5675 NP_705833 C387R not found in SNVbox database
7815 NP_705833 V989D not found in SNVbox database
7956 NP_705833 S625F not found in SNVbox database
106 NP_705833 G653A not found in SNVbox database
551 NP_705833 G605C not found in SNVbox database
584 NP_001070868 D575H not found in SNVbox database
1274 NP_001070868 D77N not found in SNVbox database
1517 NP_705833 A127T not found in SNVbox database
2170 NP_705833 P330L not found in SNVbox database
2514 NP_705833 P711S not found in SNVbox database
2756 NP_001070868 S714L not found in SNVbox database
3550 NP_705833 E511D not found in SNVbox database
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:9000290 C>T maps to NM_144670.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr3:137849688 A>C did not map to a codon.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr3:151475279 T>C maps to NM_207365.3 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:12711236 G>T maps to NM_001013630.1 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:69757188 G>A maps to NM_014911.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:70301661 G>A maps to ENST00000418685 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr17:79094951 A>T maps to NM_001080395.2 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr9:107578435 C>T maps to NM_005502.3 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:67189984 T>C maps to NM_080282.3 K497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:215840567 A>G maps to NM_173076.2 Y1774Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr2:215880303 G>T maps to NM_173076.2 C622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr7:48284202 G>A maps to NM_152701.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:48506567 C>T maps to NM_152701.3 N4277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr7:48411808 C>A maps to NM_152701.3 A3616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr9:139908395 G>C maps to ENST00000355090 V1475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr9:139907276 C>G maps to ENST00000355090 V1686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr1:94548961 G>A maps to NM_000350.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:94528185 A>T maps to NM_000350.2 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:94522329 A>G maps to NM_000350.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr1:94486857 A>G maps to NM_000350.2 Y1652Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:94546178 G>A maps to NM_000350.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:1059068 G>T maps to NM_019112.3 G1816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr17:66981099 G>A maps to NM_080283.3 I1435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:87051486 A>G maps to NM_018849.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr7:20778603 A>G did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:220074989 G>A maps to NM_005689.2 I794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr16:48210874 G>A maps to NM_032583.3 R1166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr10:101569943 C>T maps to NM_000392.3 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr10:101559079 G>A maps to NM_000392.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr17:48734447 C>T maps to NM_003786.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:21962861 G>A maps to NM_005691.2 C1413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:146041305 G>A did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr4:89039326 A>G maps to NM_004827.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr14:51368557 C>T maps to ENST00000337334 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr3:43744052 T>C maps to NM_016006.4 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr3:58242369 A>T maps to NM_020676.5 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:47299546 T>C maps to NM_016428.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr9:133748370 C>T maps to NM_007313.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr9:133759488 C>A maps to NM_007313.2 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr9:133759485 G>A maps to NM_007313.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr7:150553626 G>C maps to ENST00000416793 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:26597327 A>T maps to NM_013375.2 K40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr3:127396050 C>A maps to NM_172027.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr17:35615280 A>T maps to NM_198834.1 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr12:109692083 C>T maps to NM_001093.3 L2037L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:112183961 T>C maps to NM_001136538.1 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr2:211057526 C>G did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr10:124800166 G>A maps to NM_001609.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr17:7127678 T>C maps to ENST00000356839 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr15:89398461 C>T maps to NM_013227.3 F882F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr15:89399907 T>C maps to NM_013227.3 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:7250506 G>A maps to NM_014716.3 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:195006525 T>C maps to NM_012287.5 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr11:44079984 C>T maps to NM_001031854.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr17:61561774 G>C maps to NM_000789.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr17:61566073 C>T maps to NM_000789.3 R791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:19435059 C>T maps to NM_001010887.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:23549775 T>C maps to NM_014977.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:40025022 T>C maps to ENST00000401700 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:40028341 A>T maps to ENST00000401700 I956I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr22:41911895 T>C maps to ENST00000396512 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr6:24701749 A>T maps to NM_018473.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr1:6399499 G>T maps to NM_007274.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:23723160 G>A did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:23723675 G>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:58517531 C>A maps to NM_003500.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:48541576 A>G did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr4:185724471 A>T did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:20559487 G>A maps to NM_182617.3 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr16:20787238 C>T maps to NM_005622.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr15:35083347 G>T maps to NM_005159.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:35085734 G>A maps to NM_005159.4 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr17:79478135 T>C did not map to a codon.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr2:74128512 T>C maps to NM_001615.3 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr3:179298769 G>T maps to NM_004301.3 G307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr20:37383624 T>C maps to NM_024855.3 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr3:53913971 T>C maps to NM_022899.4 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr1:2938840 C>A maps to NM_080431.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr3:38519722 G>A maps to NM_001106.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr3:52023048 G>C maps to ENST00000463937 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:52022537 A>C did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr11:67412338 A>G maps to NM_080658.1 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr16:84228708 G>A maps to NM_139174.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr8:39550200 T>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:24209519 T>C maps to NM_014265.4 H733H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr8:39044453 A>G maps to NM_145004.5 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:38871522 C>T maps to NM_003816.2 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:33658353 A>G maps to NM_030955.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr9:136305498 G>T maps to NM_139025.3 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:100871169 G>A maps to NM_139057.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr16:77325308 C>A maps to NM_199355.2 G1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr5:128797257 G>C maps to NM_133638.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:128983498 T>C maps to NM_133638.3 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr5:178553060 G>T maps to NM_014244.4 A896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr21:28338044 A>T maps to NM_007038.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr15:79058943 A>T maps to ENST00000258883 A1103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr9:136419612 C>T maps to ENST00000393061 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr15:84581895 C>T maps to NM_207517.2 Q585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr15:84592740 T>C maps to NM_207517.2 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:1506085 G>A maps to NM_213604.2 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr7:45747950 T>C maps to NM_021116.2 A940A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr5:7816983 C>T maps to NM_020546.2 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:24793366 C>A maps to NM_139247.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:50338446 C>T maps to NM_001114.3 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr8:132052525 G>A maps to NM_001115.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr16:4029167 G>A maps to NM_001116.3 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr16:4164713 G>A maps to NM_001116.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:111878342 A>G did not map to a codon.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr4:100231923 T>C maps to NM_000668.4 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:100057628 G>T maps to ENST00000505590 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr15:73045221 C>A maps to NM_031284.4 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr20:4229280 A>G maps to NM_000678.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr2:96781258 C>T maps to NM_000682.5 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr12:19665399 G>C did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr4:7811365 T>C maps to NM_001134647.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr10:116100455 G>A maps to NM_001001936.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:88053422 C>T maps to NM_001166693.1 C1058C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr4:88029421 A>T maps to NM_001166693.1 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:100623249 G>A maps to NM_001025108.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr5:132270291 T>G maps to NM_014423.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:75457453 T>C maps to NM_001144000.1 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr15:87217501 A>G did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:48999846 A>G maps to NM_032785.3 *504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr2:27291527 A>G maps to NM_021831.5 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr2:228399579 C>G maps to NM_001135187.1 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr7:100160552 C>T maps to NM_006076.4 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr1:100327976 C>G maps to ENST00000311030 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr9:139581686 G>A maps to NM_006412.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:41467378 C>T maps to NM_178819.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr1:984365 C>T maps to NM_198576.2 L1409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:957702 C>A maps to NM_198576.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr23:115303623 T>G did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr5:177642284 C>T maps to NM_153373.2 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr5:177649896 T>C maps to NM_153373.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr20:32880314 T>C did not map to a codon.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr20:32873356 G>T maps to NM_000687.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:110561172 G>A did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr6:135644422 C>A maps to NM_017651.4 E1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr11:62301414 C>T maps to NM_001620.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr14:105410342 C>A maps to NM_138420.2 V3815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr14:105412622 A>G maps to NM_138420.2 A3055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:105413290 C>A maps to NM_138420.2 E2833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:105409721 G>A maps to NM_138420.2 S4022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr14:105406109 A>C maps to NM_138420.2 G5226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr5:353962 C>T maps to NM_020731.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:129270134 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr6:106960431 C>G maps to NM_001624.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr17:55197615 G>A maps to ENST00000427138 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:19845194 C>G maps to NM_007202.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr15:86269659 C>G maps to NM_006738.4 L2259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:91631867 A>G maps to NM_005751.4 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr7:91631220 A>T maps to NM_005751.4 K664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr1:46032693 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr7:134133230 T>C maps to NM_001628.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:134260619 C>T maps to ENST00000418096 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:19611545 A>G maps to NM_012067.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:243800912 C>T maps to NM_005465.