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr14:38679208 G>A maps to NM_001049.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:71166309 C>T maps to NM_001050.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:71166354 C>T maps to NM_001050.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr22:37603254 G>A maps to NM_001051.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:23017172 C>A maps to NM_001052.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr20:23016245 G>A maps to NM_001052.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:48117189 G>T did not map to a codon.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr23:48123287 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:48116745 G>A did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:48117230 G>A did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:48208992 A>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:48049697 G>A did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:48054485 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:52681919 C>G did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr22:41240868 G>A maps to NM_003932.3 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:41240913 C>T did not map to a codon.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr11:130058528 C>T maps to NM_021978.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:130059705 C>T maps to NM_021978.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr11:130078331 C>T maps to NM_021978.3 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr11:130060364 C>A maps to NM_021978.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:53084517 C>T maps to NM_014682.2 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr8:53049181 T>C maps to NM_014682.2 K756K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr8:53045824 C>G maps to NM_014682.2 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr8:53062327 A>T maps to NM_014682.2 Y672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:53045842 G>A maps to NM_014682.2 C773C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr8:53062468 G>A maps to NM_014682.2 D625D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr8:53025817 G>T maps to NM_014682.2 S1028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr8:53092795 T>A maps to NM_014682.2 K55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr8:53030948 C>G maps to NM_014682.2 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr8:134474116 C>A did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:44201936 G>T maps to NM_174963.2 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:44303968 G>A maps to NM_174963.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:44365305 T>A maps to NM_174963.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:126283416 G>C maps to ENST00000356132 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:86075250 A>T maps to NM_003896.3 L132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:86071527 G>A maps to NM_003896.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:86071516 A>G did not map to a codon.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr2:86071563 G>A maps to NM_003896.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:98512550 C>G maps to ENST00000493584 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr3:98506993 G>A maps to ENST00000493584 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr11:8752422 C>T maps to NM_005418.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:8752203 C>T maps to NM_005418.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr11:8739407 A>G maps to NM_005418.3 D503D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr11:8739319 G>A maps to NM_005418.3 Q533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr11:8728694 C>T maps to NM_005418.3 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:8724163 G>C maps to NM_005418.3 S892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr11:8751709 G>T maps to NM_005418.3 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:8737200 G>C maps to NM_005418.3 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:8737228 G>C maps to NM_005418.3 S589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr3:186760907 C>T maps to NM_003032.2 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:186793539 C>T maps to NM_003032.2 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:107459974 G>A maps to NM_001142351.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:107460127 G>T maps to NM_001142351.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr2:107446570 C>T maps to NM_001142351.1 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:74625171 C>T maps to NM_018414.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:74625489 C>G maps to NM_018414.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:74639687 C>G maps to NM_018414.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:74621570 G>A maps to NM_018414.3 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:74625777 C>T maps to NM_018414.3 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr17:74569350 G>A maps to NM_006456.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:74564814 G>A maps to NM_006456.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:74564835 G>A maps to NM_006456.2 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr1:77094302 A>G did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:76877997 G>A maps to NM_152996.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:76878003 G>A maps to NM_152996.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:77094489 G>C maps to NM_152996.2 *306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr9:130658592 C>A maps to NM_013443.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr7:116593614 C>G maps to ENST00000323984 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr15:92981808 C>T maps to NM_006011.3 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr15:93007599 C>T maps to NM_006011.3 C371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr18:55020119 C>T maps to NM_015879.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:55020181 G>A maps to NM_015879.2 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:55024149 A>G maps to NM_015879.2 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr18:44261972 C>T maps to NM_013305.4 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr18:44272160 C>T maps to NM_013305.4 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:52558126 T>C maps to NM_015136.2 D2518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr3:52544477 T>C maps to NM_015136.2 G914G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr3:52552019 G>C did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:52539120 C>A maps to NM_015136.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:104044338 G>T maps to NM_017564.9 G414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr12:104033918 G>T maps to NM_017564.9 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr12:104107481 C>A maps to NM_017564.9 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:104067820 C>T maps to NM_017564.9 F836F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:104063326 G>A maps to NM_017564.9 K727K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:104063401 A>G maps to NM_017564.9 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr12:104031884 C>G maps to NM_017564.9 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr3:36587703 G>T maps to NM_003149.1 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr3:36587779 G>T maps to NM_003149.1 *403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:36570190 A>T maps to NM_003149.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:36545897 A>T maps to NM_003149.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr17:37368613 G>A maps to NM_198993.3 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:37369369 G>T maps to NM_198993.3 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr17:37371436 G>A maps to NM_198993.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr3:136240235 G>C maps to NM_005862.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:136141362 G>A maps to NM_005862.2 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr23:123164833 C>T did not map to a codon.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr23:123200244 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr23:123217392 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:123159746 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:123181322 A>C did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:123217343 C>T did not map to a codon.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr23:123195627 A>G did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:123196816 C>A did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:123197010 C>T did not map to a codon.
Multiple mappings detected for codon TCGA-IQ-A61G-01A-11D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr7:74301261 T>A did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr7:66771027 C>T maps to NM_022906.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:17737123 C>T maps to NM_003473.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:17747603 C>G maps to NM_003473.2 S358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr10:90682923 G>C did not map to a codon.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr10:90665315 A>G maps to NM_020799.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr19:4329962 T>G maps to ENST00000314714 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr8:38006157 C>T did not map to a codon.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr8:38006272 C>A did not map to a codon.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:38003512 G>A maps to NM_000349.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:38005822 G>C maps to NM_000349.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr13:33679798 T>A maps to NM_178007.2 A1083A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr13:33701583 G>A maps to NM_178007.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:33703292 G>T maps to NM_178007.2 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr13:33703124 A>G maps to NM_178007.2 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr13:33701604 C>G maps to NM_178007.2 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr13:33703784 C>T maps to NM_178007.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr13:33760036 C>A maps to NM_178007.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr13:33859649 G>A maps to NM_178006.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:37813325 C>T maps to NM_006804.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr5:110835646 C>T maps to NM_139164.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr15:81614832 G>A maps to NM_181900.2 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr15:81605704 G>T maps to NM_181900.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr15:81614836 C>T maps to NM_181900.2 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr15:81605704 G>C maps to NM_181900.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr18:51851188 A>T maps to NM_139171.1 L179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr18:51851062 C>T maps to NM_139171.1 *221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:96858994 C>T maps to NM_020151.3 W215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:67939132 C>A did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr23:67938279 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:67942408 T>C did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:67938002 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:191845387 G>A maps to NM_007315.3 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:191873690 G>A maps to NM_007315.3 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:191872312 C>A maps to NM_007315.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:191874722 G>A maps to NM_007315.3 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:191859794 G>C maps to NM_007315.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr2:191843714 G>A maps to NM_007315.3 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr12:56743975 T>A did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr12:56740684 G>A maps to NM_005419.3 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:56740693 C>A maps to NM_005419.3 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr12:56748399 T>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:191929549 G>A maps to NM_003151.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr2:191929663 G>T maps to NM_003151.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr17:40461400 G>A maps to NM_003152.3 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr17:40453424 C>T maps to NM_003152.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr17:40453382 G>A maps to NM_003152.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr17:40458299 G>T maps to NM_003152.3 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr17:40368064 G>A maps to NM_012448.3 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr20:47752435 G>C maps to NM_017453.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:47733707 C>G maps to NM_017453.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr8:23702399 A>C maps to NM_003155.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:23709898 T>A did not map to a codon.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr7:89856754 C>G maps to NM_152999.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr7:89861766 T>G maps to NM_152999.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:89854671 T>C maps to NM_152999.3 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:89856304 T>C maps to NM_152999.3 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr2:119988593 G>A maps to NM_182915.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr7:87910313 C>T maps to NM_024636.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr7:87910250 C>T maps to NM_024636.2 W376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:87913171 G>C maps to NM_024636.2 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr7:87912009 C>A maps to NM_024636.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:47717389 G>A maps to NM_001048166.1 S1095S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr11:4112584 C>T maps to NM_003156.3 Q539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr11:3988830 C>G maps to NM_003156.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:4112526 C>T maps to NM_003156.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr4:27009226 C>T maps to ENST00000382009 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:63967639 G>T did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr5:171481611 C>T maps to NM_005990.3 A871A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr5:171491741 C>T maps to NM_005990.3 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:171534827 C>G maps to NM_005990.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr5:171520514 C>T maps to NM_005990.3 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr19:1218422 C>T maps to NM_000455.4 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:220111833 G>C did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr7:43663373 A>G maps to NM_004760.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr13:99127077 C>T maps to NM_003576.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr2:242441063 C>T maps to NM_006374.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr7:23825152 C>T maps to NM_031414.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:23825128 A>G maps to NM_031414.3 E727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr7:23827672 A>G maps to NM_031414.3 S854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr7:23871840 C>T maps to NM_031414.3 F972F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:23830530 C>G maps to NM_031414.3 S909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:23809340 C>A maps to NM_031414.3 S560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:23871924 G>A maps to NM_031414.3 T1000T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr5:146730661 G>A maps to NM_001112724.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr4:5170099 G>A maps to NM_018401.1 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr4:5458559 G>A maps to NM_018401.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr10:134038744 G>A maps to NM_173575.2 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr10:134039103 G>T maps to NM_173575.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr11:8483357 C>G maps to NM_030906.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr11:8494818 G>C maps to NM_030906.2 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr11:8414254 A>C maps to NM_030906.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr11:8478906 T>A maps to NM_030906.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr2:219543896 C>T maps to NM_015690.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr2:219559300 C>T maps to NM_015690.3 D818D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr2:219540847 C>T maps to NM_015690.3 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:219543984 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:219563389 C>T maps to NM_015690.3 A1041A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:36475337 C>T maps to NM_007271.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr12:27467946 G>A did not map to a codon.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr12:27468246 G>A maps to NM_015000.3 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:169023848 G>A maps to NM_013233.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr8:80577107 G>A maps to NM_007029.3 *180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:27099980 C>A maps to NM_030795.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr15:74284509 G>A maps to NM_004809.3 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:48809195 C>G maps to NM_172311.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr14:81744352 G>T maps to NM_033104.2 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr14:81743533 C>T maps to NM_033104.2 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:70646266 C>T maps to NM_001130161.2 N905N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:184930440 C>G maps to NM_020225.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr4:184938289 C>T maps to NM_020225.1 N878N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr4:184931952 G>A maps to NM_020225.1 K654K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr4:184931157 G>T maps to NM_020225.1 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr15:74472516 C>T maps to ENST00000449139 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:134916759 C>G maps to NM_182489.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr2:202337800 T>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:202343225 A>G maps to NM_018571.5 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr2:202343120 G>A maps to NM_018571.5 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr12:16048403 A>G maps to ENST00000025399 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr9:125921432 G>A maps to NM_018387.4 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:125890529 T>A maps to NM_018387.4 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:43910165 C>A maps to NM_153700.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr15:43896332 C>T maps to NM_153700.2 E1412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr2:37152276 T>C maps to NM_003162.2 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:31420118 T>C maps to NM_001083893.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr19:47231983 G>A maps to NM_001039877.1 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr23:7268020 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:7171342 G>C did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr23:7268166 G>C did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:125484216 A>G did not map to a codon.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr11:125479464 C>T maps to NM_152713.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr3:31674464 T>C maps to NM_178862.1 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr16:731285 C>T maps to NM_005861.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:732455 C>T maps to NM_005861.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:144507959 G>T maps to NM_003764.3 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr1:28144384 G>A maps to ENST00000373939 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr1:28148833 G>A maps to ENST00000373939 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:28120124 C>T maps to ENST00000373939 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:28138697 G>A maps to ENST00000373939 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr20:57246298 C>T maps to NM_001001433.1 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr9:102722404 C>T maps to NM_017919.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:4458948 G>T maps to NM_016930.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr7:73117213 G>A maps to NM_004603.3 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr16:31012507 C>A maps to NM_052874.3 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:131285790 G>A maps to NM_194356.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr16:31051060 C>T maps to NM_004604.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:31046324 C>T maps to NM_004604.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:180959167 G>C maps to NM_005819.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:132785160 G>A maps to NM_003569.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr17:9448487 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:7705801 G>C maps to ENST00000441779 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:109342873 A>G maps to NM_007269.2 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:109318957 A>G maps to NM_007269.2 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:53108626 T>C did not map to a codon.
Sequencing variant TCGA-KU-A6H8-01A-21D-A34J-08 chr17:53156044 A>T did not map to a codon.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr17:53237244 T>C maps to NM_178509.5 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:147684645 G>A maps to NM_001127715.1 Q907Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:120998663 G>T maps to NM_014980.2 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr3:121132061 G>A maps to NM_014980.2 R1026R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:120998726 C>T maps to NM_014980.2 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:10783758 T>C maps to NM_018423.2 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:10774548 G>A maps to NM_018423.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:75643193 G>A maps to NM_016086.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr13:48563042 G>A maps to NM_003850.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr3:151597695 G>A did not map to a codon.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr12:118838507 C>T maps to NM_022491.2 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr10:104359283 C>T maps to NM_016169.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:70476366 C>T maps to NM_001128206.1 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr8:70570761 G>T maps to NM_001128206.1 E870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:70517084 C>G maps to NM_001128206.1 S432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:70501298 C>T maps to NM_001128206.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:70512982 G>T maps to NM_001128206.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr8:70514019 T>G maps to NM_001128206.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr20:46313261 G>C maps to NM_001161841.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr20:46386014 C>G maps to NM_001161841.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr20:46301110 C>A maps to NM_001161841.1 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr20:46307420 G>T maps to NM_001161841.1 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:28617419 G>A maps to NM_177529.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:28617425 G>A maps to NM_177529.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr4:70620402 C>A maps to NM_014465.3 G88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr4:70596324 G>T maps to NM_014465.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:108924877 A>G maps to ENST00000437390 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr2:108863793 T>C maps to NM_001008743.1 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr4:70707743 C>A maps to NM_005420.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr19:49079248 C>T maps to NM_177973.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr19:49094969 G>C maps to NM_177973.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr22:44234791 G>A maps to NM_014351.3 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr22:44237687 G>A maps to NM_014351.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr2:37410657 C>G did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr7:56147374 C>T maps to NM_001130069.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr7:56145841 C>T maps to ENST00000395437 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr21:46226907 C>T maps to ENST00000411651 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:912966 G>A maps to ENST00000456758 *975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:912961 C>G maps to ENST00000456758 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr7:891655 G>A maps to ENST00000456758 W465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr7:883125 G>A maps to ENST00000456758 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr22:39138355 C>A maps to ENST00000405018 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:39148609 G>A maps to ENST00000405018 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr20:31572919 C>T maps to NM_080675.3 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr20:31590694 C>T maps to NM_080675.3 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr20:31571671 G>A maps to NM_080675.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:56397409 G>A maps to NM_001032387.1 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr14:21831283 G>A maps to NM_007192.3 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:21831309 T>G did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr14:21825366 C>T maps to NM_007192.3 K883K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr17:56429451 G>A maps to NM_003168.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:39962115 C>T maps to NM_003169.3 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr17:27027530 G>T did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr17:27010308 C>T maps to NM_003170.3 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr17:27005864 G>A maps to NM_003170.3 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:27880481 G>C maps to NM_014860.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr10:70940260 C>T maps to NM_003171.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr10:70958210 C>T maps to NM_003171.3 C369C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr9:136220668 G>A maps to NM_003172.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr9:136227942 C>G maps to NM_017503.3 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:136226862 T>C maps to NM_017503.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:136234222 G>A maps to NM_033161.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr9:136234282 C>T maps to NM_033161.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr9:136234195 G>A maps to NM_033161.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr9:136199073 C>T maps to NM_006753.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:114875120 G>C maps to NM_022486.3 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:114886645 G>A maps to NM_022486.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr9:114886702 G>A maps to NM_022486.3 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr9:114911524 T>A maps to NM_022486.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr22:24580745 C>G maps to NM_019601.3 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:24582116 G>A maps to NM_019601.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr22:24583659 C>G maps to NM_019601.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:24580230 G>A maps to NM_019601.3 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr9:95838219 C>T maps to NM_145006.2 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:223438080 C>T maps to NM_017982.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr1:223396789 G>A maps to NM_017982.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:223465978 G>A maps to NM_017982.3 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr1:223401021 G>A maps to NM_017982.3 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:33195133 G>A maps to NM_015551.1 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:33255547 C>T maps to NM_015551.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr23:48558588 G>A did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:48564735 C>A did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr23:48564701 G>A did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:48558859 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:48565905 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:67925547 G>A maps to NM_017635.3 N755N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:67926429 C>T maps to NM_017635.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:55853366 C>T maps to NM_032701.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr17:30302526 T>C maps to NM_015355.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:149879360 T>C maps to NM_014849.3 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:149880766 A>T maps to NM_014849.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr1:149882447 C>T maps to NM_014849.3 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr1:149879276 G>A maps to NM_014849.3 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr15:91769846 C>A maps to NM_014848.4 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr15:91835754 A>G maps to NM_014848.4 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr15:91835658 C>A maps to NM_014848.4 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr15:91827365 C>G maps to NM_014848.4 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr15:91835658 C>T maps to NM_014848.4 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:91795214 C>T maps to NM_014848.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:75490759 C>T maps to NM_014979.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr5:75490834 C>A maps to NM_014979.1 C224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr9:113168735 G>A maps to ENST00000374463 A3051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr9:113168501 C>T maps to ENST00000374463 P3129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:113261432 C>T maps to ENST00000374463 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:113220759 G>A maps to ENST00000374463 I1189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr9:113148249 G>A maps to ENST00000374463 L3392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr9:113170490 G>C maps to ENST00000374463 L2466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr9:113228229 T>A maps to ENST00000374463 P1079P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:113168895 C>T maps to ENST00000374463 W2998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:113265468 C>T maps to ENST00000374463 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr9:113170217 G>T maps to ENST00000374463 I2557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr9:113171186 A>G maps to ENST00000374463 C2234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:113189971 A>G maps to ENST00000374463 C1961C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr9:113170973 C>T maps to ENST00000374463 W2305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr9:113171108 C>G maps to ENST00000374463 L2260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:29762805 C>G maps to NM_021738.2 A1830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr10:29801692 G>A maps to NM_021738.2 Q1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr10:29776151 G>C maps to NM_021738.2 L1475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr10:29775130 G>C maps to NM_021738.2 L1554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr10:29762805 C>T maps to NM_021738.2 A1830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:9759762 C>T maps to NM_015055.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:9749697 G>C maps to NM_015055.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr11:9750957 C>T maps to NM_015055.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr23:16737952 G>C did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:16774793 C>T did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:16775365 G>A did not map to a codon.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr8:110631185 G>A maps to NM_001099744.1 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:110655122 A>G maps to NM_001099744.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr8:110590242 A>G maps to NM_001099744.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:135369530 C>T maps to NM_001143764.1 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr19:39694789 C>T maps to NM_001080468.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:115527423 A>T maps to NM_003176.2 K880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr1:115438111 A>G maps to NM_003176.2 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr20:58449031 G>T maps to NM_014258.2 S1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr20:58457210 G>A maps to NM_014258.2 Q847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr20:58467455 A>G maps to NM_014258.2 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr19:15220101 C>T maps to NM_033025.4 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:15224467 G>A maps to NM_033025.4 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:85630215 G>A maps to NM_032184.1 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr1:85666169 G>A maps to NM_032184.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:93650071 G>A maps to NM_003177.5 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr9:93641136 C>T maps to NM_003177.5 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:93650033 C>T maps to NM_003177.5 Q529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr19:46330776 C>T maps to NM_004819.2 E724E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr19:46328446 C>G maps to NM_004819.2 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:46341721 A>G maps to NM_004819.2 N413N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr1:33149860 A>G maps to NM_030786.2 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr6:86328537 T>C maps to NM_006372.4 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:86324794 G>A maps to NM_006372.4 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr6:152451871 G>A maps to NM_182961.2 V8712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:152605235 C>G maps to NM_182961.2 L6028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:152639308 C>A maps to NM_182961.2 L5493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:152647534 G>A maps to NM_182961.2 I5063I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:152711563 T>C maps to NM_182961.2 E2676E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr6:152469387 A>G maps to NM_182961.2 N8256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:152702404 C>G maps to NM_182961.2 G2915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:152720762 T>A maps to NM_182961.2 K2409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:152510446 G>A maps to NM_182961.2 I7747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:152453255 C>A did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:152638074 A>T maps to NM_182961.2 L5540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr6:152469312 G>A maps to NM_182961.2 I8281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr6:152605241 C>T maps to NM_182961.2 E6026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr6:152461284 G>A maps to NM_182961.2 R8420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:152644704 G>C maps to NM_182961.2 T5275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr6:152639351 A>T maps to NM_182961.2 L5479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:152786533 G>C maps to NM_182961.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:152826447 C>A maps to NM_182961.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:152623105 G>A maps to NM_182961.2 T5813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:152757236 C>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr6:152456261 G>A maps to NM_182961.2 Q8589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:152443675 G>T maps to NM_182961.2 C8763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:152674535 C>T maps to NM_182961.2 Q3705Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr6:152651116 C>T maps to NM_182961.2 R4901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr6:152539538 C>A did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr6:152631903 T>C maps to NM_182961.2 Q5605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:152786397 T>A maps to NM_182961.2 K643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr6:152665275 G>T maps to NM_182961.2 V4055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr6:152536194 C>A maps to NM_182961.2 G7398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:152737754 G>A maps to NM_182961.2 I1939I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr6:152651123 C>T maps to NM_182961.2 W4899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:152485447 C>T maps to NM_182961.2 L7880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:152647474 C>T maps to NM_182961.2 Q5083Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:152674484 G>A maps to NM_182961.2 G3722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:152708395 C>T maps to NM_182961.2 L2766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr6:152675907 C>T maps to NM_182961.2 E3604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr6:152527353 T>C maps to NM_182961.2 S7656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr6:152832196 G>T maps to NM_182961.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr14:64493343 C>T maps to NM_182914.2 I2100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr14:64494409 C>T maps to NM_182914.2 Q2205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr14:64656946 C>T maps to NM_182914.2 I6010I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr14:64491049 C>T maps to NM_182914.2 L1905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr14:64468756 A>G maps to NM_182914.2 G1248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr14:64564716 A>G maps to NM_182914.2 K4053K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr14:64522879 C>T maps to NM_182914.2 S3321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:64421610 C>T maps to NM_182914.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr14:64497901 A>T maps to NM_182914.2 K2350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr14:64493337 G>A maps to NM_182914.2 E2098E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:64626097 C>G maps to NM_182914.2 L5344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:64596824 T>C maps to NM_182914.2 P4733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:64565539 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr14:64416649 C>T maps to NM_182914.2 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr14:64473775 C>T maps to NM_182914.2 I1471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr14:64682002 G>A did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr6:33402926 A>T did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr6:33400551 C>T maps to NM_006772.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr6:33391281 C>T maps to NM_006772.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr17:76167594 C>T maps to NM_004710.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr21:34011283 T>A maps to NM_003895.3 P1322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr21:34003712 G>A maps to NM_003895.3 I1477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr21:34011424 G>A maps to NM_003895.3 F1275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr21:34011984 C>T maps to NM_003895.3 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr6:158450034 T>G maps to NM_003898.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:158483058 G>A maps to NM_003898.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:158516990 T>C maps to NM_003898.3 N1362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr6:158449944 C>G maps to NM_003898.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr6:158509795 C>T maps to NM_003898.3 Q1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:158487491 G>T maps to NM_003898.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:158492711 G>A maps to NM_003898.3 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr6:158510942 G>T maps to NM_003898.3 E1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr6:158516915 G>A maps to NM_003898.3 K1337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr14:70855192 G>T maps to NM_018373.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr5:150027824 C>T maps to NM_001166209.1 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr5:150029325 G>T maps to NM_001166209.1 E741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr4:119952080 A>T maps to NM_133477.2 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:119951384 A>G maps to NM_133477.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr4:119952398 C>T maps to NM_133477.2 N823N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:75407450 T>C maps to NM_001114133.1 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr17:35913811 T>A maps to NM_007247.4 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:35932027 T>C maps to NM_007247.4 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:35913448 G>A maps to NM_007247.4 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr17:35932000 C>T maps to NM_007247.4 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:35902353 G>C maps to NM_007247.4 T974T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr23:49049870 G>A did not map to a codon.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:110022064 G>C maps to NM_001040709.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr1:110019529 C>T maps to NM_001040709.1 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr12:79837862 G>A maps to NM_005639.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr12:33559822 T>C maps to NM_198992.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:33532865 G>T maps to NM_198992.3 C467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr12:33579230 C>T maps to NM_198992.3 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr1:155837783 C>T maps to NM_152280.4 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:155851055 G>A maps to NM_152280.4 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr1:155837975 T>G maps to NM_152280.4 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:155851256 C>T maps to NM_152280.4 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:66811230 C>T maps to NM_001177880.1 N248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr11:66811317 G>A maps to NM_001177880.1 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:45274136 G>A maps to NM_020826.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr11:45277358 C>G maps to NM_020826.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:210334215 G>A maps to NM_001146261.1 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr10:46968668 C>T maps to NM_031912.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr10:46962029 G>A maps to NM_031912.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr10:46969271 C>G maps to NM_031912.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr14:62550912 G>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr14:62547850 T>C maps to NM_031914.2 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr14:62567239 C>T maps to NM_031914.2 Q585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr14:62551059 C>A maps to NM_031914.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:62547862 C>T maps to NM_031914.2 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr16:19278267 C>A maps to NM_016524.2 S432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:19236020 C>T maps to NM_016524.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:202569512 G>C maps to NM_177402.4 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:51133411 G>A maps to NM_001160329.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:51133334 G>A maps to NM_001160329.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr19:51135874 C>G maps to NM_001160329.1 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr18:40850485 G>T maps to NM_020783.3 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr18:40853628 C>T maps to NM_020783.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr18:40853922 G>C maps to NM_020783.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr18:40850344 C>T maps to NM_020783.3 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr18:40854063 G>C maps to NM_020783.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:55686277 C>T maps to NM_003180.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:114682430 G>A maps to ENST00000369545 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr1:114640423 G>A maps to ENST00000369545 N480N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr1:114680203 A>G maps to ENST00000369545 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:61291311 G>A maps to NM_004200.2 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr11:1858220 G>A maps to NM_138567.3 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr11:7324465 C>T maps to NM_175733.3 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:7334937 A>G maps to NM_175733.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr11:7324588 G>A maps to NM_175733.3 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:27676948 G>A maps to NM_001193308.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:85436773 C>T maps to ENST00000359152 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr11:85409098 T>C maps to ENST00000359152 G1638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:85436428 C>A maps to ENST00000359152 V881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr11:85420459 A>G maps to ENST00000359152 Y1484Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr11:85456723 G>A maps to NM_001162953.1 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:85445198 C>T maps to NM_001162953.1 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr23:99942201 C>A did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr23:99945601 T>C did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:99931172 C>A did not map to a codon.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr23:99931102 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:99956597 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr23:37985954 G>A did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr23:37984587 A>G did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:37969685 C>T did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:37913469 C>A did not map to a codon.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr23:37965887 G>C did not map to a codon.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr23:37955444 T>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:166581040 C>G maps to NM_003181.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:166571921 C>A maps to NM_003181.2 G397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:166578114 G>A maps to NM_003181.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:166571970 G>A maps to NM_003181.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:132892294 T>C maps to NM_175067.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr6:132891603 T>C maps to NM_175067.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:132859538 C>T maps to NM_175057.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr6:132859646 G>A maps to NM_175057.3 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr22:39826097 C>T maps to NM_006116.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:149691181 C>T maps to NM_015093.4 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:30872654 G>T did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:30873378 G>A did not map to a codon.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr23:30872590 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:30872790 G>A did not map to a codon.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr10:123970123 C>T maps to NM_206862.2 Q2062*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CN-6024-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:123844324 G>C maps to NM_206862.2 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr10:123970683 G>A maps to NM_206862.2 S2248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr10:124001516 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:123842302 C>T maps to NM_206862.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr10:124008653 G>A maps to NM_206862.2 A2881A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr10:123970458 G>A maps to NM_206862.2 T2173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr10:123846479 C>T maps to NM_206862.2 L1489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr10:123844396 G>C maps to NM_206862.2 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:1729443 C>T maps to NM_006342.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr4:1730163 C>T maps to NM_006342.1 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr4:1733023 T>A maps to NM_006342.1 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr2:75347731 C>T maps to NM_001058.3 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr10:71166837 A>G did not map to a codon.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr10:71175905 G>T maps to NM_001057.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:71164841 T>C did not map to a codon.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr10:71168821 G>A maps to NM_001057.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:104640370 G>C maps to NM_001059.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr4:104511030 G>A maps to NM_001059.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:104512795 G>T maps to NM_001059.2 C311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr4:104579370 C>T did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:104512752 G>A maps to NM_001059.2 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr4:104511050 G>T maps to NM_001059.2 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:59042501 G>A maps to NM_002353.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr17:35800746 A>G maps to NM_001166105.1 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:35818659 C>T maps to NM_001166105.1 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr4:7056306 C>G maps to NM_152293.2 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr4:7056453 G>A maps to NM_152293.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr3:9828793 C>T did not map to a codon.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr3:9831512 C>T maps to NM_006354.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr23:70617100 A>T did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:70618459 A>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr23:70612766 A>G did not map to a codon.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr23:70598235 G>A did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr23:70604856 A>G did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:70607297 G>A did not map to a codon.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr23:70613165 C>T did not map to a codon.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr23:70618518 G>C did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:70612526 T>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:70614022 A>G did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr23:70674607 T>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:70644010 C>G did not map to a codon.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr23:70607208 G>A did not map to a codon.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr23:70617221 G>C did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:70603877 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:70613189 C>T did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr11:6632500 G>A maps to NM_006284.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr17:34171896 G>T maps to NM_139215.1 G532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:34171940 T>C maps to NM_139215.1 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:10008538 C>T maps to NM_005680.2 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr16:84214951 C>T maps to NM_005679.2 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr9:32635463 C>T maps to NM_153809.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr9:32633171 G>A maps to NM_153809.2 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr9:32635388 C>T maps to NM_153809.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr9:32632973 G>A maps to NM_153809.2 C868C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:32633159 G>A maps to NM_153809.2 P806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:32634230 A>T maps to NM_153809.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:32632799 G>A maps to NM_153809.2 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr9:32631587 A>G maps to NM_153809.2 D1330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr9:32635508 C>T maps to NM_153809.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr9:32630546 C>T maps to NM_153809.2 T1677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:120772952 G>A maps to NM_003184.3 Q862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:120831747 T>G did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:8006136 C>T maps to NM_031923.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:8007659 G>A maps to NM_031923.2 E729E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr10:8006039 G>T maps to NM_031923.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr20:60581805 T>C maps to NM_003185.3 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr20:60584188 A>T maps to NM_003185.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr20:60581736 C>T maps to NM_003185.3 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr20:60575777 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr20:60578313 G>A maps to NM_003185.3 P796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr20:60584178 T>A maps to NM_003185.3 K605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr18:23873439 C>T maps to ENST00000418698 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr10:105133310 C>T maps to NM_006951.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:105139421 G>T maps to NM_006951.3 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr1:229730403 G>A maps to NM_014409.3 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:229730337 C>T maps to NM_014409.3 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr7:99707582 C>T maps to ENST00000472509 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr7:99711568 C>T maps to ENST00000472509 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr7:99711748 G>A maps to ENST00000472509 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:99711344 G>A maps to ENST00000472509 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:99710523 C>T maps to ENST00000472509 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr7:99711748 G>A maps to ENST00000472509 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr7:99707618 C>T maps to ENST00000472509 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr5:140698573 G>C maps to NM_005642.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr23:100538562 G>A did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr23:100547853 G>A did not map to a codon.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr23:100524181 C>T did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:100532639 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:100547781 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:100533087 C>T did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr6:42036203 G>A maps to NM_138572.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:68660865 T>C maps to NM_001015892.1 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:77395060 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:77392459 G>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:77393353 T>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:159462433 C>T maps to NM_054114.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr6:159457884 G>A maps to NM_054114.3 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr1:159890212 G>A maps to ENST00000368096 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr1:159889092 G>C maps to ENST00000368096 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr3:111732319 A>C maps to NM_001008272.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:47691449 G>A maps to ENST00000371883 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:47685628 C>T maps to ENST00000371883 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:47689751 C>T maps to ENST00000371883 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:747534 C>G maps to NM_006755.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr11:755975 G>A maps to NM_006755.1 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr11:763490 G>A maps to NM_006755.1 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr2:160053171 G>T maps to NM_033394.2 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:160084426 T>A maps to NM_033394.2 L1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:160031501 C>G maps to NM_033394.2 Y514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:160019982 C>G maps to NM_033394.2 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:160028630 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:160086253 C>T maps to NM_033394.2 S1439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr2:160082197 G>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:61499144 C>T maps to ENST00000389520 L1944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr2:162091950 A>G maps to NM_004180.2 Q400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr17:27837970 G>A maps to NM_020791.2 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:27829691 C>G maps to NM_020791.2 S430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr17:27849480 C>T maps to NM_020791.2 R698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:27861162 G>T maps to NM_020791.2 E797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:29999288 C>T maps to NM_016151.2 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:29996844 C>T maps to NM_016151.2 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:29996845 C>T maps to NM_016151.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr16:29998226 G>A maps to NM_016151.2 E878E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr16:29994472 C>T maps to NM_016151.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr12:118650750 G>A maps to NM_016281.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:118590136 G>A maps to NM_016281.3 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr12:118682748 C>A maps to NM_016281.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:32818144 G>C maps to NM_000593.5 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:32815406 G>A maps to NM_000593.5 Q656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr6:32813459 G>A maps to NM_000593.5 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr6:32816570 G>C maps to NM_000593.5 S535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr6:32798442 T>C maps to ENST00000452392 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:32805815 C>G maps to ENST00000452392 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:32797313 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:33281480 G>A maps to NM_172208.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr6:33281026 G>A maps to NM_172208.2 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:234546227 G>C maps to NM_005646.3 S1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:234586267 G>A maps to NM_005646.3 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr1:234529143 G>A maps to NM_005646.3 L1508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:53899913 C>T maps to NM_134323.1 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr12:53895897 C>G maps to NM_134323.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr12:53899502 C>G maps to NM_134323.1 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr1:11078817 C>G maps to NM_007375.3 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr7:38305121 C>G maps to ENST00000443402 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:38305105 C>A maps to ENST00000443402 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:33461069 G>A maps to ENST00000455217 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:33457372 G>A maps to ENST00000455217 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:33455162 C>T maps to ENST00000455217 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:102264440 G>C maps to NM_152334.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr15:102242580 G>C maps to NM_152334.2 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:6635142 C>T maps to NM_138697.3 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:19181195 G>A maps to NM_152232.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr1:19166790 G>A maps to NM_152232.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr1:19180754 G>A maps to NM_152232.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr1:19166329 G>A maps to NM_152232.2 F761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:1267465 C>A maps to NM_152228.1 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr5:9629958 G>A maps to NM_019599.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr5:9629280 T>C maps to NM_019599.2 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr5:9629541 C>T maps to NM_019599.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:10978172 G>A maps to NM_023921.1 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr12:11061486 G>A maps to NM_023920.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:11061285 G>A maps to NM_023920.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr12:11061429 C>T maps to NM_023920.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:11091368 T>C maps to NM_023922.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr7:122635250 A>T maps to NM_016945.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr12:11175080 T>A maps to NM_176888.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr12:11174443 G>A maps to NM_176888.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr7:141464575 C>T maps to NM_016943.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:11183778 C>T maps to NM_176885.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:11183043 C>G maps to NM_176885.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:141672667 G>A maps to NM_176817.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr7:141672583 G>A maps to NM_176817.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:141673225 C>T maps to NM_176817.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr7:141673456 G>C maps to NM_176817.4 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:141478515 G>A maps to NM_016944.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr7:142919245 C>T maps to NM_176882.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr7:142919269 C>T maps to NM_176882.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr7:143175525 C>A maps to NM_176883.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:143175186 C>A maps to NM_176883.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr7:143175435 A>G maps to NM_176883.2 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:11214110 G>A maps to ENST00000422992 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:11214515 C>T maps to NM_176887.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr7:141490604 C>T maps to NM_018980.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr12:11138841 G>C maps to NM_176890.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:11139066 C>T maps to NM_176890.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:11138871 C>T maps to NM_176890.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:11138910 C>T maps to NM_176890.2 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:143141255 C>A maps to NM_177437.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr7:143140946 G>A maps to NM_177437.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:143140715 G>A maps to NM_177437.1 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:143141133 C>T maps to NM_177437.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr12:10954989 G>A maps to NM_023919.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:10959147 G>C maps to NM_023918.1 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:10959183 C>T maps to NM_023918.1 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr20:13371099 C>T did not map to a codon.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr8:125506160 G>C maps to NM_032026.3 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:10291084 G>A maps to NM_014760.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr23:153649015 G>A did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:153648420 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:153641565 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:153648396 C>T did not map to a codon.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr4:38138874 G>A maps to NM_015173.2 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:38016215 G>A maps to NM_015173.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:38047457 G>A maps to NM_015173.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:37903766 C>A maps to NM_015173.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr4:38051363 G>A maps to NM_015173.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr22:30689979 G>A maps to ENST00000403477 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr22:30690931 C>A maps to ENST00000403477 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr22:30722696 G>A maps to ENST00000403477 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr22:30691790 C>T maps to ENST00000403477 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr22:30722747 G>A maps to ENST00000403477 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr22:30695462 C>T maps to ENST00000403477 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr22:30691031 T>C maps to ENST00000403477 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr16:30369852 C>T maps to NM_015527.3 E613E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:30376482 G>A maps to NM_015527.3 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr11:67172898 G>A maps to NM_198517.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr10:96162459 G>A maps to NM_015188.1 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr4:6925211 C>T maps to NM_001113361.1 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr4:6925442 C>T maps to NM_001113361.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:7011632 T>C maps to NM_001113361.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr12:72312229 G>T did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:72278769 G>T maps to NM_022771.4 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr12:72289856 T>C did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:77914882 G>A maps to NM_019020.2 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:77984302 G>T maps to NM_019020.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr19:50385366 C>T maps to NM_024682.2 H199H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr4:26719589 G>A maps to NM_018317.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr9:100973014 C>T maps to NM_018421.3 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:100971110 C>T maps to NM_018421.3 E663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:428598 C>A maps to ENST00000246077 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr15:74178504 T>A maps to NM_153356.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr6:37247259 C>T maps to NM_017772.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:2547030 C>T maps to ENST00000434757 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr16:2550907 C>T maps to ENST00000434757 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2546622 C>T maps to ENST00000434757 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr16:2546544 C>T maps to ENST00000434757 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr23:48417354 G>C did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:48418231 G>A did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr23:48419317 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:48418192 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr23:48417604 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:34499236 G>A maps to NM_001001417.5 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr13:75936701 C>T maps to ENST00000431480 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:75898413 C>T maps to ENST00000431480 Q719Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:101624354 G>A maps to NM_001102426.1 I1117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr23:106066677 C>T did not map to a codon.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr23:106097446 A>G did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr4:141543408 C>A maps to NM_015130.2 R1247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr4:141590934 G>A maps to NM_015130.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr4:141583130 A>T maps to NM_015130.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr4:141555228 T>C maps to NM_015130.2 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr4:141543480 C>T maps to NM_015130.2 E1223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:179296769 T>A maps to NM_198868.2 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr5:179291041 G>T maps to NM_198868.2 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr19:36616422 C>G maps to NM_001281.