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr9:116151741 G>A maps to ENST00000277315 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr9:116153878 C>T maps to ENST00000277315 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr23:55046922 C>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr23:55051150 C>A did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:105433492 C>T maps to NM_001034173.3 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr11:67787233 A>T maps to NM_001161473.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr12:34179834 A>G maps to NM_032834.3 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr23:110987896 G>T did not map to a codon.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr9:101980773 G>A maps to NM_033087.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr13:37539813 C>T maps to NM_013338.4 W224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr11:43905564 T>C maps to NM_139178.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:73680676 T>C maps to NM_015120.4 N2340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr2:73827934 T>C maps to NM_015120.4 R3932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr2:73836706 C>T maps to NM_015120.4 Q4158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr2:73675808 A>T maps to NM_015120.4 R718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:4542863 G>A maps to NM_001140.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr15:85407684 G>A maps to NM_020778.4 L1706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:21889673 C>A maps to NM_000478.4 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:202626256 G>A maps to NM_020919.3 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr3:46725270 C>T did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:203848265 A>G maps to NM_024744.14 Q699Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:110604110 G>T maps to NM_006492.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr17:7386124 C>T maps to NM_001102614.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr5:33998824 A>G maps to NM_001167595.1 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr11:46419221 G>A maps to ENST00000458649 G1225G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A4-8312-01A-11D-2396-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr16:56396895 A>G maps to NM_001144.4 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr19:2251511 T>A maps to NM_000479.3 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:112022637 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:112022643 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:134080583 C>A maps to ENST00000514516 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr1:115221049 A>G maps to NM_000036.2 Y365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr1:115218254 G>C maps to NM_000036.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr2:112615902 T>C maps to NM_022662.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:112608403 A>G maps to NM_022662.2 D533D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr4:25398291 G>C maps to ENST00000510092 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr12:110813920 T>C maps to NM_016238.2 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr9:129870362 T>G maps to NM_012098.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr8:41547821 G>A maps to ENST00000415018 L1343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:61830132 G>A maps to NM_020987.2 F3502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:61830688 G>C maps to NM_020987.2 S3317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr15:65223119 T>G did not map to a codon.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:139864823 T>C maps to ENST00000253810 H663H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr5:139876315 A>G maps to ENST00000253810 E819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:91957149 T>C maps to NM_019004.1 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr7:92019369 T>C maps to NM_019004.1 Y664Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr19:17396341 C>T maps to NM_152363.4 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:241465101 C>T maps to ENST00000401804 Q445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr16:89345491 G>A maps to NM_013275.4 L2486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:89345818 G>A maps to NM_013275.4 D2377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr18:9257290 T>C maps to NM_015208.3 T1342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:15765924 G>A maps to NM_015199.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr18:21214113 C>T did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr1:145561664 C>T maps to NM_144698.3 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr2:198001336 C>A maps to NM_001195144.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:197889958 T>C maps to NM_001195144.1 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr11:94231478 C>T maps to NM_017704.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr4:125592786 A>G maps to NM_020337.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:110373073 C>T maps to NM_023016.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr6:35051231 C>A maps to NM_015245.2 I982I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr12:100048988 C>G did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:99640157 G>A maps to NM_152788.3 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr7:36445952 T>C maps to NM_018685.2 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr15:69072439 C>A maps to NM_006305.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr12:48866683 C>T maps to NM_012404.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:69409662 T>G maps to NM_032208.2 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr4:80992808 C>A did not map to a codon.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr4:169108557 C>A maps to NM_007193.3 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr4:79531259 A>T maps to NM_005139.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:79516548 A>G maps to NM_005139.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr2:70037723 A>G did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr5:150518239 G>T maps to NM_001155.4 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:201478583 C>T maps to NM_001159.3 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr16:71789971 C>T maps to ENST00000423132 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr14:24032847 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr14:24032630 A>T maps to NM_003917.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr14:24030556 T>C maps to NM_003917.2 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:50305817 C>T maps to NM_014203.2 S714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr11:984671 C>T maps to ENST00000332231 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr3:183898701 T>G maps to ENST00000411763 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:75898089 T>C maps to NM_207012.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr15:51294807 T>G maps to NM_007347.3 T1121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:99093183 A>C did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr15:29368273 C>A maps to NM_005503.3 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:40818109 T>A maps to NM_004307.1 *760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:1468066 C>T maps to NM_005883.2 P1589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr19:1460856 G>T did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr19:1469818 G>C maps to NM_005883.2 T2173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:10471913 G>A maps to ENST00000423585 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr14:20925020 T>C did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr11:43350299 A>T maps to NM_001142930.1 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr19:36362559 T>A maps to NM_001024807.1 L195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr2:21251316 G>A maps to NM_000384.2 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:21260847 G>A maps to NM_000384.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr22:39482534 C>G maps to NM_021822.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr22:36661664 C>T maps to NM_145343.2 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr22:36055618 C>G maps to NM_030641.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr6:31625013 C>G maps to NM_019101.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr21:27348293 A>C maps to NM_000484.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr21:27328003 G>C maps to NM_000484.3 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr9:32988091 T>A maps to NM_001195248.1 K71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr1:154294467 C>T maps to NM_080429.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr15:35189881 T>G maps to NM_014691.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:66765166 A>T did not map to a codon.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr23:47426119 T>G did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr4:36152574 G>T maps to NM_015230.2 I948I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr5:141033933 T>C maps to NM_022481.5 P1406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr12:49334776 T>C maps to NM_001659.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr22:43213793 A>G maps to NM_014570.4 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr20:47628618 C>A maps to NM_006420.2 R1306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr20:47587773 C>G maps to NM_006420.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:47641989 C>T maps to NM_006420.2 Y1632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:46702649 G>A maps to NM_004308.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:32916474 C>T maps to NM_014783.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr15:32929466 T>C maps to NM_014783.3 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr10:24873802 T>C maps to NM_020824.3 G1805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr10:49667743 C>T maps to ENST00000417912 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:128933814 A>G maps to NM_001142685.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:36279063 C>T maps to ENST00000007510 P1199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr23:130215817 G>A did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr1:17939551 G>T did not map to a codon.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr1:17907126 G>T maps to NM_018125.3 G13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr11:120300473 C>T maps to NM_015313.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr11:73066675 C>G maps to NM_014786.3 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:73073119 G>T maps to NM_014786.3 P1510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr3:56787576 G>C maps to NM_001128615.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr23:135754262 G>C did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr23:135825891 A>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr13:111885552 G>A maps to NM_001113511.1 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr1:27107194 C>A maps to NM_006015.4 S2269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr1:27100917 T>C maps to NM_006015.4 P1400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:157527599 G>A maps to ENST00000367148 K1815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:46285792 G>A did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr19:971935 C>G maps to NM_005224.2 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr14:58827677 G>T maps to NM_002892.3 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr1:235386543 T>C maps to NM_016374.5 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr2:97216936 G>A maps to NM_212481.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr10:63852306 C>A maps to NM_032199.2 R1029R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr10:63699985 A>G maps to NM_032199.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr10:28270469 T>C maps to NM_018076.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr16:31475858 C>T maps to ENST00000408912 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr3:137982981 C>T maps to ENST00000469044 H409H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr23:101857943 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr1:150804345 A>G maps to NM_001668.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr7:98988629 A>G maps to NM_005720.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr7:98990334 C>T maps to NM_005720.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr23:2826884 T>C did not map to a codon.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr23:2861168 C>T did not map to a codon.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr23:3028195 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr12:14993940 C>T maps to NM_021071.2 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:150878301 C>G maps to ENST00000422024 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr4:177136795 T>C maps to NM_080874.3 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr9:132400145 T>A maps to NM_017873.2 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr6:101296248 T>A maps to NM_006828.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr12:103352210 G>C maps to NM_004316.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:155451418 T>C maps to ENST00000368346 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr1:155313420 G>A maps to ENST00000368346 R2703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr8:37978551 G>A maps to NM_004674.3 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:1540610 G>C did not map to a codon.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr14:104565245 C>T maps to NM_001080464.1 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr8:62460749 C>T maps to NM_004318.3 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:197069638 G>A maps to NM_018136.4 I2914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr1:197111689 G>T maps to NM_018136.4 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr9:133342186 G>C did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:96789882 G>C maps to NM_001002036.