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr17:80763846 C>T maps to NM_005993.4 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:80865684 G>A maps to NM_005993.4 Q657Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:80863818 G>A maps to NM_005993.4 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:80726330 C>T maps to NM_005993.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr17:80772797 C>T maps to NM_005993.4 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr4:107016737 T>G maps to NM_001163436.1 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:45787868 G>C maps to NM_014726.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:9679749 C>T did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:9673049 G>A did not map to a codon.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr23:9659729 T>G did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr23:9683005 G>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr23:9660273 G>T did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:9652148 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:9665462 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr23:9679710 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr3:176765337 C>G did not map to a codon.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr24:6939822 G>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr24:6958153 C>A did not map to a codon.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr24:6911084 G>T did not map to a codon.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr24:6955317 G>C did not map to a codon.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr24:6938312 C>T did not map to a codon.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr7:72987686 G>A maps to NM_012453.2 H187H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:72988771 G>T maps to NM_012453.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:72985160 G>A maps to NM_012453.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:72985580 G>A maps to NM_012453.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr16:2025057 C>T maps to NM_006453.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:170871030 G>A maps to NM_003194.4 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr6:170873696 C>T maps to NM_003194.4 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:134305617 G>A did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr14:55903568 A>G maps to NM_199047.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr2:162273104 C>T maps to NM_006593.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:162276741 A>G maps to NM_006593.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:45141454 G>A maps to ENST00000404564 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:19766782 G>A maps to NM_080646.1 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr22:19766860 C>T maps to NM_080646.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:67399080 G>A maps to NM_005995.4 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:67399228 C>G maps to NM_005995.4 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:119474282 G>A maps to ENST00000369429 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:119427861 G>A maps to ENST00000369429 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:119466121 C>T maps to ENST00000369429 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr1:119427567 C>T maps to ENST00000369429 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr6:85469989 C>G maps to NM_001080508.1 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr6:85472389 C>G maps to NM_001080508.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:168281972 C>T maps to NM_005149.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:168260634 G>T maps to NM_005149.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr1:168274252 C>A maps to NM_005149.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:168250507 G>A maps to NM_005149.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr17:59482065 C>T maps to NM_005994.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:35242186 G>T maps to NM_001077653.2 S400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:35242347 G>C maps to NM_001077653.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr17:45820479 G>A maps to NM_013351.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:45821646 C>T maps to NM_013351.1 N285N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr23:79281197 G>A did not map to a codon.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr23:79279641 C>T did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr23:79281104 C>T did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr23:79282238 G>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:79281193 G>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:79286014 C>T did not map to a codon.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr23:79286051 G>T did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr23:79281178 A>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:79286535 G>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:79286336 T>G did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:79281157 T>A did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:79283535 T>C did not map to a codon.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr23:79282318 C>A did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr23:79281107 C>G did not map to a codon.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr23:79279588 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:79286154 C>T did not map to a codon.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr23:79281234 C>A did not map to a codon.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr12:115112611 G>A maps to NM_016569.3 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:114837438 T>G did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:114793738 G>T maps to NM_000192.3 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr12:114804165 G>C maps to NM_000192.3 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr16:30100022 C>T maps to NM_004608.3 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr19:3600020 G>A maps to NM_201636.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr14:92266696 G>A maps to NM_001128596.1 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr14:92265367 G>C maps to NM_001128596.1 S201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IF-01A-11D-A31L-08 chr14:92266687 G>A maps to NM_001128596.1 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr20:62701951 C>A maps to NM_003195.4 C261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr20:62701611 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:23751108 C>T maps to NM_003196.1 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:101382451 C>T did not map to a codon.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr23:101381888 G>T did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr23:101382141 A>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:101381992 C>T did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr23:101382276 G>T did not map to a codon.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr23:101381929 A>G did not map to a codon.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr23:102864203 G>A did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:102842016 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:102528930 C>G did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr23:102528983 A>C did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr23:102528877 T>G did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:101396189 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:101396230 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:101395945 C>T did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:101396020 G>A did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:102586457 C>T did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:102586385 A>T did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr23:102508842 C>T did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr8:74858963 C>T maps to NM_005648.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr1:24078973 C>T maps to NM_003198.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr1:24077646 C>A maps to NM_003198.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr1:24078327 C>G maps to NM_003198.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr1:24082409 T>C maps to NM_003198.2 Y649Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr18:44560255 T>C maps to NM_016427.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr18:44559811 G>T maps to NM_016427.2 Y608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr18:44559421 C>T maps to NM_016427.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr18:44561302 G>T maps to NM_016427.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:44561203 C>T maps to NM_016427.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr18:44555172 G>A maps to NM_145653.3 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr18:44555157 G>A maps to NM_145653.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:44555184 C>T maps to NM_145653.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:145838778 A>G maps to NM_006706.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:145838592 G>A maps to NM_006706.3 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:132965058 C>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:132965137 T>C maps to NM_174937.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr15:57565365 T>A maps to NM_207036.1 C628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr22:42607168 C>A maps to NM_005650.1 T1381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr22:42606031 G>A maps to NM_005650.1 S1760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr6:134210615 G>A maps to NM_003206.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:134210543 C>T maps to NM_003206.3 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr6:134210906 G>A maps to NM_003206.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr6:134210906 G>A maps to NM_003206.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:89977644 G>C maps to NM_014972.2 *677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr19:1619316 G>A maps to NM_003200.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr18:52901890 G>A maps to ENST00000398339 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:133481890 G>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:85536503 C>T maps to NM_031283.2 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:114910774 C>T maps to NM_030756.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr10:114919706 G>A maps to NM_030756.4 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr20:61492824 C>T maps to NM_006602.2 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr20:61488772 C>T maps to NM_006602.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr20:61488811 C>T maps to NM_006602.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IH-01A-11D-A25Y-08 chr1:152081315 A>G maps to NM_007113.2 R1459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr1:152082605 T>C maps to NM_007113.2 E1029E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:152083790 C>T maps to NM_007113.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:152083256 C>T maps to NM_007113.2 P812P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:152085380 G>A maps to NM_007113.2 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:152079983 G>A maps to NM_007113.2 S1903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr1:152081456 G>A maps to NM_007113.2 R1412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr1:152058472 G>C maps to NM_001008536.1 S562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:67818100 C>A maps to NM_006019.3 S795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr11:67815026 C>T maps to NM_006019.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:96152887 G>A maps to NM_004918.3 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:59622210 T>C maps to NM_001062.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:59622198 A>G maps to NM_001062.3 N349N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr11:59629132 C>A maps to NM_001062.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr5:149754238 C>A maps to ENST00000451292 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr5:149775922 C>G maps to ENST00000451292 S1324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr5:149754328 G>A maps to ENST00000451292 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:167787922 G>C maps to NM_004610.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr6:167786680 G>A maps to NM_004610.3 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr21:33954616 G>A maps to ENST00000431216 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:33954557 C>T maps to ENST00000431216 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr6:167595388 G>A maps to NM_001145121.1 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr6:167592605 T>A maps to NM_001145121.1 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:35088706 C>A maps to NM_001093728.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr11:33076193 C>T maps to NM_001145541.1 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:33094116 G>A maps to NM_001145541.1 E475E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr12:106708239 C>T maps to NM_152772.1 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:106708195 C>G maps to NM_152772.1 S73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:44254174 C>G maps to NM_182539.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr6:44247947 A>T maps to NM_182539.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr6:44254021 C>T maps to NM_182539.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:44254207 G>A maps to NM_182539.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr6:170140340 A>G maps to NM_174910.1 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:67236138 G>A maps to NM_152665.2 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr1:45271806 C>T maps to NM_001013632.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:111078306 G>C maps to NM_001082538.2 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:124156102 C>T maps to NM_024809.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr10:97440279 C>T maps to ENST00000371217 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr4:156825276 T>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:156841120 C>T maps to NM_005651.2 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr14:90433739 C>T maps to NM_018319.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr14:90458310 C>T maps to NM_018319.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr14:90450868 G>A maps to NM_018319.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:24658076 G>A maps to NM_016614.2 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr10:115962044 G>A maps to NM_198795.1 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:115973129 G>A maps to NM_198795.1 W619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr10:115947745 T>C maps to NM_198795.1 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr10:115980378 G>A maps to NM_198795.1 Q849Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr10:115978257 C>T maps to NM_198795.1 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr10:115970472 A>G maps to NM_198795.1 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:154492808 C>T maps to NM_001098475.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:154516994 T>A did not map to a codon.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr13:61034584 T>G maps to NM_001146070.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:179587801 A>G maps to ENST00000444136 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:179603611 G>T maps to ENST00000444136 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:179562646 G>A maps to ENST00000444136 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:179609567 G>A maps to ENST00000444136 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr1:179561884 C>G maps to ENST00000444136 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:46657052 G>A maps to NM_001010870.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr6:46661018 G>A maps to NM_001010870.2 Q1718Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:46657373 G>A maps to NM_001010870.2 W503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr6:46658978 C>T maps to NM_001010870.2 T1038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr6:46661853 G>T maps to NM_001010870.2 E1997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:46660212 G>T maps to NM_001010870.2 E1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr6:46661853 G>T maps to NM_001010870.2 E1997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr6:46657034 G>A maps to NM_001010870.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:46659965 T>C maps to NM_001010870.2 N1367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr6:46658912 A>G maps to NM_001010870.2 S1016S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:104474747 A>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:49850455 G>C maps to NM_003598.1 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:35443390 G>A maps to ENST00000357281 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:3149529 G>A did not map to a codon.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:48172262 A>C did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:48152890 G>C maps to NM_003215.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr7:97873900 G>A maps to ENST00000379795 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr7:97852364 G>T maps to ENST00000379795 L957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:97872808 C>A maps to ENST00000379795 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:97874005 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:97861193 G>A maps to ENST00000379795 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr7:97851779 G>A maps to ENST00000379795 I996I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr14:102898196 G>T maps to NM_014844.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr14:102874943 G>C maps to NM_014844.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr14:102900896 G>T maps to NM_014844.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:102963964 C>T maps to NM_014844.3 N1330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr4:65175549 C>T maps to NM_001010874.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr4:65147242 G>A maps to NM_001010874.4 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr4:65240896 G>A maps to NM_001010874.4 H93H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:120998983 G>A maps to NM_005422.2 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:121000846 T>G maps to NM_005422.2 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr11:121000525 C>T maps to NM_005422.2 C849C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr11:121016544 C>A maps to NM_005422.2 T1275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:120989054 G>A maps to NM_005422.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:121058639 C>T maps to NM_005422.2 Y2033Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr11:121016586 C>T maps to NM_005422.2 A1289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr11:121008283 G>A maps to NM_005422.2 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:120998602 C>T maps to NM_005422.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:121008260 C>T maps to NM_005422.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr11:120984287 C>T maps to NM_005422.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:121008715 C>A maps to NM_005422.2 Y1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr11:120989411 C>T maps to NM_005422.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr11:120980008 C>T maps to NM_005422.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr11:121028674 C>T maps to NM_005422.2 R1477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr11:120998953 G>A maps to NM_005422.2 K756K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr10:114044407 C>T maps to NM_058222.1 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:27218814 G>T maps to NM_000459.3 G1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr9:27220086 C>T maps to NM_000459.3 Y1048Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:6722666 G>C maps to NM_053285.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:6703348 G>A maps to NM_053285.1 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:6704169 C>T maps to NM_053285.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:36552863 G>T maps to NM_014466.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:15231308 C>A maps to NM_031898.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:15215749 G>C maps to NM_031898.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr2:95537572 G>A maps to NM_144705.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr16:10788292 C>G maps to NM_144674.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr16:10729667 C>G maps to NM_144674.1 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:1544452 C>T maps to NM_016111.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr16:1550119 G>T maps to NM_016111.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr16:1559927 G>A maps to NM_016111.3 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr12:53455638 G>A maps to NM_170754.2 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:53453557 G>A maps to NM_170754.2 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr12:53450796 G>A maps to NM_170754.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr14:20849088 C>T did not map to a codon.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr14:20836998 C>T maps to NM_007110.4 K2573K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:20849804 G>A maps to NM_007110.4 L1489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr14:20837658 G>A maps to NM_007110.4 T2500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20845879 G>A maps to NM_007110.4 P1918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr14:20852262 C>T maps to NM_007110.4 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr14:20836705 G>A maps to NM_007110.4 R2592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr14:20848552 G>C maps to NM_007110.4 S1615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:20876529 A>G maps to NM_007110.4 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:20844027 C>T did not map to a codon.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr14:20852059 G>A maps to NM_007110.4 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:73942627 G>A maps to NM_017489.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr8:73942568 A>G did not map to a codon.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr8:73921393 C>T maps to NM_017489.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:75681827 T>C maps to NM_018975.3 H16H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr5:1253932 C>A maps to NM_198253.2 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:1282689 C>A maps to NM_198253.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr5:1272361 G>T maps to NM_198253.2 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr5:1268651 C>T maps to NM_198253.2 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr5:1264628 G>A maps to NM_198253.2 D911D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr7:115892373 G>A maps to NM_015641.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:35609310 C>T maps to NM_006285.2 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr9:35609463 C>A maps to NM_006285.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr1:45923295 C>T maps to NM_007170.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr10:70441246 T>C did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:70406097 T>C maps to NM_030625.2 H1204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:70405629 C>A maps to NM_030625.2 C1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:70406352 G>A maps to NM_030625.2 T1289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr10:70333693 C>T maps to NM_030625.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr10:70451318 C>T maps to NM_030625.2 N2053N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr4:106157589 C>T maps to ENST00000513237 Q852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr4:106156861 C>A maps to ENST00000513237 S609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr4:106156607 G>A maps to ENST00000513237 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr4:106158041 T>A maps to ENST00000513237 I1002I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:106156427 A>G maps to ENST00000513237 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:106156785 G>T maps to ENST00000513237 G584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr4:106156746 C>T maps to ENST00000513237 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr4:106158209 C>A maps to ENST00000513237 A1058A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr2:74274964 C>T maps to ENST00000409262 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr2:74274705 T>A maps to ENST00000409262 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:103109583 G>A maps to NM_017746.3 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr23:69826835 C>T did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr23:69749730 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:69871333 G>A did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr23:70026594 G>T did not map to a codon.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr23:69811632 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr23:70080743 G>C did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:104464878 G>A did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr23:104464802 C>A did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:104465005 C>A did not map to a codon.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr23:104464899 C>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:104463829 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:104464079 C>T did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr23:104464102 G>T did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr23:104463740 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:104464338 G>C did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr23:104464967 A>T did not map to a codon.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr23:104463773 G>A did not map to a codon.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr23:107225291 G>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:107224686 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr17:56651594 T>C maps to ENST00000240361 Q1158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:56700248 T>A maps to ENST00000240361 K126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:56664946 C>T maps to ENST00000240361 W934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:30702708 C>G maps to NM_031271.3 V1275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr8:30703494 T>C maps to NM_031271.3 T1013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr8:30695297 C>T maps to NM_031271.3 K2451K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:30694436 A>G maps to NM_031271.3 P2738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr8:30699681 A>G maps to NM_031271.3 N2284N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:62291205 T>C maps to NM_018469.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr17:62238186 C>T maps to NM_018469.3 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:62232278 G>A maps to NM_018469.3 S958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr3:133486975 A>G maps to NM_001063.3 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr3:133478160 C>T maps to NM_001063.3 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr6:10398700 G>A maps to ENST00000379613 H423H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr6:50810825 G>A maps to ENST00000263046 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr6:50810852 G>A maps to ENST00000263046 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr6:50786669 C>T maps to ENST00000263046 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:50803960 C>T maps to ENST00000263046 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:50803948 C>G maps to ENST00000263046 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:50696656 G>A maps to NM_172238.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr6:50740384 G>A maps to NM_172238.3 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr6:50740408 T>A maps to NM_172238.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:50740573 C>T maps to NM_172238.3 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:155618125 T>C maps to NM_016020.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:246704440 T>C maps to NM_022366.2 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr1:246704443 C>T maps to NM_022366.2 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr2:122038714 C>T maps to NM_014553.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:121995389 G>A maps to NM_014553.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr2:121989536 G>A maps to NM_014553.2 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:114294438 C>T maps to NM_007111.4 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr3:141692898 C>T maps to NM_001178139.1 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:132351547 A>T did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr23:132351158 C>A did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr23:48888087 G>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:48891045 C>T did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr23:48891648 C>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:41653830 G>T maps to ENST00000343317 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:41653836 G>A maps to ENST00000343317 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr6:41658472 G>C maps to ENST00000343317 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr6:41653975 C>G did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr7:115624313 A>G did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr21:43786544 G>A maps to NM_003225.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:100463728 G>A maps to NM_001007565.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:26894917 G>A maps to NM_012143.2 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:26895393 G>A maps to NM_012143.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr22:26895270 G>T maps to NM_012143.2 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr22:26902302 G>A maps to NM_012143.2 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr19:54611506 C>T maps to NM_013342.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr19:54617895 G>T maps to NM_013342.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:100229800 G>A maps to NM_003227.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr7:100238306 A>G did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:195782121 C>G maps to NM_001128148.1 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr3:195792458 T>C maps to NM_001128148.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr3:195798985 C>A maps to NM_001128148.1 G158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:195798887 A>T maps to NM_001128148.1 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr8:133909915 C>G maps to NM_003235.4 R1008R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr8:133925508 C>T maps to NM_003235.4 C1459C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr8:134042150 C>T maps to NM_003235.4 G2374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr8:134144070 G>A maps to NM_003235.4 A2626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr8:133978853 C>A maps to NM_003235.4 V1866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr8:134030137 C>T maps to NM_003235.4 D2226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr8:133898694 G>T maps to NM_003235.4 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:133898882 C>G maps to NM_003235.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:133885313 G>A maps to NM_003235.4 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:134034303 G>A maps to NM_003235.4 P2315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:133899038 G>A maps to NM_003235.4 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:133984059 G>A maps to NM_003235.4 R1999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:134147016 C>T maps to NM_003235.4 G2762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr8:133899062 G>A maps to NM_003235.4 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:133895230 G>A maps to NM_003235.4 E354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr8:133899689 A>G maps to NM_003235.4 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr19:41854244 C>A maps to NM_000660.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:41854274 G>A maps to NM_000660.4 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr16:31488683 G>A maps to NM_001042454.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr1:218609453 G>A maps to NM_001135599.2 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr1:218614595 C>A maps to NM_001135599.2 C407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:135379744 A>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:135394833 G>T maps to NM_000358.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr5:135385249 C>T maps to NM_000358.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr9:101907134 T>C maps to NM_004612.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:101900208 C>T maps to NM_004612.2 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr3:30713558 C>G maps to NM_001024847.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr3:30729874 G>A did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:30713697 C>T maps to NM_001024847.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr3:30691946 C>G maps to NM_001024847.2 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr3:30732962 G>T maps to NM_001024847.2 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:30691946 C>G maps to NM_001024847.2 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr3:30713558 C>G maps to NM_001024847.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:30713871 G>A maps to NM_001024847.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr3:30729916 G>T maps to NM_001024847.2 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr3:30729874 G>A did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:92177865 C>A maps to NM_003243.4 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr1:92177928 C>T maps to NM_003243.4 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:105912814 G>A maps to NM_004257.4 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:105897017 G>A maps to NM_004257.4 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6I0-01A-11D-A31L-08 chr2:105892031 C>T maps to NM_004257.4 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr2:105915091 C>T maps to NM_004257.4 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr23:89177311 C>G did not map to a codon.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr23:89177195 G>A did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:89177111 G>T did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr23:89177579 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:89177626 G>T did not map to a codon.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr23:89177093 G>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr14:24723869 C>G maps to NM_000359.2 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr20:36767844 C>T maps to NM_004613.2 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:2293572 C>T maps to NM_003245.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr20:2297757 C>T maps to NM_003245.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr20:2315840 G>A maps to NM_003245.3 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:2308910 G>A maps to NM_003245.3 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:44951843 G>A maps to NM_003241.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr15:43552358 C>G maps to NM_201631.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr15:43545011 G>C maps to NM_201631.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr15:43526972 C>T maps to NM_201631.3 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr20:2375140 C>T maps to NM_198994.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr20:2413287 G>T maps to NM_198994.2 *707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr20:2397911 G>T maps to NM_198994.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr15:43585694 G>T maps to NM_052955.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr2:85554338 C>T maps to ENST00000409015 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr8:56699251 G>A maps to NM_024831.6 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:2189384 G>T maps to NM_199292.2 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr11:2190936 G>A maps to NM_199292.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr20:57568726 C>T maps to NM_198976.1 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:43801883 C>T maps to ENST00000330266 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:43808910 C>T maps to ENST00000330266 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr2:43819111 T>C maps to ENST00000330266 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:43779472 T>A maps to ENST00000330266 K895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr2:43547612 G>T maps to ENST00000330266 L1471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr2:43755034 G>A maps to ENST00000330266 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:42693173 G>A maps to NM_018105.2 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr8:42693376 G>A maps to NM_018105.2 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr12:72070611 G>A maps to NM_031435.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:242576354 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:242576369 G>C maps to NM_015963.5 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr2:242573431 C>T maps to NM_015963.5 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr2:242572368 G>A maps to NM_015963.5 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:83838783 G>C maps to NM_024672.4 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr20:23028617 C>A maps to NM_000361.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr20:23029289 C>G maps to NM_000361.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr20:23029298 G>A maps to NM_000361.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr15:39881287 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:39880793 G>A maps to NM_003246.2 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr15:39874093 G>C maps to NM_003246.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr6:169632833 G>A maps to NM_003247.2 C619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr6:169640558 C>G maps to NM_003247.2 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr6:169648544 C>T maps to NM_003247.2 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr6:169640615 C>T maps to NM_003247.2 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:155167906 G>T maps to NM_007112.3 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:155167838 G>T maps to NM_007112.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:155174871 C>T maps to NM_007112.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:155172168 G>A maps to NM_007112.3 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:155165633 A>G maps to NM_007112.3 *957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr5:79372722 C>T maps to NM_003248.4 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr5:79372809 G>A maps to NM_003248.4 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr19:375820 C>T maps to NM_016585.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:362331 G>A maps to NM_016585.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr19:371323 T>A did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr19:374408 G>A maps to NM_016585.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:128134450 C>T maps to NM_001164685.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr6:128134537 G>A maps to NM_001164685.1 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr6:128176228 G>A maps to NM_001164685.1 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr5:157166326 A>T did not map to a codon.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr2:88474335 C>T maps to NM_018271.3 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:88478356 G>A maps to NM_018271.3 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:88472780 T>C maps to NM_018271.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr23:122747345 G>C did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:122799666 A>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:122866839 C>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr23:122755303 C>T did not map to a codon.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr23:122774414 T>C did not map to a codon.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr23:122805560 G>C did not map to a codon.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr23:122759891 T>C did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr23:122765597 G>C did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:122802033 T>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:122778701 G>A did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr23:122820423 G>C did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:122866816 G>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:122767862 C>T did not map to a codon.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr23:122767907 T>C did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:122837337 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:122755257 C>T did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr23:122747942 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:122757983 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:122778705 G>C did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:79847181 C>T maps to NM_005782.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:79846021 C>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:29927883 G>A maps to NM_003678.4 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr19:2810357 G>A maps to NM_003249.3 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr19:2811698 G>A maps to NM_003249.3 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr3:184090792 G>C maps to NM_000460.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:36755246 G>T maps to NM_005119.3 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:36752625 C>T maps to NM_005119.3 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr3:24193919 G>T maps to NM_001128177.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:77775067 C>G maps to NM_003251.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr13:52960271 C>A maps to NM_018676.3 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr13:52971384 G>A maps to NM_018676.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr15:72023536 G>A maps to NM_024817.2 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:11450925 C>A maps to ENST00000423059 E1236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr7:11441596 T>A did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr7:11630168 C>T maps to ENST00000423059 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr7:11464387 G>A maps to ENST00000423059 I1106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr7:11676025 G>C maps to ENST00000423059 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:11675952 T>A maps to ENST00000423059 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr7:11630195 G>A maps to ENST00000423059 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:11676129 G>T maps to ENST00000423059 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr7:11468651 C>G maps to ENST00000423059 V1055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:11501729 G>A maps to ENST00000423059 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:11521553 G>A maps to ENST00000423059 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:11633119 C>T maps to ENST00000423059 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr7:11676004 C>A maps to ENST00000423059 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr7:11675890 G>A maps to ENST00000423059 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:11446682 C>T did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:11446682 C>A did not map to a codon.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr7:11500388 C>T maps to ENST00000423059 W835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr2:138169278 A>G maps to ENST00000272643 G932G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:138376010 C>T maps to ENST00000272643 V1208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:137852676 G>A maps to ENST00000272643 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr2:138169407 A>G maps to ENST00000272643 G975G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:137872795 G>A maps to ENST00000272643 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:137814024 G>T maps to ENST00000272643 G59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:138169329 A>C maps to ENST00000272643 G949G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr16:20748522 G>A maps to ENST00000431224 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr3:9412932 G>T maps to NM_015453.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr3:9426230 A>G maps to NM_015453.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:9426355 G>A maps to NM_015453.2 W503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:70451686 C>T maps to NM_022173.2 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr2:70475553 G>A maps to NM_022173.2 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr10:121336172 C>T maps to NM_001033925.1 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr10:121339444 A>T did not map to a codon.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr10:121342099 G>C maps to NM_001033925.1 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr21:32582411 C>G maps to NM_003253.2 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr21:32638553 T>G maps to NM_003253.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr21:32639126 C>G maps to NM_003253.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr21:32639147 C>T maps to NM_003253.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:32492802 G>C maps to NM_003253.2 L1553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:32513498 G>A maps to NM_003253.2 I1237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr21:32595907 C>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:32585737 A>G maps to NM_003253.2 F731F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:155578188 C>G maps to ENST00000456144 V1709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:155450863 G>T maps to ENST00000456144 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr6:155569308 G>C maps to ENST00000456144 L1276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:4817883 G>T maps to NM_182919.2 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:43778210 C>G maps to NM_005424.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:43770796 C>A maps to NM_005424.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr1:43777408 G>A maps to NM_005424.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:43778830 C>T maps to NM_005424.2 H651H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:43774666 C>T maps to NM_005424.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr4:113199440 G>A maps to NM_052864.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr11:65123650 G>A maps to NM_145719.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr11:65124616 A>G maps to NM_145719.2 E446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr4:153691670 C>T maps to NM_145720.2 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:144681056 G>T maps to NM_032862.4 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr5:156390191 G>A maps to NM_138379.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr5:156346536 T>A maps to NM_138379.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr5:156381552 C>T maps to NM_138379.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr5:156381756 A>C maps to NM_138379.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr12:56815187 C>A maps to NM_003920.3 E939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr12:56827432 C>T maps to NM_003920.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:56815167 C>T maps to NM_003920.3 K945K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:7999065 C>A maps to NM_006351.3 E151*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-7568-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:39972551 T>C maps to NM_001001563.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:39976375 G>T maps to NM_001001563.1 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr23:47442864 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr23:47445925 C>T did not map to a codon.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr17:76851859 G>A maps to NM_003255.4 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr22:33253267 G>C maps to NM_000362.4 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr3:12198896 G>T maps to NM_003256.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:12198974 C>T maps to NM_003256.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr6:54254653 A>G maps to NM_014464.3 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:54214630 C>T maps to NM_014464.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:54245332 A>T maps to NM_014464.3 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr1:32049107 G>T maps to NM_022164.2 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr1:32051465 C>G maps to NM_022164.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:24710318 G>A maps to NM_001099274.1 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr14:24711352 C>T maps to NM_001099274.1 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:156411958 A>T maps to NM_015508.4 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr15:66645272 G>A maps to NM_017858.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:126162996 A>T maps to NM_148910.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr6:43472752 G>A maps to NM_001146016.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr6:43469293 C>G maps to NM_001146016.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr15:30018666 A>G maps to NM_003257.3 N776N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr15:30011210 G>A maps to NM_003257.3 Y1045Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr15:30025363 C>T maps to NM_003257.3 W557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:30058574 T>C maps to NM_003257.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:71845072 G>C maps to NM_004817.3 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:71866154 G>T maps to NM_004817.3 E1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:3747952 G>A maps to NM_014428.1 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:3740699 C>T maps to NM_014428.1 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr17:76170974 G>A maps to NM_003258.4 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr16:66562952 C>T maps to ENST00000299697 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr3:53263449 C>T maps to ENST00000423516 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:153539313 C>G did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:153533682 T>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:153524311 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:153539192 G>A did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:153524216 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr23:153539341 G>A did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:153555957 G>T did not map to a codon.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr4:164394487 T>A maps to NM_032136.4 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr4:164393620 C>G maps to NM_032136.4 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:164394268 G>A maps to NM_032136.4 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr9:84226785 C>T maps to NM_005077.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:84230974 C>T maps to NM_005077.3 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:84205763 G>A maps to NM_005077.3 D595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:84208112 C>A maps to NM_005077.3 G470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr19:3005476 C>A maps to NM_003260.4 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:3009611 C>A maps to NM_003260.4 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr19:3011065 G>A maps to NM_003260.4 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:3028340 C>A maps to NM_003260.4 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr15:70351091 G>A maps to NM_005078.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr15:70368498 T>C did not map to a codon.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr9:82333858 G>A maps to ENST00000376537 K553K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:2993527 C>T maps to NM_001143986.1 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr17:60657495 T>C maps to ENST00000326270 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr17:60663566 G>A maps to ENST00000326270 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:166981313 G>T maps to ENST00000507499 E684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:166910617 C>A maps to ENST00000507499 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:166916210 A>G did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:98170211 C>T maps to NM_012465.3 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:98133494 C>T maps to NM_012465.3 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr10:98188452 G>C maps to NM_012465.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:98157000 C>T maps to NM_012465.3 W442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:98127952 A>G maps to NM_012465.3 G980G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr10:98129947 G>T maps to NM_012465.3 Y929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr9:35717215 A>T maps to NM_006289.3 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr9:35724887 C>T maps to NM_006289.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr15:63076077 G>T maps to NM_015059.2 E1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:62993360 T>C maps to NM_015059.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr15:62942334 G>A maps to NM_015059.2 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr15:62939592 C>G maps to NM_015059.2 Y28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:63017194 G>C maps to NM_015059.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:63068994 C>T maps to NM_015059.2 A1800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:63125773 C>T maps to NM_015059.2 S2358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr15:62989910 C>T maps to NM_015059.2 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr4:38800206 C>T maps to NM_003263.3 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr4:38799111 G>A maps to NM_003263.3 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr4:38776140 A>G maps to NM_030956.3 N357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr4:38776632 C>A maps to NM_030956.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr4:38776527 A>G maps to NM_030956.3 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr4:187004612 C>T maps to NM_003265.2 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:187004930 A>G maps to NM_003265.2 K697K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr4:187004654 C>G maps to NM_003265.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr4:187004156 C>T maps to NM_003265.2 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr4:187004363 G>A maps to NM_003265.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:120476115 T>C maps to NM_138554.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:120470942 C>T maps to NM_138554.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr9:120475764 C>T maps to NM_138554.3 D453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:120470932 C>T maps to NM_138554.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr9:120470944 G>A maps to NM_138554.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:120476304 C>T maps to NM_138554.3 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:120475060 C>T maps to NM_138554.3 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:120476799 G>A maps to NM_138554.3 E798E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr9:120476221 C>T maps to NM_138554.3 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr1:223285719 T>C maps to NM_003268.5 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr1:223284504 A>G maps to NM_003268.5 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr1:223284666 T>C maps to NM_003268.5 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr1:223284384 G>A maps to NM_003268.5 F663F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:38829446 C>A maps to NM_006068.3 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr23:12905766 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr23:12904895 G>C did not map to a codon.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr23:12905258 G>C did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:12905662 A>G did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:12904443 T>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:12906381 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:12906089 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:12906090 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:12904438 C>T did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:12903861 G>C did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:12904933 C>G did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:12904322 C>G did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:12905258 G>C did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:12938836 G>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:12937727 C>A did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr23:12938008 C>G did not map to a codon.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr23:12937992 A>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr23:12939288 T>C did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:12938749 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:12939676 A>G did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:12939040 G>T did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:12939372 G>A did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:12939091 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr3:52257251 G>A maps to ENST00000494383 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr3:52255721 G>A maps to ENST00000494383 Y1023Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr3:52255538 G>A maps to ENST00000494383 R1084R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr2:74743314 G>C maps to NM_016170.4 *285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:74742934 G>A maps to NM_016170.4 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:149039270 G>A maps to NM_138786.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr3:149216508 G>C maps to NM_004617.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr17:4686421 G>A maps to NM_003963.2 *198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr15:83793512 C>T maps to NM_023003.3 C231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr15:83796129 T>C maps to NM_023003.3 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr19:19377412 C>G maps to NM_001001524.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr11:64883455 G>A maps to NM_003273.2 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr11:64881044 G>C maps to NM_003273.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:105367307 C>T maps to NM_030788.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr8:105361224 C>T maps to NM_030788.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:105361228 G>A maps to NM_030788.2 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr14:24662132 G>A maps to NM_006405.5 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr14:24658621 C>G maps to NM_006405.5 *607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr13:100193873 C>A maps to NM_004800.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:100193036 C>T maps to NM_004800.1 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:98311120 A>G maps to NM_020123.3 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr20:30723920 C>G maps to NM_014742.3 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr20:30729429 C>T maps to NM_014742.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:30730847 C>T maps to NM_014742.3 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr12:66531826 G>A maps to ENST00000286424 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:50152484 G>A maps to NM_001098576.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:75435902 C>T maps to NM_138691.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr9:75435994 C>T maps to NM_138691.2 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr20:2542576 C>T maps to NM_080751.2 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr20:2577847 C>T maps to NM_080751.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:2560665 T>A maps to NM_080751.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr20:2517942 G>A maps to NM_080751.2 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr20:2593869 C>T maps to NM_080751.2 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:54664093 G>C maps to NM_001145303.1 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:54668179 G>A maps to NM_001145303.1 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr16:19501761 C>T maps to NM_001105248.1 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr16:19460862 G>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:19488759 A>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:19477441 C>T maps to NM_001105248.1 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr16:19501747 C>T maps to NM_001105248.1 R869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:76121047 C>T maps to NM_007267.6 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr16:19033065 G>A maps to NM_024847.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr16:19058453 T>C maps to NM_024847.3 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr16:19047108 G>A maps to NM_024847.3 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr16:19056250 G>T maps to NM_024847.3 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr17:76133868 C>T maps to NM_152468.4 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr17:76128899 G>T maps to NM_152468.4 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:76134711 G>A maps to NM_152468.4 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:76130014 G>A maps to NM_152468.4 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr17:76137078 G>A maps to NM_152468.4 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:205238350 C>T maps to NM_014858.3 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:205238547 C>T maps to NM_014858.3 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:205238142 C>T maps to NM_014858.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr1:205240254 C>A maps to NM_014858.3 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:94975822 C>T maps to NM_020698.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:165737483 G>A maps to NM_019026.3 Y31Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:165721336 A>G did not map to a codon.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr13:114150216 A>G maps to NM_017905.4 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:20027337 C>A maps to NM_181719.4 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:20009577 G>A maps to NM_181719.4 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr1:20027286 G>A maps to NM_181719.4 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr5:140023220 T>C maps to ENST00000252100 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:68961607 C>A maps to NM_024562.1 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr16:68894424 G>T maps to NM_024562.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr12:124069242 C>G maps to NM_006815.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr7:44619143 G>A maps to NM_182547.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr16:69385575 T>A maps to NM_144676.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:69377540 G>A maps to NM_144676.3 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:69377543 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr14:77809653 C>A maps to NM_213601.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr5:177022350 C>T maps to NM_017510.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr2:192818508 T>C maps to NM_016192.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr2:193049122 C>T maps to NM_016192.2 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:42092251 G>A maps to NM_032376.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr17:72791737 C>T maps to NM_017728.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr17:72832684 G>A maps to NM_017728.3 Q450Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr7:12258147 G>A did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr7:12263953 A>G maps to NM_018374.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr7:12263944 C>T maps to NM_018374.3 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr17:8077875 C>T maps to NM_032354.3 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr3:133109138 G>A maps to NM_001136469.1 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr11:60689393 G>C maps to NM_024092.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr3:52877739 G>C maps to ENST00000504329 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:50392779 C>T maps to NM_007024.4 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:112374540 G>A maps to NM_001193531.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr12:112369502 C>T maps to NM_001193531.1 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr12:44781845 G>A maps to NM_032256.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr12:108985565 C>T maps to NM_181724.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr12:122213540 C>T maps to NM_001080825.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr12:122181638 G>A maps to NM_001080825.2 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr14:105995410 C>T maps to NM_025268.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:102272785 G>C maps to NM_052932.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:85365268 C>T maps to NM_032273.3 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr11:85366749 C>G maps to NM_032273.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr4:1719931 G>A maps to NM_001127266.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr7:98453742 G>A maps to NM_001134450.1 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr7:98446237 G>T maps to NM_001134450.1 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr7:98446223 C>T maps to NM_001134450.1 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:98449122 C>T maps to NM_001134450.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:98457824 G>A maps to NM_001134450.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr2:98408978 C>T maps to NM_015348.1 A1338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr2:98411467 A>C maps to NM_015348.1 L1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:98422127 G>A maps to NM_015348.1 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr2:98421911 A>G maps to NM_015348.1 I737I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr2:98543937 G>C maps to NM_015348.1 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:60694841 G>A maps to NM_017870.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:60696150 C>T maps to NM_017870.3 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr11:60702151 C>T maps to NM_017870.3 H585H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr11:60699156 G>A did not map to a codon.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr11:60699311 C>T maps to NM_017870.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:126138490 G>A maps to NM_052907.2 Q824Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:126128736 G>A maps to NM_052907.2 W513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:125834436 C>T maps to NM_052907.2 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr12:126138781 G>A maps to NM_052907.2 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr12:130184674 C>T maps to NM_133448.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr12:130184677 G>A maps to NM_133448.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr12:130184665 C>T maps to NM_133448.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr12:129694086 G>T maps to NM_133448.2 S474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr12:129558509 C>T maps to NM_133448.2 E1070E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr12:130185046 G>A maps to NM_133448.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:130185031 G>A maps to NM_133448.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr12:129569217 G>T maps to NM_133448.2 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr12:130184734 C>G maps to NM_133448.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr12:130184664 C>A maps to NM_133448.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:129559165 C>A maps to NM_133448.2 G852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr12:130185207 T>G maps to NM_133448.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr12:129563219 C>A maps to NM_133448.2 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:129558524 G>A maps to NM_133448.2 I1065I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:32964776 G>A maps to NM_207313.1 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr17:32953440 G>A maps to NM_207313.1 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr17:32962096 C>G maps to NM_207313.1 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr17:32964776 G>A maps to NM_207313.1 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:86868384 C>T maps to NM_022918.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:87032373 G>A maps to NM_022918.3 *459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr11:61131944 C>G maps to NM_016464.4 S28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:139686221 C>T maps to NM_032928.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:42827883 C>T maps to ENST00000406159 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:42820841 C>T maps to ENST00000406159 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr19:5749194 G>A did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr19:5776179 G>A maps to NM_152784.3 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:5768220 C>G maps to NM_152784.3 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:5776248 C>A maps to NM_152784.3 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr19:5749164 C>T maps to NM_152784.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:5754219 G>A maps to NM_152784.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr19:5772835 G>T maps to NM_152784.3 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:5776272 C>T maps to NM_152784.3 F681F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr19:5772957 C>T maps to NM_152784.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr19:36037695 G>A maps to NM_032635.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:36037924 C>T maps to NM_032635.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:36037858 A>G maps to NM_032635.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:55824412 G>A maps to NM_001085488.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr19:55831442 C>A maps to NM_001085488.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr19:55824406 G>T maps to NM_001085488.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr19:55824418 G>A maps to NM_001085488.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:55824271 G>A maps to NM_001085488.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr4:83411226 G>A maps to NM_001080506.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr11:66062448 C>T maps to NM_153266.3 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:153565565 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:153565594 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:39000473 A>C maps to NM_024943.1 Y48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:21181822 C>T maps to ENST00000451578 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:19230816 G>A maps to NM_017814.1 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:19231607 G>A maps to NM_017814.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr19:19232401 G>A maps to NM_017814.1 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr23:109310601 C>T did not map to a codon.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr4:56291573 G>A maps to NM_018475.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr7:112407740 G>C maps to NM_022484.4 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr7:112407305 C>T maps to NM_022484.4 W680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:72427520 A>T maps to NM_173490.6 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:138858007 G>A maps to NM_198282.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:946234 G>C maps to NM_032326.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr4:941649 C>T maps to NM_032326.2 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:39944276 C>T maps to NM_152390.2 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr2:39934240 C>T maps to NM_152390.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr14:105070799 G>A maps to NM_207379.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr11:62557443 G>A maps to NM_199337.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr10:104233471 C>A maps to NM_024789.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr10:104233348 T>C maps to NM_024789.3 H316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr6:158957801 C>G maps to NM_020823.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr6:159050834 G>A maps to NM_020823.1 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr2:103414409 C>T maps to NM_144632.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr7:1590489 G>T maps to NM_001097620.1 Y116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr7:1588284 G>A maps to NM_001097620.1 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr7:1586683 C>T maps to NM_001097620.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr23:148693014 C>G did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr23:153248202 G>A did not map to a codon.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr23:153247751 T>C did not map to a codon.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr23:153247559 G>C did not map to a codon.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr16:50063657 C>G maps to NM_153261.4 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:48744599 G>C maps to NM_199203.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr20:48760045 G>C maps to NM_199203.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr12:72090219 A>G maps to NM_018279.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr12:72094708 G>T maps to NM_018279.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:72091108 A>G maps to NM_018279.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr19:55889197 G>A maps to NM_139172.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:55889465 C>T maps to NM_139172.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:57454715 C>T maps to NM_001130963.1 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr12:57457025 G>A maps to NM_001130963.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:15601452 G>T maps to NM_001004320.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:19765223 G>T maps to NM_152774.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr7:19765250 G>A maps to NM_152774.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr2:220412471 C>T maps to NM_001005209.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:220412741 C>T maps to NM_001005209.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:220409615 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:74365159 G>A maps to NM_013390.2 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr9:74332990 G>A maps to NM_013390.2 R758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:74360280 T>C maps to NM_013390.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr9:74313119 C>T maps to NM_013390.2 G1126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:95658361 C>T maps to NM_001134658.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:130762866 G>T maps to NM_052913.2 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr6:130762718 C>G maps to NM_052913.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr6:130762241 C>G maps to NM_052913.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:130762040 A>T maps to NM_052913.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:5891897 G>A maps to NM_001080209.1 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:5891786 C>T maps to NM_001080209.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr18:5891792 C>G maps to NM_001080209.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:9657023 G>A maps to NM_001130924.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:72691139 A>G maps to NM_001080462.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr15:72690696 T>C maps to NM_001080462.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr15:72700047 C>G maps to NM_001080462.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr9:140099677 G>A maps to NM_053045.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr1:212583848 C>T maps to NM_001198862.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr9:32784252 T>A maps to NM_212558.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr3:136573475 G>C maps to NM_025246.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:136573800 C>T maps to NM_025246.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr3:136573745 G>C maps to NM_025246.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:27661902 C>T maps to NM_032125.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:62559382 C>T maps to NM_001080501.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:123756045 G>A maps to NM_001013743.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:123753940 T>C maps to NM_001013743.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:75579248 C>T did not map to a codon.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr10:63170316 G>A maps to NM_178505.6 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr23:15682495 C>A did not map to a codon.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr6:75968510 A>G maps to NM_018247.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr14:61746908 G>A maps to NM_001017970.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:102968634 A>T did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:102968692 G>C did not map to a codon.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr23:102968787 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:41946931 T>C maps to NM_018126.2 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:100334062 G>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:100334028 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr23:100349724 T>C did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr23:100349901 C>G did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:100334068 C>A did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:120194889 C>G maps to NM_183240.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr19:16799058 C>T maps to NM_024074.1 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:119156655 G>A maps to NM_018266.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr3:119156859 C>T maps to NM_018266.1 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr3:119176975 A>G maps to NM_018266.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:32542919 G>A did not map to a codon.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:12777057 C>A maps to ENST00000431022 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:9321189 A>G maps to NM_015012.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:44903511 G>C maps to NM_144638.1 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:44903589 G>A maps to NM_144638.1 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:194336359 T>A maps to NM_001166305.1 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:194344009 C>A maps to NM_001166305.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:194309350 C>G maps to NM_001166305.1 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:34657457 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:54269610 G>C maps to NM_018087.4 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:64173778 C>T maps to NM_014254.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr21:34823151 A>G maps to NM_006134.5 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr21:34839411 C>T maps to NM_006134.5 W39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr21:34841095 A>G maps to NM_006134.5 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr1:15541865 G>T maps to NM_018022.2 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:15545932 G>A maps to NM_018022.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:45120815 G>T maps to NM_024587.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:33363921 T>A did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:33360938 C>G maps to NM_033504.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:92032431 G>A maps to NM_018710.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:20928403 A>T maps to NM_001100814.1 C136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:25810759 G>A maps to NM_018202.4 Q436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:18729055 C>T maps to NM_012109.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:18726930 G>T maps to NM_012109.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr19:18731325 C>T maps to NM_012109.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:226041386 G>C maps to NM_014698.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7596-01A-11D-2229-08 chr1:226059714 G>C maps to NM_014698.2 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr1:226034851 C>T maps to NM_014698.2 Q771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr6:44122112 G>A maps to NM_018426.1 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr14:77715180 G>A maps to NM_020431.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr14:77709308 C>G maps to NM_020431.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:29931571 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr8:94776142 T>C maps to NM_153704.5 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:94797541 A>G maps to NM_153704.5 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr1:156255505 G>T maps to NM_032323.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:156255559 G>A maps to NM_032323.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr1:205053121 G>A maps to NM_203376.1 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:18723411 C>T maps to NM_153347.1 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr2:112821763 T>C maps to NM_032824.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr2:112865404 C>A maps to NM_032824.2 S522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr16:426288 C>T maps to NM_021259.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr16:424220 C>T maps to NM_021259.2 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr9:136380684 G>A maps to NM_001080483.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:74874372 C>T maps to NM_001105579.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr14:74874294 G>C maps to NM_001105579.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:74874629 G>A maps to NM_001105579.1 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr20:24524080 C>T maps to NM_024893.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr17:3572586 C>G maps to NM_031298.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:7259354 T>C maps to NM_198154.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr17:7259783 G>A maps to NM_198154.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:31267869 G>A maps to NM_015544.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:69088018 G>A maps to NM_007114.2 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr3:69097183 G>A maps to NM_007114.2 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:69097621 A>G maps to NM_007114.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr17:28645839 C>T maps to NM_206832.1 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:4292862 G>A maps to NM_144615.2 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr23:154736699 G>T did not map to a codon.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr23:154736594 T>C did not map to a codon.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr9:100331210 G>A maps to NM_003275.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr9:100331219 G>A maps to NM_003275.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr9:100328170 G>A maps to NM_003275.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:52069168 C>T maps to NM_014548.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr15:52188668 A>T maps to NM_014547.4 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:151146930 C>T maps to NM_013353.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:98926625 G>A maps to NM_003276.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr12:98931316 A>T maps to NM_001032283.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:98941404 T>C maps to NM_001032283.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr12:98909803 C>T maps to NM_003276.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:33135675 G>A maps to NM_001039770.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr4:68812201 C>A maps to NM_182606.3 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr4:69096988 G>A maps to NM_182502.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:69095161 G>T maps to NM_182502.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr4:68698965 C>G maps to NM_004262.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:68725341 G>A maps to NM_004262.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr4:68703946 G>A maps to NM_004262.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:69327604 C>T maps to NM_014058.3 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr4:69341982 C>T maps to NM_014058.3 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:68919653 A>G maps to NM_207407.2 D430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr11:117780579 G>A maps to ENST00000413475 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr21:19653539 T>A did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr21:19704464 C>G maps to NM_002772.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr21:19666657 G>A maps to NM_002772.2 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr21:19666723 T>C maps to NM_002772.2 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:19666639 G>A maps to NM_002772.2 G811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr21:19713856 A>G maps to NM_002772.2 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr21:19737461 G>T maps to NM_002772.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr21:42861455 G>A maps to NM_001135099.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr21:42866454 C>T maps to NM_001135099.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr22:37462242 G>A maps to ENST00000381792 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:111797613 G>A maps to ENST00000443106 Q738Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:111769614 T>C maps to ENST00000443106 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr19:2415713 C>T maps to NM_182973.1 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr19:2408470 G>A maps to NM_182973.1 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr24:15816244 C>G did not map to a codon.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr12:29670382 G>A maps to NM_001193451.1 Q716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr12:83251022 C>A maps to NM_152588.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr12:83289633 T>A maps to NM_152588.1 L231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr12:83250974 C>T maps to NM_152588.1 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr12:83360727 C>T maps to NM_152588.1 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:83358811 T>C maps to NM_152588.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:88589181 C>G maps to NM_181783.3 S834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:88586521 C>T maps to NM_181783.3 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A7BN-01A-12D-A34J-08 chr12:88584340 C>T maps to NM_181783.3 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr13:101287319 C>T maps to NM_032813.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr13:101266633 G>T maps to NM_032813.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr13:101320925 C>T maps to NM_032813.2 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr13:101257364 G>A maps to NM_032813.2 D722D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr13:101266642 C>T maps to NM_032813.2 W626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr7:150779329 C>T maps to NM_031434.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr17:42268084 C>T maps to NM_001076674.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr11:57480108 C>T maps to NM_015959.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr9:117848971 G>T maps to NM_002160.2 C346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:117849087 C>A maps to NM_002160.2 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:117797485 G>C maps to NM_002160.2 V1928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:117848983 C>T maps to NM_002160.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:31544998 G>A maps to NM_000594.2 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:138201247 C>T maps to NM_006290.2 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:138202170 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:138200105 C>T maps to NM_006290.2 H508H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr5:118728830 C>T maps to NM_014350.2 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:151131544 G>A maps to NM_024575.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr8:23049473 C>T maps to NM_003844.3 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr8:23069662 C>T maps to NM_003844.3 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:22886090 G>T maps to NM_003842.4 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr8:119938850 G>A maps to NM_002546.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:119945203 C>T maps to NM_002546.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:119945374 G>A maps to NM_002546.3 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:119945254 G>A maps to NM_002546.3 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:3071625 C>T maps to NM_016639.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr17:16843025 C>T maps to NM_012452.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr22:42322237 G>C maps to NM_052945.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:6438762 G>A maps to NM_001065.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr12:6438513 G>A maps to NM_001065.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr12:6438570 G>C maps to NM_001065.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:12251957 G>A maps to NM_001066.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr6:47254184 G>T maps to NM_014452.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr1:6526161 C>T maps to ENST00000355862 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr1:6522207 G>A maps to ENST00000355862 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:1147456 C>A maps to NM_003327.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr20:62328364 G>A maps to ENST00000482936 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr20:62328211 C>T maps to ENST00000482936 G1333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:7999953 C>T did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr13:43180975 G>A maps to NM_003701.3 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr13:43180864 G>C maps to NM_003701.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr17:7463378 G>A maps to NM_003808.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:6670017 G>A maps to NM_003807.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:173155864 G>A maps to NM_003326.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr1:173155696 C>G maps to NM_003326.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr19:6532807 G>A maps to NM_003811.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:170843829 C>A maps to NM_015028.2 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:170912382 C>G maps to NM_015028.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr3:170802910 G>A maps to NM_015028.2 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:170789098 C>T maps to NM_015028.2 R1154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:170819287 C>T maps to NM_015028.2 E847E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:170802064 T>C maps to NM_015028.2 E1016E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:150415256 G>A maps to NM_006058.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr5:150410274 C>G maps to NM_006058.3 *637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:2757794 G>A maps to NM_024309.3 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:2746660 G>C maps to NM_024309.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr4:2746143 G>A maps to NM_024309.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:122075746 C>A maps to ENST00000509841 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:122068284 T>C maps to ENST00000509841 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:122078302 C>T maps to ENST00000509841 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr17:7290419 A>G maps to NM_003985.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr3:195608989 C>T maps to NM_001010938.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr3:195599247 C>T maps to NM_001010938.1 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr3:195595560 C>A maps to NM_001010938.1 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:195606027 C>G maps to NM_001010938.1 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr8:9605598 G>A maps to NM_003747.2 A903A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr11:57076223 C>A maps to NM_033396.2 E1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr11:57087949 C>A maps to NM_033396.2 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr11:57085294 A>G maps to NM_033396.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr11:57080222 C>A maps to NM_033396.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:57069956 G>A maps to NM_033396.2 P1553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr11:57085348 G>A maps to NM_033396.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7596-01A-11D-2229-08 chr11:57076680 C>T maps to NM_033396.2 R1168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:57076248 A>G maps to NM_033396.2 G1312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr11:57070012 G>A maps to NM_033396.2 Q1535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr10:93602104 C>T maps to NM_025235.3 C672C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:99854534 C>A did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr23:99852544 G>C did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:175092650 T>A maps to NM_022093.1 A922A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:175048550 C>A maps to NM_022093.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr1:175046802 C>T maps to NM_022093.1 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:175049389 C>A maps to NM_022093.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:175097244 T>G maps to NM_022093.1 L1041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr1:175105996 G>A maps to NM_022093.1 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr1:175105984 C>T maps to NM_022093.1 T1152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:175066727 A>G maps to NM_022093.1 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr20:44453473 C>A did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:1862065 G>A maps to ENST00000381906 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:1862047 G>A did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr19:55663240 C>G maps to ENST00000344887 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:74833000 T>C maps to NM_001112808.2 C514C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:201333479 G>T maps to ENST00000421663 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr1:201334339 G>A maps to ENST00000421663 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:1959665 A>G did not map to a codon.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr11:1956070 G>A maps to ENST00000397301 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr11:1959682 G>A maps to ENST00000397301 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr11:1950353 C>T maps to ENST00000397301 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr16:11362921 G>A maps to NM_005425.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr16:11363038 G>C maps to NM_005425.4 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:12817448 G>A maps to NM_001136196.1 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:12822152 C>T maps to NM_001136196.1 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:12830099 G>A maps to NM_001136196.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:128640491 A>T maps to ENST00000471166 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr7:128640536 C>T maps to ENST00000471166 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr1:175372558 G>A maps to NM_003285.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr1:175355318 G>A maps to NM_003285.2 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:175348703 G>A maps to NM_003285.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr1:175334301 T>G maps to NM_003285.2 R811R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:175360469 C>G maps to NM_003285.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:175375751 C>A maps to NM_003285.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:175299263 C>A maps to NM_003285.2 E1247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:175375397 C>A maps to NM_003285.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr1:175365922 G>A maps to NM_003285.2 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr7:5427939 G>A maps to NM_001080495.2 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr7:5410483 C>T maps to NM_001080495.2 V1247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr7:5353144 C>T maps to NM_001080495.2 E2459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:5391492 C>T maps to NM_001080495.2 A1809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:5348801 G>A maps to NM_001080495.2 P2862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:5427891 C>T maps to NM_001080495.2 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr7:5410491 G>A maps to NM_001080495.2 L1245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr16:24801450 A>T maps to NM_014494.2 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr16:24802569 C>A maps to NM_014494.2 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr22:40660899 G>A maps to ENST00000454349 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr22:40669447 C>T maps to ENST00000454349 D1009D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr17:76046390 G>A maps to NM_001142640.1 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr2:218674658 C>T maps to NM_022648.4 Q1616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr2:218700799 G>A maps to NM_022648.4 Q923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr2:218683175 A>G maps to NM_022648.4 T1189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr7:47385790 G>C maps to NM_022748.11 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:47319948 G>C maps to NM_022748.11 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr7:47342761 G>A maps to NM_022748.11 H1081H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:47408664 G>T maps to NM_022748.11 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:47474984 C>T maps to NM_022748.11 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:47408307 C>T maps to NM_022748.11 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr7:47408862 G>T maps to NM_022748.11 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr7:47317712 G>A maps to NM_022748.11 F1433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr17:38638645 G>T maps to NM_032865.5 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:38640844 C>T maps to NM_032865.5 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr17:38636059 C>T maps to NM_032865.5 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr17:38645177 G>A maps to NM_032865.5 H161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:38638441 G>A maps to NM_032865.5 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:32037925 A>C maps to ENST00000375244 P1752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr6:32020543 G>A maps to ENST00000375244 T3006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr6:32020729 C>T maps to ENST00000375244 T2944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr6:32032667 C>T maps to ENST00000375244 K2257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:32036476 C>T maps to ENST00000375244 E1970E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:32024531 G>A maps to ENST00000375244 F2658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr6:32024588 G>A maps to ENST00000375244 A2639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:32029985 G>A maps to ENST00000375244 Y2372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:32032760 G>A maps to ENST00000375244 V2226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:32041535 G>A maps to ENST00000375244 D1523D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr6:32017904 C>T maps to ENST00000375244 A3103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr17:48941306 A>G maps to NM_005749.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr11:1309865 G>A maps to ENST00000382211 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr11:1310006 C>T did not map to a codon.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr11:1298421 G>A maps to ENST00000382211 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr22:35726366 C>T maps to ENST00000451197 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A499-01A-11D-A24D-08 chr17:52993151 C>T maps to NM_005486.2 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr17:17788010 C>T maps to NM_001082968.1 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr17:17754215 C>T maps to NM_001082968.1 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr17:17766142 G>A maps to NM_001082968.1 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr1:235292009 G>A maps to NM_014765.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:58869468 G>A maps to NM_207377.2 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:43572213 G>A maps to NM_006809.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:45406350 G>A maps to NM_006114.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:45395689 C>A maps to NM_006114.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr1:161198033 G>A maps to NM_032174.4 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:37592508 G>C maps to NM_001134485.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:100093900 G>T maps to NM_014820.3 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:100087928 T>C maps to NM_014820.3 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr3:100093990 T>A maps to NM_014820.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr20:39706250 G>A maps to NM_003286.2 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr20:39744052 G>T maps to NM_003286.2 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:39729956 T>C maps to NM_003286.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr8:144392335 C>T maps to NM_052963.1 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr8:144400208 G>A maps to NM_052963.1 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:38567941 T>C maps to ENST00000357601 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr17:38569175 G>T maps to ENST00000357601 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:38568019 A>G maps to ENST00000357601 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:25670594 G>A maps to ENST00000264331 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr3:25639815 A>G maps to ENST00000264331 D1621D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr3:133372360 C>T maps to NM_007027.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:133368366 G>C maps to NM_007027.3 S455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:133347418 C>T maps to NM_007027.3 E893E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr9:32543993 G>A maps to NM_005802.4 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr1:179851876 G>A maps to ENST00000398836 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:179815799 C>T maps to NM_145034.4 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:179834002 A>T maps to NM_022347.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr9:132565577 C>T maps to NM_014506.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:132566418 G>A maps to NM_014506.1 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:179063233 C>T maps to NM_022371.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr8:59764238 C>G maps to NM_014729.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:59851884 T>G maps to NM_014729.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr8:59728262 G>A maps to NM_014729.2 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr20:42694518 G>A maps to ENST00000348077 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr20:42694467 G>A maps to ENST00000348077 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr16:52497887 G>A maps to ENST00000407228 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr16:52473856 G>T maps to ENST00000407228 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:52473777 G>A maps to ENST00000407228 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr14:21957420 T>C maps to NM_014828.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:21955827 G>A maps to NM_014828.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr17:7577016 A>C did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr17:7578246 A>T maps to NM_001126112.1 L201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr17:7573925 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr17:7579311 C>G maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr17:7578401 G>A maps to NM_001126112.1 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr17:7577016 A>C did not map to a codon.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:7579309 A>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:7578418 C>A maps to NM_001126112.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr17:7578523 G>A maps to NM_001126112.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr17:7579590 C>T did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr17:7576852 C>T maps to NM_001126112.1 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:7578246 A>T maps to NM_001126112.1 L201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:7574033 C>A did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr17:7577497 C>T did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr17:7578523 G>A maps to NM_001126112.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr17:7577141 C>A maps to NM_001126112.1 G266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr17:7577609 T>A did not map to a codon.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr17:7579371 G>A maps to NM_001126112.1 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:7579697 A>C did not map to a codon.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr17:7576926 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:7578432 G>C maps to NM_001126112.1 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr17:7579385 T>A maps to NM_001126112.1 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr17:7577024 T>A maps to NM_001126112.1 K305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr17:7578176 C>T maps to NM_001126112.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:7577017 C>A did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:7579414 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr17:7579520 C>A maps to NM_001126112.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr17:7576852 C>T maps to NM_001126112.1 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr17:7576927 T>C did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr17:7577141 C>A maps to NM_001126112.1 G266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr17:7577142 C>A maps to NM_001126112.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:7578418 C>A maps to NM_001126112.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:7578419 C>A maps to NM_001126112.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr17:7579574 G>A maps to NM_001126112.1 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:7579532 G>A maps to NM_001126112.1 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr17:7579377 G>C maps to NM_001126112.1 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr17:7578548 G>A maps to NM_001126112.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:7579376 G>A maps to NM_001126112.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr17:7579721 C>G did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr17:7579698 C>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr17:7578289 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr17:7577081 C>A maps to NM_001126112.1 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr17:7578368 A>C did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr17:7579484 C>A maps to NM_001126112.1 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:7574020 C>A maps to NM_001126112.1 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr17:7579520 C>A maps to NM_001126112.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr17:7579310 C>A did not map to a codon.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr17:7574033 C>A did not map to a codon.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr17:7578238 C>A maps to NM_001126112.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr17:7573009 T>A did not map to a codon.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr17:7579310 C>A did not map to a codon.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H8-01A-21D-A34J-08 chr17:7579591 T>A did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr17:7578440 G>C maps to NM_001126112.1 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr17:7578233 A>T maps to NM_001126112.1 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr17:7577084 C>A maps to NM_001126112.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:7578369 C>T did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr17:7577608 C>G did not map to a codon.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr17:7577156 T>G did not map to a codon.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr17:7579484 C>A maps to NM_001126112.1 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr17:7578253 C>A maps to NM_001126112.1 G199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr15:43705365 G>A maps to NM_001141980.1 S1752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr15:43771644 C>T maps to NM_001141980.1 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr15:43748854 C>A maps to NM_001141980.1 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr15:43738702 C>T maps to NM_001141980.1 G974G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr15:43766889 T>C maps to NM_001141980.1 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr15:43783897 C>A maps to NM_001141980.1 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:223984131 G>C maps to NM_001031685.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:223990486 C>G maps to NM_001031685.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr1:223991101 G>A maps to NM_001031685.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr11:44957115 G>A maps to NM_006034.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr11:44956497 G>T maps to NM_006034.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr11:44959880 C>T maps to NM_006034.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr17:27896355 C>T maps to NM_138349.2 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr2:24305860 A>T maps to NM_147184.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:24302331 C>T maps to NM_147184.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:95952350 C>T maps to NM_033285.3 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:95942724 C>T maps to NM_033285.3 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr20:33296572 C>T maps to NM_021202.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr20:33298027 C>A maps to NM_021202.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:189586431 G>A maps to NM_003722.4 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr3:189582019 G>A did not map to a codon.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr3:189526080 G>T maps to NM_003722.4 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr3:189526212 C>A maps to NM_003722.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr3:189607207 C>T maps to NM_003722.4 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr3:189582019 G>T did not map to a codon.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr3:189582019 G>T did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr3:189597915 T>C maps to NM_001114979.1 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr1:3599707 C>T maps to NM_005427.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:83075787 C>T maps to NM_006670.4 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:113730844 G>T maps to NM_001143819.1 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:113714795 C>T maps to NM_001143819.1 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr12:113715133 C>T maps to NM_001143819.1 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:113711397 C>T maps to NM_001143819.1 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:68830380 C>A maps to NM_139075.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr11:68822186 A>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:68830446 G>A maps to NM_139075.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr11:68846463 C>T maps to NM_139075.3 D505D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr11:68822820 G>A did not map to a codon.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr8:80954858 A>T maps to NM_001025252.1 L184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr6:125569433 G>A maps to NM_003287.2 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr20:62505151 C>T maps to NM_199360.1 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr9:6330997 G>A maps to NM_001001874.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr9:6328606 C>G maps to NM_033516.5 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr11:18057545 G>C maps to ENST00000341556 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr12:72372828 C>T maps to ENST00000389376 Y307Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr12:72425342 C>T maps to ENST00000389376 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr12:72366469 C>G maps to ENST00000389376 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:72335506 C>G maps to ENST00000389376 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr12:72425054 G>A maps to ENST00000389376 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr12:72388284 A>G maps to ENST00000389376 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:6979495 T>C maps to NM_001159287.1 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr7:144463006 A>T maps to NM_022445.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:154144522 C>G maps to NM_153649.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:18148146 C>G did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:1497616 G>A maps to NM_000547.5 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:1440051 C>A maps to NM_000547.5 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr2:1459984 A>G maps to NM_000547.5 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr2:1488597 C>T maps to NM_000547.5 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr2:1507768 G>A maps to NM_000547.5 A812A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:6636693 C>T maps to ENST00000453338 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr13:103279444 C>T maps to ENST00000376052 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr13:103275225 G>C did not map to a codon.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr13:103249402 G>A maps to ENST00000376052 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr5:666135 G>A maps to NM_007030.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:665267 G>A maps to NM_007030.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr14:21499179 C>T maps to NM_173846.4 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr14:21499311 C>A maps to NM_173846.4 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:186315361 G>A maps to NM_003292.2 Q1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:127294642 G>A maps to NM_001136053.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:127298672 G>A maps to NM_001136053.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr3:127298652 C>T maps to NM_001136053.1 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr3:127292390 G>A maps to NM_001136053.1 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr1:3545079 C>T maps to NM_182752.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:73959361 G>C maps to ENST00000409716 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr9:140087089 G>A maps to NM_001128228.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:48305448 G>C maps to NM_198479.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:48305271 G>A maps to NM_198479.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:48305261 G>A maps to NM_198479.2 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr19:48305073 C>T maps to NM_198479.2 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:1279655 C>G maps to ENST00000445910 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr7:65751527 G>A maps to NM_003596.3 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr7:65706140 C>T maps to NM_003596.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr22:26928675 C>T maps to NM_003595.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr21:10959801 T>C did not map to a codon.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr21:10933917 C>A maps to NM_199261.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr21:10933852 T>A maps to NM_199261.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr21:10920131 T>A maps to NM_199261.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr21:10951320 G>A maps to NM_199261.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr21:10951399 C>T maps to NM_199261.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr21:10906976 T>A maps to NM_199261.2 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:10910381 T>C maps to NM_199261.2 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:10969097 G>T maps to NM_199261.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr21:10970039 C>A maps to NM_199261.2 G30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr13:20039643 A>T maps to NM_199254.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr13:20000606 A>G maps to NM_199254.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr13:20041461 A>G maps to NM_199254.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr13:20024300 C>T maps to NM_199254.2 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:23556038 C>G maps to NM_013293.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:185636150 A>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:50636359 C>T maps to NM_025204.2 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr9:139820215 C>T maps to ENST00000359662 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr14:103357699 C>T maps to NM_145725.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr14:103363705 C>T maps to NM_145725.2 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr14:103363737 G>A maps to NM_145725.2 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:103369698 C>T maps to NM_145725.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:103372012 C>T maps to NM_145725.2 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:239237416 T>C maps to NM_015650.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr6:111912596 G>A maps to ENST00000340026 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:209949071 C>A maps to NM_025228.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:27075533 C>T maps to NM_004295.3 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr1:211534066 T>C maps to ENST00000427925 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr16:2218132 C>T maps to NM_032271.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:112578684 C>G maps to NM_006700.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr12:112586050 T>C maps to NM_006700.2 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:112579999 G>T maps to NM_006700.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:42132990 C>G maps to NM_001042646.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr3:42229592 C>T maps to NM_001042646.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:42264823 G>A maps to NM_001042646.1 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:71520407 C>T maps to NM_014294.5 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr8:71495488 G>A maps to NM_014294.5 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr8:71508496 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:118005949 A>T maps to NM_152402.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr4:118006318 G>C maps to NM_152402.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr3:36873987 G>C maps to NM_014831.2 L2318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr3:36899180 G>A maps to NM_014831.2 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr3:36872598 T>C maps to NM_014831.2 E2781E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:36884181 G>A maps to NM_014831.2 F1693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:36898413 C>A maps to NM_014831.2 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr3:36876398 C>A did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr3:36873735 G>A maps to NM_014831.2 I2402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:36873774 G>A maps to NM_014831.2 F2389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr16:3724417 G>A maps to NM_016292.2 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr16:3736065 G>A maps to NM_016292.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr16:3722788 C>T maps to NM_016292.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr16:3726127 G>A maps to NM_016292.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr16:3739109 G>A maps to NM_016292.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:3712054 G>A maps to NM_016292.2 Q625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr16:3727504 G>C maps to NM_016292.2 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr17:7834415 G>A maps to NM_001166621.1 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr23:13734172 C>T did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:88925145 C>A maps to NM_016209.3 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:7747351 G>A maps to NM_001042461.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr8:140743396 G>T maps to NM_031466.5 I1216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr8:140922440 C>A maps to NM_031466.5 E1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr8:141370155 C>G maps to NM_031466.5 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr8:141461049 G>A maps to NM_031466.5 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr8:140744266 G>A maps to NM_031466.5 H1176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr8:141263008 G>A maps to NM_031466.5 F864F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr8:141445298 G>A maps to NM_031466.5 H355H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr8:141297719 C>T maps to NM_031466.5 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr10:17199511 G>T maps to NM_004412.5 S272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr10:17199504 C>T maps to NM_004412.5 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr6:123869614 G>A maps to NM_006073.2 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:123687328 T>C did not map to a codon.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr6:41130790 G>C maps to NM_018965.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:41126779 G>A maps to NM_018965.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:41162311 G>A maps to ENST00000373108 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr6:41160554 C>T maps to ENST00000373108 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr6:41162431 G>C maps to ENST00000373108 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:42227371 C>T maps to NM_033502.2 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:42231258 C>A maps to NM_033502.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:42222640 C>T maps to NM_033502.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:42224468 C>T maps to NM_033502.2 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr6:42225913 C>A maps to NM_033502.2 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr6:42196407 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr23:152710806 C>T did not map to a codon.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr23:152710828 G>A did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:152710317 C>T did not map to a codon.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr3:129695950 C>T maps to NM_007117.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr12:73014919 T>C maps to NM_013381.2 Y789Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:73056936 G>T maps to NM_013381.2 E1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:72666977 C>T maps to NM_013381.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr12:72667101 C>T maps to NM_013381.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:72866929 T>C maps to NM_013381.2 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:72936126 G>A maps to NM_013381.2 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr12:72969047 A>C maps to NM_013381.2 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:72667121 G>A maps to NM_013381.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr12:72956691 C>A maps to NM_013381.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:110100016 C>A maps to NM_003301.4 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr8:110099851 C>A maps to NM_003301.4 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:110131278 C>T maps to NM_003301.4 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr8:110099807 G>T maps to NM_003301.4 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:120882719 C>T maps to NM_016399.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:12880595 C>T maps to NM_021643.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:12880893 G>T maps to NM_021643.3 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr20:377163 C>A maps to ENST00000422053 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr20:368669 C>T maps to ENST00000422053 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr20:372178 G>A maps to ENST00000422053 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr20:376919 G>A maps to ENST00000422053 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:30122126 C>A maps to NM_006778.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr1:228582786 G>A maps to NM_145214.2 H342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr1:228584660 C>T maps to NM_145214.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr13:50586099 C>G maps to NM_001007278.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:100862395 G>C maps to NM_033219.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr9:100862404 G>A maps to NM_033219.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr6:30131820 C>T maps to NM_033229.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:30140092 G>A maps to NM_033229.2 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:15554473 G>A maps to ENST00000455584 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:15554854 G>C maps to ENST00000455584 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:18638706 C>A maps to NM_001037330.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr17:18635350 G>C did not map to a codon.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:228596741 T>C maps to NM_001134855.1 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr4:154249704 C>T maps to NM_015271.3 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr4:154197119 C>T maps to NM_015271.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:4409646 C>T maps to NM_003141.3 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr11:5730847 C>T maps to NM_006074.4 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:5730670 G>A maps to NM_006074.4 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:5730526 G>A maps to NM_006074.4 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:64910039 G>C maps to NM_001656.3 S84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:138235860 G>A maps to NM_015905.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:138261115 A>T did not map to a codon.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr7:138265312 G>A maps to NM_015905.2 E864E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:138209984 G>C did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr17:54990923 G>A maps to NM_005082.4 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:30166208 C>T maps to NM_003449.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:30154333 C>T maps to NM_003449.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr11:120008394 C>T maps to NM_012101.3 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr11:6477632 G>A maps to NM_033278.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr11:6478167 G>T maps to NM_033278.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:6472239 G>A maps to NM_033278.2 D584D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:6477355 G>A maps to NM_033278.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:30076800 A>G did not map to a codon.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:119461760 C>T maps to NM_012210.3 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:119460353 C>T maps to NM_012210.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr9:119460323 G>T maps to NM_012210.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:119461730 G>A maps to NM_012210.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:119461805 T>C maps to NM_012210.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:5653888 G>T maps to NM_001003819.3 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr11:5655104 C>A maps to NM_001003819.3 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr5:114499268 G>A maps to NM_018700.3 R82*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D6-A74Q-01A-11D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:57165710 T>C maps to NM_015294.3 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr17:57125152 G>A maps to NM_015294.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr17:57093002 C>T maps to NM_015294.3 A848A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr6:25983470 C>T maps to NM_006355.2 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr6:25983647 G>A maps to NM_006355.2 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:30297213 C>T maps to NM_021253.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:30309966 C>T maps to NM_021253.3 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:99489923 C>T maps to NM_033017.3 G455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr3:140401990 G>A maps to NM_152616.4 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr3:140401412 C>A maps to NM_152616.4 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:35747620 C>A maps to NM_017583.4 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:117656089 C>G maps to NM_025188.3 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr1:117663358 G>A maps to NM_025188.3 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:117659367 C>T did not map to a codon.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:155152366 C>T maps to NM_025058.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:73871027 C>A maps to NM_033452.2 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr11:55036774 G>T maps to ENST00000357530 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr11:55032762 C>A maps to ENST00000357530 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr11:55036717 G>A maps to ENST00000357530 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr11:55036812 G>T maps to NM_024114.3 *225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr11:55036771 A>C maps to ENST00000357530 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:5701230 C>G maps to NM_033034.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:5688929 G>A maps to NM_033034.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr7:72738497 G>C maps to NM_178125.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr2:27521505 G>A maps to NM_032546.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr2:27527837 C>T maps to NM_032546.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr8:67039640 G>T maps to NM_184085.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr8:67066570 T>G did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:67067882 T>A maps to NM_033058.2 L517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:100732059 C>T maps to NM_030961.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:248028107 G>A maps to NM_015431.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr1:248020625 G>A maps to NM_015431.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:33625293 G>A maps to NM_018207.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:73887414 C>T maps to NM_173547.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:231335943 C>T maps to NM_001004342.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr1:231339745 G>T maps to NM_001004342.3 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:231351158 G>A maps to NM_001004342.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:231298756 T>C maps to NM_001004342.3 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:231337180 T>C maps to NM_001004342.3 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:4621895 G>A maps to NM_018073.5 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:4624491 G>A maps to NM_018073.5 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr15:45047400 A>T maps to NM_182985.3 K104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr15:45059954 C>T maps to NM_182985.3 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr5:180627054 C>T maps to NM_203293.1 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr3:32933122 T>C maps to NM_001039111.1 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:32933212 G>A maps to NM_001039111.1 G839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:32932009 G>T maps to NM_001039111.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr10:104416555 C>T maps to NM_030912.2 C367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr10:104415876 G>A maps to NM_030912.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:104404916 C>T maps to NM_030912.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:51561182 G>A maps to ENST00000338969 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr14:51464788 G>A maps to ENST00000338969 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:189060747 G>A maps to NM_178556.3 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:189060942 C>T maps to NM_178556.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr4:189060729 G>C maps to NM_178556.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr5:14419990 G>T maps to NM_007118.2 R1688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr5:14401069 A>G did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:14291309 G>A maps to NM_007118.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:14387623 G>A maps to NM_007118.2 E1216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:14387878 C>T maps to NM_007118.2 I1268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:14368962 C>G maps to NM_007118.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr5:14488245 G>C maps to NM_007118.2 P2503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:14487612 G>C maps to NM_007118.2 G2292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:14488149 G>A maps to NM_007118.2 E2471E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr5:14492731 G>A maps to NM_007118.2 T2563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr5:14291173 C>G maps to NM_007118.2 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr22:38154057 G>A maps to NM_001039141.2 K2042K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr22:38119915 C>T maps to NM_001039141.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr22:38154081 C>G maps to NM_001039141.2 L2050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr22:38121553 C>T maps to NM_001039141.2 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr22:38165091 G>A maps to NM_001039141.2 Q2211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:38121031 C>T maps to NM_001039141.2 I823I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:38130788 G>A maps to NM_001039141.2 R1482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr22:38121379 C>T maps to NM_001039141.2 L939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr22:38120198 C>T maps to NM_001039141.2 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:6743835 C>T maps to ENST00000313244 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr19:6742998 C>T maps to ENST00000313244 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:92469777 C>T maps to NM_004239.3 L1514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:92469840 C>T maps to NM_004239.3 L1493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:92471130 C>T maps to NM_004239.3 Q1063Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr14:92491670 G>A maps to NM_004239.3 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr14:92436037 C>T maps to NM_004239.3 L1973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:230652325 T>C maps to ENST00000389044 A1603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:230652348 G>A maps to ENST00000389044 Q1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:230636254 G>A maps to ENST00000389044 Q1903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr2:230675761 C>G did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr2:230672974 G>A maps to ENST00000389044 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr2:230744732 G>A maps to ENST00000389044 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr2:230655843 C>T maps to ENST00000389044 W1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr5:908534 C>T maps to NM_004237.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr5:908528 C>T maps to NM_004237.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr15:64716266 C>T maps to NM_016213.4 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr7:100466241 G>A maps to NM_003302.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:100468202 T>C maps to NM_003302.2 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:100468205 T>C maps to NM_003302.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:13223746 G>A maps to NM_001136035.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr6:126334220 C>T maps to NM_001031712.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr11:64084792 G>A maps to NM_016404.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr22:20103245 C>T maps to ENST00000439169 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr23:100275561 G>A did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr23:100290612 G>C did not map to a codon.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr23:100265667 T>C did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:100274272 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr20:5921953 G>A maps to NM_015939.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:29092864 C>T maps to NM_017910.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr2:29092738 T>C maps to NM_017910.3 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr2:29092442 A>G did not map to a codon.