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:119202961 G>T maps to ENST00000313400 V1236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr20:31024235 G>T maps to ENST00000375687 E1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:25972918 C>T maps to NM_018263.4 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr18:31263417 A>G maps to NM_030632.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr18:31318453 G>C maps to NM_030632.1 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr1:1458173 C>G maps to NM_018188.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr17:29220518 A>T maps to NM_024857.3 K1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr17:29162088 T>A maps to NM_024857.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr12:53931333 A>T maps to NM_001130059.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr12:14613822 C>T maps to NM_018179.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr2:234173558 T>C maps to ENST00000392018 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:150720229 G>A maps to NM_173681.5 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr11:108155201 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:7046364 C>G maps to NM_001940.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:85981695 G>T maps to NM_032827.6 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr15:25959388 C>G did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr15:25972304 A>T did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr15:25981204 G>A maps to NM_024490.3 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:47538505 C>A maps to NM_020453.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr13:113474212 G>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr23:138857090 C>G did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr23:138880881 A>C did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:160105303 C>A maps to NM_000702.3 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr3:141626057 T>C maps to NM_001679.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr3:10387741 G>A maps to NM_001001331.2 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr23:152826335 C>T did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr23:152823736 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:130673863 C>T maps to NM_001001486.1 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr12:57036239 A>G did not map to a codon.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:153657421 C>A did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr16:67487538 G>A maps to NM_004691.4 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr5:172410943 C>T maps to NM_003945.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr23:77268390 T>A did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr13:52548107 A>T maps to NM_000053.2 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr13:52548875 G>A maps to NM_000053.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:154314971 C>T maps to NM_020452.3 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr20:50221536 C>G maps to NM_006045.1 A942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr3:142274791 A>T maps to NM_001184.3 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:142238532 G>A maps to NM_001184.3 L1454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr3:48488464 C>T maps to NM_130384.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr10:117075178 G>A maps to NM_207303.2 E990E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr23:76777833 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr12:112036796 C>T maps to NM_002973.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:112036796 C>T maps to NM_002973.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr12:111926344 A>G maps to NM_002973.3 V885V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BQ-5875-01A-11D-1589-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr17:42275085 C>A maps to NM_020218.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:74756586 G>C maps to ENST00000258081 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr7:70229863 C>G maps to NM_015570.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr7:70255843 A>G maps to NM_015570.2 T1214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr7:70231265 G>A maps to NM_015570.2 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr16:354432 G>A maps to NM_003502.3 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr13:31821209 A>G maps to NM_194318.3 A107A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G7-6792-01A-21D-1961-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-IZ-8195-01A-31D-2396-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr16:67183947 C>T maps to NM_033309.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:67184130 G>C maps to NM_033309.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr3:118945880 C>T maps to NM_212543.1 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr18:29218693 G>A maps to NM_004775.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr9:104125252 T>C maps to NM_001701.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:90660213 G>A maps to NM_001170794.1 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:104027516 A>T maps to NM_001015049.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr21:11097540 C>A did not map to a codon.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr17:79425868 G>T maps to ENST00000436173 E1827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:32207415 C>A maps to NM_001703.2 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr1:32203281 G>A maps to NM_001703.2 T949T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr7:97933660 G>A maps to NM_018842.4 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:38483171 G>T maps to NM_025045.4 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr16:1398015 C>G maps to NM_003933.4 Y1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:88105727 G>A maps to NM_001173543.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr1:171501661 A>C maps to ENST00000392078 R479R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A4-A5DU-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:49464329 T>C maps to NM_004324.3 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr14:35295322 A>G maps to NM_013448.2 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:35242929 A>G maps to NM_013448.2 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr14:35269497 T>A maps to NM_013448.2 K354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr7:72907198 T>C maps to NM_032408.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr4:123664663 T>C maps to NM_152618.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:56531662 G>A maps to NM_031885.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:56518731 G>A maps to NM_031885.3 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr19:45322836 A>C did not map to a codon.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr1:94054730 C>T maps to NM_003567.2 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr1:94054977 T>C did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr20:30253880 A>G maps to NM_138578.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr14:23776984 C>A maps to NM_004050.4 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:30899186 C>T maps to NM_004765.2 *218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:147086308 A>C maps to NM_004326.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr11:118771982 C>T maps to NM_182557.2 Q823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:118773515 C>A maps to NM_182557.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr23:39932879 G>T did not map to a codon.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr23:39932147 A>G did not map to a codon.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr23:39923131 G>T did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr22:23656858 T>A maps to NM_004327.3 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr5:70800507 C>T maps to NM_018429.2 Q768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:101012902 G>A maps to NM_020836.3 H37H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr23:18195782 A>T did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:61730353 C>T maps to NM_001139443.1 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr16:14755822 G>T maps to NM_016561.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr16:14738463 C>T maps to NM_016561.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr23:102004857 G>C did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:22488016 G>A maps to NM_018688.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr2:32664735 T>C maps to NM_016252.3 A1264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:32626578 C>T maps to NM_016252.3 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr23:50658964 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr23:50658767 A>T did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr4:79786782 T>C maps to NM_198892.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr10:88681452 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr10:43312104 A>G maps to NM_014753.3 S796S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr9:16419220 A>G maps to NM_017637.5 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:26240663 C>G maps to NM_004331.2 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr6:3137662 C>T maps to NM_004332.2 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr12:112098448 G>C maps to NM_006768.3 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr12:112096634 G>A maps to NM_006768.3 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:41203098 G>A maps to ENST00000471181 P1793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr13:32906982 G>A maps to NM_000059.3 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr23:154299903 A>C did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr6:32944713 G>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr6:32945958 C>G maps to ENST00000395289 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr6:32947798 C>G maps to ENST00000395289 S714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr6:32945265 T>C maps to ENST00000395289 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:15350518 C>T maps to NM_058243.2 E1132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:15353720 G>T maps to NM_058243.2 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr5:137506597 C>T maps to NM_139199.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:125509639 C>A maps to NM_080626.5 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr6:166778931 T>C maps to ENST00000360961 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:55805596 G>T maps to NM_032430.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr11:1466622 C>T maps to NM_003957.2 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr11:1466526 G>C maps to NM_003957.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr21:40665926 G>T maps to NM_018963.3 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr23:79932815 G>T did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:80001212 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr11:62458108 C>T maps to NM_001130702.1 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr3:49689058 C>A maps to NM_003458.3 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr12:107713244 G>A maps to NM_001018072.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:1986876 C>G maps to NM_017797.3 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr19:1986957 G>A maps to NM_017797.3 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr1:203274778 C>T maps to NM_006763.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr1:203276559 C>T maps to NM_006763.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr5:180338540 C>T maps to NM_001040462.2 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr2:111399712 G>A maps to NM_004336.3 Q816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:45472881 G>A maps to NM_007021.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr10:115917413 G>A maps to NM_018017.2 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr10:121598083 A>G maps to NM_024834.2 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr10:98741938 T>G maps to NM_015652.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr10:5781660 C>T maps to NM_017782.4 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr10:50532032 G>A maps to NM_001135196.1 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr10:103789496 C>T maps to NM_024541.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr10:105928499 A>T did not map to a codon.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr11:30352521 C>T maps to NM_152316.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:77580811 G>A maps to NM_024684.2 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr12:110207029 G>A maps to NM_032829.2 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr12:21680691 G>C maps to NM_030572.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr12:112668607 G>A maps to NM_001109662.2 P1901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:48888592 T>C maps to NM_152319.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr12:64615825 G>C maps to ENST00000311915 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr13:42031875 G>A maps to NM_014059.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr13:46946277 G>A maps to NM_025113.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr13:39596541 A>T maps to NM_025138.3 Y217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr14:57960295 T>A maps to NM_018168.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr14:45711248 A>C maps to NM_018353.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr14:93670050 C>T maps to NM_032490.4 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr14:91681815 C>T maps to NM_001102368.1 H544H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr14:73959008 G>A maps to NM_024644.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:77844645 G>A maps to NM_001010860.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr14:77846825 T>C did not map to a codon.