Sequencing variant TCGA-BA-A4IH-01A-11D-A25Y-08 chr22:46733800 C>T maps to NM_018006.4 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:46752901 G>A maps to NM_018006.4 *422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr22:46746282 C>T maps to NM_018006.4 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr3:3170786 C>T maps to NM_182916.2 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr23:54957427 G>T did not map to a codon.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr23:54957318 G>A did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr23:54951478 G>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:54949661 A>G did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr23:54955856 T>G did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr23:54955307 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:54955272 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr23:54955076 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr23:54955077 G>A did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:49719905 C>T maps to NM_005480.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:49719906 C>T maps to NM_005480.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr12:49725030 G>A maps to NM_005480.3 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr1:193045124 A>G maps to NM_004600.5 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr8:72967822 G>T maps to NM_007332.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr8:72971645 T>C maps to NM_007332.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr8:72948638 C>A maps to NM_007332.2 T813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:72942204 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:72981314 G>A maps to NM_007332.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr8:72973951 G>T maps to NM_007332.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr8:72963051 T>A maps to NM_007332.2 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr8:72946533 G>T maps to NM_007332.2 I878I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:142525008 C>T maps to ENST00000476941 R772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:142467158 C>T maps to ENST00000476941 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:122828720 A>T maps to NM_001130698.1 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr4:122836026 G>A maps to NM_001130698.1 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr4:122854051 C>A maps to NM_001130698.1 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:122828483 C>T maps to NM_001130698.1 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr13:38320379 G>C maps to NM_003306.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr13:38320427 G>T maps to NM_003306.1 C181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr13:38211558 C>T maps to NM_003306.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr13:38320193 C>T maps to NM_003306.1 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr13:38357100 C>A maps to NM_003306.1 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr20:33632353 C>T maps to NM_015638.2 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:111078161 T>C did not map to a codon.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr23:111195419 C>A did not map to a codon.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr23:111078214 G>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:111090411 T>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:111097123 T>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr23:111078300 G>T did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr23:111097061 T>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:111090556 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr23:111025197 C>G did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr23:111025356 C>T did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:111025208 C>G did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:111020091 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:111155910 G>C did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr23:111022219 T>G did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:111019936 G>C did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:111155685 A>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:101344379 C>G maps to NM_004621.5 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr5:135587502 C>T maps to NM_020389.2 W471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:135692538 G>A maps to NM_020389.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:135693000 G>A maps to NM_020389.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr15:31294735 T>C maps to NM_002420.4 R1367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:31339442 C>T maps to NM_002420.4 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:31354780 C>G did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:31323258 C>T maps to NM_002420.4 W996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:31324987 G>A maps to NM_002420.4 I930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr15:31295038 G>A maps to NM_002420.4 S1266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:31358387 G>A maps to NM_002420.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr15:31324972 G>A maps to NM_002420.4 I935I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:45838390 C>T maps to ENST00000397932 F1138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr21:45843585 G>T maps to ENST00000397932 E1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr21:45821617 C>T maps to ENST00000397932 F792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr21:45833912 C>G maps to ENST00000397932 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr21:45819233 C>T maps to ENST00000397932 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr21:45786767 G>T maps to ENST00000397932 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr9:73254077 G>T maps to ENST00000419692 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr9:73399061 C>T maps to ENST00000419692 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr9:73151798 C>A maps to ENST00000419692 S1364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr9:73151900 T>A maps to ENST00000419692 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr9:73151426 G>A maps to ENST00000419692 S1488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:73235149 G>A maps to ENST00000419692 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:73477821 A>T did not map to a codon.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr9:73152299 C>T maps to ENST00000419692 R1197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr9:73235023 G>A maps to ENST00000419692 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:49684705 C>T maps to NM_017636.3 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:49692329 T>C maps to NM_017636.3 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:49671538 T>C maps to NM_017636.3 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr19:49703923 C>T maps to NM_017636.3 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr11:2434716 G>A maps to ENST00000452833 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:2433447 C>T maps to ENST00000452833 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr9:77397709 C>T maps to NM_017662.4 V993V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr9:77377560 G>T maps to NM_017662.4 G1342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:77411724 G>A maps to NM_017662.4 Q775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:77354767 G>A maps to NM_017662.4 V1786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:77370355 G>A maps to NM_017662.4 Q1607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:77436730 G>T maps to NM_017662.4 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:77354740 G>A maps to NM_017662.4 L1795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr9:77431588 C>T maps to NM_017662.4 W435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:50929754 C>A maps to NM_017672.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr15:50888512 G>A maps to NM_017672.4 Q1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr15:50906376 G>A maps to NM_017672.4 C526C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr15:50903316 C>T maps to NM_017672.4 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:234862640 C>T maps to NM_024080.4 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:234888875 G>T maps to NM_024080.4 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:234871982 C>T maps to NM_024080.4 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:234905029 C>T maps to NM_024080.4 F1000F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:116599314 A>C maps to NM_014112.2 A871A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr8:116631646 T>G maps to NM_014112.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr8:116631734 G>C maps to NM_014112.2 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr11:63992033 T>C maps to NM_001160393.1 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr17:3470182 G>A maps to ENST00000399756 R827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr17:3493396 C>A maps to ENST00000399756 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr17:3494381 C>T maps to ENST00000399756 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr17:3481023 C>T maps to ENST00000399756 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DD-01A-12D-A31L-08 chr17:16336964 C>T maps to NM_016113.4 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:3438900 G>A maps to ENST00000381913 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr17:3448489 G>C maps to ENST00000381913 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr12:110236714 C>A maps to NM_021625.4 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:110246197 G>C maps to NM_021625.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:110252301 C>T maps to NM_021625.4 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:110246112 C>A maps to NM_021625.4 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:110230483 C>A maps to NM_021625.4 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr12:110232202 G>A maps to NM_021625.4 N474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr12:110238455 G>A maps to NM_021625.4 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:110240844 G>A maps to NM_021625.4 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr12:110252319 C>T maps to NM_021625.4 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr12:110230549 C>T maps to NM_021625.4 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:142612692 G>A maps to NM_019841.4 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:142606702 G>A maps to NM_019841.4 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:142605908 G>C maps to NM_019841.4 S654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr7:142605865 G>T maps to NM_019841.4 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr7:142605774 G>A maps to NM_019841.4 R699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr7:142571365 G>A maps to NM_018646.2 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:142574507 C>T maps to NM_018646.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr7:98608796 C>A maps to ENST00000359863 T3673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr7:98522760 G>A maps to ENST00000359863 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:98545956 G>C maps to ENST00000359863 L1547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr7:98609010 C>T maps to ENST00000359863 D3716D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:98501138 C>T maps to ENST00000359863 N345N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr7:98552767 C>T maps to ENST00000359863 I1919I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:98574263 A>G maps to ENST00000359863 T2699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr7:98515049 G>A maps to ENST00000359863 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr7:98606090 C>T maps to ENST00000359863 C3601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:131084582 C>G maps to NM_015679.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr9:131076090 G>T maps to NM_015679.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr7:141955073 C>A maps to NM_001001317.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:141952097 G>T maps to NM_001001317.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:141952172 C>T maps to NM_001001317.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:141955029 G>T maps to NM_001001317.2 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr7:141952345 G>T maps to NM_001001317.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr7:141955353 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr9:135798765 G>A maps to NM_000368.4 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr16:2134998 C>G maps to NM_000548.3 S1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr16:2111961 C>T maps to NM_000548.3 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr16:2127658 C>T maps to NM_000548.3 F966F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr16:2135262 C>T maps to NM_000548.3 L1534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:45008998 C>T maps to NM_183422.2 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr13:45010653 C>T maps to NM_006022.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr13:45149169 A>G maps to NM_183422.2 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr23:106960003 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:106957809 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:106957810 G>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:100065213 T>C maps to NM_030935.3 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:18505527 C>T maps to NM_006292.2 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr2:99725294 C>T did not map to a codon.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr7:130038841 T>A maps to NM_018718.1 K338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:115576667 C>A maps to NM_000549.3 Y79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr14:81610640 C>T maps to NM_000369.2 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:81610459 G>A maps to NM_000369.2 Q686Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr14:81610330 T>A maps to NM_000369.2 Y643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr18:72999254 G>A maps to NM_005786.4 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr18:73000484 C>T maps to NM_005786.4 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:72999356 C>T maps to NM_005786.4 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr18:72999677 G>A maps to NM_005786.4 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:72997952 C>T maps to NM_005786.4 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr18:72999602 C>T maps to NM_005786.4 S702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr18:73000280 C>T maps to NM_005786.4 N928N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr19:31769408 G>A maps to NM_020856.2 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr19:31770590 C>T maps to NM_020856.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:31769228 C>T maps to NM_020856.2 K490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr19:31770257 G>A maps to NM_020856.2 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr19:31769048 G>A maps to NM_020856.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr19:31768177 C>A maps to NM_020856.2 E841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:31768094 G>A maps to NM_020856.2 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr19:31768177 C>A maps to NM_020856.2 E841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:31769771 G>T maps to NM_020856.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:50243128 G>A maps to NM_021733.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:50250009 G>A maps to NM_021733.1 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:76507403 T>C maps to NM_015516.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:122514813 A>C did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr8:143396414 C>T maps to ENST00000445818 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:143425408 G>T maps to ENST00000445818 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr8:143425642 G>A maps to ENST00000445818 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr8:143399952 G>A maps to ENST00000445818 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:231678280 C>G maps to NM_005999.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr16:67860094 T>G maps to ENST00000339830 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr16:67859619 C>A maps to ENST00000339830 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr16:67860626 C>T maps to ENST00000339830 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr1:46649972 G>A maps to NM_005727.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:79612250 G>A maps to NM_031945.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:79612448 C>T maps to NM_031945.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:31116807 G>A maps to NM_001080509.2 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr10:82264527 C>T maps to NM_030927.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:82269157 C>T maps to NM_030927.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr10:82269076 C>T maps to NM_030927.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr10:71258082 G>A maps to NM_012339.3 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr12:3387621 G>A maps to ENST00000407263 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:41011349 G>A maps to NM_001159726.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr24:9305926 C>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr24:6114390 G>T did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr24:6115621 G>C did not map to a codon.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr23:53114819 A>T did not map to a codon.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr23:53114238 G>A did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr8:98290054 C>A maps to NM_033512.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:98289087 G>A maps to NM_033512.2 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:98289088 G>A maps to NM_033512.2 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr2:54483228 C>T maps to NM_001003937.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr17:2238188 T>A maps to NM_018128.4 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:2238907 C>T maps to NM_018128.4 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr17:2234279 G>T maps to NM_018128.4 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr17:2233880 G>A maps to NM_018128.4 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:54469924 G>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:3193184 G>A maps to ENST00000398659 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr11:2424708 G>A maps to NM_005706.2 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr5:112769744 G>A maps to NM_032028.3 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr22:19119172 C>G maps to NM_053006.4 Y87*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DQ-5630-01A-01D-1870-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-T2-A6WX-01A-12D-A34J-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-UF-A71E-01A-31D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:32829352 G>A maps to NM_052841.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr19:19625861 G>A maps to NM_032037.2 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr22:37407205 G>A maps to NM_003312.4 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr9:100388078 T>G maps to NM_139246.4 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr9:100388015 G>A maps to NM_139246.4 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr9:100380036 A>G did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:43222388 C>T maps to NM_032538.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:43220479 A>T maps to NM_032538.1 K38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr6:43230733 C>A maps to NM_032538.1 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:43214424 G>A maps to NM_032538.1 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr15:43044497 C>A maps to ENST00000263802 L1387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr15:43102901 G>A maps to ENST00000263802 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:43038280 C>T maps to ENST00000263802 R1554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:231064750 G>A maps to NM_024525.4 H463H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr1:231061287 G>A maps to NM_024525.4 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:231047214 C>T did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr3:180321092 A>T maps to NM_133462.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr3:180322056 G>A maps to NM_133462.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr3:180328269 G>A maps to NM_133462.3 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr3:180321059 G>A maps to NM_133462.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr3:180324049 C>T maps to NM_133462.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:3391501 C>T maps to NM_016030.5 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr2:3469399 G>T maps to NM_016030.5 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:3469390 G>C maps to NM_016030.5 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr2:3392314 C>T maps to NM_016030.5 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr9:130485520 C>T maps to NM_144965.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr9:130482359 C>T maps to NM_144965.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:130493458 C>A maps to NM_144965.1 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr9:130479957 C>T maps to NM_144965.1 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr9:130487068 C>G maps to NM_144965.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr9:130493005 G>A maps to NM_144965.1 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:43428726 G>T maps to NM_018259.5 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr11:43419531 G>T maps to NM_018259.5 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr10:75051479 C>T maps to NM_145170.3 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr10:75082774 T>C maps to NM_145170.3 R356R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-6951-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr17:15902869 C>G maps to NM_017775.2 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr15:99758830 C>T maps to NM_022905.4 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:34863072 G>A maps to NM_144725.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr5:34867131 G>A maps to NM_144725.3 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr5:34867132 C>T maps to NM_144725.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:156554970 A>G maps to NM_001105669.2 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:40094864 G>T maps to ENST00000377543 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:40091558 G>A maps to ENST00000377543 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:138827002 T>C maps to NM_024926.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr2:32927944 A>G maps to NM_017735.4 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr2:33036233 G>A maps to NM_017735.4 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr2:32855701 T>C maps to NM_017735.4 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:147861011 C>A maps to ENST00000513335 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr21:38538337 C>G maps to NM_003316.3 V1274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr21:38560887 G>A maps to NM_003316.3 L1672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:38538151 G>A maps to NM_003316.3 R1212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr21:38523185 T>C did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr21:38529113 G>A maps to NM_003316.3 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr21:38520907 G>A maps to NM_003316.3 K693K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:40747076 G>C maps to NM_012382.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr8:109462083 G>T maps to NM_014673.3 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:109491299 T>G maps to NM_014673.3 Y256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr8:109482342 G>T maps to NM_014673.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:94842672 G>A maps to NM_014639.3 Y1019Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:94876456 C>T maps to NM_014639.3 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:94860295 C>T did not map to a codon.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr5:94833131 T>C maps to NM_014639.3 Q1208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr5:94820489 G>A maps to NM_014639.3 Q1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr9:15199905 G>A maps to NM_152574.2 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:15190561 G>A maps to NM_152574.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr9:15214243 T>C maps to NM_152574.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr9:15172091 A>G maps to NM_152574.2 D658D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr18:21703802 C>T maps to NM_001135993.1 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr18:21649176 C>A maps to NM_001135993.1 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr18:21660588 G>A maps to NM_001135993.1 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr14:20768885 C>A maps to NM_138376.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:47300992 C>T maps to ENST00000394850 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr2:47278894 G>A maps to ENST00000394850 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:47278982 C>T maps to ENST00000394850 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr14:91142992 G>A maps to NM_001010854.1 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr14:91084370 C>T maps to NM_001010854.1 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:89305908 A>G maps to NM_144596.2 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr19:40723997 C>T maps to NM_152479.5 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr9:135277017 G>A maps to NM_007344.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr9:135273708 G>A maps to NM_007344.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr9:135267529 C>T maps to NM_007344.2 K640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr1:117618363 C>T maps to NM_003594.3 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:117644142 C>T maps to NM_003594.3 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr1:117624535 A>T maps to NM_003594.3 K624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr1:117631429 C>G maps to NM_003594.3 S723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr6:80720549 A>G maps to NM_003318.4 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr6:80749471 G>A maps to NM_003318.4 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:113251797 C>G maps to NM_153712.4 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:43460218 C>T maps to NM_012263.4 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:1120450 C>A maps to NM_001130045.1 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:1118412 G>A maps to NM_001130045.1 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:124794103 C>T maps to NM_001139442.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr9:124751884 G>A maps to NM_001139442.1 C376C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr22:43576831 G>A maps to NM_015140.3 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr22:43576770 G>A maps to NM_015140.3 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:43575867 G>A maps to NM_015140.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:90801268 G>A did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:167753591 G>C did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr6:167754656 G>A maps to NM_031949.4 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr6:167754935 G>C maps to NM_031949.4 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr6:167753960 C>T maps to NM_031949.4 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:9877029 C>T maps to NM_001025930.3 R869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:219602783 C>T maps to NM_014640.4 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr2:219610492 C>T maps to NM_014640.4 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr14:76249856 C>T maps to NM_015072.4 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:76245980 C>T maps to NM_015072.4 F817F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr17:46847447 G>A maps to NM_001130918.1 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr17:46862374 G>A maps to NM_001130918.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr1:84387019 G>C maps to NM_024686.4 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr20:30497541 G>T maps to NM_001008409.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:30522679 G>A maps to NM_001008409.2 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:179537202 C>A maps to NM_133378.4 E10320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:179553840 G>C maps to NM_133378.4 P9434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:179583700 C>G did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:179659843 G>T maps to NM_133378.4 Y350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:179583154 G>T maps to NM_133378.4 T6982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr2:179659933 A>G maps to NM_133378.4 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:179400543 C>A maps to NM_133378.4 E31032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr2:179593404 C>A maps to NM_133378.4 V5172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr2:179655563 C>T maps to NM_133378.4 Q557Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr2:179575888 G>C maps to NM_133378.4 L8114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:179569096 C>G maps to NM_133378.4 L8756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:179497259 G>A maps to NM_133378.4 I11923I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:179466433 G>A maps to NM_133378.4 A15893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:179597006 T>A maps to NM_133378.4 L4319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:179598041 G>A maps to NM_133378.4 H4082H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:179605072 G>T maps to NM_133437.3 S4125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr2:179455599 A>G maps to NM_133378.4 T17716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr2:179483377 C>G maps to NM_133378.4 G13065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:179616569 T>C maps to ENST00000375038 E3521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:179650576 G>A maps to NM_133378.4 Q790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr2:179399514 C>A maps to NM_133378.4 E31375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr2:179428691 C>A maps to NM_133378.4 L24821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr2:179497063 C>T maps to NM_133378.4 E11951E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr2:179436107 G>C maps to NM_133378.4 V22349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr2:179476144 G>A maps to NM_133378.4 S14369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr2:179641975 G>A maps to NM_133378.4 R1572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:179598557 G>T maps to NM_133378.4 T3942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:179478782 C>T maps to NM_133378.4 Q13879Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:179482707 G>T maps to NM_133378.4 I13222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:179669321 C>T maps to NM_133378.4 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr2:179650466 G>A maps to NM_133378.4 I791I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:179437568 C>T maps to NM_133378.4 L21862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr2:179475026 C>A maps to NM_133378.4 G14508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr2:179535850 A>T maps to NM_133378.4 T10457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr2:179443830 G>T maps to NM_133378.4 G20074G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:179611823 C>T maps to ENST00000375038 E5103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:179412920 C>T maps to NM_133378.4 R28576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:179638441 C>G maps to NM_133378.4 V2447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr2:179603910 G>A maps to NM_133437.3 S4512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:179482530 G>T maps to NM_133378.4 P13281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr2:179444519 A>G maps to NM_133378.4 C19900C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr2:179469533 G>T maps to NM_133378.4 G15526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr2:179586739 T>C maps to NM_133378.4 K6306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:179417225 G>C maps to NM_133378.4 S27566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr2:179431565 A>T maps to NM_133378.4 I23863I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:179470317 G>T maps to NM_133378.4 R15334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:179439362 G>T maps to NM_133378.4 T21264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:179579977 G>A maps to NM_133378.4 F7401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr2:179404535 T>C maps to NM_133378.4 A30184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr2:179539080 T>G maps to NM_133378.4 P10255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr2:179481234 G>A maps to NM_133378.4 R13527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:179392224 A>G maps to NM_133378.4 N33308N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:179482515 A>T maps to NM_133378.4 A13286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:179438978 G>T maps to NM_133378.4 I21392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:179474459 A>G maps to NM_133378.4 I14662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:179584097 G>A maps to NM_133378.4 R6763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:179659663 G>A maps to NM_133378.4 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:179430728 A>G maps to NM_133378.4 D24142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:179462733 C>A maps to NM_133378.4 E16487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:179642180 G>T maps to NM_133378.4 G1537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:179647598 G>A maps to NM_133378.4 R1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr2:179428333 G>T maps to NM_133378.4 R24941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr2:179599566 G>A maps to NM_133378.4 V3784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr2:179571655 G>T maps to NM_133378.4 T8445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:179411787 A>T maps to NM_133378.4 A28920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:179581891 G>T maps to NM_133378.4 A7279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179419417 G>T maps to NM_133378.4 T26984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179442238 T>C did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179490066 T>C maps to NM_133378.4 L12259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179578834 C>T maps to NM_133378.4 E7606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179617887 A>G maps to NM_133378.4 H3441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:179423145 G>T maps to NM_133378.4 R26446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:179604399 A>G maps to NM_133437.3 T4349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:179436458 G>T maps to NM_133378.4 T22232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr2:179635015 C>G maps to NM_133378.4 V2804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr2:179638097 T>C did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr2:179592513 T>C maps to NM_133378.4 L5353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:179467096 C>T maps to NM_133378.4 K15776K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr2:179600757 T>C maps to NM_133378.4 T3561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr2:179463493 C>T maps to NM_133378.4 A16413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:179413403 C>T maps to NM_133378.4 V28415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:179414055 C>T maps to NM_133378.4 W28198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:179416807 C>T maps to NM_133378.4 K27705K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:179489446 C>A maps to NM_133378.4 E12286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:179598473 G>A maps to NM_133378.4 I3970I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:179600388 G>A maps to NM_133378.4 L3684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:179604009 G>A maps to NM_133437.3 F4479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:179606172 C>T maps to NM_133437.3 L3758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:179633553 C>T maps to NM_133378.4 K3003K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr2:179566973 T>A did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr2:179593062 A>G maps to NM_133378.4 S5252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:179462704 T>C maps to NM_133378.4 R16496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:179599096 C>A maps to NM_133378.4 E3908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:179654191 A>T maps to NM_133378.4 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:179659888 C>A maps to NM_133378.4 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:179451301 C>T maps to NM_133378.4 A18874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:179586796 A>G maps to NM_133378.4 S6287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr2:179587664 C>A did not map to a codon.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:179435189 T>A maps to NM_133378.4 T22655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr2:179413859 T>G maps to NM_133378.4 T28263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:179612931 G>T maps to ENST00000375038 S4734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr2:179648931 C>T maps to NM_133378.4 Q880Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179439623 G>A maps to NM_133378.4 T21177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179446508 G>A maps to NM_133378.4 F19594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179486277 G>A maps to NM_133378.4 N12523N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179590732 G>A maps to NM_133378.4 T5528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179594213 C>T maps to NM_133378.4 T4979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179605332 A>T maps to NM_133437.3 P4038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179616728 C>T maps to ENST00000375038 R3468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr2:179434640 T>C maps to NM_133378.4 P22838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr2:179452441 C>T maps to NM_133378.4 V18630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:179437280 C>T maps to NM_133378.4 L21958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:179578645 G>T maps to NM_133378.4 C7669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:179639114 T>C maps to NM_133378.4 P2292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:179399559 G>A maps to NM_133378.4 Q31360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:179579025 G>T maps to NM_133378.4 S7581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:179616518 A>G maps to ENST00000375038 T3538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr2:179537197 T>C maps to NM_133378.4 V10321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:179426381 A>G maps to NM_133378.4 G25591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:179463271 G>A maps to NM_133378.4 I16456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr2:179588169 A>T maps to NM_133378.4 S5975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:179615717 C>T maps to ENST00000375038 Q3805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr2:179604204 A>G maps to NM_133437.3 T4414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr2:179433971 C>T maps to NM_133378.4 G23061G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr2:179441373 G>T maps to NM_133378.4 C20631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr2:179452803 C>T maps to NM_133378.4 A18542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr2:179594421 C>A maps to NM_133378.4 T4942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr2:179391792 C>T maps to NM_133378.4 G33406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr2:179571292 G>A maps to NM_133378.4 R8526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr2:179496027 C>A did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr2:179641979 A>G maps to NM_133378.4 G1570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr2:179589209 C>G maps to NM_133378.4 T5720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr2:179594237 G>A maps to NM_133378.4 D4971D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr2:179476183 A>G maps to NM_133378.4 Y14356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr2:179615320 G>A maps to ENST00000375038 R3938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr2:179480378 G>C maps to NM_133378.4 S13582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr2:179615426 T>A maps to ENST00000375038 I3902I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr2:179588289 T>C maps to NM_133378.4 K5935K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr2:179628973 G>A maps to NM_133378.4 I3348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr2:179455353 G>A maps to NM_133378.4 C17798C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr2:179498021 G>A maps to NM_133378.4 Y11758Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr20:43108866 C>T maps to NM_024331.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:54930384 C>T maps to ENST00000391739 C70C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr19:54930405 C>T maps to ENST00000391739 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr17:72233623 C>T maps to NM_032646.5 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:2686530 G>A maps to NM_025250.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr11:8123159 C>T maps to NM_003320.4 C560C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr12:49580116 G>A maps to NM_006009.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr12:49580523 G>A maps to NM_006009.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr12:49579179 C>A maps to NM_006009.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:49521799 C>A maps to NM_006082.2 E433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr12:49522571 G>A maps to NM_006082.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr13:19751081 G>T maps to NM_006001.1 C347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr13:19755883 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr13:19752451 G>A maps to NM_006001.1 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr13:19751432 C>G maps to NM_006001.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr2:220116385 G>A maps to NM_006000.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:220116736 C>T maps to NM_006000.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr2:220115610 G>T maps to NM_006000.1 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr10:5435650 C>T maps to NM_024803.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:5437376 C>T maps to NM_024803.2 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:5442962 G>A maps to NM_024803.2 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr9:140137530 C>T maps to NM_006088.5 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:140137605 G>A maps to NM_006088.5 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr9:140136999 G>A maps to NM_006088.5 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr16:90001359 C>T maps to ENST00000304984 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:6495567 G>A maps to NM_006087.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr18:12325642 C>A maps to NM_032525.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr18:12311044 C>T maps to NM_032525.1 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr10:93791 C>A maps to NM_177987.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr10:93287 G>A maps to NM_177987.2 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr17:57955639 G>C maps to NM_016261.3 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr17:57958323 C>T maps to NM_016261.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr17:57955548 A>G maps to NM_016261.3 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr17:57955575 G>A maps to NM_016261.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr10:135094820 A>G maps to NM_006659.2 Y843Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr10:135096617 G>A maps to NM_006659.2 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:135106654 C>T maps to NM_006659.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr10:135106019 G>A maps to NM_006659.2 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr10:135094860 G>C maps to NM_006659.2 S830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr13:113200120 C>T maps to NM_006322.4 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr13:113213690 G>C maps to NM_006322.4 S92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:113210455 G>A maps to NM_006322.4 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr15:43668715 C>T maps to ENST00000399460 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr15:43687328 G>T maps to ENST00000399460 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8569-01A-11D-2394-08 chr15:43670085 A>G maps to ENST00000399460 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:22850971 C>T maps to NM_052903.4 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr15:22866730 T>C maps to NM_052903.4 F781F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr22:50656374 G>A maps to NM_020461.3 F1780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr22:50682456 C>A maps to NM_020461.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr22:50662571 C>T maps to NM_020461.3 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr22:50659211 A>C maps to NM_020461.3 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr16:28856349 G>A maps to NM_003321.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr16:28854442 C>T maps to NM_003321.4 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr6:35479473 G>A maps to NM_003322.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr6:35473537 C>T maps to NM_003322.3 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:49391428 C>A maps to NM_003323.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:49398632 C>T maps to NM_003323.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:49387076 C>T maps to NM_003323.2 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr6:158923679 G>A maps to NM_020245.3 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr6:158923367 C>T maps to NM_020245.3 F891F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr6:158924159 G>A maps to NM_020245.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:15480729 C>T maps to NM_006765.2 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr8:15601045 G>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:15601075 C>T maps to NM_006765.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:1183396 G>A maps to NM_172367.2 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr11:62343618 C>T maps to NM_022830.2 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr11:62348580 G>A maps to NM_022830.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:44191150 G>A maps to NM_002822.3 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr3:52263739 G>A maps to ENST00000494383 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:19156445 C>A maps to NM_000474.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr7:19748630 T>A maps to NM_001002926.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr18:9360007 C>G maps to NM_020648.5 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr18:9396465 G>T maps to NM_020648.5 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr4:48096213 C>A maps to NM_003328.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr4:48096214 C>A maps to NM_003328.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr4:48081952 C>T maps to NM_003328.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:32660618 G>C maps to NM_175852.3 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:139576739 C>T maps to ENST00000358430 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr6:139563751 G>A maps to ENST00000358430 R656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:113006437 T>C maps to NM_003329.2 *106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr16:11785383 C>T maps to ENST00000356957 E581E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr16:11794370 C>T maps to ENST00000356957 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr14:53010230 G>C maps to NM_020784.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr18:9887609 A>G maps to NM_001098529.1 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr18:9887576 C>T maps to NM_001098529.1 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr18:9886721 C>T maps to NM_001098529.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:37903064 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:37903046 C>A maps to NM_016616.4 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr6:7884681 T>C maps to NM_030810.3 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr3:138023769 G>A maps to ENST00000333911 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr3:138037034 G>A maps to ENST00000333911 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr2:99949493 C>T maps to NM_005783.3 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:54293688 C>A did not map to a codon.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr16:72122886 C>A maps to NM_001142318.1 G95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr12:104732984 G>A maps to NM_001093771.1 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:104645323 T>A maps to NM_001093771.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr22:19868177 G>A maps to NM_006440.3 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr22:19868159 C>A maps to NM_006440.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:19865924 C>T maps to NM_006440.3 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr22:19864629 A>G maps to NM_006440.3 *525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:126291215 C>A maps to NM_001039783.1 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:10464799 C>A maps to NM_003331.4 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:10475628 C>T maps to NM_003331.4 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr19:10476498 C>G maps to NM_003331.4 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr19:10488919 C>A maps to NM_003331.4 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:10464865 G>A maps to NM_003331.4 N920N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:10475300 G>A maps to NM_003331.4 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr19:10477148 G>C maps to NM_003331.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr19:10461533 G>A maps to NM_003331.4 A1180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr22:50967606 G>A maps to ENST00000395681 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr18:670728 C>A maps to NM_001071.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr11:88911534 C>T maps to NM_000372.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr11:88911459 A>C maps to NM_000372.4 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:88911531 C>A maps to NM_000372.4 Y137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr15:41864734 C>T maps to NM_006293.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr15:41870396 C>T maps to NM_006293.3 Q866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:36398447 C>A maps to NM_003332.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr10:71903625 G>T maps to NM_173555.2 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr10:71902545 G>C maps to NM_173555.2 S454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr7:66660170 C>T maps to NM_018264.2 C608C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr7:66660158 C>T maps to NM_018264.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr7:72159742 G>A maps to NM_001145440.1 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:72267522 G>A maps to NM_001145440.1 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:36234911 C>T did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:56166481 C>T maps to NM_007279.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr19:56180836 C>T maps to NM_007279.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr15:70959586 G>A maps to NM_018003.2 Q1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr15:70960220 C>A maps to NM_018003.2 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:162536138 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr1:162569110 C>T maps to ENST00000367925 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr1:162557311 A>G maps to ENST00000367925 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr9:139974546 C>T maps to NM_207309.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:47074276 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:47060899 C>T did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:47069516 G>C did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:47058239 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr3:69105054 G>T maps to NM_003968.3 S417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr3:132390724 G>A maps to NM_024818.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr4:68543385 T>A maps to NM_018227.5 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr3:49842757 G>A maps to NM_003335.2 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr3:49847985 G>C maps to NM_003335.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr13:100037587 G>A maps to NM_001144072.1 *345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr9:33933497 G>A maps to NM_018449.2 Q700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:154197668 C>T maps to NM_014847.3 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:154223668 C>T maps to NM_014847.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:154223758 A>T maps to NM_014847.3 K486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:154223769 G>A maps to NM_014847.3 K489K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr1:154239019 G>A maps to NM_014847.3 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr21:43862565 C>G maps to NM_018961.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr21:43833585 C>T maps to NM_018961.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr21:43857619 T>C maps to NM_018961.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr11:122666899 C>T maps to NM_032873.4 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr17:16285799 G>A maps to NM_018955.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr12:125397264 T>C maps to NM_021009.5 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr12:125397962 A>G maps to NM_021009.5 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr12:125397971 G>A maps to NM_021009.5 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:125397804 G>C maps to NM_021009.5 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:125398023 G>A maps to NM_021009.5 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr12:125397651 T>C maps to NM_021009.5 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr12:125396268 C>G maps to NM_021009.5 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr12:125397147 A>G maps to NM_021009.5 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr12:125397153 C>G maps to NM_021009.5 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr6:29523953 G>T maps to NM_006398.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:83767584 T>G maps to NM_198920.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr5:138994174 C>T maps to NM_003339.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:103723795 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:23932087 C>A maps to NM_003341.3 Y191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr3:23574160 C>T maps to NM_152653.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr21:46193488 G>A maps to NM_003343.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr16:1374784 G>T maps to NM_194259.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr16:1364313 A>C maps to NM_194259.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:59068276 C>T maps to NM_003969.3 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:142967295 G>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:142967282 A>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:142967600 C>A did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr23:142967321 T>A did not map to a codon.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr23:142967436 C>A did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:74392379 C>A maps to NM_022066.3 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr17:74387542 G>A maps to NM_022066.3 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr1:154524643 G>A maps to NM_017582.6 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:154523417 T>C maps to NM_017582.6 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr1:154527221 C>A maps to NM_017582.6 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr15:76171513 T>G maps to NM_173469.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr15:76183294 C>T maps to NM_173469.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr9:33917125 C>G maps to NM_017811.3 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr9:33900203 G>T maps to NM_017811.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:55915772 G>A maps to NM_014501.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:55915801 G>A maps to NM_014501.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr12:109972412 G>T maps to NM_183415.1 L1011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:109945504 G>A maps to NM_183415.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:109972427 G>A maps to NM_183415.1 R1016R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr12:109937498 C>T maps to NM_183415.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr12:109921469 C>T maps to NM_183415.1 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr7:157046700 G>C maps to NM_014671.2 R916R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr7:156979547 A>G maps to NM_014671.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:118239344 G>C did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:118260438 G>A did not map to a codon.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr11:118263535 G>A maps to NM_004788.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr11:118267058 C>T maps to NM_004788.2 P1042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr11:118253481 G>T maps to NM_004788.2 E737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr11:118250275 C>T maps to NM_004788.2 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:10207076 G>A maps to NM_001105562.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr1:10239992 G>A maps to NM_001105562.2 E1296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:10132156 C>A maps to NM_001105562.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:10166446 T>G maps to NM_001105562.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:10231323 A>G maps to NM_001105562.2 Q1154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr1:10197128 C>T maps to NM_001105562.2 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr16:23570828 C>T maps to ENST00000219638 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:23570849 G>A maps to ENST00000219638 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:23569514 C>T maps to ENST00000219638 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr16:23574001 G>A maps to ENST00000219638 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:11334043 G>C maps to NM_013319.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:153713957 G>A did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr15:74738532 G>A maps to NM_201265.1 D347D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr15:74740854 C>T maps to NM_201265.1 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr15:74748952 G>A maps to NM_201265.1 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr15:74741682 G>A maps to NM_201265.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr16:4925362 G>T maps to NM_016936.3 V984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr16:4924258 G>A maps to NM_016936.3 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:138969090 C>G maps to NM_173569.3 S1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:138946204 C>T maps to NM_173569.3 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:138964103 A>T maps to NM_173569.3 K689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:138968644 C>T maps to NM_173569.3 P998P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr7:138957169 C>T maps to NM_173569.3 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr7:138968053 G>A maps to NM_173569.3 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:33481235 G>A maps to NM_001128161.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr23:56591209 G>A did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr23:56591222 A>T did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:56590908 G>T did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:5530479 T>G maps to NM_017481.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:5529405 A>G maps to NM_017481.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:156021498 C>T maps to NM_020131.3 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr15:43363030 C>T maps to NM_174916.2 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr15:43350595 G>A maps to NM_174916.2 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:42637958 G>T maps to NM_015255.2 A1337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr6:42559957 T>C maps to NM_015255.2 H136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:42574325 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr6:42573561 G>T maps to NM_015255.2 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:19487410 C>T maps to ENST00000375267 Q1802Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr1:19525297 G>C maps to ENST00000375267 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr1:19451154 A>G maps to ENST00000375267 Y3156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:19453066 G>C maps to ENST00000375267 S3104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:19505573 G>A maps to ENST00000375267 D775D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7100-01A-11D-2012-08 chr1:19451142 T>G maps to ENST00000375267 L3160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr1:19487580 G>A maps to ENST00000375267 Q1746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr1:19478947 C>T maps to ENST00000375267 V2285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:19440288 G>T maps to ENST00000375267 S3787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:19447896 G>A maps to ENST00000375267 F3309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:103289201 G>A maps to NM_015902.4 F2169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr8:103305963 G>C maps to NM_015902.4 V1486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr8:103301698 A>T maps to NM_015902.4 V1565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr8:103281236 C>A maps to NM_015902.4 E2444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr8:103305834 G>A maps to NM_015902.4 S1529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:103297761 G>C maps to NM_015902.4 Y1821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr8:103291307 G>A maps to NM_015902.4 L2044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr8:103287968 T>A maps to NM_015902.4 V2199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr8:103317372 A>G maps to NM_015902.4 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr8:103324677 T>C maps to NM_015902.4 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:103310704 C>T maps to NM_015902.4 G1113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:103326145 T>C did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:103293653 A>G maps to NM_015902.4 D1930D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr8:103293650 C>T maps to NM_015902.4 E1931E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr17:42290279 A>G maps to NM_014233.2 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:42287533 C>T maps to NM_014233.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr17:42288699 C>G did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr17:42293956 T>C maps to NM_014233.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr11:62445535 C>T maps to NM_015853.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:62444319 G>C maps to NM_015853.3 S270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr1:20517145 C>A maps to NM_152376.3 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr1:26609383 C>T maps to NM_183008.2 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr8:59352287 G>A maps to NM_001077619.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr2:136499549 G>A maps to NM_014607.3 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr2:136511786 A>G maps to NM_014607.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr19:4447567 C>T maps to NM_025241.2 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr19:4446696 G>A maps to NM_025241.2 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr19:4445518 C>A maps to NM_025241.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:196098826 G>A maps to NM_015562.1 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:30620833 G>A maps to ENST00000265616 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr4:41265297 C>T maps to NM_004181.4 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr1:193028339 G>C maps to ENST00000367450 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr20:62575961 G>T maps to NM_017859.3 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr10:13275759 C>T maps to NM_145314.1 Q33Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:5415733 C>G maps to NM_053049.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr11:73689423 G>C did not map to a codon.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr11:73716904 T>C maps to NM_003356.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr13:38924168 G>T maps to NM_016617.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr9:114676953 G>A maps to NM_003358.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:114676935 C>T maps to NM_003358.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr2:128865572 C>G maps to NM_020120.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:128890737 T>C maps to NM_020120.3 D467D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:128937401 G>C maps to NM_020120.3 V1286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr2:128910375 C>T maps to NM_020120.3 Q679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:234669409 C>T maps to NM_000463.