Alternatively spliced codon TCGA-B1-5398-01A-02D-1589-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr14:60921716 A>T did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr14:77493793 T>C maps to NM_024496.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr14:77493793 T>C maps to NM_024496.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr14:77493793 T>C maps to NM_024496.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr14:65053587 G>A maps to NM_172365.1 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr14:103570686 G>A maps to NM_001077594.1 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr14:23467860 A>C maps to NM_021944.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr15:24923230 T>A maps to NM_018958.2 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr15:24921073 A>G maps to NM_018958.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr15:24923446 T>A maps to NM_018958.2 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr15:24923341 C>T maps to NM_018958.2 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr15:93016233 T>C maps to NM_153040.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr15:75499126 C>A maps to NM_015492.4 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr15:75499666 C>T maps to NM_015492.4 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr15:90138744 T>C maps to NM_152259.3 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:90118912 C>A maps to NM_152259.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr15:90167320 G>A maps to NM_152259.3 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr15:65871973 G>T maps to ENST00000420799 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:38988924 G>C maps to NM_207444.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr15:73843451 A>G maps to NM_001042367.1 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr15:73735651 G>T maps to NM_001042367.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr16:81094971 G>A maps to NM_152337.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:2511751 C>T maps to NM_025108.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:67168084 T>C maps to NM_025187.3 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr16:67702136 C>G maps to NM_001012984.2 Y196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr17:42228327 G>C did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:80405454 C>T did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr17:79518168 A>G maps to NM_025161.5 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr17:71231746 T>G maps to NM_017941.4 Y42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr17:74729097 C>A maps to ENST00000317409 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr18:71816321 C>G maps to NM_014177.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr19:757668 C>T maps to NM_173481.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:3546267 G>A maps to NM_021731.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr19:36253152 G>A did not map to a codon.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:13996868 C>G did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:159781880 G>A maps to NM_031908.4 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:119210070 G>C maps to NM_015645.3 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr1:200860814 A>G maps to NM_018265.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:210006561 G>T maps to NM_014388.6 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:162344113 T>C maps to NM_182581.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:169806132 C>T maps to NM_018186.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr1:231474335 C>T maps to NM_032018.4 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr1:24105127 A>G maps to NM_020362.4 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:182922004 C>G maps to ENST00000287709 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr1:182921875 C>T maps to ENST00000287709 L200L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G7-7501-01A-11D-2201-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr1:156309582 G>C did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:11771906 G>A did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:11775242 C>T maps to NM_198545.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr1:109649720 G>A maps to NM_001122961.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:184476744 G>T maps to NM_030806.3 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:23696042 A>C maps to ENST00000507744 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr1:186355193 T>C maps to NM_017847.5 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:150258999 T>A maps to NM_144697.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr1:16332450 G>C maps to NM_178840.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:223567035 C>T maps to NM_152610.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:156706430 T>C maps to NM_015997.3 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr1:156897771 A>G maps to NM_144702.2 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr1:34677971 A>G maps to NM_001134734.1 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr20:31892697 G>A did not map to a codon.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr20:18414379 C>T maps to NM_001099407.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr20:35772167 G>A maps to ENST00000343811 H455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr20:61427955 G>A maps to NM_018270.4 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr20:1161647 G>A maps to NM_018354.1 Y205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr20:1161560 C>T maps to NM_018354.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:17950810 C>A maps to NM_052865.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr21:45949792 G>A maps to ENST00000443468 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr21:33651271 C>T maps to NM_018944.2 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr22:24106286 G>A maps to NM_182520.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr2:24261377 G>C maps to NM_025203.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr2:219222407 C>T maps to NM_198559.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:219222363 C>T maps to NM_198559.1 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr2:54587527 G>T maps to NM_001100396.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:62317064 T>A maps to NM_020685.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr3:48956090 T>A maps to NM_001123040.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr4:170658831 G>T maps to NM_017867.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:123783918 C>G maps to NM_001735.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr5:102611691 C>T maps to NM_033211.2 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr5:43490824 C>A maps to NM_198566.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr5:156770120 C>A maps to NM_001001343.3 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr5:37121779 A>G maps to NM_023073.3 L2988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr5:64956552 T>G maps to NM_001093755.1 Y242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr6:43193767 C>A maps to NM_199184.1 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:53989446 T>C maps to ENST00000502396 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr6:3751741 G>T maps to NM_183373.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr6:31079877 G>T maps to NM_014070.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr6:74135069 A>G maps to NM_138441.2 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr6:42994981 C>T maps to NM_033112.2 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr6:97629853 A>T maps to NM_198468.2 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr6:121433800 G>T maps to ENST00000275159 C1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr6:121576520 T>A maps to ENST00000275159 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr6:2623683 C>A maps to NM_152554.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr6:36294404 G>C maps to NM_001010903.4 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr6:31627424 A>G maps to NM_021184.3 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr7:66410207 T>C maps to NM_017994.4 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr7:99753404 G>A maps to NM_018275.3 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr7:100033304 G>C maps to NM_145030.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr7:100087002 C>T maps to ENST00000423930 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:48081006 C>A maps to ENST00000430738 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr7:120629776 C>G maps to NM_024913.4 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr7:47698324 G>A maps to NM_001123065.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr8:67405942 T>A maps to NM_152765.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr8:12879057 T>C maps to NM_020844.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr9:99413723 T>C maps to NM_153698.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr9:34397496 C>T maps to NM_032596.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr9:111853339 G>A maps to NM_032012.3 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:214550 G>T maps to NM_152569.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr9:215108 G>T maps to NM_152569.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:136333114 G>A maps to NM_017586.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr9:132593304 G>T maps to NM_016520.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr9:90501483 C>T maps to NM_178828.4 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr9:117400850 T>C maps to ENST00000374049 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr9:15745612 C>T maps to NM_173550.2 D885D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr8:61192347 C>T maps to NM_004056.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr22:24447424 T>A maps to NM_012295.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr18:20814664 G>A maps to NM_001100619.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr20:60967981 C>G maps to NM_031215.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr20:60982023 C>T maps to NM_031215.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:13346024 G>A maps to NM_023035.2 Q1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr9:140943669 T>C maps to ENST00000277549 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:2716230 C>T maps to NM_199460.2 D1117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr12:2763056 C>T maps to NM_199460.2 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:181701627 G>A maps to ENST00000357570 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr16:1251874 C>T maps to NM_021098.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:201034980 G>T maps to NM_000069.2 G946G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:50513566 G>T maps to ENST00000435965 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr17:37341118 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:27440796 C>A maps to NM_004341.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr1:159169658 G>A maps to NM_021189.3 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr1:159170697 G>T maps to NM_021189.3 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr3:62499342 A>G maps to NM_183394.2 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr7:122081598 A>G maps to NM_001167940.1 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr7:122269334 A>G maps to NM_001167940.1 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr14:90870814 C>T maps to NM_006888.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:114434487 G>A maps to ENST00000515496 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:48266892 T>C maps to NM_004345.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:67699343 G>A maps to NM_018448.3 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:17507927 T>C maps to NM_006366.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr6:44148400 T>G did not map to a codon.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr19:39226898 G>A maps to NM_144691.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:39226165 G>T maps to NM_144691.3 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:39226802 G>A maps to NM_144691.3 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr19:36631957 C>G maps to NM_001749.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr12:30888128 C>T maps to NM_001002259.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr19:5914494 G>T maps to ENST00000394521 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr22:37898634 C>G maps to NM_014550.3 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:2959067 G>A maps to NM_032415.4 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr7:2956955 G>A maps to NM_032415.4 R891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr19:11019855 G>A maps to NM_199141.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:38319004 G>A maps to NM_007359.4 W212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:40913800 A>T maps to NM_170589.3 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr23:41448781 G>C did not map to a codon.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr11:104901191 A>C maps to NM_033292.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr19:15164632 C>T maps to NM_012114.2 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr4:185552221 G>T maps to NM_032991.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:10713662 G>A maps to NM_001079843.1 T817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:10714627 G>A maps to NM_001079843.1 Y562Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr11:65788965 C>T did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr15:43940127 G>A maps to NM_172095.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:38850107 A>T did not map to a codon.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr7:116166676 C>T maps to NM_001753.4 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr7:107398635 C>T maps to NM_024814.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr4:169931207 G>T maps to NM_032783.4 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr9:69206733 C>T maps to NM_001085457.1 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:46152377 G>A maps to ENST00000442683 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr7:26251699 A>T did not map to a codon.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr22:39066950 G>A maps to NM_015373.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr10:70547738 T>G maps to NM_018237.2 L979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr16:57562849 C>A maps to NM_033212.