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr2:234669124 C>T maps to NM_000463.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr2:234669574 C>T maps to NM_000463.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr2:234637858 A>G maps to NM_019093.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr2:234637865 T>C maps to NM_019093.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:234638470 C>T maps to NM_019093.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:234627537 C>G maps to NM_007120.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr2:234622485 C>T maps to NM_019078.1 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr2:234621861 C>T maps to NM_019078.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:234602465 C>T maps to NM_001072.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:234591191 C>T maps to ENST00000373460 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:234527111 G>A maps to NM_019076.4 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:70513299 C>T maps to ENST00000514019 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:70512978 G>A maps to ENST00000514019 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr4:70460412 T>C maps to ENST00000514019 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:70455167 A>G maps to ENST00000514019 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr4:70513155 C>G maps to ENST00000514019 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr4:70512981 A>G maps to ENST00000514019 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr4:70455335 A>T maps to ENST00000514019 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr4:69795743 T>C maps to NM_024743.3 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:70079864 G>T maps to NM_001073.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr4:70079795 G>A maps to NM_001073.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr4:69535642 T>A maps to NM_001076.2 K232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr4:69536138 G>A maps to NM_001076.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr4:69513061 A>G maps to NM_001076.2 H451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:69519768 G>T maps to NM_001076.2 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:69519825 G>A maps to NM_001076.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr4:70160520 A>G maps to NM_053039.1 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr4:70156308 G>A did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr4:70156430 T>A maps to NM_053039.1 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr4:70156461 C>T maps to NM_053039.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr4:70155438 G>T maps to NM_053039.1 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr4:70360856 A>G did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:70355208 G>T maps to NM_021139.2 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:70361537 C>T maps to NM_021139.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr4:70360952 C>T maps to NM_021139.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr4:70346486 G>A maps to NM_021139.2 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr4:70346426 C>T maps to NM_021139.2 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr4:70361129 T>C maps to NM_021139.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:69978303 C>A maps to NM_001074.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr4:69962246 G>A maps to NM_001074.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:69962534 C>T maps to NM_001074.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C6-01A-11D-A25D-08 chr5:35991264 C>T maps to NM_152404.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr5:35965517 C>T maps to NM_152404.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr5:35957443 A>G maps to NM_152404.3 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:35954386 G>A maps to NM_152404.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr5:35991317 G>A maps to NM_152404.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:36037912 G>T maps to NM_174914.3 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:36066837 C>A maps to NM_174914.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:115544563 C>T maps to NM_003360.3 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr4:115544354 C>T maps to NM_003360.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr1:162469841 C>G maps to NM_175866.4 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr1:162467789 G>A did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:4950896 G>T maps to ENST00000398240 G582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr19:4932905 G>A maps to ENST00000398240 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr19:4950634 C>G maps to ENST00000398240 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:34827075 C>T maps to NM_017754.3 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:34835328 G>A maps to NM_017754.3 E1218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr6:34826613 C>T maps to NM_017754.3 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:34838700 G>A maps to NM_017754.3 E1263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr6:34789447 C>T maps to NM_017754.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:100492320 T>C did not map to a codon.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr9:6460621 C>T maps to NM_152896.1 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:6506133 G>A maps to NM_152896.1 Q788Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr5:176396608 G>T maps to ENST00000377219 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr5:176370345 C>T maps to ENST00000377219 E529E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:176396023 G>A maps to ENST00000377219 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:150263228 C>A maps to NM_025217.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:150267511 C>T maps to NM_025217.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr6:150267598 C>A maps to NM_025217.2 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:132404536 G>A maps to NM_003565.2 L939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr12:132404648 G>T maps to NM_003565.2 E977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr12:132405860 C>T maps to NM_003565.2 C1036C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:19699442 C>T maps to NM_014683.3 Q654Q. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-6942-01A-21D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr17:19683937 G>A maps to NM_014683.3 V921V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr3:41795980 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:41977349 A>G maps to NM_017886.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr21:43529774 C>T maps to NM_173568.3 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr21:43531074 C>T maps to NM_173568.3 L581L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BB-7863-01A-11D-2229-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CN-A498-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:43508452 C>G maps to NM_173568.3 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr21:43531074 C>T maps to NM_173568.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr21:43547844 C>T maps to NM_173568.3 F1326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr21:43531710 G>A maps to NM_173568.3 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr21:43547901 C>A maps to NM_173568.3 L1345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:124462849 C>T maps to NM_000373.3 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:124456710 G>T maps to NM_000373.3 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr17:26874806 G>C maps to NM_005148.3 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:17740102 T>A maps to ENST00000428389 A1321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:17768872 G>T maps to ENST00000428389 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:17740046 A>G did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr19:17768989 C>T maps to ENST00000428389 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:35389841 G>C did not map to a codon.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr9:35398239 G>A maps to ENST00000396787 L1192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr9:35231141 G>A maps to ENST00000396787 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:35385811 T>C did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:35403455 C>T maps to ENST00000396787 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:35243342 C>T maps to ENST00000396787 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr9:35377546 C>T maps to ENST00000396787 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:54307584 T>C maps to ENST00000260323 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr15:54305603 C>T maps to ENST00000260323 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:54307971 C>T maps to ENST00000260323 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr15:54919299 G>T maps to ENST00000260323 E2212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:54305277 A>T maps to ENST00000260323 K60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr15:54542505 G>A maps to ENST00000260323 T1104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr15:54586183 G>T maps to ENST00000260323 E1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr15:54914564 T>C maps to ENST00000260323 H2049H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr15:54847644 G>T maps to ENST00000260323 E1965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr15:54306701 C>T maps to ENST00000260323 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:54804024 G>A maps to ENST00000260323 K1818K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr15:54307053 G>T maps to ENST00000260323 E652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr15:54542487 C>T maps to ENST00000260323 H1098H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr15:54586114 C>T maps to ENST00000260323 R1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr15:54435231 G>T maps to ENST00000260323 E1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr15:54542532 G>A maps to ENST00000260323 E1113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr15:54685244 G>C did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:73831828 C>T maps to ENST00000412096 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr17:73831564 C>T maps to ENST00000412096 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:91488218 C>T maps to NM_018671.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:91490131 C>T maps to NM_018671.3 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr15:91479548 C>G maps to NM_018671.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr17:33507655 G>A maps to NM_173167.2 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:176304607 C>T maps to NM_133369.2 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:176306885 G>A maps to NM_133369.2 *843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr10:73039770 C>T maps to NM_170744.3 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr10:73053605 G>T maps to NM_170744.3 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr10:73039677 G>A maps to NM_170744.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr10:73046444 G>A did not map to a codon.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr4:96091408 G>A maps to NM_003728.3 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr4:96256762 T>C maps to NM_003728.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:96256639 G>T maps to NM_003728.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:96222796 C>A maps to NM_003728.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:96469981 C>T maps to NM_003728.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr4:96106221 C>T maps to NM_003728.3 K754K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr4:96124061 C>T maps to NM_003728.3 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr4:96091387 C>T maps to NM_003728.3 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr4:96166281 C>T maps to NM_003728.3 W263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr4:96163589 A>G maps to NM_003728.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr4:96469912 G>A maps to NM_003728.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr4:96091444 C>T maps to NM_003728.3 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:35588528 G>A did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:35624526 C>A maps to ENST00000416672 C812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr8:35541102 A>G maps to ENST00000416672 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr8:35608197 C>A maps to ENST00000416672 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:35608236 G>T maps to ENST00000416672 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:35616847 C>G maps to ENST00000416672 S730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr8:35541165 G>T maps to ENST00000416672 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr8:35425629 G>T maps to ENST00000416672 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:35583802 G>A maps to ENST00000416672 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr8:35583898 C>T maps to ENST00000416672 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:167708042 G>T maps to NM_018974.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr6:167728906 G>A maps to NM_018974.3 Q447Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51X-01A-11D-A25Y-08 chr11:67765216 C>T maps to NM_030930.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:73815858 C>T maps to NM_001080419.1 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr19:18968193 C>T maps to ENST00000418384 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr19:18963798 C>T maps to ENST00000418384 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:18976382 G>A maps to ENST00000418384 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:18961673 G>A maps to ENST00000418384 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:12070766 G>C maps to NM_015542.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr10:12006124 C>T did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:11994185 A>G maps to NM_015542.2 D971D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr10:12041913 C>G maps to NM_015542.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr10:12042008 C>T did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr23:118985731 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:118971738 C>T did not map to a codon.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr23:118972411 G>A did not map to a codon.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr23:118977251 C>T did not map to a codon.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr23:118968978 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr11:118828849 G>A maps to NM_006760.3 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr22:45689059 A>T did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr7:76140091 C>A maps to NM_030570.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr7:76140987 C>G maps to ENST00000434948 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr7:48146982 C>G maps to NM_003364.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:48147941 G>T maps to NM_003364.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr2:158962649 G>A maps to NM_001135098.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:74519709 C>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:74494241 C>A did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr23:74494188 C>T did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr23:74494380 G>C did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:74519597 C>T did not map to a codon.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr22:30163554 C>T maps to ENST00000406782 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:29698649 C>T maps to NM_006003.2 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:229772123 G>C maps to NM_014777.2 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr1:229773395 C>A maps to NM_014777.2 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:229773041 C>T maps to NM_014777.2 I894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:229772432 C>T maps to NM_014777.2 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:229770965 C>T maps to NM_014777.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr7:43918731 A>C maps to NM_001077663.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr9:131140338 C>T maps to NM_001135947.1 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:126219701 G>A maps to NM_001165974.1 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:126219566 A>T maps to NM_001165974.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr3:126219695 C>T maps to NM_001165974.1 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr3:126220059 C>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:126220751 G>T maps to NM_001165974.1 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr3:126224561 G>A maps to NM_001165974.1 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:45478995 C>T maps to NM_000374.4 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:45480409 C>A maps to NM_000374.4 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr19:17327090 G>A maps to NM_018467.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr1:161011573 C>T maps to NM_007122.3 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:161011564 A>G maps to NM_007122.3 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr11:17537814 G>A maps to NM_153676.3 Y411Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr11:17548773 C>T maps to NM_153676.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr17:72915895 C>G maps to NM_173477.2 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:215848780 G>A maps to ENST00000366943 Q4158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:216019334 A>T maps to ENST00000366943 L2962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:215824102 C>T maps to ENST00000366943 W4725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:216074209 G>A maps to ENST00000366943 A2446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr1:216348687 A>T maps to ENST00000366943 A1511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:216373029 C>T maps to ENST00000366943 K1250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:216040364 C>G maps to ENST00000366943 V2943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:215901488 C>T maps to ENST00000366943 L3983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:215848508 A>G maps to ENST00000366943 H4248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:216052139 G>A maps to ENST00000366943 Q2842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr1:216498644 A>G did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:215955410 C>G maps to ENST00000366943 T3571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:215847663 G>T maps to ENST00000366943 S4530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:215847914 G>A maps to ENST00000366943 N4446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:215823957 G>A maps to ENST00000366943 S4773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:215848241 C>G maps to ENST00000366943 T4337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:215914856 C>T maps to ENST00000366943 R3857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr1:216420041 C>T maps to ENST00000366943 Q898Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:216260109 G>C maps to ENST00000366943 V1646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:215963414 C>A maps to ENST00000366943 G3390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:215990529 G>A maps to ENST00000366943 Q3127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:216040364 C>A maps to ENST00000366943 V2943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:215820915 G>A maps to ENST00000366943 N4913N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr1:216258089 C>T maps to ENST00000366943 W1706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:215914772 A>T maps to ENST00000366943 I3885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61V-01A-11D-A28R-08 chr1:216420131 A>G maps to ENST00000366943 C868C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr1:216595552 G>A maps to ENST00000366943 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A634-01A-11D-A28R-08 chr1:216258154 C>T maps to ENST00000366943 P1684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr1:215848733 C>G maps to ENST00000366943 L4173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr1:216108137 C>A did not map to a codon.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr1:216251524 G>A maps to ENST00000366943 S1826S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:17373675 C>T maps to NM_031941.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr4:76721830 A>C maps to NM_003715.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr4:76708300 G>A maps to NM_003715.2 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr4:76725348 C>G maps to NM_003715.2 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:62908867 G>A maps to NM_003368.4 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:62907260 T>C maps to NM_003368.4 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr1:62913121 C>T maps to NM_003368.4 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr16:84808829 A>T maps to NM_005153.2 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr23:47098751 G>C did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:47101691 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:47092373 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr23:47102103 G>A did not map to a codon.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr23:47100674 G>T did not map to a codon.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr23:47107269 G>T did not map to a codon.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr23:47104855 G>A did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:27649389 T>C maps to NM_182488.3 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:179472518 G>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr3:179399664 G>C did not map to a codon.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr3:179439329 C>T maps to NM_003940.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr18:202938 C>T maps to NM_005151.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:62786083 A>G maps to ENST00000280377 K779K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr21:30414332 G>C did not map to a codon.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr8:11995294 G>A maps to NM_201402.2 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr22:18650682 G>A maps to NM_017414.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:49155174 G>C maps to ENST00000434032 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7072-01A-21D-A30E-08 chr3:49153321 T>C maps to ENST00000434032 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:49149393 G>A maps to ENST00000434032 A949A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:49152478 G>A maps to ENST00000434032 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr11:119243869 G>T maps to NM_004205.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:119229765 A>T maps to NM_004205.4 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr9:132637881 C>T maps to NM_001008563.3 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr1:161133692 T>C maps to NM_012475.4 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:55545228 C>A maps to NM_015306.2 G2394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:55598229 G>C maps to NM_015306.2 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:55599817 C>T maps to NM_015306.2 R1102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:55559720 G>A maps to NM_015306.2 S2081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-8568-01A-11D-2394-08 chr1:55614213 T>A maps to NM_015306.2 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr21:17236766 T>A did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:132159532 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:132162178 C>G did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr23:132161247 G>T did not map to a codon.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr23:132161098 G>C did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:132159730 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:132159686 C>A did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr11:113683211 C>T maps to NM_020886.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr11:113712436 A>G maps to NM_020886.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr11:113711430 G>A maps to NM_020886.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr11:113679957 G>C maps to NM_020886.2 S664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr11:113673936 C>T maps to NM_020886.2 G935G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C4-01A-11D-A30E-08 chr11:113684606 C>T maps to NM_020886.2 Q581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr19:57640563 C>A maps to NM_020903.2 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:57641828 G>T maps to NM_020903.2 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:57640144 G>A maps to NM_020903.2 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:57641737 C>A maps to NM_020903.2 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:57641803 C>T maps to NM_020903.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:57641575 G>A maps to NM_020903.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr19:57641824 C>A maps to NM_020903.2 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr15:63855162 A>G maps to NM_006537.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:109522851 C>T maps to NM_032663.3 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr12:109520484 G>A maps to NM_032663.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr16:23116890 G>A maps to NM_020718.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr17:58329764 C>T maps to NM_032582.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:58288741 G>C maps to NM_032582.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr17:58258921 C>T maps to NM_032582.3 Q1437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr17:58262996 C>A maps to NM_032582.3 E1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr1:78183705 G>A maps to NM_015017.3 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr1:78200090 A>G maps to NM_015017.3 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr2:61415539 A>G maps to NM_014709.3 D3446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr2:61597494 C>T maps to NM_014709.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr2:61597671 A>G maps to NM_014709.3 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:61508320 C>T maps to NM_014709.3 L1685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:61570971 A>G maps to NM_014709.3 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr2:61597521 C>T maps to NM_014709.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:61492561 A>T maps to NM_014709.3 P1916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr2:61566563 G>T maps to NM_014709.3 S889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr2:61575591 G>A maps to NM_014709.3 D566D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QE-01A-11D-A28R-08 chr2:61430322 G>A maps to NM_014709.3 R3154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr11:77924729 C>A maps to NM_020798.2 I976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:77911808 C>T maps to NM_020798.2 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:77921126 G>A maps to NM_020798.2 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr2:219324527 C>G maps to NM_020935.2 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr2:219341589 G>A maps to NM_020935.2 N672N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr3:49329941 C>G did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:49321936 G>C maps to NM_003363.3 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr3:49343282 G>A maps to NM_003363.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:234465563 C>A maps to NM_018218.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr2:234460154 A>C maps to NM_018218.2 L247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:6182586 T>C maps to ENST00000404835 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:9631982 C>G maps to NM_153210.3 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr17:9578274 C>T maps to NM_153210.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:95927269 G>A maps to NM_032147.2 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:99883591 T>C maps to NM_001080481.1 *815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:11964240 T>C maps to ENST00000399455 P898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr11:11913621 C>G maps to ENST00000399455 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:22016568 A>G maps to NM_032236.5 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr1:22056205 G>A maps to NM_032236.5 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:41767598 G>A maps to ENST00000373009 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr6:41773476 G>C maps to ENST00000373009 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:6966014 G>A maps to NM_001098536.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:6973917 C>T maps to NM_001098536.1 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:50830916 G>A maps to ENST00000456636 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr23:55514101 G>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:55513446 A>T did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr23:55513553 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:55513684 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:55515082 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr23:55513640 C>T did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:120190942 A>G maps to NM_019050.2 Q462Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr4:120177468 A>G maps to NM_019050.2 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr4:120190940 C>T maps to NM_019050.2 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr4:120188599 C>T maps to NM_019050.2 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:75331187 G>A maps to NM_152586.3 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr17:5042700 T>G maps to NM_004505.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr17:5064822 T>A maps to NM_004505.2 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:11505306 C>T maps to NM_001080491.2 E557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr15:50769167 G>A maps to NM_005154.3 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:50791261 C>T maps to NM_005154.3 R1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr15:50788055 G>C maps to NM_005154.3 R890R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr15:50784948 T>A maps to NM_005154.3 I762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr15:50763973 G>C maps to NM_005154.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr23:41007693 G>A did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr23:41007736 G>T did not map to a codon.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr23:41000631 A>G did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:41075703 G>C did not map to a codon.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr23:41077798 G>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:41077826 G>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:41069828 G>T did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:41048593 C>T did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:41000591 G>A did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:41031205 C>G did not map to a codon.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr23:40990714 G>T did not map to a codon.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr23:40994015 C>T did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:41002597 C>T did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:41027467 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:41077794 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:41082518 T>A did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr23:40988322 C>T did not map to a codon.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr23:41075167 G>A did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr23:41027442 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr23:41088842 G>A did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:41027442 G>T did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:41088906 C>T did not map to a codon.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr23:41056743 G>C did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:41089763 A>G did not map to a codon.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr23:41000615 G>T did not map to a codon.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr24:14885610 C>G did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr24:14958425 T>C did not map to a codon.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr24:14832659 A>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr13:31233366 A>G maps to NM_005800.4 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr13:31205138 C>T maps to NM_005800.4 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr1:38484940 C>T maps to NM_016037.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:129053150 G>T did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:129059036 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:129063381 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr23:129059975 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr23:129045062 A>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:129059901 A>G did not map to a codon.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr23:129060289 G>A did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr23:129059986 A>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:72868353 A>T maps to NM_032175.2 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr17:49371298 C>T maps to NM_016001.2 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr12:101732714 A>G maps to NM_014503.2 K1331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:101679590 C>T maps to NM_014503.2 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr12:101680211 G>A maps to NM_014503.2 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:117782553 G>T maps to NM_032334.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr17:30214305 A>G maps to NM_018428.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:30213065 A>G maps to NM_018428.2 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr17:30192411 A>G maps to NM_018428.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:144843113 A>G did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:145093084 C>A maps to NM_007124.2 T2846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr6:145069595 G>A maps to NM_007124.2 K2718K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr6:144837952 G>T maps to NM_007124.2 E1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:144875971 C>G maps to NM_007124.2 L2359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:144779940 G>T maps to NM_007124.2 E774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr6:145093096 A>G maps to NM_007124.2 Q2850Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr6:145021234 G>A maps to NM_007124.2 E2555E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr6:144769777 C>T maps to NM_007124.2 Q649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:144844226 G>T maps to NM_007124.2 E1937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr6:145093099 C>T maps to NM_007124.2 S2851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr6:145142115 G>A maps to NM_007124.2 L3152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:144780130 T>A maps to NM_007124.2 L837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr6:145095468 C>T maps to NM_007124.2 I2867I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr11:75715073 C>G maps to NM_003369.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:47516686 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr23:47518278 T>C did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr23:47518283 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr16:70721965 G>C maps to NM_018052.3 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:6575057 C>A maps to ENST00000396308 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:6575057 C>A maps to ENST00000396308 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr2:85818954 G>A maps to NM_006634.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:155169400 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr23:155171681 C>G did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr1:160389069 C>T maps to NM_020335.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr1:160394930 G>A maps to NM_020335.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr18:9936134 G>A maps to NM_003574.5 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:57015991 C>T maps to NM_004738.4 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:31750117 G>C maps to NM_006295.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:31749636 G>A maps to NM_006295.2 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr6:31747891 G>A maps to NM_006295.2 R988R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:31759486 G>A maps to NM_006295.2 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr6:31747295 G>A maps to NM_006295.2 P1102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr6:30890715 T>C maps to NM_001167734.1 D746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr6:30888895 C>T maps to NM_001167734.1 Q542*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-5248-01A-01D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:213134596 G>T did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:213147382 C>T maps to NM_001136474.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr16:4432461 C>T maps to NM_138440.2 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr16:4431561 G>A maps to NM_138440.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:41170068 C>T maps to NM_006373.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr17:41170801 C>T maps to NM_006373.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:77910305 C>T maps to NM_020927.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:6828658 C>G maps to NM_005428.2 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:6854108 G>T maps to NM_005428.2 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:136641199 C>A maps to NM_001134398.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:136671216 G>A maps to NM_001134398.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:136635536 C>A maps to NM_001134398.1 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr9:136671255 G>A maps to NM_001134398.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr1:108417603 C>A maps to NM_006113.4 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:108116683 T>A maps to NM_006113.4 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr1:108307727 C>T maps to NM_006113.4 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:108298047 C>T did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:118896128 G>A maps to NM_001112704.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr10:118897432 C>T maps to NM_001112704.1 K45K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr23:154467051 G>C did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:101194798 G>A maps to NM_001078.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:101194831 C>T maps to NM_001078.3 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr1:101190243 G>A maps to NM_001078.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr1:101203718 C>T maps to NM_001078.3 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DG-01A-21D-A30E-08 chr5:82815555 C>A maps to NM_004385.4 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr5:82837878 C>T maps to NM_004385.4 I3019I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:82833069 C>T maps to NM_004385.4 L1416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr5:82817079 G>A maps to NM_004385.4 V985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr5:82834902 C>T maps to NM_004385.4 P2027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr5:82789363 G>A did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr5:82834174 G>T maps to NM_004385.4 E1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr5:82815924 C>G maps to NM_004385.4 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr5:82815482 C>G maps to NM_004385.4 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr5:82834811 C>A maps to NM_004385.4 S1997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr5:82843856 C>T maps to NM_004385.4 F3149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:75855483 G>A maps to NM_014000.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr10:75854094 G>T maps to NM_014000.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:35061119 C>T maps to NM_007126.3 E417E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr9:35061621 C>T maps to NM_007126.3 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr8:67546741 G>A maps to NM_025054.4 H1221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:67547414 G>C maps to NM_025054.4 S997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:67578143 G>A maps to NM_025054.4 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr8:67578152 C>T maps to NM_025054.4 W347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:8434163 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:8434193 G>A did not map to a codon.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr5:133326806 G>C maps to NM_003374.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:48238537 C>T maps to NM_001017535.1 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr6:43749749 G>A maps to NM_001025366.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SG-01A-12D-A34J-08 chr11:64004682 G>T maps to NM_003377.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:177650750 G>C maps to NM_005429.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:177649123 T>A did not map to a codon.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr10:135053282 C>G maps to NM_014468.2 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:156978934 G>C maps to NM_001167912.1 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:157146230 C>T maps to NM_001167912.1 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:157146251 T>C maps to NM_001167912.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:157146113 G>A maps to NM_001167912.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr3:157131747 C>T maps to NM_001167912.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr3:156979060 G>A maps to NM_001167912.1 F788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr17:56060237 G>A maps to NM_007146.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr17:56058053 G>A maps to NM_007146.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:95660257 T>A maps to NM_017599.3 L187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:95676360 G>A maps to NM_017599.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr7:100806474 G>A maps to NM_003378.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr7:100807316 G>A maps to NM_003378.3 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:135630909 G>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:135618204 T>A did not map to a codon.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr6:117586935 C>T maps to NM_182645.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:87018112 C>A maps to NM_016206.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:87018031 C>A maps to NM_016206.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr3:87027678 G>A maps to NM_016206.2 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr3:11643422 G>T maps to NM_014667.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr3:11600119 G>A maps to NM_014667.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr3:11600091 G>A maps to NM_014667.2 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr3:11744451 G>A maps to NM_014667.2 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:10188210 C>T maps to NM_000551.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr1:156268970 T>G maps to NM_001004319.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr2:219314034 C>G maps to NM_007127.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:219289046 C>T maps to NM_007127.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:219292993 C>T maps to NM_007127.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr3:38040428 G>A maps to NM_015873.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:17278347 G>A maps to NM_003380.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr10:17277250 C>A maps to NM_003380.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr10:17277251 C>T maps to NM_003380.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr10:17278315 C>T maps to NM_003380.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr6:153073383 G>A maps to NM_003381.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:158823438 C>G maps to ENST00000402066 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:158896489 G>A maps to ENST00000402066 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:36956605 G>A maps to NM_053276.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr2:36970261 C>T maps to NM_053276.3 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr16:31105903 G>A maps to ENST00000319788 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr9:2643959 G>A did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr17:4688866 G>A maps to NM_182566.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr19:57967605 C>T maps to NM_020633.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr19:57967711 G>T maps to NM_020633.2 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:57967614 C>T maps to NM_020633.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr19:53762719 T>C maps to NM_173856.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr19:53762611 C>T maps to NM_173856.2 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr19:53762521 C>A maps to NM_173856.2 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:133013715 G>T maps to NM_004666.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:133014448 G>A maps to NM_004666.2 N180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:133073774 A>G maps to NM_004665.2 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr6:133078595 T>A maps to NM_004665.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:51457834 A>G maps to ENST00000273612 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr3:51517820 C>A maps to ENST00000273612 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr3:51497225 C>G maps to ENST00000273612 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr22:22599469 C>T maps to NM_007128.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr11:118942469 C>T maps to NM_021729.4 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr9:79959941 A>T maps to ENST00000376646 A2391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr9:79824393 C>T maps to ENST00000376646 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:79910534 T>G maps to ENST00000376646 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr9:79960035 G>T maps to ENST00000376646 E2423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr9:79852967 C>A maps to ENST00000376646 S549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr9:79954476 C>T maps to ENST00000376646 Q2142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr8:100146858 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:100866326 G>A maps to NM_017890.3 L3595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr8:100829988 G>T maps to NM_017890.3 V2798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr8:100779108 C>T maps to NM_017890.3 I2411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr8:100133445 C>T maps to NM_017890.3 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:100443888 A>T maps to NM_017890.3 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:100115241 C>G maps to NM_017890.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr8:100533239 T>A did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr8:100789143 G>A maps to NM_017890.3 L2488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr8:100523669 G>A maps to NM_017890.3 L1546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:100147837 C>T maps to NM_017890.3 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:100523502 G>T maps to NM_017890.3 E1491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:100831005 G>A maps to NM_017890.3 E2862E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr8:100147901 C>T maps to NM_017890.3 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:100831672 C>T maps to NM_017890.3 P2910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:100847875 A>G maps to NM_017890.3 L3309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:100880544 G>A maps to NM_017890.3 P3773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr8:100493855 C>A maps to NM_017890.3 I1232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr8:100796679 C>T maps to NM_017890.3 S2664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr8:100479780 G>A maps to NM_017890.3 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr8:100286453 T>G maps to NM_017890.3 T848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr8:100654569 C>T maps to NM_017890.3 R1943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr8:100523441 G>A maps to NM_017890.3 E1470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr8:100883891 G>A maps to NM_017890.3 Q3929Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:62312737 C>A did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:62258316 G>A maps to NM_020821.2 Q1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr15:62299581 G>C maps to NM_020821.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr15:62146685 C>G maps to NM_020821.2 V3744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:62182497 G>A maps to NM_020821.2 A3069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr15:62165561 T>C maps to NM_020821.2 K3487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:12336510 C>T maps to NM_015378.2 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:12304643 C>A maps to NM_015378.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr1:12331120 G>A maps to NM_015378.2 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:12418559 G>T maps to NM_015378.2 P3348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr1:12395846 G>A maps to NM_015378.2 W2838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:12343294 A>G maps to NM_015378.2 S1712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr1:12569057 C>T maps to NM_015378.2 Q4383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:12460257 T>C maps to NM_015378.2 G3885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr1:12328838 C>G maps to NM_015378.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr1:12337587 C>T maps to NM_015378.2 R1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr1:12322006 G>A maps to NM_015378.2 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:2841159 C>A maps to NM_022575.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr15:41191579 C>G maps to NM_020857.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:41191636 C>T maps to NM_020857.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr17:40925507 C>T maps to NM_032353.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:70922188 A>G maps to NM_004896.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:134095033 C>T maps to NM_052875.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr12:122748186 C>T maps to NM_022916.4 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr12:122729265 C>T maps to NM_022916.4 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr15:91557071 G>A maps to NM_018668.3 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:91546341 G>T maps to NM_018668.3 Y415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr15:91557625 G>A maps to NM_018668.3 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr13:53001178 G>C maps to NM_016075.2 S195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:17142025 A>T maps to NM_152415.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr12:123380552 G>A maps to NM_024667.2 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:60906238 C>A maps to NM_017966.4 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr15:42457993 C>T maps to ENST00000348544 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr15:42470703 C>T maps to ENST00000348544 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr15:42481356 C>T maps to ENST00000348544 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr15:42457993 C>T maps to ENST00000348544 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr7:38796566 C>T maps to NM_014396.3 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:38765890 A>C maps to NM_014396.3 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:38816314 A>G maps to NM_014396.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr16:69349972 G>T maps to NM_013245.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr16:69350017 C>T maps to NM_013245.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:61066521 C>T maps to NM_004869.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr18:61064455 C>T maps to NM_004869.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr18:61074673 G>A maps to NM_004869.3 Q119*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-6019-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr6:33236965 G>A maps to NM_022553.4 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:463773 G>A maps to NM_001128159.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:455170 G>A maps to NM_001128159.2 Q603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr2:64174525 G>A maps to NM_016516.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr2:64208796 G>A maps to NM_016516.2 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:151150568 C>T maps to ENST00000354473 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr1:151149263 C>T maps to ENST00000354473 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:184714190 G>T maps to ENST00000437079 S1246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr2:58362326 C>T maps to NM_001130480.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:58276055 A>T maps to NM_001130480.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr2:58386583 C>G maps to NM_001130480.2 S428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:58373461 A>G maps to NM_001130480.2 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:50510832 G>C maps to NM_016440.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr19:50512577 G>A maps to NM_016440.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr23:107301343 C>G did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr23:107310363 G>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:124617496 G>A maps to NM_014312.3 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:124618356 C>T maps to NM_014312.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr11:124619697 C>G maps to NM_014312.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:65253340 C>A did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr23:65253532 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:65252478 A>G did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:36572480 C>T maps to NM_080607.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr20:25060073 G>A maps to NM_014588.4 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr20:25057163 C>A maps to NM_014588.4 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr6:142539728 T>A maps to NM_016485.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:1372442 C>T maps to NM_022834.4 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JS-01A-11D-A34J-08 chr1:1372484 C>T maps to NM_022834.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:116045995 T>C maps to NM_198496.1 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr16:22134932 G>T did not map to a codon.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr16:22161161 G>A maps to NM_173615.3 V1013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr2:98851129 G>T maps to NM_144992.4 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:98828425 A>T maps to NM_144992.4 K591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:98916585 T>C maps to NM_144992.4 F1109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr2:98914448 C>T maps to NM_144992.4 S1079S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr2:98736106 C>T maps to NM_144992.4 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr2:98744736 T>A maps to NM_144992.4 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr11:123993787 C>T maps to NM_014622.4 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr2:215440474 T>C maps to NM_001080500.2 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:215301350 A>T did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:61032010 C>A maps to NM_152718.2 R726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr11:61042027 G>C maps to NM_152718.2 Y508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr11:61026509 T>C maps to NM_152718.2 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:6103291 G>A maps to NM_000552.3 Q2112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:6103364 G>T maps to NM_000552.3 I2087I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr12:6219669 A>G maps to NM_000552.3 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr12:6173439 G>A maps to NM_000552.3 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr12:6076765 G>T maps to NM_000552.3 P2591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr12:6128368 C>T maps to NM_000552.3 K1405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr12:6105332 G>A maps to NM_000552.3 F1966F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr12:6103626 C>A maps to NM_000552.3 L2070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr10:28905157 C>G maps to NM_016628.3 S538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:28872435 T>G did not map to a codon.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr10:28905263 A>T maps to NM_016628.3 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr10:88277385 T>C maps to ENST00000342368 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:88277757 G>C maps to ENST00000342368 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr10:88259532 C>T maps to ENST00000342368 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:88260012 C>T maps to ENST00000342368 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr10:88211792 G>A maps to ENST00000342368 I1100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr14:100826919 G>A maps to NM_173701.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:119683179 G>A maps to NM_015836.3 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:119575538 G>A maps to NM_015836.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr23:48544017 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:48542679 C>A did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr23:48542319 C>G did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:48549499 G>A did not map to a codon.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:110423256 T>G maps to NM_003931.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:110423088 C>T maps to NM_003931.2 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:27736339 A>G maps to NM_006990.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr1:27742574 G>C maps to NM_006990.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr13:27216529 G>A maps to NM_006646.5 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr13:27257004 G>A maps to NM_006646.5 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:123346844 A>G maps to NM_003941.2 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:14940262 A>G maps to NM_016312.2 I554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr12:14947540 A>G maps to NM_016312.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr22:42423139 C>T maps to NM_152613.2 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr22:42418310 T>A maps to NM_152613.2 Y155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr22:42422962 A>T maps to NM_152613.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr22:42415410 C>G maps to NM_152613.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr13:41639313 C>T maps to NM_007187.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:102612734 A>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:70881050 T>C did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:70853352 G>A maps to NM_022479.1 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:70880891 C>T maps to NM_022479.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:70800593 T>C maps to NM_022479.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr7:71130574 G>A maps to NM_022479.1 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr7:73254879 C>A did not map to a codon.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr7:73275544 C>G maps to NM_182504.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:224765919 C>T maps to NM_020830.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr2:224749379 C>G maps to NM_020830.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:85600084 G>A maps to NM_014991.4 S3378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr4:85731059 T>A maps to NM_014991.4 V775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr4:85748034 T>A maps to NM_014991.4 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr4:85752749 C>T maps to NM_014991.4 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:85657474 C>A maps to NM_014991.4 E2255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr4:85707146 T>C maps to NM_014991.4 K1349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr4:85742693 C>G maps to NM_014991.4 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr4:85748078 G>A maps to NM_014991.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr14:55457984 C>T maps to NM_007086.3 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr14:55454020 G>T maps to NM_007086.3 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr14:55411048 C>T did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr4:10083022 G>A maps to NM_017491.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:10100635 C>A maps to NM_017491.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:10117802 G>A maps to NM_017491.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:122668113 G>A maps to NM_018117.11 K1188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr10:122612035 G>A maps to NM_018117.11 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr10:122622271 C>T maps to NM_018117.11 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:122662635 G>A maps to NM_018117.11 Q941Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr2:203745630 T>C maps to NM_018256.3 K408K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:203747436 T>C maps to NM_018256.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:203776181 T>A maps to NM_018256.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr2:203748996 G>A maps to NM_018256.3 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr23:48458092 G>A did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr23:48457987 G>A did not map to a codon.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr23:48457206 A>C did not map to a codon.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr23:48460485 A>T did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr17:9532072 C>T maps to NM_145054.4 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr17:9515646 C>A maps to NM_145054.4 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr4:177067238 T>C maps to NM_170710.4 H565H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr4:177056260 A>T maps to NM_170710.4 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:177056353 T>C maps to NM_170710.4 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr4:177081213 G>A maps to NM_170710.4 V889V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr4:177071266 A>G maps to NM_170710.4 E731E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr4:177077228 G>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:177041153 C>T maps to NM_170710.4 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:177077241 C>T maps to NM_170710.4 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr4:39233471 G>T maps to NM_025132.3 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr4:39230268 C>T maps to NM_025132.3 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:39276494 C>T maps to NM_025132.3 F1211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:102675277 G>T maps to ENST00000454394 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr14:100995421 C>T maps to NM_001161476.1 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr6:170033069 C>T maps to NM_182552.3 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:118497251 T>C did not map to a codon.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr9:116082636 C>A maps to NM_001012361.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr9:116083792 G>A maps to NM_001012361.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr9:116094224 T>C maps to NM_001012361.2 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr2:128480907 G>A maps to NM_018383.4 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr2:128481926 T>A maps to NM_018383.4 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:20145564 G>A maps to NM_001006657.1 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:20130162 T>A maps to NM_001006657.1 K1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:20130163 C>T maps to NM_001006657.1 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:20138032 G>A maps to NM_001006657.1 R697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr21:44299515 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:29158442 C>T maps to NM_015131.1 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr23:117530988 G>C did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr23:117582908 G>A did not map to a codon.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr23:117538392 G>C did not map to a codon.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr23:117532357 C>T did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr23:117527108 C>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:117527101 G>A did not map to a codon.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr23:117575440 C>G did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:117526617 G>C did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr23:117526861 G>C did not map to a codon.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr23:117578414 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr23:117582898 C>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:48933526 C>G did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr23:48934115 C>G did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:48935371 C>A did not map to a codon.
Sequencing variant TCGA-MZ-A5BI-01A-31D-A34J-08 chr17:80588875 G>A maps to NM_019613.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr6:33247106 C>T maps to NM_005452.5 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:109538249 G>C maps to NM_001142550.1 S556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:109554139 G>T maps to NM_001142550.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr1:109553760 G>A maps to NM_001142550.1 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr3:167240191 T>C maps to NM_178824.3 E543E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr3:167240196 T>A maps to NM_178824.3 K542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr3:167278010 G>A maps to NM_178824.3 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr9:137017112 G>A maps to NM_052821.3 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr3:113146034 T>G maps to NM_001164496.1 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:113098398 C>G did not map to a codon.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr3:113099871 G>A maps to NM_001164496.1 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr3:196288328 C>T maps to NM_182627.1 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:196288298 C>G maps to NM_182627.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr3:196281249 G>A maps to NM_182627.1 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr3:196281516 A>G maps to NM_182627.1 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:74652826 G>C maps to NM_032118.2 *335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:74652066 A>T maps to NM_032118.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr16:74972116 G>A maps to NM_030581.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:74951880 C>T maps to NM_030581.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr16:74957841 G>C maps to NM_030581.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr16:74949803 G>C maps to NM_030581.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:74985405 G>A maps to NM_030581.3 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr16:74951891 G>A maps to NM_030581.3 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr3:122133835 G>T maps to NM_019069.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr7:158738289 G>T maps to NM_018051.4 A1007A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr7:158704238 A>G did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr19:36562558 C>T maps to NM_001083961.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:36558320 C>T maps to NM_001083961.1 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:36595902 C>T maps to NM_001083961.1 A1515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:36573967 C>T maps to NM_001083961.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IH-01A-11D-A31L-08 chr19:36572336 G>A maps to NM_001083961.1 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:43672568 C>G maps to NM_001195831.1 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr12:122369653 C>T maps to NM_144668.4 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:122396264 G>A maps to NM_144668.4 K606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr8:124105862 C>T maps to NM_145647.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:228786233 C>A maps to NM_178821.1 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr2:228769655 C>T maps to NM_178821.1 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:54448879 C>A maps to NM_015285.2 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr18:54385257 C>T maps to NM_015285.2 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr18:54483273 C>G maps to NM_015285.2 S1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr18:54358526 C>G maps to NM_015285.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr18:54423843 C>T maps to NM_015285.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:37479939 C>T maps to NM_018034.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr5:37605165 G>T maps to NM_018034.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr5:37605303 G>A maps to NM_018034.2 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr5:37480010 G>A maps to NM_018034.2 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr5:37396548 C>T maps to NM_018034.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr15:53992034 A>C maps to NM_182758.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr15:53992088 G>A maps to NM_182758.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr15:53889438 C>T maps to NM_182758.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr15:53998226 T>C maps to NM_182758.2 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:53994480 G>C maps to NM_182758.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr15:54003098 G>T maps to NM_182758.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71E-01A-31D-A34J-08 chr15:54025295 G>A maps to NM_182758.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr15:85188752 G>A maps to NM_032856.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:111989743 G>A maps to NM_024102.2 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:111990151 G>A maps to NM_024102.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:67340501 G>A maps to NM_024763.4 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr1:67292603 A>T maps to NM_024763.4 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr1:67370925 C>A maps to NM_024763.4 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:1635681 C>T maps to NM_001163809.1 L1407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr17:1634160 C>T maps to NM_001163809.1 L1296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr17:1639388 C>T maps to NM_001163809.1 I1794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:1635705 G>A maps to NM_001163809.1 E1415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr9:140473184 G>A maps to NM_138778.2 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr9:140469250 C>T maps to NM_138778.2 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:33623311 G>A maps to NM_173479.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr19:33647372 C>T maps to NM_173479.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:706410 C>G maps to NM_145294.4 Y692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:711777 C>T maps to NM_145294.4 I1285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:716484 C>T maps to NM_145294.4 L1591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A460-01A-21D-A25D-08 chr16:711666 C>A maps to NM_145294.4 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr16:716722 G>A maps to NM_145294.4 G1645G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:68365915 G>C maps to NM_138458.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr2:160128238 G>T maps to NM_001128212.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:27627908 G>A maps to ENST00000319394 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr1:27621044 G>A maps to ENST00000319394 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:141424932 C>A maps to NM_001105558.1 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49A-01A-11D-A24D-08 chr7:141414205 G>T did not map to a codon.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr7:141427198 C>G maps to NM_001105558.1 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:44416544 T>C maps to NM_080614.1 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr20:44166662 G>A maps to ENST00000396669 C154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr16:682655 C>A maps to NM_053284.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr17:48916921 C>A maps to NM_175575.5 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr17:48917854 G>A maps to NM_175575.5 W402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr4:6302535 C>T maps to NM_006005.3 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:6302727 G>C maps to NM_006005.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr4:6296870 C>T maps to NM_006005.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr15:83478537 C>T maps to NM_001080435.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr4:1941402 A>G maps to NM_133335.3 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr4:1902731 C>T maps to NM_133335.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:38162180 G>A maps to NM_023034.1 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:38172975 C>T maps to NM_023034.1 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr8:38172931 A>T did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr8:38148152 C>A maps to NM_023034.1 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IF-01A-11D-A25Y-08 chr4:1985045 C>T maps to NM_005663.3 *540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:65461538 G>C maps to NM_007191.4 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JT-01A-11D-A31L-08 chr12:65445209 G>C maps to NM_007191.4 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:175427286 G>A maps to NM_003387.4 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr17:38416863 G>A maps to NM_133264.4 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr17:66429703 G>A maps to NM_017983.5 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:5232765 C>G maps to NM_015610.3 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:134225120 C>A maps to NM_003882.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr8:134237783 C>A maps to NM_003882.2 C254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr8:134232845 C>T maps to NM_003882.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:15547893 G>A maps to ENST00000389282 F773F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:15537871 C>A maps to ENST00000389282 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:15535765 G>A maps to ENST00000389282 L1420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:15535766 G>A maps to ENST00000389282 H1419H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:15559027 C>A maps to ENST00000389282 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr19:15538234 G>A maps to ENST00000389282 G1070G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:68659749 G>A maps to NM_024911.6 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr1:68564315 C>T maps to NM_001002292.3 *544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr1:68620826 C>T maps to NM_024911.6 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr12:970336 A>G maps to NM_001184985.1 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:988981 C>T maps to NM_018979.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:996422 C>T maps to NM_001184985.1 L2033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:993326 G>A maps to NM_001184985.1 A1514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr12:1005292 A>G maps to NM_001184985.1 A2140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr12:994622 C>A maps to NM_001184985.1 S1811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr12:939274 T>C maps to NM_001184985.1 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr9:96051727 C>T maps to ENST00000297954 H1601H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr9:96021457 T>C maps to ENST00000297954 I876I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:96025976 G>T maps to ENST00000297954 R1180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr9:96051364 G>A maps to ENST00000297954 P1480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr9:96069101 T>C maps to ENST00000297954 S2123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr23:54319738 C>G did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr23:54359589 C>A did not map to a codon.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr23:54335723 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:54324817 G>C did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr23:54334450 A>G did not map to a codon.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr23:54324750 C>G did not map to a codon.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr23:54359868 T>C did not map to a codon.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr23:54259279 T>A did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr23:54321096 G>C did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr23:54259358 G>T did not map to a codon.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr23:54228470 G>T did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:54337719 C>G did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:54275518 G>C did not map to a codon.
Sequencing variant TCGA-KU-A6H8-01A-21D-A34J-08 chr23:54276494 C>T did not map to a codon.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr23:54276530 C>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:40937376 G>T maps to NM_032387.4 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr17:40946993 C>G maps to NM_032387.4 S852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr17:40947761 C>T maps to NM_032387.4 Q1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:40936503 C>T maps to NM_032387.4 Y359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr12:49373451 G>A maps to NM_005430.3 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr12:49373478 C>T maps to NM_005430.3 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr7:116963001 C>A maps to NM_003391.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr7:116962986 G>A maps to NM_003391.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr17:44851058 G>A maps to NM_030753.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr17:44845706 G>A maps to NM_030753.3 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:228210571 C>T maps to ENST00000366753 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr1:228210481 C>T maps to ENST00000366753 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:55513546 A>T maps to NM_003392.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:1741946 C>T maps to NM_032642.2 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr2:219736444 C>T maps to NM_006522.3 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr3:13896226 G>T maps to NM_004625.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr3:13860851 C>G maps to NM_004625.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:137426350 G>A maps to NM_058244.2 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr5:137426395 C>T maps to NM_058244.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:137426722 C>T maps to NM_058244.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr10:102242119 C>T maps to NM_003393.3 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:44954071 C>A maps to NM_003396.1 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr17:7604803 G>T maps to NM_018081.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr17:7592166 A>G maps to NM_018081.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr8:30977860 G>T maps to NM_000553.4 E851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr17:25631812 C>A maps to NM_015626.8 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr12:118480754 G>A maps to ENST00000441406 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr17:6021410 G>A maps to NM_015253.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr17:5998440 C>T maps to NM_015253.1 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr17:5984265 G>A maps to NM_015253.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr12:108620879 G>A maps to ENST00000261400 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:108589737 C>T maps to ENST00000261400 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr12:108589737 C>T maps to ENST00000261400 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr12:108618514 G>T did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr12:108634151 C>T maps to ENST00000261400 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr12:108589887 C>T maps to ENST00000261400 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr11:32417946 G>A maps to NM_024426.4 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:32417878 G>A maps to NM_024426.4 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr6:160174646 G>C did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:160164725 G>T maps to NM_004906.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:160176432 T>C maps to NM_004906.3 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr19:34984492 G>T maps to ENST00000270288 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr5:167887708 C>T maps to NM_001161661.1 R960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr5:167896015 C>T maps to NM_001161661.1 D1118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:167850579 C>G maps to NM_001161661.1 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr5:167812358 C>T maps to NM_001161661.1 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:167812283 C>T maps to NM_001161661.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr5:167855065 G>C maps to NM_001161661.1 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr4:184174978 G>A maps to ENST00000448232 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr23:10102534 C>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr23:10106853 T>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:10092368 G>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:10096606 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:10085584 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:10098007 G>A did not map to a codon.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr23:10094265 G>A did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:10109514 C>G did not map to a codon.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr23:10109535 G>A did not map to a codon.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr23:10085538 G>A did not map to a codon.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr23:10084512 C>T did not map to a codon.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:78133747 A>T maps to NM_016373.1 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:78458950 C>T maps to NM_016373.1 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:87414409 A>G maps to NM_007013.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr8:87423944 A>G maps to NM_007013.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr8:87393859 T>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:69874158 G>A maps to NM_007014.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr16:69922038 C>A maps to NM_007014.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:69874158 G>C maps to NM_007014.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr16:69963427 C>T maps to NM_007014.3 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:69874116 G>A maps to NM_007014.3 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr3:149243912 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr19:7688058 G>A maps to NM_020196.2 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr19:7689196 G>A maps to NM_020196.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr19:7690906 G>C maps to NM_020196.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61O-01A-11D-A30E-08 chr19:7685212 G>A maps to NM_020196.2 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:6665480 A>G maps to NM_017523.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr17:6674068 G>A maps to NM_017523.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:52844168 G>T did not map to a codon.
Sequencing variant TCGA-RS-A6TO-01A-32D-A34J-08 chr23:52841624 G>T did not map to a codon.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr23:52844130 C>A did not map to a codon.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr1:168545889 C>T maps to NM_002995.2 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:46062614 G>A maps to NM_005283.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr3:46063049 C>T maps to NM_005283.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:31598257 C>T maps to NM_000379.3 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:31621532 G>A maps to NM_000379.3 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:31600013 T>A maps to NM_000379.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:31572646 C>T maps to NM_000379.3 Q958Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr2:31598410 C>T maps to NM_000379.3 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr23:123019595 T>C did not map to a codon.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr23:123040863 C>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:123019597 G>C did not map to a codon.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr3:39230225 C>T maps to NM_194293.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr3:39228920 G>A maps to NM_194293.2 G672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:39230362 T>G maps to NM_194293.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:39229739 C>A maps to NM_194293.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr3:39229310 C>T maps to NM_194293.2 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr3:39227312 C>T maps to NM_194293.2 G1208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr2:168101808 G>T maps to NM_152381.5 E1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr2:168103463 G>A maps to NM_152381.5 Q1854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:168100145 G>T maps to NM_152381.5 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr2:168100278 C>A maps to NM_152381.5 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr2:168106778 G>A maps to NM_152381.5 S2959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:168103754 T>G maps to NM_152381.5 A1951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:168107804 G>A maps to NM_152381.5 V3301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:168105476 A>T maps to NM_152381.5 P2525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr2:168106862 G>C maps to NM_152381.5 L2987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:168102260 T>G maps to NM_152381.5 T1453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr2:168102824 A>G maps to NM_152381.5 L1641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:168100277 C>T maps to NM_152381.5 V792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:168100278 C>T maps to NM_152381.5 R793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:168115395 G>A maps to ENST00000420519 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr2:168107252 C>T maps to NM_152381.5 R3117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr2:168100466 A>G maps to NM_152381.5 E855E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:168105299 A>G maps to NM_152381.5 V2466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr23:37587031 G>C did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:37586995 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:37545252 G>C did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr22:17280838 G>A maps to NM_175878.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr22:17288844 G>C maps to NM_175878.3 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:17288750 G>A maps to NM_175878.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr22:17264946 A>G maps to NM_175878.3 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:56015533 C>T maps to NM_052898.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:56015392 C>T maps to NM_052898.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr8:56015683 G>A maps to NM_052898.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr8:56270345 G>T maps to NM_052898.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr8:56015383 C>A maps to NM_052898.1 C112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr8:56015560 C>T maps to NM_052898.1 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr8:6690389 C>A maps to NM_207411.4 G31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:10755965 C>T maps to NM_173683.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr8:10755635 G>C maps to NM_173683.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr20:30584929 G>A maps to NM_001011718.1 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:30584821 C>G maps to NM_001011718.1 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr1:28293494 C>T maps to NM_018053.2 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr8:71619347 C>G maps to NM_001011720.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr8:71619233 C>T maps to NM_001011720.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr23:100169655 C>A did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr23:100177996 T>A did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:100169569 G>C did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:100183243 G>A did not map to a codon.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr23:100183280 A>G did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr23:100183209 G>T did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr23:100177938 C>G did not map to a codon.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr3:14187458 G>A maps to NM_004628.4 F935F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr23:128895150 G>A did not map to a codon.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr23:128881675 A>G did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr23:128896687 A>T did not map to a codon.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr23:128887211 C>G did not map to a codon.
Sequencing variant TCGA-D6-A6EQ-01A-11D-A31L-08 chr23:128879211 G>A did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:128885795 C>T did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:41253201 C>A maps to NM_022098.2 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:61760929 A>G maps to NM_003400.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr2:61720110 C>T maps to NM_003400.3 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr13:21382701 T>C maps to NM_022459.4 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr13:21357968 G>A maps to NM_022459.4 L1116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45R-01A-11D-A24D-08 chr16:28145176 G>A maps to NM_015171.2 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IH-01A-11D-A25Y-08 chr8:21843167 G>T maps to ENST00000434536 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr8:21857169 G>T maps to ENST00000434536 G932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr8:21851878 T>A maps to ENST00000434536 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr8:21843103 G>A maps to ENST00000434536 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:64818848 G>T maps to NM_007235.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr12:64813911 G>A maps to NM_007235.3 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr1:180794072 C>G maps to NM_004736.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:44051049 T>A maps to NM_006297.2 K427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr19:44050065 C>A maps to NM_006297.2 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr7:152346253 C>A maps to NM_005431.1 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr14:104174901 C>T maps to NM_005432.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr5:82648964 A>C maps to NM_022406.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:42046860 C>T maps to NM_001469.3 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:142098953 G>A maps to NM_019001.3 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:142048323 G>A maps to NM_019001.3 S1451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr3:142078759 G>A maps to NM_019001.3 A1136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr20:21346225 A>T maps to NM_012255.3 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr11:74617423 G>T maps to NM_182969.1 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr11:74559186 C>T maps to NM_182969.1 K559K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr16:17221546 G>A maps to NM_022166.3 D733D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr16:17221564 G>A maps to NM_022166.3 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr16:17211719 C>T maps to NM_022166.3 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr12:32908352 C>T maps to NM_001040436.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:7192916 G>A maps to NM_015982.3 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:7192917 G>A maps to NM_015982.3 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:183493895 C>T maps to NM_018023.4 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A47Z-01A-11D-A24D-08 chr3:183474439 G>A maps to NM_018023.4 Q505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr3:183470000 G>A maps to NM_018023.4 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr18:743307 G>A maps to NM_005433.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:38800242 G>A maps to NM_001039672.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:54332511 T>C maps to NM_018982.4 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr1:54344377 C>T maps to NM_018982.4 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr19:11038314 G>A maps to NM_024029.3 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:11036434 G>A maps to NM_024029.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:43480833 G>A maps to ENST00000506469 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:43483628 G>A maps to ENST00000506469 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr4:44638053 C>T maps to NM_182592.2 E79E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr7:44251861 C>G maps to NM_006555.3 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr7:44246047 A>G maps to NM_006555.3 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr14:75230941 G>T maps to NM_019589.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr14:75266306 T>G maps to NM_019589.2 L1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr14:75266068 C>T maps to NM_019589.2 R1357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:27403473 T>C maps to NM_139312.1 E718E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr10:27423859 G>A maps to NM_139312.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr10:27406522 C>A maps to NM_139312.1 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr1:207222775 C>T maps to NM_018566.3 W212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr1:207222564 G>A maps to NM_018566.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr22:22057703 G>A maps to NM_013313.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr17:57466718 A>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:38272868 T>C maps to NM_024640.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr2:135744716 C>A maps to NM_025052.3 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr2:135744392 C>T maps to NM_025052.3 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:135745718 G>C maps to NM_025052.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:135745304 G>A maps to NM_025052.3 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:135745628 C>T maps to NM_025052.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:135738605 G>T maps to NM_025052.3 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:69184562 G>A maps to NM_001031732.2 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:112917311 G>T maps to NM_022828.3 E1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr5:112868638 C>T maps to NM_022828.3 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:112889015 C>T maps to NM_022828.3 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr5:112878078 G>A maps to NM_022828.3 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr20:61833965 C>A maps to NM_017798.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:61846953 C>G did not map to a codon.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr1:29069498 G>A maps to NM_016258.2 W239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:64099526 C>T maps to ENST00000339066 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr20:43530338 C>T maps to NM_139323.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr17:1264555 G>A maps to NM_006761.4 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr7:75959451 G>T maps to NM_012479.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr7:75988083 G>T maps to NM_012479.3 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr2:9770491 G>C maps to NM_006826.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr2:9725446 C>A maps to NM_006826.2 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr8:101936266 T>C maps to NM_003406.3 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:100743852 C>T maps to NM_003403.3 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:100706060 C>T maps to NM_003403.3 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:155629558 C>T maps to ENST00000368339 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:155629471 T>A maps to ENST00000368339 T881T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:155630377 G>A maps to ENST00000368339 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr1:155630073 T>A maps to ENST00000368339 K681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr23:21875243 G>A did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr23:21875472 G>C did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:21875521 G>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr23:21875296 C>T did not map to a codon.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr23:21874966 C>G did not map to a codon.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr23:21875099 G>A did not map to a codon.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr23:21874754 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr17:74076045 C>G maps to NM_180990.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:74077660 C>T maps to NM_180990.3 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr17:74076446 C>G maps to NM_180990.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr18:72914174 A>G maps to NM_175907.4 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6D8-01A-31D-A31L-08 chr7:100370986 G>A maps to ENST00000349350 P1835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:100365620 C>G maps to ENST00000349350 L1676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr7:100345236 C>G maps to ENST00000349350 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:100344230 G>A maps to ENST00000349350 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr7:100345254 A>G maps to ENST00000349350 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr7:100350535 C>T maps to ENST00000349350 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr7:100358064 C>T maps to ENST00000349350 L1250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr7:100345977 C>T maps to ENST00000349350 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:100350373 G>A maps to ENST00000349350 T882T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:100391589 G>A maps to ENST00000349350 Q2645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr2:98354061 G>A maps to NM_001079.3 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr2:98341613 T>A maps to NM_001079.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr2:98355849 C>A maps to NM_001079.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:98354269 C>T maps to NM_001079.3 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr2:98354245 C>G maps to NM_001079.3 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr2:98351028 G>T maps to NM_001079.3 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr4:48496197 C>T maps to NM_175619.1 C404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr3:167023496 G>T maps to ENST00000307529 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr3:167045804 G>A maps to ENST00000307529 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr3:167039992 G>A maps to ENST00000307529 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr3:167031786 A>G maps to ENST00000307529 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr3:167077759 C>A maps to ENST00000307529 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:167016197 G>A maps to ENST00000307529 Q592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:2407921 G>A did not map to a codon.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr23:2408367 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:2408096 C>T did not map to a codon.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr23:2408254 G>C did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:2408483 C>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr22:50279256 C>T maps to NM_014838.2 Y649Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:56188386 C>G did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr20:56189964 T>C maps to NM_030776.2 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr20:56186818 C>A maps to NM_030776.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:64989073 C>T maps to NM_001123329.1 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr14:64988827 T>C maps to NM_001123329.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr8:81411835 A>G maps to NM_001105539.1 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:101373662 C>A maps to NM_014415.3 E732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:101390838 T>A maps to NM_014415.3 K177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr3:101395453 C>T maps to NM_014415.3 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr3:101370489 A>G maps to NM_014415.3 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr11:113934864 G>T maps to NM_001018011.1 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:114027107 C>A maps to NM_001018011.1 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:113934660 C>G maps to NM_001018011.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr11:114121087 C>A maps to NM_001018011.1 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr11:113934354 C>A maps to NM_001018011.1 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:114117977 C>A maps to NM_001018011.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:16273490 G>C maps to ENST00000375733 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:16269652 G>T maps to ENST00000375733 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:151694703 C>T maps to NM_020861.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:114069346 G>A maps to NM_001164342.1 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr3:114070459 A>T maps to NM_001164342.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:114069726 G>T maps to NM_001164342.1 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr3:114058211 G>T maps to NM_001164342.1 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:33283757 C>A maps to NM_001145338.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:33284360 G>A maps to NM_001145338.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr6:109802665 C>G maps to NM_014797.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr14:64954377 G>A maps to NM_006977.2 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr14:64954650 G>A maps to NM_006977.2 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr11:62520233 C>G maps to NM_024784.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T6-01A-11D-A34J-08 chr11:62520866 C>G maps to NM_024784.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:36205788 T>C maps to NM_014383.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr19:36205626 C>T maps to NM_014383.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr23:119388596 G>C did not map to a codon.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr23:119388775 A>G did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:119388365 A>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:119389151 G>C did not map to a codon.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr23:119387864 T>A did not map to a codon.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:173839374 T>C maps to NM_001122770.1 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr1:173840133 G>A maps to NM_001122770.1 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:141161523 C>G maps to NM_001080412.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr3:141164304 C>T maps to NM_001080412.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:141161622 G>A maps to NM_001080412.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:141163752 G>A maps to NM_001080412.2 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr17:7370045 G>T maps to NM_020899.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:7366416 C>A maps to NM_020899.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:7370090 C>T maps to NM_020899.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr17:7365711 G>A maps to NM_020899.3 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:22837769 C>T maps to NM_014870.3 C644C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:22816680 G>A maps to NM_014870.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr1:22848020 C>A maps to NM_014870.3 T1027T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:22838592 T>C maps to NM_014870.3 C809C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:22843856 C>T maps to NM_014870.3 H911H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr1:22850915 C>T maps to NM_014870.3 A1168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:197128770 C>T maps to NM_194314.2 Q816Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr9:129595075 C>T maps to NM_014007.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:59028614 C>T maps to NM_032792.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr19:59028059 C>T maps to NM_032792.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:59028821 C>T maps to NM_032792.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr20:62421366 G>A maps to NM_025224.2 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr20:62421835 G>C maps to NM_025224.2 S92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:6648383 C>T maps to NM_005341.2 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:6642210 C>T maps to NM_005341.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr4:4322502 C>A maps to NM_145291.3 C586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr4:4304615 A>G maps to NM_145291.3 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr9:125673994 G>A maps to NM_006626.4 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr19:4054876 G>A maps to NM_015898.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:154987573 A>C maps to ENST00000417934 L180L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-7404-01A-11D-2129-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DQ-5624-01A-01D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:33058777 C>T maps to NM_001040441.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:33116073 C>T maps to NM_178547.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr6:33422990 G>A maps to NM_152735.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr1:203816648 A>T maps to NM_014827.4 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr1:37949127 G>C maps to NM_025079.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:37948749 G>A maps to NM_025079.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr1:37941402 C>G maps to NM_025079.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr1:37948896 C>T maps to NM_025079.2 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr23:64722773 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:64722485 A>T did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr23:64722217 C>G did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr23:64709218 C>G did not map to a codon.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr13:46542133 T>A maps to ENST00000242848 R1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:46542017 C>T maps to ENST00000242848 E1314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr13:46562942 G>A maps to ENST00000242848 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr13:46619637 G>C maps to ENST00000242848 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr14:89039314 G>A maps to NM_024824.4 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:89041108 G>T maps to NM_024824.4 G312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr14:89069314 C>G maps to NM_024824.4 S553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr2:187370221 T>A maps to NM_018471.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr16:88691021 G>A maps to ENST00000452588 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr16:88643836 C>T maps to ENST00000452588 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr16:88664700 C>T maps to ENST00000452588 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr16:88689625 G>A did not map to a codon.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr8:144557589 G>T maps to NM_015117.2 G627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:47585471 G>A maps to NM_015168.1 C433C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:47597669 C>T maps to NM_015168.1 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr19:47570689 G>A maps to NM_015168.1 P945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:47570605 G>A maps to NM_015168.1 F973F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:47597292 G>A maps to NM_015168.1 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:47572550 G>C maps to NM_015168.1 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr2:113074097 C>T maps to NM_198581.2 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:11845265 C>T maps to NM_014153.3 K941K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr22:41753276 G>C maps to ENST00000351589 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:41738567 C>T maps to ENST00000351589 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr22:41752803 C>G maps to ENST00000351589 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr22:41738576 C>T maps to ENST00000351589 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:112994206 G>A maps to NM_032494.2 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr7:138764701 T>G maps to ENST00000464606 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr7:138738293 G>A maps to ENST00000464606 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:138764846 G>A maps to ENST00000464606 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45O-01A-21D-A24D-08 chr7:138764923 G>A maps to ENST00000464606 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr7:138764669 G>C maps to ENST00000464606 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr7:138711579 C>G did not map to a codon.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr7:129679337 C>T maps to NM_016478.3 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr23:64141700 T>C did not map to a codon.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr23:64141758 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr5:132334526 G>C maps to ENST00000509437 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr1:52897048 A>C maps to NM_001009881.2 S1449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr1:52896751 G>A maps to NM_001009881.2 H1548H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr1:52901117 G>A maps to NM_001009881.2 N1394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr1:52941094 C>A maps to NM_001009881.2 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr23:117959417 G>A did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr23:117959640 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:117959997 T>C did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr23:117960076 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr23:117960305 G>A did not map to a codon.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr23:73524173 G>C did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:73524499 C>A did not map to a codon.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr23:73524269 G>T did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:73524385 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr16:87445944 A>G maps to NM_015144.2 C657C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr16:87525409 G>A maps to NM_015144.2 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr16:87446151 G>C maps to NM_015144.2 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr23:111698149 A>G did not map to a codon.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr23:111698733 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr1:31811835 C>T maps to NM_016505.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:103359850 C>T did not map to a codon.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr23:103359009 G>C did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:60212053 C>G maps to NM_017742.4 S383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr18:60242730 C>T maps to NM_017742.4 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:25314460 C>A maps to NM_024936.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr4:25363859 G>A maps to NM_024936.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr23:77913338 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:77913598 C>T did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr23:77913881 C>T did not map to a codon.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr23:77913744 G>T did not map to a codon.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr23:77912861 C>G did not map to a codon.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr23:77913256 C>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:77912703 G>A did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr23:77913907 C>G did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr9:88925619 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr9:37356933 G>A maps to NM_032226.2 W434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:122962394 G>A maps to NM_017612.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr12:122975113 C>T maps to NM_017612.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:122958595 C>T maps to NM_017612.2 Q524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr12:42707674 C>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:99998660 G>A maps to NM_017984.3 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr3:28562600 A>G maps to NM_001040432.1 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:28520394 G>T maps to NM_001040432.1 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr3:28454849 T>A maps to NM_001040432.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:825359 T>C maps to NM_024786.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:837491 T>C maps to NM_024786.2 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr5:825359 T>C maps to NM_024786.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr5:801278 C>T maps to NM_024786.2 G394G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CN-A6V3-01A-12D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr6:158093958 G>A maps to NM_024630.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr23:74644540 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr23:74670645 C>A did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr23:74742781 G>A did not map to a codon.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr23:74670661 C>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:99215801 G>C did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr10:99213335 T>C maps to NM_198046.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:77216298 G>A maps to NM_015336.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr9:14674242 G>T maps to NM_178566.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr3:113672829 C>T maps to NM_173570.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:44986675 G>A maps to NM_016598.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:44986676 G>A maps to NM_016598.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr3:44974658 G>A maps to NM_016598.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr7:6621829 G>T maps to NM_018106.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:114192219 G>T maps to NM_022494.1 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr10:114194099 T>C maps to NM_022494.1 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr22:20127355 C>T maps to NM_013373.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr22:20127040 G>A maps to NM_013373.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr22:20127071 C>T maps to NM_013373.3 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr23:128963074 T>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr10:31816026 A>G maps to NM_001174096.1 E1071E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:31815598 G>T did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr10:31810428 A>G maps to NM_001174096.1 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr10:31809261 G>A maps to NM_001174096.1 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61L-01A-11D-A30E-08 chr10:31812947 C>A maps to NM_001174096.1 R898R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr10:31815882 G>C maps to NM_001174096.1 S1023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UM-01A-12D-A34J-08 chr2:145161593 G>A maps to NM_014795.3 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:145147398 C>T maps to NM_014795.3 R1088R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:145156647 A>G maps to NM_014795.3 N702N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:145156365 G>T maps to NM_014795.3 S796S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A465-01A-11D-A25Y-08 chr2:145157726 G>A maps to NM_014795.3 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A652-01A-11D-A30E-08 chr2:145187366 G>A maps to NM_014795.3 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr9:131515597 C>T maps to NM_006336.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CB-01A-11D-A25D-08 chr8:82626244 G>A maps to NM_024699.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr8:82627223 C>T maps to NM_024699.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr8:82615266 C>T maps to NM_024699.2 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:135612759 C>T maps to NM_020863.3 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr8:135614793 C>A maps to NM_020863.3 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr8:135533179 C>T maps to NM_020863.3 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr8:135621015 G>A maps to NM_020863.3 Y247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr8:135614101 G>A maps to NM_020863.3 H620H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr12:72057342 C>T maps to NM_144982.4 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr12:72008697 G>T maps to NM_144982.4 S1759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:72005624 C>G maps to NM_144982.4 L1890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:72020215 C>A maps to NM_144982.4 E1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr12:72050968 C>T maps to NM_144982.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A6UO-01A-12D-A34J-08 chr16:72984481 G>A maps to NM_006885.3 I1034I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr16:72992973 G>A maps to NM_006885.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr16:72831513 C>T maps to NM_006885.3 G1689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr16:72984802 C>T maps to NM_006885.3 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr16:72984463 G>C maps to NM_006885.3 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:72822415 G>A maps to NM_006885.3 P3253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr16:72828996 G>A maps to NM_006885.3 I2528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr16:72821071 G>A maps to NM_006885.3 F3701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:72821728 G>A maps to NM_006885.3 S3482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:72829089 C>T maps to NM_006885.3 S2497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr16:72828432 G>A maps to NM_006885.3 C2716C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7H4-01A-21D-A34J-08 chr16:72822727 C>T maps to NM_006885.3 P3149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr8:77617963 T>C maps to NM_024721.4 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr8:77768486 C>T maps to NM_024721.4 P3110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:77618581 C>A maps to NM_024721.4 C753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:77617903 G>A maps to NM_024721.4 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:77764910 T>C maps to NM_024721.4 F1918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr8:77763746 G>C maps to NM_024721.4 T1530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:77764851 C>A maps to NM_024721.4 R1899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr8:77764943 G>A maps to NM_024721.4 Q1929Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr8:77616340 C>G maps to NM_024721.4 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr8:77618401 G>C maps to NM_024721.4 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:77775783 C>A maps to NM_024721.4 L3278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr8:77763206 G>C maps to NM_024721.4 P1350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:77775693 T>C maps to NM_024721.4 N3248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr8:77618161 C>T maps to NM_024721.4 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr8:77767247 G>A maps to NM_024721.4 R2697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr8:77764067 C>T maps to NM_024721.4 S1637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr8:77618656 C>A maps to NM_024721.4 V778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:77766125 G>A maps to NM_024721.4 R2323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr8:77618443 T>C maps to NM_024721.4 S707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr8:77766926 C>T maps to NM_024721.4 C2590C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:77764097 G>A maps to NM_024721.4 Q1647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:77767871 G>A maps to NM_024721.4 A2905A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr8:77616691 C>T maps to NM_024721.4 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr8:77767190 G>C maps to NM_024721.4 P2678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:75203754 C>T maps to NM_153688.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr16:75203913 A>G maps to NM_153688.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:75203688 C>T maps to NM_153688.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr15:42743328 G>A maps to NM_022473.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr15:42729428 C>T did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr15:42734334 C>T maps to NM_022473.1 E1210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:42731745 G>A maps to NM_022473.1 T1320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:44831902 G>A maps to ENST00000412927 Q820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:44833879 G>A maps to ENST00000412927 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr19:44833907 G>A maps to ENST00000412927 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr19:36831736 G>A maps to NM_020917.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:36832352 G>T maps to NM_020917.2 C125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:36853090 C>T maps to NM_020917.2 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:36853053 C>T maps to NM_020917.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr19:36831233 G>A maps to NM_020917.2 H498H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr18:5291780 A>G maps to NM_003409.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:178359094 C>T maps to NM_030613.2 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:178359012 G>A maps to NM_030613.2 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:57066550 C>T maps to NM_020828.1 H799H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:38127000 C>G maps to NM_014898.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr19:38134168 G>A maps to NM_014898.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:39898585 C>T maps to NM_003407.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr14:69256567 G>A maps to NM_004926.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr14:69256576 A>T maps to NM_004926.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr14:69257035 G>A maps to NM_004926.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:69257125 C>A maps to NM_004926.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:43451805 C>T maps to NM_006887.4 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:43451841 C>A maps to NM_006887.4 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8634-01A-11D-2394-08 chr9:115805688 C>T maps to NM_003408.1 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr9:115805120 G>A maps to NM_003408.1 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:188924026 C>A maps to NM_174900.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr4:188923975 G>A maps to NM_174900.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:50705114 G>A maps to NM_199427.2 H348H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr20:50769881 C>A maps to NM_018197.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A76A-01A-51D-A34J-08 chr20:50769806 G>A maps to NM_018197.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:36884836 T>C maps to NM_133466.2 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr19:36883702 C>T maps to NM_133466.2 K513K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr16:68598393 C>T maps to NM_133458.2 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:68591908 G>A maps to NM_133458.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr11:64854193 C>T maps to NM_006782.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61S-01A-11D-A28R-08 chr16:88601257 G>T maps to NM_153813.2 T964T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr8:106814629 C>T maps to NM_012082.3 Q774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr8:106815639 T>C maps to NM_012082.3 G1110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr8:106814844 G>A maps to NM_012082.3 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Y-01A-11D-A25D-08 chr8:106815540 G>A maps to NM_012082.3 S1077S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr5:32407028 A>T maps to NM_016107.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr5:32407028 A>T maps to NM_016107.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr19:3816704 C>T maps to NM_015174.1 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:24229431 G>A did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr23:24228853 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr24:2829477 A>T did not map to a codon.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr24:2829237 C>T did not map to a codon.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr14:73437691 G>A maps to NM_021260.2 F744F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr14:73448573 G>A maps to NM_021260.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:73490961 C>T maps to NM_021260.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr14:73464705 A>T maps to NM_021260.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr5:79734564 C>T maps to NM_014733.3 I687I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:79770504 G>A maps to NM_014733.3 Q1439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr15:41102894 C>T maps to NM_001077268.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:15115501 G>T maps to NM_022340.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr3:15137555 C>T maps to NM_022340.2 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr14:68274301 C>A maps to NM_015346.3 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr14:68252947 G>A maps to NM_015346.3 R1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr14:68215204 C>T maps to NM_015346.3 W2523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr14:68272335 C>A did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr14:68272336 T>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:2306179 G>T maps to NM_020972.2 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr4:2306242 C>T maps to NM_020972.2 E608E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:52705123 G>T maps to NM_004799.2 G679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:52729529 C>G maps to NM_004799.2 S755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:52759158 C>T maps to NM_004799.2 F1020F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr1:52705056 C>A maps to NM_004799.2 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr1:52810540 C>G maps to NM_004799.2 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:2880711 G>T maps to NM_145252.2 G60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr16:2880773 T>G maps to NM_145252.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr19:10415871 G>A maps to NM_001103167.1 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr20:62340306 C>T maps to NM_032527.4 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr20:62339986 C>T maps to NM_032527.4 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:62340462 G>A maps to NM_032527.4 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr8:124268126 T>A maps to NM_007222.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr8:124267751 T>C maps to NM_007222.3 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr8:123966104 C>T maps to NM_014943.3 N785N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:123965798 G>A maps to NM_014943.3 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr8:123965009 T>A maps to NM_014943.3 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr20:39831672 C>T maps to NM_015035.3 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:147131167 C>T maps to NM_003412.3 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:147131265 C>A maps to NM_003412.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr3:147128417 G>A maps to NM_003412.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr3:147131304 G>T maps to NM_003412.3 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V7-01A-12D-A34J-08 chr3:147128360 G>A maps to NM_003412.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:147131244 G>T maps to NM_003412.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr3:147128516 G>A maps to NM_003412.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr3:147131220 C>T maps to NM_003412.3 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr13:100635304 C>T maps to NM_007129.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr13:100635349 C>T maps to NM_007129.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr13:100637245 C>T maps to NM_007129.2 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr23:136649542 G>T did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr23:136652133 A>C did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr23:136649735 G>A did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr23:136652128 C>A did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr23:136649665 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45X-01A-21D-A25D-08 chr23:136649291 C>A did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr23:136649479 C>G did not map to a codon.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr23:136649866 T>C did not map to a codon.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr23:136649785 G>T did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:147108848 C>T maps to NM_001168379.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr3:147114185 G>A maps to NM_001168379.1 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:147113921 G>C maps to NM_001168379.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:147114161 G>C maps to NM_001168379.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr3:147113699 C>A maps to NM_001168379.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:100622423 G>A maps to NM_033132.3 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr13:100622741 G>A maps to NM_033132.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:58101556 T>G maps to NM_001010879.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:58102360 C>A maps to NM_001010879.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr19:57293444 C>T maps to NM_001146326.1 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:57647165 G>C maps to NM_052882.1 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:57646829 G>C maps to NM_052882.1 S292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr19:57647236 G>A maps to NM_052882.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:57648259 C>T maps to NM_052882.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:57646306 C>T maps to NM_052882.1 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:57646876 C>T maps to NM_052882.1 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:57646325 G>T maps to NM_052882.1 S460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr19:57648306 A>G maps to NM_052882.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:25258085 G>A maps to NM_001012981.4 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:25263317 G>A maps to NM_001012981.4 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr6:28333969 C>T maps to NM_024493.2 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr6:28333341 C>T maps to NM_024493.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr6:28327419 G>A maps to NM_024493.2 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr6:28214795 G>A maps to NM_019110.3 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:99124009 A>G maps to NM_014569.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr7:99117509 C>A maps to NM_014569.3 S205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:99128781 C>G maps to NM_014569.3 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr23:101139764 T>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr23:101139593 C>G did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr23:101139286 G>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr23:101139206 C>G did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr23:101139650 A>T did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr23:101159302 T>C did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr23:101139014 C>T did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr23:101152891 A>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:101139504 C>T did not map to a codon.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr23:101138796 A>G did not map to a codon.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr23:101139590 G>C did not map to a codon.