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr2:219868975 T>C maps to NM_194302.2 P1751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr4:186382295 A>G maps to NM_152775.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr22:21989094 C>G maps to NM_152612.2 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr2:179701994 A>T maps to NM_173648.3 A1317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr4:24838060 G>T maps to NM_001130726.2 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr23:133379027 T>C did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:46086773 G>T maps to NM_001114938.2 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:3679838 A>G maps to NM_152492.2 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:96273431 G>A maps to NM_182496.2 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr17:28512532 G>T maps to NM_032141.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr17:80115740 C>T maps to ENST00000445854 E708E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr3:122102041 A>G maps to NM_001017928.2 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:120428097 C>T maps to NM_207311.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr16:3081003 G>A maps to NM_001103175.1 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:56649977 A>C maps to NM_001141947.1 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr10:32854548 G>T did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:32676506 T>C maps to NM_001008391.2 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:118869165 C>T maps to NM_198489.1 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr11:65658487 C>T maps to NM_006848.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr11:60609626 G>T maps to NM_024098.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:55566740 T>G maps to ENST00000436346 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr14:91776234 C>G maps to NM_001080414.2 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr9:36170074 C>T maps to NM_005893.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr17:34340314 G>A maps to NM_005064.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:45112358 C>T maps to NM_001029835.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr4:78082687 C>T maps to NM_004354.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr5:132084159 C>A maps to NM_001039780.2 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:1334455 G>A maps to NM_030937.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr3:46415325 C>T maps to NM_001100168.1 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr1:156294857 A>G maps to NM_005998.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:10263418 G>A maps to NM_012073.3 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:7654023 A>C maps to NM_004244.4 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:7528455 T>A maps to ENST00000416109 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr12:7527335 G>T maps to ENST00000416109 R1047R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr6:109690200 C>T maps to NM_006016.4 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr5:66478707 T>G maps to NM_005582.2 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:7810713 G>A maps to NM_021155.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:35828751 C>T maps to NM_001771.3 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr9:5457409 G>A maps to NM_014143.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr7:80302112 A>T maps to NM_001127444.1 K385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:26646660 G>T did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:43828620 G>A did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr17:45247408 C>T did not map to a codon.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:10506723 G>C maps to NM_007065.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:4706078 A>G maps to NM_017913.2 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:22413229 C>G maps to NM_001039802.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:22413328 C>G maps to NM_001039802.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr14:103430981 C>T maps to NM_006035.3 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:44390389 T>C maps to NM_001253.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr2:174231882 G>A maps to NM_031942.4 W397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr16:68853182 A>C maps to NM_004360.3 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:66949282 T>A did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr10:73406334 C>T maps to ENST00000398860 Y475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr14:23524348 T>A maps to NM_022478.3 K139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr5:31323225 T>G maps to NM_004932.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr16:61851549 C>T maps to NM_001796.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr16:89760631 C>T maps to NM_052988.4 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:1638913 G>T maps to NM_024011.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr7:40134551 A>G maps to NM_003718.4 R1504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr7:40134338 T>C maps to NM_003718.4 P1433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr17:30815100 C>T maps to NM_003885.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr17:46058012 C>T maps to NM_176096.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr4:76521461 G>T maps to ENST00000307465 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:76532404 T>C maps to ENST00000307465 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr4:76529104 T>A maps to ENST00000307465 K231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:18646491 G>C did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr9:21971183 T>G maps to NM_001195132.1 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr9:22006243 G>A maps to NM_004936.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr23:139866439 A>G did not map to a codon.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:139866439 A>G did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr20:5157343 C>A maps to NM_003818.2 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr16:80654829 G>T maps to NM_152342.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:33793107 G>T maps to NM_004364.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:33793119 G>T maps to NM_004364.3 Y67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr22:18028579 T>A maps to ENST00000400579 P1180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr22:18021910 C>T maps to ENST00000400579 C672C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:15793928 C>T maps to ENST00000375924 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:22310246 C>T maps to NM_007352.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr1:151678721 T>C maps to NM_007185.4 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr1:151678721 T>C maps to NM_007185.4 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr22:46765597 A>G maps to NM_014246.1 A2621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr22:46930991 G>A maps to NM_014246.1 Y692Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr22:46931729 G>A maps to NM_014246.1 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr1:109801210 G>C maps to NM_001408.2 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:109792761 T>C maps to NM_001408.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr1:109792761 T>C maps to NM_001408.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr3:48692762 T>A maps to NM_001407.2 T1602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr3:48699893 G>A maps to NM_001407.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr4:104117118 A>C maps to NM_001813.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:214815374 G>T maps to NM_016343.3 E1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:214813547 A>T maps to NM_016343.3 K623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr22:42342455 C>G maps to NM_024053.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr12:88471485 G>T maps to NM_025114.3 T1858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:88514779 A>C maps to NM_025114.3 Y451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:180044160 C>T maps to NM_014810.4 L1858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:196654323 A>G maps to NM_000186.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:151509761 C>T maps to NM_020770.2 Y1184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:57808994 G>T maps to NM_032866.3 A807A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr19:4433328 G>A maps to NM_005483.2 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr1:146747122 C>A maps to NM_004284.3 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:6707539 G>A maps to ENST00000309577 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr1:6204187 G>A maps to NM_015557.2 Y610Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr20:40143494 C>A maps to NM_032221.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr20:40033766 G>A maps to NM_032221.3 L2538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr8:61654761 T>C maps to NM_017780.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr20:5903026 A>G maps to NM_001819.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr20:5903929 T>C maps to NM_001819.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:111862961 C>T maps to NM_201653.2 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr22:51018474 A>C maps to NM_005198.4 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr16:89713673 C>A maps to NM_001083314.1 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:89717998 G>C maps to NM_001083314.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr15:41535938 T>C did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr2:220404815 A>T maps to NM_024536.5 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr3:184098192 A>C maps to NM_003741.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr2:175614799 G>A maps to NM_001039523.2 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:154544110 C>A maps to NM_000748.2 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr23:46434587 A>C did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr5:129241298 C>T maps to NM_175856.4 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:24775202 G>C maps to NM_014430.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr15:65490141 G>A maps to NM_003613.3 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr15:65494240 C>A maps to NM_003613.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr2:175215407 T>C maps to NM_004882.3 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr12:120150414 G>C maps to ENST00000392521 L1555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr6:139694868 A>G maps to NM_006079.3 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr11:46799003 G>C maps to ENST00000415402 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:86890014 C>T maps to NM_006536.5 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr11:67135056 G>T maps to NM_013246.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr7:143049048 G>A maps to NM_000083.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr3:184071154 C>A maps to NM_004366.4 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr23:10162969 C>G did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:16378295 A>C maps to NM_000085.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr16:3063764 C>A maps to NM_020982.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr14:38724315 C>T maps to NM_175060.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:71036917 G>A maps to NM_173535.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr21:36042940 C>T maps to ENST00000360731 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:73752799 A>T maps to NM_003388.4 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr2:201719789 T>G maps to NM_001162407.1 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr5:178050362 C>A maps to NM_020666.2 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr4:56301653 A>T maps to NM_004898.2 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr1:9809528 G>A maps to NM_001009566.1 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr12:7302197 T>C maps to NM_014718.3 D718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr9:36209296 C>T maps to NM_007096.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr17:57746159 C>T maps to NM_004859.3 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr16:3554720 T>C maps to NM_015041.1 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr16:66612902 G>A maps to NM_052999.3 *287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr16:66670439 T>A maps to NM_178818.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr3:32433538 G>C maps to NM_138410.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr5:79032747 T>C maps to NM_153610.3 T2720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr23:150912595 C>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:150906985 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr23:150911738 G>A did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:97428004 C>A maps to NM_020184.3 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:70704757 C>T maps to NM_014515.5 Y44Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr19:54648052 G>A maps to NM_014516.3 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr9:17394560 T>C maps to NM_017738.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:17332673 G>A maps to NM_017738.2 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:41316145 C>T maps to NM_001843.2 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:205028741 C>A maps to NM_005076.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:40849968 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:39140599 G>A maps to NM_033655.3 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr17:40717243 G>T did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr9:140158761 G>A maps to NM_015456.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr14:31355024 C>T maps to NM_004086.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:71196857 G>A maps to NM_018714.2 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr1:103428307 G>A maps to NM_080629.2 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:75861880 T>C maps to ENST00000322507 A1267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:121170483 A>G maps to NM_021110.