Sequencing variant TCGA-BA-A6DL-01A-21D-A30E-08 chr5:140084080 G>A maps to NM_144723.1 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:140080471 C>G maps to NM_144723.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr8:40532343 G>T maps to NM_024645.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr8:40554762 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:40532264 A>G maps to NM_024645.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr8:40532358 A>G maps to NM_024645.2 C147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr8:40554785 C>T maps to NM_024645.2 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A4C1-01A-11D-A24D-08 chr22:30138422 C>T maps to NM_019103.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr10:81072504 G>A maps to NM_020338.3 *1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr10:81051987 C>T maps to NM_020338.3 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr10:81063877 C>T maps to NM_020338.3 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:81058852 C>T maps to NM_020338.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:81050777 G>C maps to NM_020338.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr10:81058891 G>A maps to NM_020338.3 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50I-01A-11D-A28R-08 chr10:81064918 A>G did not map to a codon.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr10:81056364 C>T maps to NM_020338.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr10:81051995 G>A maps to NM_020338.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:44797688 C>G maps to NM_031449.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:44801093 T>C maps to NM_031449.3 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:44804987 C>T maps to NM_031449.3 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:44805101 C>T maps to NM_031449.3 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr1:40758217 A>G maps to NM_005857.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr1:35559685 T>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr13:20567601 G>A maps to NM_001190965.1 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr23:70472944 G>A did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr23:70463730 C>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr23:70463740 G>A did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr23:70461116 G>A did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr23:70470528 C>T did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr23:70470532 G>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr23:70467680 T>G did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr23:70470283 C>T did not map to a codon.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr23:70466244 C>T did not map to a codon.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr23:70467619 C>A did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:70464696 G>A did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr1:35476585 G>A maps to NM_007167.3 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr1:35485179 G>A maps to NM_007167.3 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr1:35484993 G>A maps to NM_007167.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:35452857 T>C maps to NM_007167.3 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr1:35485039 G>C maps to NM_007167.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr10:267289 T>C maps to NM_006624.4 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:294370 G>A maps to NM_006624.4 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr17:4647996 C>G maps to NM_001136046.1 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr20:45905247 C>T maps to ENST00000471951 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr20:45875010 G>A maps to ENST00000471951 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr20:45927649 T>C maps to ENST00000471951 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:45874947 G>A maps to ENST00000471951 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:133733347 A>T maps to NM_015394.4 K506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr12:133727682 C>T maps to NM_015394.4 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr19:21910042 G>A maps to NM_173531.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:21948579 C>T maps to NM_173531.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr19:21910213 C>T maps to NM_173531.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:19790617 A>C maps to NM_033204.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:19790799 A>T maps to NM_033204.2 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:19790751 C>G maps to NM_033204.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:64168430 A>G maps to NM_016220.3 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:64167168 G>T maps to NM_016220.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:48785740 C>T maps to NM_153608.1 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr7:64438978 T>A maps to NM_015852.3 K324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:6731675 A>T maps to ENST00000330442 C356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr7:6731083 C>A maps to ENST00000330442 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr7:6732044 G>C maps to ENST00000330442 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:6730808 C>T maps to ENST00000330442 Q645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr1:247323031 A>G maps to NM_003431.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:43161389 A>T maps to ENST00000509156 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:58945238 G>A maps to NM_003433.3 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr19:58131570 G>A maps to NM_003435.3 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:58578598 A>G maps to NM_007134.1 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:58578349 G>A maps to NM_007134.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A620-01A-11D-A28R-08 chr19:58578598 A>G maps to NM_007134.1 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr19:58579418 G>T maps to NM_007134.1 E547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr19:12297982 C>T maps to NM_003437.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr19:12297489 G>A maps to NM_003437.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr19:19822313 A>T maps to NM_021030.2 C592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:19823300 G>T maps to NM_021030.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:133682775 G>T maps to NM_003440.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr4:337650 G>A maps to NM_003441.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr4:367158 C>T maps to NM_003441.2 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:219510997 C>T maps to NM_001105537.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr2:219510939 T>A maps to NM_001105537.1 K469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr2:219520927 G>A maps to NM_001105537.1 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:36727788 C>T maps to NM_007145.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:124951512 G>C maps to NM_021964.2 S686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr3:124998091 C>A did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr3:124952000 C>T maps to NM_021964.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:58213788 G>C maps to NM_001085384.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:47272913 G>T did not map to a codon.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr23:47272939 A>G did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr23:47272965 T>G did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr23:47271930 A>C did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:47272114 G>C did not map to a codon.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr23:47272086 C>T did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:146157134 C>T maps to NM_006958.2 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:146157371 G>A maps to NM_006958.2 C267C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr8:146157089 G>A maps to NM_006958.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:53572904 A>G maps to NM_001102603.1 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EN-01A-11D-A31L-08 chr19:53573248 G>A maps to NM_001102603.1 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:44612215 C>G maps to NM_018651.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr3:44612533 C>T maps to NM_018651.2 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:44609917 C>T maps to NM_018651.2 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:44609920 C>T maps to NM_018651.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr9:97062207 C>A maps to NM_194320.2 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr19:57931030 G>A maps to NM_006959.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:57931541 A>C maps to NM_006959.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:52091026 G>A maps to NM_007147.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:9489657 A>G maps to NM_001172651.1 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:11895760 C>T maps to NM_144680.2 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr17:11895777 G>A maps to NM_144680.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr19:44981989 A>G maps to NM_013256.3 H236H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:44981194 G>A maps to NM_013256.3 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr19:35230524 A>T maps to ENST00000392232 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr23:47837081 C>G did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr23:47837108 T>C did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr23:47836066 G>C did not map to a codon.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr23:47836980 C>A did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:27424700 C>T did not map to a codon.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr23:152113984 C>T did not map to a codon.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr23:152088888 G>A did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:152113853 G>A did not map to a codon.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr23:152085678 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr9:104171025 C>T maps to NM_003452.2 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:71512137 G>A maps to NM_006961.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:28121668 G>C maps to NM_006298.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr6:28121662 A>G maps to NM_006298.2 Q535Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr11:3380842 G>T maps to NM_001130520.1 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr2:95846872 C>T maps to ENST00000453539 H113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr19:12243776 A>C maps to NM_021143.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:12244367 G>C maps to NM_021143.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr11:123601371 C>T maps to NM_003455.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr11:123597652 C>G maps to NM_003455.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr11:123598958 C>T maps to NM_003455.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr11:123601254 G>A maps to NM_003455.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr16:3169974 C>T maps to NM_001042428.1 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr17:30692367 A>T maps to ENST00000394679 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:30688522 C>T maps to ENST00000394679 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:22155687 A>T maps to NM_007153.3 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr19:22156524 G>A maps to NM_007153.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:22170087 C>T maps to NM_007153.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:22155423 G>T maps to NM_007153.3 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr19:22156074 G>T maps to NM_007153.3 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:22156014 T>C maps to NM_007153.3 K607K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr19:22154038 G>C maps to NM_007153.3 S1266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:22155675 G>C maps to NM_007153.3 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr19:22156896 G>T maps to NM_007153.3 Y313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr19:22156524 G>A maps to NM_007153.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:22154136 G>A maps to NM_007153.3 A1233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:22155222 T>C maps to NM_007153.3 K871K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61J-01A-11D-A30E-08 chr19:22157110 G>T maps to NM_007153.3 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr19:22154847 A>T maps to NM_007153.3 T996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:148947392 G>A maps to NM_012256.3 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr16:3187478 C>T maps to NM_001134655.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr11:7022031 C>T maps to NM_013249.2 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr11:6977594 C>T maps to NM_013250.2 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-8501-01A-11D-2394-08 chr11:6977362 G>A maps to NM_013250.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:52188283 C>G maps to NM_006526.2 *1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr20:52199331 G>A maps to NM_006526.2 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr20:52192995 A>T maps to NM_006526.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr20:52199197 G>A maps to NM_006526.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr14:21561410 C>A maps to NM_001102454.1 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:45498927 C>T maps to NM_006963.4 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr19:44471150 C>A maps to NM_013359.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr19:44536828 C>G maps to NM_001129996.1 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:44536051 A>G maps to NM_001129996.1 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr19:44536635 C>A maps to NM_001129996.1 S310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr19:44536388 C>T maps to NM_001129996.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr19:44611164 G>A maps to NM_013398.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr19:44610696 T>A maps to NM_013398.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:44605295 A>C maps to NM_013398.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:44635981 T>A maps to NM_013362.2 C405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr19:44636170 C>T maps to NM_013362.2 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr19:44635585 C>T maps to NM_013362.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr19:44680434 T>C maps to NM_001032372.1 C340C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:44680225 C>T maps to NM_001032372.1 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr19:44739551 T>C maps to NM_182490.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr19:44738976 C>T maps to NM_182490.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr19:44933308 G>A maps to NM_014518.2 C549C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:44933284 G>T maps to NM_014518.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr19:44933968 G>A maps to NM_014518.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:44936399 G>A maps to NM_014518.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr16:71483727 G>C maps to NM_145911.1 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IG-01A-11D-A31L-08 chr16:71483480 G>A maps to NM_145911.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:44515024 G>A maps to NM_006300.3 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr19:44515252 T>C maps to NM_006300.3 H354H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:44513051 G>A maps to NM_006300.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr17:5012302 C>T maps to NM_014519.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:5012862 C>T maps to NM_014519.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr17:5009728 G>T maps to NM_014519.2 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:44778657 G>T maps to NM_181756.1 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr19:44777131 C>T maps to NM_181756.1 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:44777859 G>A maps to NM_181756.1 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr19:44777754 T>C maps to NM_181756.1 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:44777199 G>A maps to NM_181756.1 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:44661806 G>A maps to NM_006630.2 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JU-01A-11D-A31L-08 chr19:44661767 T>C maps to NM_006630.2 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:44791700 A>G maps to NM_004234.4 C629C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:44791651 G>A maps to NM_004234.4 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:44792213 T>A maps to NM_004234.4 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr1:244217658 C>T maps to NM_205768.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr1:244218371 C>T maps to NM_205768.2 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:244217658 C>T maps to NM_205768.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr1:244218341 G>A maps to NM_205768.2 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:44052300 C>T maps to NM_001099284.1 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:44053167 C>A maps to NM_001099284.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr10:38121208 C>G maps to NM_021045.1 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr10:38120758 A>T maps to NM_021045.1 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:38242023 T>A maps to NM_145011.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr10:38242686 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:146108150 C>T maps to NM_021061.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr8:146107268 C>G maps to NM_021061.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:145948231 C>T maps to NM_138367.1 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:20002712 G>A maps to NM_021047.2 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:20002665 G>T maps to NM_021047.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:20002337 C>T maps to ENST00000427401 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:20002338 C>T maps to ENST00000427401 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:20002531 C>G maps to ENST00000427401 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:24309075 C>T maps to NM_203282.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JV-01A-11D-A34J-08 chr19:24310304 A>G maps to NM_203282.2 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:22255702 G>T maps to NM_033468.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr19:22271901 G>A maps to NM_033468.2 K450K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr19:37005171 C>G maps to NM_001166038.1 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr19:57723538 C>T maps to NM_003417.4 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67D-01A-31D-A30E-08 chr19:57716771 T>A maps to NM_003417.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:9525074 T>A maps to NM_006631.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr16:31896533 G>A maps to NM_003414.4 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:58718243 G>A maps to NM_133502.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:58718243 G>C maps to NM_133502.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JO-01A-11D-A34J-08 chr16:89804287 C>T maps to NM_001113525.1 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr7:111846845 G>T maps to NM_021994.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr19:53304911 C>G maps to NM_006969.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr19:53303096 T>C maps to NM_006969.3 E667E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr22:22868976 C>T maps to NM_080740.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr22:22869675 C>G maps to NM_080740.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr22:22869588 T>C maps to NM_080740.3 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr22:22868459 G>A maps to NM_080740.3 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr22:22868742 C>T maps to NM_080740.3 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr15:56961079 G>A maps to NM_017661.2 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr15:56974507 C>T maps to NM_017661.2 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:200377872 G>A maps to NM_012482.3 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:148903832 G>T maps to NM_003575.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:44341278 G>A maps to NM_181845.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:44590113 C>A maps to NM_001037813.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr19:44590485 G>A maps to NM_001037813.2 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:44891416 G>A maps to NM_152354.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr19:44891919 G>A maps to NM_152354.3 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr17:15620348 C>T maps to NM_020652.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:18565408 A>G maps to NM_001145045.1 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:16455378 G>A maps to NM_020653.2 Q693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr17:16455847 A>G maps to NM_020653.2 Y536Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BA-4078-01A-01D-1434-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BA-A6DE-01A-22D-A31L-08 chr6:87968971 A>G maps to NM_015021.1 K1875K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:87969023 C>T maps to NM_015021.1 Q1893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr6:87969526 T>C maps to NM_015021.1 I2060I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr6:87966216 C>G maps to NM_015021.1 S957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:87967021 T>C maps to NM_015021.1 G1225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr6:87968275 T>G maps to NM_015021.1 A1643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr6:87969625 A>G maps to NM_015021.1 K2093K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr21:43412299 C>G maps to NM_020727.4 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:45579001 G>C maps to NM_145288.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr19:45579616 C>T maps to NM_145288.1 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45P-01A-11D-A24D-08 chr19:45575431 C>T maps to NM_145288.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr19:35435247 G>T maps to NM_001099438.1 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:150275861 A>G maps to NM_001172831.1 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr5:150276464 C>T maps to NM_001172831.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr19:35175565 A>G maps to ENST00000221282 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr19:35173683 G>A maps to ENST00000221282 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:35175541 C>T maps to ENST00000221282 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:35175529 T>C maps to ENST00000221282 N275N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:28962831 G>A maps to NM_001010877.2 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr19:9271902 A>T maps to NM_020933.4 K528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:43307215 G>C maps to NM_014345.2 S1507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:43306785 C>A maps to NM_014345.2 L1650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:43322833 T>C maps to NM_014345.2 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr6:43305057 A>G maps to NM_014345.2 D2226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr6:43323361 C>G maps to NM_014345.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SW-01A-11D-A34J-08 chr6:43305921 G>C maps to NM_014345.2 L1938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr16:58030906 G>A maps to NM_020807.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr16:58031443 C>T maps to NM_020807.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr16:58031158 G>A maps to NM_020807.1 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:58032105 G>A maps to NM_020807.1 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr10:44140202 T>C maps to NM_006973.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:53385153 C>T maps to NM_207333.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr6:28294188 G>A maps to NM_030899.4 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr19:58982599 C>A maps to NM_014347.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr19:58983226 G>A maps to NM_014347.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:58980560 T>C maps to NM_014347.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A642-01A-12D-A30E-08 chr19:58967399 C>T maps to NM_207395.2 H363H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:58967711 G>T maps to NM_207395.2 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:58967528 C>T maps to NM_207395.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:58967042 C>T maps to NM_207395.2 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6V9-01A-11D-A34J-08 chr1:90473297 C>T maps to NM_182976.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:58639325 C>T maps to NM_024620.3 Q515Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:58639937 C>G maps to NM_024620.3 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr19:58639244 T>C maps to NM_024620.3 *542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr19:54080932 C>T maps to NM_001079907.1 H373H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr19:54080197 G>A maps to NM_001079907.1 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:54081121 G>A maps to NM_001079907.1 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:14829869 C>T maps to NM_032433.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:14805945 G>A did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:14829048 C>T maps to NM_032433.2 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr20:45130307 G>C maps to NM_018102.3 S557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr20:44579140 G>A maps to NM_022095.3 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr20:44581028 G>A maps to NM_022095.3 C982C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:44589502 C>A maps to NM_022095.3 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:44588037 G>A maps to NM_022095.3 F685F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr20:25657008 G>C maps to NM_015655.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr20:25655810 T>G maps to NM_015655.2 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr10:38306270 G>A maps to NM_006954.1 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr10:38344244 C>A maps to NM_006954.1 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr10:38344195 G>T maps to NM_006954.1 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr10:38344048 G>T maps to NM_006954.1 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr10:38305867 C>T maps to NM_006954.1 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr10:43088342 T>C maps to NM_006955.1 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr10:43088924 G>A maps to NM_006955.1 H491H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr10:43127880 G>A maps to NM_006955.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr20:32378905 C>T maps to ENST00000375200 C716C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr20:32379112 C>A maps to ENST00000375200 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:2474451 C>T maps to NM_024325.4 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:2464517 G>A maps to NM_024325.4 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr20:2464241 G>A maps to NM_024325.4 H455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A61W-01A-11D-A28R-08 chr20:2463923 T>C maps to NM_024325.4 K561K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr20:2464781 C>T maps to NM_024325.4 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50G-01A-11D-A25Y-08 chr19:37369177 C>T maps to NM_003419.3 C482C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:176489128 C>T maps to ENST00000503039 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr19:53643890 G>A maps to NM_001172674.1 I731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr19:53644778 G>A maps to NM_001172674.1 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:53643935 C>T maps to NM_001172674.1 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:53644811 G>A maps to NM_001172674.1 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:52468505 T>C maps to ENST00000391795 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:52468148 G>A maps to NM_021632.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:178152446 C>T maps to NM_005649.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:178140026 G>A maps to NM_005649.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr5:178310088 A>G maps to NM_058230.2 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:178503531 G>T maps to NM_014594.1 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:178507031 C>T maps to NM_014594.1 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr5:178506329 G>A maps to NM_014594.1 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr1:33745944 C>T maps to NM_152493.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr10:64148196 G>A maps to NM_199451.2 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr10:64416232 C>T maps to NM_199451.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:64415347 C>G maps to NM_199452.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr10:64159481 C>T maps to NM_014951.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr5:71756159 C>T maps to NM_152625.1 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:71756258 G>A maps to NM_152625.1 H355H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr5:71739681 G>A maps to NM_152625.1 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr5:71756462 C>G maps to NM_152625.1 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr5:71739684 G>A maps to NM_152625.1 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr5:71743154 G>A maps to NM_152625.1 C538C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr9:99150719 C>T maps to NM_153695.3 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr10:38406774 A>G maps to NM_003421.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:38407108 C>T maps to NM_003421.2 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr10:38404179 G>A maps to NM_003421.2 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:38406834 C>T maps to NM_003421.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T8-01A-11D-A34J-08 chr10:38407506 C>T maps to NM_003421.2 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:37118347 G>T maps to NM_032825.3 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:37117311 C>G maps to NM_032825.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr19:37117053 T>C maps to NM_032825.3 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:37118396 C>G maps to NM_032825.3 S533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:37733491 A>T maps to NM_152604.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:37734226 G>A maps to NM_152604.1 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr12:6788349 C>G did not map to a codon.
Multiple mappings detected for codon TCGA-CV-7568-01A-11D-2229-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CV-A468-01A-11D-A25Y-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CV-A468-01A-11D-A25Y-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr12:6781535 G>A maps to NM_001135734.1 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr12:54764734 G>A maps to NM_001130967.1 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:180383317 G>T maps to NM_152520.4 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:21465511 G>T maps to NM_024697.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:21606086 G>T maps to NM_024697.2 C85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr3:21478514 G>T maps to NM_024697.2 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:21478594 G>A maps to NM_024697.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr6:27369063 C>T maps to NM_001076781.1 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:99097389 C>T maps to NM_032164.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:99091988 A>G maps to NM_032164.2 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr7:99091604 C>T maps to NM_032164.2 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A718-01A-22D-A34J-08 chr7:99091496 G>A maps to NM_032164.2 C447C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr18:32949529 A>G maps to NM_145756.2 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr18:32949318 G>A maps to NM_145756.2 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr7:148876661 C>A maps to NM_170686.2 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:148876805 G>T maps to NM_170686.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:148876541 G>A maps to NM_170686.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:44376784 T>C maps to ENST00000324394 E525E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-A4AQ-01A-11D-A25D-08 chr19:44377477 C>T maps to ENST00000324394 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr18:72343889 A>G maps to NM_017757.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr18:72345758 T>C maps to NM_017757.2 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr23:47307708 C>G did not map to a codon.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr23:47308009 C>G did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:47308125 A>G did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:74371736 G>A maps to NM_021188.1 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:53612313 G>T maps to NM_001164309.1 Y328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:53612342 G>A maps to NM_001164309.1 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:53612055 G>A maps to NM_001164309.1 C414C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr19:53619584 G>A maps to NM_001164309.1 Y39Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr19:53611914 G>A maps to NM_001164309.1 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr19:58420412 C>T maps to NM_152475.2 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C7-01A-11D-A25D-08 chr19:58420103 A>G maps to NM_152475.2 H514H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr19:58420555 T>A maps to NM_152475.2 K364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:58438231 G>T maps to NM_133460.1 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr19:58001540 A>C maps to NM_001098491.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:58005262 A>G maps to NM_001098491.1 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:37619639 G>T maps to NM_144689.3 G583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:37619743 C>T maps to NM_144689.3 C617C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr16:49764793 A>G maps to NM_015069.2 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr16:49764835 C>T maps to NM_015069.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr16:49672762 G>A maps to NM_015069.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr16:49672147 G>A maps to NM_015069.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr16:49671733 A>T maps to NM_015069.2 C443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr16:49670848 G>A maps to NM_015069.2 H738H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr16:49671870 G>T maps to NM_015069.2 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:148801942 G>A maps to NM_001001661.2 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr7:148801951 C>A maps to NM_001001661.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr19:21719157 G>A maps to NM_001001415.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:21720753 T>C maps to NM_001001415.2 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:21713484 A>T maps to NM_001001415.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4II-01A-11D-A25Y-08 chr19:21991629 A>T maps to NM_003423.2 C403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:21991839 C>T maps to NM_003423.2 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr19:21992241 C>A maps to NM_003423.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:21992316 G>A maps to NM_003423.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:21990519 T>C maps to NM_003423.2 Q773Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:21990409 T>A maps to NM_003423.2 *810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:21205624 A>T maps to NM_025189.3 K12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr19:21365729 A>G maps to NM_133473.2 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr19:21365996 C>T maps to NM_133473.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr19:52537190 C>A maps to NM_014650.2 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr19:12126250 C>T maps to NM_001080411.1 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:23688995 G>A maps to NM_001077195.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr10:31137575 C>A maps to NM_182755.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:11978655 C>T maps to NM_152262.2 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr19:11979382 A>G maps to NM_152262.2 *500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:12384319 C>T maps to NM_001164276.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:11942378 G>T maps to NM_152357.2 G130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr19:11943216 C>G maps to NM_152357.2 S409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr19:11942500 A>G maps to NM_152357.2 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr19:11943308 C>T maps to NM_152357.2 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:11943140 C>T maps to NM_152357.2 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:11943667 A>G maps to NM_152357.2 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:11942803 T>C maps to NM_152357.2 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JH-01A-21D-A34J-08 chr19:11943100 T>C maps to NM_152357.2 C370C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr19:11891445 A>C maps to NM_152355.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:12460904 A>G maps to NM_030824.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:12542084 T>A maps to NM_005815.4 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr19:12541095 G>A maps to NM_005815.4 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:44489428 G>A maps to NM_181489.5 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:58988809 G>C maps to NM_017908.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:58991810 G>A maps to NM_017908.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:134481369 G>C did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:134494648 C>G did not map to a codon.
Sequencing variant TCGA-CQ-A4CG-01A-11D-A25Y-08 chr23:134483098 C>A did not map to a codon.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr23:134494850 G>A did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr23:134493847 C>G did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr23:134494924 C>T did not map to a codon.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr23:134483237 T>G did not map to a codon.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr23:134483214 G>T did not map to a codon.