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr8:121237424 A>T maps to NM_021110.1 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr10:105793763 A>G maps to NM_000494.3 A1365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr21:46930114 G>A maps to ENST00000359759 Q1626Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr21:46924433 A>C maps to ENST00000359759 P1359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr21:46925136 T>C maps to ENST00000359759 P1401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr6:70646795 A>G maps to NM_001858.4 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr20:61945125 G>T maps to ENST00000326996 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr8:139707080 C>A maps to NM_152888.1 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr8:139767733 T>C maps to NM_152888.1 K656K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr9:117052532 C>G maps to NM_032888.2 G1430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr2:189867766 C>T maps to NM_000090.3 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr13:110827562 A>C did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:227872133 C>T maps to ENST00000396625 Q1660Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:107938133 G>A did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr23:107447617 C>G did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr23:107433649 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr23:107434728 T>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr23:107430495 T>A did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr9:137734001 G>C did not map to a codon.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr2:189912940 T>C maps to NM_000393.3 G1065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr21:47421873 G>A did not map to a codon.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr21:47542787 G>A did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:238280360 C>T maps to NM_057165.4 A1227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:238234212 A>T maps to NM_004369.3 V3161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:238275564 C>T maps to NM_004369.3 S1755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:36564105 A>G maps to NM_005202.2 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:71003974 G>A maps to NM_001851.4 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr20:61468579 C>T maps to NM_001853.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr8:120114629 A>G maps to NM_006438.3 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr10:22605387 G>A maps to NM_012071.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:160305058 A>G maps to NM_001098398.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr11:14510131 T>C did not map to a codon.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr7:99686961 T>C maps to NM_006833.4 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr17:46103805 C>G maps to NM_016429.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr6:99823845 T>A maps to NM_017421.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr9:131095204 G>A maps to NM_016035.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr17:27948313 G>A maps to ENST00000345068 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr17:14005507 T>A maps to NM_001303.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:13980320 A>G maps to NM_001303.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr14:93813724 G>T maps to NM_182971.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:129962494 T>C maps to NM_016352.3 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:17056400 G>T maps to ENST00000443236 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr10:93999657 A>C maps to NM_014912.4 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:173370038 T>G maps to NM_030627.2 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr20:34215309 G>T maps to NM_003915.5 Y381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr14:24545746 G>A maps to NM_006032.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr16:89650106 T>A maps to NM_014427.4 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:207833967 G>C maps to NM_173077.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr2:207827298 C>T maps to NM_173077.2 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:98309566 A>T maps to NM_000097.5 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:50200611 C>A maps to NM_152359.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr20:2776795 C>G maps to NM_019609.4 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr4:8607800 G>C maps to NM_001014447.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:207669653 G>C maps to NM_000651.4 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr16:1718162 C>T maps to NM_020825.3 I1101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr3:3209359 T>C maps to NM_016302.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr16:3860636 G>A maps to NM_004380.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr16:3817822 C>A maps to NM_004380.2 E1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:3779017 C>T maps to NM_004380.2 G2010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr8:67089640 C>T maps to NM_000756.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr2:36583677 C>G maps to NM_016441.2 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr6:43275359 T>C maps to ENST00000449267 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr6:43275461 T>C maps to ENST00000449267 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr16:84940196 G>A maps to NM_031476.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr20:20033151 G>A maps to NM_016652.4 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr21:44589373 C>G maps to NM_000394.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr3:97595924 A>T maps to ENST00000182096 K15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr1:115280130 A>G maps to NM_001007553.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr20:47691343 A>G maps to NM_001316.2 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr23:1407701 G>T did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr10:43651226 A>G maps to NM_018590.3 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr8:2832126 T>C maps to NM_033225.5 P2862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:33985174 T>A maps to ENST00000373381 T3573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:113249530 G>T maps to NM_198123.1 Y3505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr8:113516206 C>G did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:80202674 C>T maps to NM_001893.3 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr20:470422 C>A did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr15:75982865 G>C maps to NM_001897.4 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr20:23618487 G>A maps to NM_000099.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr20:23548868 G>T maps to NM_080610.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr18:19995947 G>C maps to NM_172241.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:70895505 T>C maps to NM_001902.5 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr5:138266341 C>T maps to ENST00000355078 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:41274904 C>T maps to NM_001904.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr17:3550807 C>T maps to NM_001031681.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr23:16685794 A>C did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr7:117375371 C>T maps to NM_033427.2 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr7:117364733 T>A maps to NM_033427.2 I1438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr7:117396641 G>A maps to NM_033427.2 I1105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:16916467 G>T maps to NM_001081.3 I3047I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr10:16941135 A>G maps to NM_001081.3 P2819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr10:35324144 G>T maps to NM_001198778.1 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr2:225449721 G>T maps to NM_003590.3 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:225422515 G>A maps to NM_003590.3 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:43008725 G>A maps to NM_001168370.1 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:43181267 T>C maps to ENST00000354495 P1817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:33384695 C>G did not map to a codon.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr7:101882762 G>A maps to ENST00000360264 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr12:111757855 C>T maps to NM_015267.3 N681N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:180810242 A>G maps to NM_020943.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr4:49032878 T>G maps to NM_025087.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:136873380 G>T maps to NM_001008540.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr23:30578341 G>T did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr23:75394773 T>C did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr23:40506302 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:134303601 A>G did not map to a codon.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr23:36156551 T>C did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr23:36103602 A>G did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:61511912 G>A maps to NM_001915.3 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr8:143957216 G>A maps to ENST00000377675 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr8:143956728 C>G did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr10:94828243 C>A maps to NM_183374.2 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr2:127950813 G>T maps to NM_001001665.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:41712374 C>T maps to NM_030622.6 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr7:99328743 T>A maps to ENST00000292414 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:15651479 C>T maps to NM_173483.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr5:39390644 A>G maps to NM_001343.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr5:39394410 T>C maps to NM_001343.2 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:39383199 A>G maps to NM_001343.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr13:72440445 G>A maps to ENST00000359684 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr23:86087131 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:109290783 G>T maps to NM_001917.4 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr4:100787279 T>G did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:136736936 C>A did not map to a codon.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr9:121930243 C>T maps to NM_014618.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr17:42828062 C>T maps to NM_145663.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr9:37800964 G>T maps to NM_024345.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:125685497 A>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr2:172333420 T>A maps to NM_025000.3 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr14:73412734 G>A maps to NM_015604.3 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr3:98600600 A>G maps to ENST00000326857 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr18:50985742 T>A maps to NM_005215.3 S1178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr6:24357768 A>T maps to NM_016356.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr13:36383186 A>G maps to NM_004734.4 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr10:115608964 A>G maps to NM_014881.3 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr3:53376260 G>T maps to ENST00000480258 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr11:126201298 G>T did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:155015934 G>T maps to NM_152494.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr16:20871249 G>A maps to NM_173475.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr4:52765462 T>C maps to ENST00000451288 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr23:110654010 C>T did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:61081865 G>A maps to NM_001923.3 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:15956838 C>T maps to NM_032341.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr1:162729663 G>A maps to NM_006182.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr12:31242980 C>A maps to NM_030653.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr23:134706892 G>T did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr23:41205658 C>A did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr23:41200809 T>C did not map to a codon.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr23:41202003 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr17:62500169 T>C maps to NM_004396.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr23:23019107 G>A did not map to a codon.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:113596867 G>C maps to NM_001111322.1 R821R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr12:113610194 G>A maps to NM_001111322.1 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr9:32459419 G>T maps to NM_014314.3 C810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr4:169382990 C>T maps to NM_001012967.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr4:169317121 C>T maps to NM_001012967.1 R1215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr16:90023965 G>A maps to NM_207514.1 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr6:49936557 T>C maps to NM_001037729.1 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr6:49931769 G>A maps to NM_001037499.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr1:197684158 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:142186772 C>T maps to NM_014957.2 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr15:66010114 C>G did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr15:66031103 A>G maps to ENST00000443035 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr15:65983019 C>T maps to ENST00000443035 V1304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:153907293 C>T maps to NM_014856.2 Q905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr12:31551283 C>T maps to NM_144973.3 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr22:32193640 A>T maps to NM_001136029.1 K275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr22:32301996 T>G maps to NM_001136029.1 S1479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr8:145540218 A>T maps to NM_012079.4 *489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:75509460 C>T maps to NM_032564.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr22:20077781 G>C did not map to a codon.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr2:234368473 C>T maps to NM_152879.2 V922V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:185960323 T>A maps to NM_001346.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:50144041 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:46401422 G>T maps to NM_001105540.1 E1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr10:99358954 C>T maps to NM_138413.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:12628410 T>C maps to NM_004753.4 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr6:30622527 C>A maps to NM_003587.4 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr6:30640453 G>T maps to NM_003587.4 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:54591350 A>G maps to NM_019030.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr3:47882519 C>A maps to NM_138615.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr19:47856880 C>G maps to NM_014681.5 Y198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr20:37623475 C>A maps to NM_021931.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr20:37653977 C>T maps to NM_021931.3 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr2:39088915 T>C maps to NM_198963.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:95556879 G>T maps to NM_177438.2 A1908A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr21:47958480 G>A maps to ENST00000318711 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr9:93375536 C>T maps to NM_017594.3 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr11:65547486 G>A maps to NM_138368.3 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr7:107556127 A>T maps to NM_000108.3 K288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:107545819 T>C maps to NM_000108.3 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr3:38159472 A>G maps to NM_007335.2 S1554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:196888576 A>T maps to NM_004087.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr11:83770382 T>C maps to NM_001142699.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr8:1513949 C>T maps to ENST00000357934 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:35331686 C>T maps to NM_001080418.1 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:101198409 C>T maps to NM_003836.5 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr10:124351861 C>A maps to ENST00000368915 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr10:124361508 T>C maps to ENST00000368915 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:31854855 T>G did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr23:31152281 C>G did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr23:32305750 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:88584222 G>A maps to NM_004407.3 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr5:118479555 T>C maps to NM_005509.4 F799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr15:51857283 C>A did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr15:51790749 T>G maps to NM_001174116.1 S1557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr15:51828387 T>G maps to NM_001174116.1 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr10:70196868 A>C maps to NM_001080449.1 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr10:70196868 A>C maps to NM_001080449.1 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr3:52432934 A>G maps to ENST00000273600 V4117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr3:52422875 C>T maps to ENST00000273600 L3204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr7:21737743 A>G maps to NM_003777.3 L2038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr7:21678589 C>A maps to NM_003777.3 Y1622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr17:76449534 G>T maps to ENST00000389840 V3459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr17:7689596 C>T maps to NM_020877.2 R2095R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr5:13727613 A>G did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr5:13814811 C>A maps to NM_001369.2 E2378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr2:84846835 T>G maps to NM_001370.1 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:84777108 A>T maps to NM_001370.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:196749320 T>C maps to NM_018897.2 Q1917Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr17:72306226 G>T maps to NM_023036.4 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr7:157177600 T>C maps to NM_058246.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr7:108212286 G>A maps to NM_012328.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr2:183594618 G>T maps to NM_018981.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:132196968 T>C maps to NM_015268.3 I898I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B1-A657-01A-11D-A31X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr12:49743365 T>C maps to NM_024902.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr9:114429093 G>A did not map to a codon.
Multiple mappings detected for codon TCGA-EV-5903-01A-11D-1589-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:27503081 A>T maps to ENST00000406962 K103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr11:6592936 G>T maps to NM_144666.2 A4661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:130982345 G>A maps to ENST00000372923 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:25469541 C>T maps to NM_175629.1 W409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr20:31375211 G>A maps to NM_006892.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr2:220239738 G>A maps to NM_012100.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr10:129209145 G>A maps to ENST00000398025 R1507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr10:128830576 T>A maps to ENST00000398025 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:117761499 T>C did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr23:117731502 A>T did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr23:117786021 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:11326076 T>C maps to ENST00000319867 S1364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr19:11312612 G>A maps to ENST00000319867 H1882H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr1:63119665 T>C maps to ENST00000371140 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:441957 C>T maps to NM_203447.3 V1813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr13:99481632 G>A maps to ENST00000428223 S1608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr13:99540612 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr4:3494663 A>C maps to ENST00000389653 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr6:83862076 A>G maps to NM_015018.2 L2040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr6:83862019 T>A maps to NM_015018.2 P2021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr19:2216710 G>A maps to ENST00000221482 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr19:2210829 C>T maps to ENST00000221482 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr11:118969111 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr11:65113197 G>A maps to NM_006268.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:116572491 T>C maps to NM_020868.3 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:66260241 G>A maps to NM_005700.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr3:109023470 T>C maps to NM_138815.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:7867785 T>A maps to NM_199286.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:98058808 T>A maps to NM_000110.3 K365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr8:105479133 C>T maps to NM_001385.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr1:111667501 G>T maps to NM_178454.4 C67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr5:174870045 G>A maps to NM_000794.3 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:113295343 A>G maps to ENST00000355319 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:113288846 C>T maps to ENST00000355319 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr4:9784111 T>C maps to NM_000798.4 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr18:28598132 C>T maps to NM_001941.3 W389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr18:65181491 A>G maps to NM_032160.2 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr18:29116285 T>C maps to NM_001943.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr18:29054159 A>G maps to NM_001944.2 G726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr6:7562979 T>A maps to NM_004415.2 Y231*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AT-A5NU-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-GL-A59R-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-HE-A5NF-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-IZ-A6M8-01A-11D-A31X-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-MH-A562-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-MH-A562-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-P4-A5EB-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-PJ-A5Z9-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-Q2-A5QZ-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr4:88536435 C>T maps to NM_014208.3 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr6:56463336 T>C maps to ENST00000361203 A3744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:56501421 C>T maps to ENST00000361203 W787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:205132070 G>A maps to NM_015375.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:7147901 A>G maps to NM_015343.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr15:45445602 G>C maps to NM_175940.1 V1150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr15:45427437 A>G maps to NM_175940.1 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:167096128 A>G maps to NM_001080426.1 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr18:46798649 C>G maps to NM_017653.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:56164456 T>A maps to NM_080677.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:207564615 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:23540827 C>T maps to NM_001083614.1 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr5:158158100 A>G maps to NM_024007.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:25715867 G>A maps to NM_022659.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr1:21546591 G>C maps to NM_001397.2 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr2:233350796 G>A maps to NM_004826.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr6:127611394 T>C maps to NM_001139510.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr1:53362194 T>C maps to ENST00000371522 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr23:69243091 G>C did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr2:109527286 C>T maps to ENST00000376651 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:67910483 G>A maps to NM_014329.3 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:67913802 C>T maps to NM_014329.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:22274499 C>T maps to NM_013302.3 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:22291587 C>T maps to NM_013302.3 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr8:49647694 G>A maps to NM_024593.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr17:60484527 T>C maps to NM_001144933.1 H326H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr17:28407884 G>C maps to NM_198529.3 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr13:22088515 C>T maps to NM_152726.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:19925988 G>C maps to NM_144715.3 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr8:132968017 C>T maps to NM_015137.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr14:23828917 G>A maps to NM_005864.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr23:13635855 T>C did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:38418271 C>A maps to ENST00000354891 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr1:231502191 T>A maps to NM_022051.2 K416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:41306602 T>A maps to NM_053046.2 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr3:184922366 G>A maps to NM_001966.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr23:20152120 C>A did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:37365710 G>A maps to NM_001135651.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:88890365 C>T maps to NM_004836.5 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr15:40284410 G>A maps to NM_001013703.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr1:36354061 G>A maps to NM_012199.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr14:67848334 T>C maps to NM_004094.4 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr23:24089814 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr8:109215295 A>T maps to NM_001568.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr19:10230529 A>G maps to NM_003755.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:78120724 C>G maps to NM_014740.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:21226357 C>A maps to NM_001198801.1 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:100015353 A>C maps to NM_015904.3 T1179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr2:99978206 A>T maps to NM_015904.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr17:12898189 A>G maps to NM_018127.6 C640C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr19:8038747 G>A maps to ENST00000351593 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr23:129201250 A>G did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:205588956 C>G maps to NM_021795.2 *406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:18557589 G>A maps to NM_006532.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr16:67236621 T>A maps to NM_024712.3 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:67233264 C>A maps to NM_024712.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:11005703 A>C maps to NM_017770.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr1:79402058 T>C maps to NM_022159.3 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr22:29627007 G>T did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr2:27305347 C>T maps to NM_007046.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr2:42488419 T>C maps to NM_019063.3 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr2:73145298 C>G maps to NM_004097.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr8:120628548 G>T maps to NM_006209.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr8:120580454 G>A maps to NM_006209.3 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr17:77710871 C>T maps to NM_178543.3 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr3:40465426 T>A maps to NM_001248.