Sequencing variant TCGA-CV-A464-01A-11D-A25Y-08 chr23:134481153 G>A did not map to a codon.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr19:44417629 G>C maps to NM_003425.3 S653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:44418405 C>T maps to NM_003425.3 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:57012575 G>T maps to NM_001031623.2 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:56999544 C>T maps to NM_001031623.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr6:57015614 C>T maps to NM_001031623.2 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr6:56997883 C>T maps to NM_001031623.2 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:57012088 C>A maps to NM_001031623.2 C402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr5:178369800 C>A maps to NM_182594.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr5:178369800 C>G maps to NM_182594.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:37129719 A>G maps to NM_153257.2 H509H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:109691070 A>G maps to NM_021224.4 E1626E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr9:109691727 A>T maps to NM_021224.4 P1845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr9:109690842 C>T maps to NM_021224.4 H1550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr9:109701311 C>A maps to NM_021224.4 I2117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr9:109687760 C>G maps to NM_021224.4 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:109687821 G>C maps to NM_021224.4 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:149462861 G>A maps to NM_207336.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr7:149461820 C>T maps to NM_207336.1 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:53344520 C>A maps to NM_001008801.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:53344688 G>A maps to NM_001008801.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr19:53344883 G>A maps to NM_001008801.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:50549103 C>T maps to NM_015428.1 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr19:50549980 C>T maps to NM_015428.1 Q761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:50549314 A>C maps to NM_015428.1 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:50549886 C>T maps to NM_015428.1 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:50548344 G>A maps to NM_015428.1 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr19:50550295 A>T maps to NM_015428.1 K866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr7:57188500 A>G maps to NM_033273.1 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8601-01A-11D-2394-08 chr7:57193796 A>G maps to NM_033273.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr7:57194302 G>T maps to NM_033273.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:57194380 C>T maps to NM_033273.1 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:57188596 A>G maps to NM_033273.1 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr7:57188353 A>G maps to NM_033273.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr7:57188620 A>G maps to NM_033273.1 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UP-A6WW-01A-12D-A34J-08 chr7:57194422 T>C maps to NM_033273.1 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:52817497 G>A maps to NM_144684.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:52825846 C>T maps to NM_144684.2 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:114304422 C>G maps to NM_133464.2 S403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr9:114289920 A>G maps to NM_133464.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:114304894 C>T maps to NM_133464.2 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:114305146 C>T maps to NM_133464.2 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61G-01A-11D-A30E-08 chr9:114304132 C>T maps to NM_133464.2 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr9:114296087 C>T maps to NM_133464.2 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr9:114296093 G>T maps to NM_133464.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr9:95609542 G>T maps to NM_031486.1 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr10:44112549 G>A maps to NM_145312.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr19:20308130 T>C maps to ENST00000428290 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr19:20307968 G>A maps to NM_052852.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr10:48371154 C>A maps to NM_153034.2 S208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:12721449 G>C maps to NM_020714.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:12721449 G>A maps to NM_020714.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7063-01A-11D-2394-08 chr19:12691748 G>A maps to NM_020714.2 H380H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr19:11917868 C>G maps to NM_152356.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:21607278 T>C maps to NM_001076678.2 C606C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr19:21606459 C>T maps to NM_001076678.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:21607092 C>A maps to NM_001076678.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr19:21607042 C>T maps to NM_001076678.2 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DB-01A-11D-A30E-08 chr1:247464554 C>A maps to NM_032752.1 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QA-01A-11D-A28R-08 chr19:58868530 G>A maps to NM_198458.1 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:19917754 G>A maps to NM_001099269.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr9:99522149 G>C maps to NM_014930.1 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr9:99521422 C>T maps to NM_014930.1 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr9:99522149 G>C maps to NM_014930.1 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr10:135123744 C>T maps to NM_145806.2 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr2:27823642 C>T maps to NM_032434.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr20:62597873 G>A maps to NM_020713.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr20:62598357 C>A did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr20:62597951 G>A maps to NM_020713.1 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr20:62598781 C>T maps to NM_020713.1 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61K-01A-11D-A30E-08 chr20:62599267 G>A maps to NM_020713.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:27601469 C>T maps to NM_144631.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr2:27601562 G>A maps to NM_144631.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr2:95815452 G>C maps to NM_032788.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr18:74154313 C>A maps to ENST00000443185 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr18:74154629 C>A maps to ENST00000443185 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr18:74154473 G>A maps to ENST00000443185 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:74154068 G>A maps to ENST00000443185 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr18:74153249 G>A maps to ENST00000443185 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr8:146033062 C>T maps to NM_213605.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:97918676 A>T maps to NM_014803.3 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr10:97917660 G>T maps to NM_014803.3 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HZ-01A-21D-A28R-08 chr10:97916586 C>T maps to NM_014803.3 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr10:97917734 T>C maps to NM_014803.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:97916166 A>C maps to NM_014803.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr10:97917389 C>T maps to NM_014803.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr10:97917854 T>C maps to NM_014803.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:10444811 G>A maps to NM_053042.2 D1047D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr4:10447433 C>T maps to NM_053042.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr4:10445504 C>T maps to NM_053042.2 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr18:14105332 T>C maps to NM_145287.3 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr18:14106205 T>C maps to NM_145287.3 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr18:14105476 G>T maps to NM_145287.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr18:14105044 G>A maps to NM_145287.3 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr18:22805753 G>A maps to NM_015461.2 Q710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr18:22805214 G>A maps to NM_015461.2 D889D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr18:22804668 G>C maps to NM_015461.2 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr18:22805792 C>A maps to NM_015461.2 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr18:22807173 C>T maps to NM_015461.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr18:22804523 G>A maps to NM_015461.2 Q1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr18:22805259 C>T maps to NM_015461.2 G874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A633-01A-11D-A28R-08 chr18:22804707 G>T maps to NM_015461.2 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A6I9-01A-11D-A31L-08 chr18:22807494 G>T maps to NM_015461.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr18:22902017 C>T maps to NM_015461.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr19:56114116 C>T maps to NM_153219.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:56114032 G>A maps to NM_153219.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:42730363 A>G maps to NM_133444.1 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr19:37880351 A>G maps to NM_032453.1 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:37879379 G>A maps to NM_032453.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:37880678 C>T maps to NM_032453.1 H576H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:52918854 C>T maps to NM_032423.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr19:52905280 G>A maps to NM_032423.2 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr19:37038094 A>G maps to NM_001145649.1 C455C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr19:58118330 C>T maps to NM_020880.3 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr18:56620895 G>A maps to NM_018181.4 K1005K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr18:56586481 C>T maps to NM_018181.4 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr18:56586562 G>A maps to NM_018181.4 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K0-01B-21D-A31L-08 chr18:56586442 G>A maps to NM_018181.4 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr18:56587477 C>G maps to NM_018181.4 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:52941052 C>T maps to NM_001143939.1 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr19:52941774 C>A maps to NM_001143939.1 Y367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:30935176 C>T maps to NM_014717.1 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:30935221 G>A maps to NM_014717.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr19:31040059 C>T maps to NM_014717.1 N1178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:30936463 C>T maps to NM_014717.1 H665H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7069-01A-11D-2394-08 chr19:31039156 T>G maps to NM_014717.1 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4C9-01A-11D-A25D-08 chr19:30935707 G>A maps to NM_014717.1 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:30934666 G>A maps to NM_014717.1 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:31039804 C>T maps to NM_014717.1 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:30936466 G>T maps to NM_014717.1 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:31025859 T>C maps to NM_014717.1 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr19:31039642 C>A maps to NM_014717.1 V1039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:30935395 T>A maps to NM_014717.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:30935482 C>A maps to NM_014717.1 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr19:30934870 C>T maps to NM_014717.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr19:31039972 C>A maps to NM_014717.1 I1149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:30935062 G>C maps to NM_014717.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:38103197 C>T maps to NM_152606.3 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr19:38102813 T>C maps to NM_152606.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:57839468 C>T maps to NM_213598.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:57839315 T>C maps to NM_213598.3 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:58773054 A>G maps to NM_014480.2 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:58758137 G>A maps to NM_014480.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr19:58757772 G>A maps to NM_014480.2 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7064-01A-11D-2394-08 chr19:40520013 G>A maps to NM_178544.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr19:40520757 T>C maps to NM_178544.3 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:57883218 C>T maps to NM_173631.2 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr19:57905566 G>A maps to NM_001172773.1 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr19:57910123 G>T maps to NM_001172773.1 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:57910605 C>T maps to NM_001172773.1 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr19:58049112 T>A maps to ENST00000376233 Y247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:58059065 G>T maps to NM_001039654.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:58067716 C>T maps to NM_001039654.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr19:58198983 T>A maps to ENST00000356715 Y447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:58199001 G>A maps to ENST00000356715 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr19:2834411 A>T maps to NM_001102651.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:2853583 C>G maps to NM_152791.4 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:9452471 A>G maps to NM_032497.1 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:9453077 G>A maps to NM_032497.1 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:9578056 C>T maps to NM_152476.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:9578248 C>T maps to NM_152476.2 K458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:9577561 G>A maps to NM_152476.2 N687N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:9580304 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:9578134 G>C maps to NM_152476.2 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:9721790 T>A maps to NM_152289.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr19:9721286 C>A maps to NM_152289.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr19:9721240 G>A maps to NM_152289.2 Q366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45V-01A-21D-A25D-08 chr19:9768730 G>C maps to NM_001130032.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:36673656 G>C maps to ENST00000355114 S425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:36673813 G>A maps to ENST00000355114 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:36964330 T>C maps to NM_001145343.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr19:36964258 C>T maps to NM_001145343.1 E37E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr19:37210996 C>A maps to ENST00000423498 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr19:37210258 A>G maps to ENST00000423498 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr19:37211353 C>G maps to ENST00000423498 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr19:37440778 C>T maps to NM_198539.2 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:37440566 C>A maps to NM_198539.2 S171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr19:37440670 G>T maps to NM_198539.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DI-01A-11D-A30E-08 chr19:37903576 G>A maps to NM_152484.2 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr19:37904956 G>A maps to NM_152484.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:37903738 T>C maps to NM_152484.2 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr19:37904368 A>T maps to NM_152484.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:37904080 G>T maps to NM_152484.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:2917425 A>G maps to NM_173480.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:38057173 C>T maps to NM_016536.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr19:38055700 T>C maps to NM_016536.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr8:125989244 A>G maps to NM_152412.2 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr8:125989608 C>T maps to NM_152412.2 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CD-01A-21D-A25D-08 chr8:125988596 A>T maps to NM_152412.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:125989716 C>T maps to NM_152412.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr8:125989979 C>T maps to NM_152412.2 H490H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr19:42584698 C>T maps to ENST00000222339 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr19:42584119 G>A maps to ENST00000222339 E544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr19:42582793 T>C maps to ENST00000222339 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:42583150 C>T maps to ENST00000222339 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61H-01A-11D-A30E-08 chr19:42582949 G>A maps to ENST00000222339 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr19:44103202 G>A maps to NM_024327.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:52376426 G>T maps to NM_032679.2 C272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr19:53015265 T>C maps to NM_001099694.1 C544C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:53015076 A>G maps to NM_001099694.1 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:56154206 C>T maps to NM_001163423.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:56896527 C>T maps to NM_144690.1 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:56901747 T>C maps to NM_144690.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:56934473 C>T maps to NM_001159861.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:58928445 C>T maps to NM_173548.1 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:58928589 T>C maps to NM_173548.1 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:37643885 T>C maps to ENST00000356958 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:37677946 C>G maps to NM_152279.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:37676275 A>G maps to NM_152279.3 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A640-01A-21D-A30E-08 chr19:58290797 G>A maps to NM_017652.2 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:58370974 C>T maps to NM_032828.2 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:58367482 G>A maps to NM_032828.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JY-01A-11D-A31L-08 chr3:48309606 A>G maps to NM_016089.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr15:85341665 C>G maps to NM_014630.2 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63V-01A-11D-A28R-08 chr15:85345395 G>A maps to NM_014630.2 A1192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:85326319 C>T maps to NM_014630.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr15:85341885 C>G maps to NM_014630.2 S935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr15:85328023 C>T maps to NM_014630.2 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:5086385 G>C maps to NM_032530.1 S389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr17:5087488 G>A maps to NM_032530.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr4:59390 C>A maps to NM_182524.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:59345 G>A maps to NM_182524.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr4:59957 G>A maps to NM_182524.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr4:59390 C>T maps to NM_182524.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:59330 A>T maps to NM_182524.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr16:3487032 G>A maps to NM_152457.1 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:3487314 T>A maps to NM_152457.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr16:2052727 G>A maps to ENST00000431526 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:2053039 C>T maps to ENST00000431526 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2049626 G>A maps to ENST00000431526 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr19:53270815 T>A maps to NM_198457.2 K65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:58489923 G>A maps to NM_025027.3 Y708Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr19:58490028 A>T maps to NM_025027.3 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:58491453 G>A maps to NM_025027.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HJ-01A-12D-A34J-08 chr19:58490064 G>A maps to NM_025027.3 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:38189042 A>G maps to NM_032689.4 H663H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:38189303 G>A maps to NM_032689.4 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T4-01A-11D-A34J-08 chr19:38189765 T>C maps to NM_032689.4 K422K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A4IG-01A-11D-A25Y-08 chr5:123983484 C>A maps to NM_020747.2 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:123983565 C>A maps to NM_020747.2 G837G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:123982854 C>A maps to NM_020747.2 L1074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JJ-01A-11D-A34J-08 chr5:123982539 C>T maps to NM_020747.2 E1179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr15:64968079 G>A maps to NM_015042.1 Q1009Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:64791722 C>T maps to NM_015042.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr19:52856993 G>C maps to NM_001161425.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:52869338 A>G maps to NM_001161425.1 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr19:53217271 A>C maps to NM_001161500.1 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A64Z-01A-11D-A30E-08 chr19:53209566 C>T maps to NM_001161500.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:52443550 C>T maps to NM_001031721.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:52448209 G>A maps to NM_001031721.3 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:52519443 G>A maps to NM_025040.3 C469C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr19:52519598 G>A maps to NM_025040.3 Q418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:52519833 C>T maps to NM_025040.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr19:52506949 C>T maps to ENST00000354939 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:52497521 G>A maps to ENST00000354939 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:52497497 T>A maps to ENST00000354939 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T3-01A-11D-A34J-08 chr19:52496986 G>A maps to ENST00000354939 R459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr19:52619804 C>T maps to NM_178523.3 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CH-01A-11D-A25Y-08 chr19:52619792 A>G maps to NM_178523.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:52619846 A>G maps to NM_178523.3 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr19:52619979 G>T maps to NM_178523.3 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A51W-01A-21D-A25Y-08 chr19:52618994 G>A maps to NM_178523.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:116764923 G>T maps to ENST00000374126 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr3:40570901 G>A maps to NM_001098414.1 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr5:16465249 C>T maps to NM_033414.2 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr8:144733583 C>T maps to NM_014789.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:144733534 C>A maps to NM_014789.3 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-8489-01A-31D-2394-08 chr8:144732345 A>C maps to NM_014789.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr17:16527242 G>C maps to NM_020787.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:16525916 G>A maps to NM_020787.3 F761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:12256888 C>T maps to ENST00000439556 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:12256681 T>A maps to ENST00000439556 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:20807481 C>A maps to NM_001076675.2 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:20807836 C>T maps to NM_001076675.2 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:11727527 C>T maps to NM_145295.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:11728613 T>C maps to NM_145295.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr19:55995169 G>A maps to NM_033113.2 V866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:30794730 G>A maps to NM_001080417.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:30794799 G>A maps to NM_001080417.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JO-01B-11D-A34J-08 chr16:30794847 G>A maps to NM_001080417.1 C267C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:30794874 G>A maps to NM_001080417.1 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T7-01A-11D-A34J-08 chr16:30794511 G>A maps to NM_001080417.1 C379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr23:47919476 G>C did not map to a codon.
Sequencing variant TCGA-CQ-7071-01A-12D-A30E-08 chr23:47917922 G>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr23:47918862 T>A did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr23:47918144 C>G did not map to a codon.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr23:47918973 G>A did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr23:47919826 A>T did not map to a codon.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr23:47920201 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr2:71629114 C>G maps to NM_014497.3 V909V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr2:71653960 C>T maps to NM_014497.3 C1654C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:179051457 C>T maps to NM_016331.1 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr3:179051423 C>T maps to NM_016331.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr3:179050800 C>G maps to NM_016331.1 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr12:48737160 T>C maps to NM_152320.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:40961661 C>T maps to NM_198494.2 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:40961127 C>T maps to NM_198494.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:40929122 C>G maps to NM_023070.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr1:40928282 C>T maps to NM_023070.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:40922675 G>T maps to NM_023070.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:91403320 G>A maps to NM_201269.1 L1137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:91403925 G>A maps to NM_201269.1 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:91405605 C>T maps to NM_201269.1 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:22291691 A>G did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:22291389 G>C did not map to a codon.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr23:22291313 G>A did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr16:31091298 C>T maps to NM_014699.3 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:31089072 C>T maps to NM_014699.3 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:182026715 G>A maps to NM_001009992.1 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr1:182026641 G>T maps to NM_001009992.1 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr1:182025762 C>T maps to NM_001009992.1 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:52394689 G>T maps to NM_023074.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:47388698 G>A maps to NM_014897.2 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr19:11598500 G>T maps to NM_138783.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:88188517 C>T maps to NM_018293.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:99159524 C>T maps to NM_024061.3 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr9:40772751 G>C maps to NM_033160.5 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr9:40774006 G>T maps to NM_033160.5 S423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HI-01A-11D-A34J-08 chr9:40774443 T>C maps to NM_033160.5 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:44635867 G>A maps to NM_173658.1 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr3:42950328 C>T maps to NM_001134656.1 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:53669069 G>A maps to NM_024733.3 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:53668206 T>C maps to NM_024733.3 K512K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:53668983 C>T maps to NM_024733.3 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:56953603 G>A maps to ENST00000342634 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr19:56973705 C>G did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:56953258 G>T maps to ENST00000342634 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:56952581 C>A maps to ENST00000342634 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:56953820 G>A maps to ENST00000342634 F309F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-5360-01A-01D-1434-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CR-7371-01A-11D-2012-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CR-7373-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HD-8224-01A-11D-2394-08 chr16:31075549 G>A maps to NM_001172669.1 S100S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-P3-A5QF-01A-11D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr1:247201302 G>A maps to NM_033213.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:247201494 A>G maps to NM_033213.3 H142H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RS-A6TP-01A-12D-A34J-08 chr19:58232844 G>A maps to ENST00000335820 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr1:249142663 C>T maps to NM_024836.1 C397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JF-01A-11D-A34J-08 chr1:249142405 C>T maps to NM_024836.1 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr19:23836306 T>A maps to NM_138330.2 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr19:23836192 G>A maps to NM_138330.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:23836954 T>C maps to NM_138330.2 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:22363717 G>A maps to NM_001001411.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr19:22363090 A>G maps to NM_001001411.2 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63T-01A-11D-A28R-08 chr19:22364065 G>T maps to NM_001001411.2 C151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:22363930 G>A maps to NM_001001411.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr19:22362825 C>A maps to NM_001001411.2 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:53740379 G>A maps to NM_182609.2 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V6-01A-12D-A34J-08 chr19:53740938 G>T maps to NM_182609.2 Y347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:227842403 A>G maps to NM_178549.3 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr7:63720696 A>G maps to NM_153363.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr7:63726908 G>T maps to NM_153363.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr7:63726350 A>C maps to NM_153363.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:23927131 G>C maps to NM_138286.2 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EK-01A-11D-A31L-08 chr19:23927978 C>A maps to NM_138286.2 G125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X2-01A-12D-A34J-08 chr19:20135092 C>T maps to NM_033196.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:26691025 G>C maps to ENST00000436292 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:26691178 C>T maps to ENST00000436292 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:41012510 T>C maps to NM_152373.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr1:151260749 G>A maps to NM_020832.1 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr1:151260524 G>A maps to NM_020832.1 K586K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr1:151261020 C>T maps to NM_020832.1 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr16:30615769 G>A maps to NM_138447.1 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr19:12014458 G>A maps to ENST00000429654 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67A-01A-11D-A30E-08 chr1:249151460 G>A maps to NM_001136036.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:247163358 C>T maps to NM_020394.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr8:144378414 C>T maps to NM_030895.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:120165543 G>A maps to NM_001080470.1 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7446-01A-11D-2229-08 chr19:9406609 G>A maps to NM_198535.1 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:9406699 C>T maps to NM_198535.1 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:146068369 G>A maps to ENST00000446747 K636K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr8:146067675 C>G maps to ENST00000446747 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:24086060 G>A maps to NM_021916.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:24086775 G>C maps to NM_021916.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr22:24086331 G>A maps to NM_021916.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr22:24087057 G>T maps to NM_021916.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:12060797 C>A maps to NM_144566.1 C653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:12060473 C>T maps to NM_144566.1 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JZ-01A-11D-A31L-08 chr19:12060398 C>T maps to NM_144566.1 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr19:53077369 G>T maps to NM_001172655.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:81605275 A>C maps to NM_001033723.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:81733813 G>A maps to NM_001033723.2 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr8:81553669 C>G maps to NM_001033723.2 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:21477071 A>G maps to NM_021269.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:21477104 C>T maps to NM_021269.2 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:12575298 T>C maps to ENST00000428311 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr19:12575148 C>T maps to ENST00000428311 E529E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:57133987 A>T maps to NM_021216.4 K445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr19:57132790 G>T maps to NM_021216.4 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:57133863 G>T maps to NM_021216.4 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:57133428 C>T maps to NM_021216.4 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr19:57134091 G>C maps to NM_021216.4 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr19:57133845 C>T maps to NM_021216.4 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:90611532 C>T maps to NM_198526.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr15:90611532 C>T maps to NM_198526.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61E-01A-22D-A30E-08 chr15:90610894 C>T maps to NM_198526.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr23:84502624 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr23:84523344 C>T did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr23:84525038 G>C did not map to a codon.
Sequencing variant TCGA-CV-A6JE-01A-11D-A31L-08 chr23:84526390 A>G did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:84520162 G>T did not map to a codon.
Sequencing variant TCGA-P3-A6T5-01A-11D-A34J-08 chr23:84525921 T>A did not map to a codon.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr7:56007146 C>T maps to NM_182633.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:56007357 C>T maps to NM_182633.1 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8314-01A-11D-2394-08 chr7:56006939 G>A maps to NM_182633.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr7:55990880 C>T maps to NM_182633.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:21300357 C>T maps to NM_182515.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr19:21300909 C>G maps to NM_182515.3 Y480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr19:21281094 C>T maps to NM_182515.3 N7N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr19:21299745 G>C maps to NM_182515.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:57529303 C>T maps to NM_001159279.1 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr7:57528991 C>G maps to NM_001159279.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr4:436362 C>T maps to NM_133474.2 Q631Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr4:437595 G>A maps to NM_133474.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr4:435876 G>C maps to NM_133474.2 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:20728195 G>A maps to NM_001159293.1 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr19:20736632 C>T maps to NM_001159293.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:20728761 G>A maps to NM_001159293.1 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:20728687 T>C maps to NM_001159293.1 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr19:20735340 G>A maps to NM_001159293.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr22:20749633 C>T maps to NM_003426.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr7:149171708 G>A maps to NM_001163474.1 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr7:149171597 C>T maps to NM_001163474.1 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71B-01A-12D-A34J-08 chr7:149191089 C>T maps to NM_001163474.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr19:57955190 G>A maps to NM_001023561.2 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:57955242 C>T maps to NM_001023561.2 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:80788497 C>T maps to NM_024702.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:80790149 G>A maps to NM_024702.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:80789424 G>C maps to NM_024702.2 Y302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A6H7-01A-11D-A31L-08 chr17:80790228 G>T maps to NM_024702.2 C34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67G-01A-11D-A30E-08 chr17:80789501 C>A maps to NM_024702.2 G277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr17:80789698 G>C maps to NM_024702.2 S211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WX-01A-12D-A34J-08 chr17:80789501 C>A maps to NM_024702.2 G277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr23:134427678 C>G did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr23:134421765 T>A did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr23:134428025 G>T did not map to a codon.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr23:134421748 C>T did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr23:134426279 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:134421320 C>T did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr6:35260715 G>A maps to NM_003427.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr6:35260406 C>T maps to NM_003427.3 H336H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:53958796 C>T maps to NM_001008401.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr19:53958192 T>C maps to NM_001008401.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr19:53959368 C>T maps to NM_001008401.3 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:53958819 T>C maps to NM_001008401.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr19:53959872 C>T maps to NM_001008401.3 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6X0-01A-11D-A34J-08 chr19:12088964 G>T maps to NM_001012753.1 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr16:30566841 C>T maps to NM_033410.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:53912280 G>A maps to NM_001040185.1 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JA-01A-12D-A34J-08 chr19:53912378 A>T maps to NM_001040185.1 *524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:52794351 G>A maps to NM_001010851.2 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:52793883 C>T maps to NM_001010851.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T0-01A-12D-A34J-08 chr19:52793355 G>A maps to NM_001010851.2 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr16:30537132 G>A maps to NM_024671.3 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:30536710 G>A maps to NM_024671.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr15:35274540 G>A maps to NM_014106.3 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:57985604 C>T maps to NM_001024596.2 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EM-01A-21D-A31L-08 chr19:57987106 C>T maps to NM_001024596.2 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45U-01A-12D-A24D-08 chr15:90903701 G>A maps to NM_001004309.2 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr7:150094921 C>T maps to NM_173680.3 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr7:150093928 G>A maps to NM_173680.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:58265187 C>A maps to NM_173632.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr19:58265260 C>T maps to NM_173632.3 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:149129493 T>C maps to ENST00000440594 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr7:149152362 G>A maps to ENST00000440594 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5Q6-01A-11D-A28R-08 chr7:149153093 G>C maps to ENST00000440594 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CE-01A-11D-A25Y-08 chr16:89294663 C>T maps to NM_182531.2 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:40580485 A>G maps to NM_001142577.1 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr19:40540671 T>A maps to NM_001005851.2 V698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JD-01A-11D-A31L-08 chr19:38160803 A>G maps to NM_152605.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr19:38160503 T>C maps to NM_152605.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr9:99581053 C>T maps to NM_001001662.1 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr9:99581235 G>A maps to NM_001001662.1 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:56133380 G>A maps to NM_203374.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr16:30594426 G>A maps to NM_152458.6 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr7:148767796 C>A maps to NM_152411.3 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr7:148768225 G>A maps to NM_152411.3 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr7:148769032 G>A maps to NM_152411.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr7:148769031 G>A maps to NM_152411.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr19:12734542 G>C maps to NM_153358.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6ES-01A-12D-A31L-08 chr19:12738612 G>A maps to NM_153358.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr19:35451805 C>T maps to NM_175872.4 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:35449807 T>C maps to NM_175872.4 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Z-01A-21D-A25D-08 chr19:12501531 A>G maps to NM_001080821.2 Y560Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:12502623 A>C maps to NM_001080821.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr3:113955699 C>T maps to NM_007136.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6SX-01A-11D-A34J-08 chr3:113955303 T>A maps to NM_007136.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C9-A480-01A-12D-A24D-08 chr7:127014573 T>C maps to NM_176814.3 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:127014178 G>C maps to NM_176814.3 S404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T2-A6WZ-01A-21D-A34J-08 chr7:127014012 T>C maps to NM_176814.3 K459K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JD-01A-11D-A34J-08 chr7:127013760 T>C maps to NM_176814.3 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:185803539 C>G maps to NM_194250.1 T1139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:185801352 T>A maps to NM_194250.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:185803104 T>A maps to NM_194250.1 Y994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:185803440 C>T maps to NM_194250.1 H1106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45W-01A-11D-A25D-08 chr2:185801871 A>G maps to NM_194250.1 K583K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr2:185798421 C>A maps to NM_194250.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:185800593 G>T maps to NM_194250.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A50J-01A-21D-A28R-08 chr2:185800791 C>T maps to NM_194250.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A6SH-01A-12D-A34J-08 chr2:185802015 G>A maps to NM_194250.1 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr7:88964687 A>T maps to NM_181646.2 K798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49C-01A-11D-A24D-08 chr7:88963927 T>C maps to NM_181646.2 D544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr7:88964092 G>A maps to NM_181646.2 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr7:88847531 G>T maps to NM_181646.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr7:88964788 C>T maps to NM_181646.2 N831N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr7:88963051 C>G maps to NM_181646.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:88963594 C>T maps to NM_181646.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:88966297 G>A maps to NM_181646.2 Q1334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr7:88956678 C>A maps to NM_181646.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr7:88963957 G>A maps to NM_181646.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr19:57765983 T>C maps to NM_001023563.3 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:53058568 C>T maps to NM_001039886.3 F800F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:53058025 A>G maps to NM_001039886.3 G619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr19:53058289 C>T maps to NM_001039886.3 Y707Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:53058460 G>A maps to NM_001039886.3 K764K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:53056774 C>T maps to NM_001039886.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:53046597 C>T maps to NM_001039886.3 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr23:47774930 C>T did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr23:47774431 A>T did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr23:47775779 G>T did not map to a codon.
Sequencing variant TCGA-CN-A641-01A-11D-A30E-08 chr19:53454526 G>T maps to NM_001031665.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr19:53453767 A>T maps to NM_001031665.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JN-01A-11D-A31L-08 chr19:53454619 A>T maps to NM_001031665.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr16:71898870 T>A maps to ENST00000425432 K83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr16:71894094 C>T maps to ENST00000425432 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:11832718 G>A maps to NM_001080493.2 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63W-01A-11D-A30E-08 chr4:146807289 C>A maps to ENST00000508784 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr4:146770711 C>T maps to ENST00000508784 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr4:146824263 C>T maps to ENST00000508784 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:115089331 G>A maps to NM_032436.2 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr13:115090168 A>T maps to NM_032436.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:37383091 G>A maps to NM_001171979.1 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:37398927 T>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:53117231 G>A maps to NM_018300.3 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr19:53116710 A>G maps to NM_018300.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr19:53117346 G>A maps to NM_018300.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-A4CI-01A-11D-A25Y-08 chr17:33289646 G>A maps to NM_052857.3 E354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr20:57766301 G>T maps to NM_178457.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-8596-01A-11D-2394-08 chr20:57767474 G>A maps to NM_178457.1 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr20:57767408 C>A maps to NM_178457.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A49B-01A-31D-A24D-08 chr20:57769097 C>T maps to NM_178457.1 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr20:57767312 C>T maps to NM_178457.1 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr20:57769025 G>T maps to NM_178457.1 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:57767537 C>T maps to NM_178457.1 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr20:57769697 G>A maps to NM_178457.1 A1208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-8635-01A-11D-2394-08 chr20:57766862 C>G maps to NM_178457.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VC-01A-23D-A34J-08 chr20:57767135 G>A maps to NM_178457.1 E354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TN-A7HL-01A-11D-A34J-08 chr20:57769307 C>T maps to NM_178457.1 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:57175753 G>A maps to NM_001005850.1 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V3-01A-12D-A34J-08 chr19:57175945 C>A maps to NM_001005850.1 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:57176559 C>A maps to NM_001005850.1 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:57175432 G>A maps to NM_001005850.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:57175081 C>T maps to NM_001005850.1 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6JM-01A-11D-A31L-08 chr19:57176107 C>T maps to NM_001005850.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr19:57175945 C>T maps to NM_001005850.1 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6II-01A-11D-A31L-08 chr19:57175282 G>A maps to NM_001005850.1 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr19:57175051 T>C maps to NM_001005850.1 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JK-01A-11D-A34J-08 chr19:57175876 C>T maps to NM_001005850.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:52659058 G>C maps to NM_001102657.1 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr19:52658815 G>C maps to NM_001102657.1 S707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:102805528 G>A maps to NM_018335.3 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:102792467 C>T maps to NM_018335.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr14:102808374 A>G maps to NM_018335.3 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:52569823 G>C maps to NM_001136499.1 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HY-01A-11D-A28R-08 chr19:12186813 C>T maps to NM_001136501.1 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr19:12187209 A>G maps to NM_001136501.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr19:53854764 C>A maps to NM_138374.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr19:53855451 A>G maps to NM_138374.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:53855799 T>C maps to NM_138374.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K1-01A-11D-A31L-08 chr19:53854693 C>T maps to NM_138374.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:53848881 C>T maps to NM_138374.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:53855646 T>C maps to NM_138374.1 H573H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:21132174 C>A maps to NM_003429.4 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr7:149545304 A>C maps to NM_001099220.1 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-A5HU-01A-11D-A28R-08 chr19:12155087 G>A maps to NM_001080404.1 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:52887775 C>T maps to NM_001145434.1 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr19:20228641 T>C maps to NM_007138.1 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:20229331 G>A maps to NM_007138.1 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:23544196 T>C maps to NM_003430.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:23545291 G>A maps to NM_003430.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr19:23543348 G>C maps to NM_003430.2 S811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MT-A67F-01A-11D-A30E-08 chr19:23557443 G>A maps to NM_003430.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr19:22574947 G>T maps to NM_001098626.1 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr19:22951155 C>A maps to ENST00000397104 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:22952080 C>A maps to ENST00000397104 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:22940816 G>A maps to ENST00000397104 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:22939864 T>C maps to ENST00000397104 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:22939422 G>T maps to ENST00000397104 Y916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63U-01A-11D-A30E-08 chr19:22939268 C>A maps to ENST00000397104 G968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5333-01A-01D-2394-08 chr19:22941701 C>A maps to ENST00000397104 G246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr19:22939993 A>G maps to ENST00000397104 C779C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:22940511 G>T maps to ENST00000397104 Y642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr19:22939798 G>A maps to ENST00000397104 A844A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr19:22941471 A>G maps to ENST00000397104 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WA-A7GZ-01A-11D-A34J-08 chr19:22941438 G>C maps to ENST00000397104 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6V1-01A-12D-A34J-08 chr20:47886749 C>T maps to NM_021035.2 Q533Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr20:47863941 C>T maps to NM_021035.2 K1873K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4Z9-01A-11D-A25D-08 chr20:47886635 T>A maps to NM_021035.2 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr20:47881312 C>G maps to NM_021035.2 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:64884390 G>C maps to NM_014205.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A6T2-01A-11D-A34J-08 chr11:64884963 G>A maps to NM_014205.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr6:30029435 C>A maps to NM_170783.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr16:75033820 G>A maps to ENST00000320619 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A6K2-01A-11D-A31L-08 chr22:29439333 G>A maps to NM_032173.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A71A-01A-22D-A34J-08 chr22:29445591 C>T maps to NM_032173.2 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:5456014 G>A maps to NM_181710.3 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr19:5456158 G>A maps to NM_181710.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr19:5455921 C>T maps to NM_181710.3 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:60637114 C>A maps to NM_207341.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EP-01A-11D-A31L-08 chr11:60640751 G>A maps to NM_207341.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:21213514 T>A maps to NM_003460.1 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:21213520 C>T maps to NM_003460.1 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A74Q-01A-11D-A34J-08 chr16:21221023 C>T maps to NM_003460.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr7:50121442 C>G maps to NM_007009.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:50070686 C>A did not map to a codon.
Sequencing variant TCGA-UF-A71D-01A-12D-A34J-08 chr7:50132757 C>A maps to NM_007009.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr17:38027759 G>C maps to NM_199321.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr3:102171892 C>A maps to NM_175056.1 C95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:102196425 A>G maps to NM_175056.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-A61I-01A-11D-A30E-08 chr1:71544246 C>T maps to NM_203350.2 E37E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:136107558 C>A maps to NM_032143.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr2:135965228 C>T maps to NM_032143.2 A928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6IJ-01A-11D-A31L-08 chr2:135965291 T>C maps to NM_032143.2 E907E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr23:15809057 C>A did not map to a codon.
Sequencing variant TCGA-UF-A7JC-01A-21D-A34J-08 chr23:15841048 G>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:58565247 C>A maps to NM_182572.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:58549383 G>A maps to NM_182572.3 W60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DA-01A-31D-A31L-08 chr16:3140534 C>A maps to NM_032805.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr16:3140552 T>G maps to NM_032805.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A6EO-01A-11D-A31L-08 chr16:3140534 C>T maps to NM_032805.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:28097415 C>T maps to NM_025231.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-A6HZ-01A-12D-A31L-08 chr6:28093442 C>T maps to NM_025231.1 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr6:28097583 C>T maps to NM_025231.1 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr19:58601583 C>T maps to NM_001145542.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:58601679 A>T maps to NM_001145542.1 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr19:58596243 C>T maps to NM_001145542.1 W503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr19:58596147 C>T maps to NM_001145542.1 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KU-A66T-01A-11D-A30E-08 chr19:58596525 G>A maps to NM_001145542.1 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:85149784 G>A maps to NM_017894.5 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr15:85165177 G>A maps to NM_181877.3 K584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr15:85164139 C>T maps to NM_181877.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-A6C5-01A-11D-A30E-08 chr15:85164613 G>A maps to NM_181877.3 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr1:33960363 C>G maps to NM_145238.3 S807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr1:33960511 C>T maps to NM_145238.3 I856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr1:33960784 C>T maps to NM_145238.3 I947I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-A4ZB-01A-11D-A25D-08 chr1:33960847 C>T maps to NM_145238.3 F968F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QK-A6VB-01A-12D-A34J-08 chr1:33954219 C>T maps to NM_145238.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr7:99654655 C>T maps to NM_145914.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A6UY-01A-12D-A34J-08 chr19:58850178 G>A maps to NM_181846.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P3-A5QF-01A-11D-A28R-08 chr19:58850484 G>A maps to NM_181846.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7JT-01A-11D-A34J-08 chr19:58850178 G>A maps to NM_181846.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MZ-A7D7-01A-21D-A34J-08 chr15:43656251 G>A maps to NM_152455.3 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:58189589 G>T maps to NM_152677.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr19:56733087 G>A maps to NM_024303.1 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr19:56734094 G>A maps to NM_024303.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A63Y-01A-11D-A30E-08 chr19:56704175 C>T maps to NM_001080456.2 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:56703217 C>A did not map to a codon.
Sequencing variant TCGA-CV-A468-01A-11D-A25Y-08 chr19:56704076 C>T maps to NM_001080456.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A7J9-01A-12D-A34J-08 chr19:56704313 G>A maps to NM_001080456.2 H36H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:44512004 C>G maps to NM_080603.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-A461-01A-41D-A25Y-08 chr2:187703738 G>T maps to NM_182521.2 C147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr2:187694507 A>G maps to NM_182521.2 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:13928081 G>A maps to NM_023072.2 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:45506090 G>A maps to NM_020883.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:116988127 C>T maps to NM_145062.2 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr11:113639608 C>T maps to NM_004724.2 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:113630935 G>C maps to NM_004724.2 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr15:66828268 A>T did not map to a codon.
Sequencing variant TCGA-BA-A6DF-01A-11D-A30E-08 chr23:57935933 G>A did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr23:57934506 G>C did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr23:57935808 G>A did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr23:57936695 G>A did not map to a codon.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr23:57935932 C>T did not map to a codon.
Sequencing variant TCGA-CV-7568-01A-11D-2229-08 chr23:57935881 C>T did not map to a codon.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr23:57935378 C>T did not map to a codon.
Sequencing variant TCGA-KU-A66S-01A-21D-A30E-08 chr23:57935134 G>T did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr23:57618965 C>T did not map to a codon.
Sequencing variant TCGA-CN-A498-01A-11D-A24D-08 chr23:57620825 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr23:57620203 G>T did not map to a codon.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr23:57619096 G>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr23:57618952 G>A did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr23:57619371 C>T did not map to a codon.
Sequencing variant TCGA-CV-A45Q-01A-11D-A24D-08 chr23:57618620 T>C did not map to a codon.
Sequencing variant TCGA-CV-A463-01A-11D-A25Y-08 chr23:57620699 C>T did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr3:126180733 G>A maps to NM_025112.4 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-A6DJ-01A-11D-A30E-08 chr1:53287267 C>T maps to NM_024646.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-A497-01A-11D-A24D-08 chr1:53237307 G>T maps to NM_024646.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:3926062 C>G maps to NM_015113.3 L2384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:3981228 C>T maps to NM_015113.3 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:4009036 G>C maps to NM_015113.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr17:3977537 A>G maps to NM_015113.3 D1197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:3928236 C>T maps to NM_015113.3 L2356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:3980239 G>A maps to NM_015113.3 S1011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A623-01A-11D-A28R-08 chr17:3937553 G>A maps to NM_015113.3 H2113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-A624-01A-22D-A30E-08 chr1:78098604 T>C maps to NM_015534.4 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UF-A719-01A-12D-A34J-08 chr1:78097598 C>A maps to NM_015534.4 E481*. Only missense variants will be evaluated by CHASM.