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr8:23294704 G>A maps to NM_004901.3 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr20:25201970 T>A maps to ENST00000443525 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr22:41543892 G>A maps to NM_001429.3 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr12:132547146 G>A maps to ENST00000333577 Q2781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr12:132522574 G>A maps to ENST00000333577 V2083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr20:34778269 C>A maps to NM_012156.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr10:32560792 A>G maps to NM_025209.2 H709H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:22927185 A>T maps to NM_020526.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:22903098 G>T maps to NM_020526.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr7:142562310 G>T maps to NM_004445.3 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr7:142561392 A>T maps to NM_004445.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr8:144940740 C>T maps to NM_031308.1 A2227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:16551693 A>G maps to ENST00000455140 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr11:723295 C>A maps to NM_022772.3 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr17:56281633 G>A maps to NM_000502.4 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr17:37876079 A>C maps to NM_004448.2 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:212295692 C>A maps to NM_005235.2 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:45868314 G>A maps to NM_000400.3 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr23:71427692 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:71426808 G>C did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr12:29502994 A>T maps to NM_016570.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr10:101911986 A>G maps to NM_001100626.1 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:23713535 C>T maps to NM_033266.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr11:124623586 C>T maps to NM_138961.2 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr13:47354150 A>G maps to NM_001984.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:53685604 A>G maps to NM_012291.4 T1884T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:6512053 C>T maps to NM_031475.2 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:152201892 A>G maps to NM_001122741.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr16:68267895 C>G did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:103499099 C>T did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:67631298 A>G maps to NM_019002.3 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:204101335 C>T maps to NM_018208.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr11:128360460 A>T maps to NM_001143820.1 C75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:13971322 C>G maps to NM_004956.4 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr4:5721078 G>A maps to NM_153717.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:5754738 G>A maps to NM_153717.2 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:7927063 C>T maps to NM_001159944.1 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr4:56765983 A>G maps to NM_018261.3 Q757Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:446364 G>A maps to ENST00000315013 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr14:57684752 C>T maps to ENST00000340918 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr8:145134931 C>T maps to NM_019037.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr4:122724129 G>A maps to NM_001034194.1 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr4:122722614 C>T maps to NM_001034194.1 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:108380879 C>T maps to NM_015065.2 W1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr11:108381025 T>G maps to NM_015065.2 T1736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr8:72182013 G>A maps to NM_000503.4 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr5:176831340 G>A maps to NM_000505.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr5:176830984 G>A maps to NM_000505.3 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:197020001 T>C maps to NM_001994.2 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr23:154159036 A>C did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:154124443 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:154130374 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr23:154157882 C>T did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr23:57313329 A>G did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr16:1877592 G>T maps to NM_001018104.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr3:138340382 T>A did not map to a codon.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr1:207085118 G>C maps to NM_005449.4 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr16:4659849 T>G maps to NM_145253.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr9:130707095 G>A maps to NM_001035254.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr5:14601481 G>A maps to NM_019018.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr19:1881549 G>A maps to NM_031213.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr19:1881549 G>A maps to NM_031213.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr19:1881549 G>A maps to NM_031213.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:59059733 C>T maps to NM_147189.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr12:47628908 G>T maps to NM_138371.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr2:203500480 A>C maps to NM_173511.3 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr12:58166554 C>T maps to NM_015433.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr23:133941689 G>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:63412719 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr23:63412032 A>G did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr23:63411695 G>A did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr2:131521381 C>A maps to NM_001105195.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:131520233 C>T maps to NM_001105195.1 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr1:1179847 G>C maps to NM_001014980.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr8:139163999 G>T maps to NM_015912.3 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr5:137289149 G>A maps to NM_016603.2 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr10:61112191 C>A maps to ENST00000442566 L76L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B1-A47M-01A-11D-A25F-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:187093140 A>T maps to ENST00000502894 K34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr23:68748895 C>T did not map to a codon.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:122128620 C>T maps to NM_014367.3 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr8:79578394 G>C maps to NM_016010.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr2:187559028 A>G maps to NM_177454.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr10:102675795 C>T maps to NM_001136123.1 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:102683798 C>T maps to NM_001136123.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:119282963 T>G maps to NM_024581.4 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr6:119282963 T>G maps to NM_024581.4 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr7:30893076 T>C did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:150421589 T>C maps to NM_152394.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr4:159092401 A>T maps to NM_001128424.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr7:193540 C>T maps to NM_020223.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr7:193560 T>A maps to NM_020223.2 L121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:97081336 C>A maps to NM_017561.1 G561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr9:97082578 G>A maps to NM_017561.1 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:99700840 G>T maps to NM_001170741.1 G546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr10:88911775 C>G maps to ENST00000298786 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr18:10691259 T>A maps to NM_022068.2 K2325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr6:82461774 G>T maps to ENST00000369756 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:82461789 T>G maps to ENST00000369756 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr1:27332863 G>A maps to NM_052943.3 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr23:34148841 G>A did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr23:34148835 C>T did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr23:34148935 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr23:34961453 G>A did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr23:24381694 G>A did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr23:24381816 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr8:130883631 C>A maps to NM_016623.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr11:114401162 C>T maps to ENST00000424269 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:190067268 A>T maps to NM_199051.1 L727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr15:59139572 A>T maps to NM_001040450.1 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr20:49219115 G>A maps to NM_080829.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr5:156590093 T>A maps to NM_130899.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:78325732 T>C maps to NM_198549.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr9:90534183 C>T maps to NM_001145124.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr2:38156860 A>G maps to NM_001170792.1 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr15:41043763 G>T maps to NM_018145.1 C128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr20:37555363 G>A maps to NM_030919.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr20:37570603 G>A maps to NM_030919.2 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:49114032 G>A maps to NM_017708.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr8:144808645 T>C maps to NM_198488.3 Q995Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr8:144810121 G>A maps to NM_198488.3 D503D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:144809116 G>C maps to NM_198488.3 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:71507082 G>A maps to NM_018172.2 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr8:124787417 C>A maps to NM_144963.2 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:33810280 T>C maps to ENST00000395190 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:33813449 A>G maps to ENST00000395190 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:33813425 T>C maps to ENST00000395190 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr15:38776826 T>A maps to NM_173611.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr3:10089632 G>A maps to NM_033084.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:89856163 A>T maps to NM_001113378.1 G1227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr2:58386911 T>C maps to NM_001114636.1 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:58431303 A>G maps to NM_001114636.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr2:163046172 A>G maps to NM_004460.2 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr12:29485565 T>C maps to NM_018099.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:29469909 T>A maps to NM_018099.3 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr13:98865555 G>A maps to NM_005766.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr13:99092298 T>A did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:242407763 C>G maps to NM_014808.2 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:242433434 G>C maps to NM_014808.2 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr17:80053199 G>A maps to NM_004104.4 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr17:80047602 C>G did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:207655322 T>C maps to NM_014929.3 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr5:7867620 A>G maps to NM_024091.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr5:7867845 A>G maps to NM_024091.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:187530417 T>A maps to ENST00000260147 I3378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr5:150911352 G>A maps to NM_001447.2 G3202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr11:92533291 C>T maps to ENST00000298047 F2371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr4:126411929 C>A maps to NM_024582.4 I4651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:126239107 T>C maps to NM_024582.4 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr23:150891104 T>G did not map to a codon.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr23:150889895 G>A did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:73916510 C>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr19:40330914 G>A maps to NM_001436.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr19:40331278 G>A maps to NM_001436.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr14:92349358 G>T maps to ENST00000267620 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr15:48748936 G>T maps to NM_000138.4 I1773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:8183904 G>A maps to NM_032447.3 D1071D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr16:30676957 G>C did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr7:102553613 G>A maps to NM_145032.3 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:33415409 C>T maps to NM_012157.3 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:48050457 T>G maps to NM_001190274.1 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr1:11710790 C>G maps to NM_012168.4 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr1:224302058 C>G maps to NM_015176.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr16:87377236 G>C maps to NM_024735.3 Y208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr14:55818481 C>T maps to NM_152231.1 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr2:230875428 A>G maps to NM_174899.4 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr6:153293426 G>A maps to NM_012177.3 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr17:18653136 T>A maps to ENST00000395665 L258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr9:123527052 G>A maps to NM_012164.3 D383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr10:103454328 G>C maps to ENST00000331272 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:55385757 C>T maps to NM_002000.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:40419756 A>G maps to NM_003890.2 H1079H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr19:40395977 G>A maps to NM_003890.2 G2473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:40366037 C>G maps to NM_003890.2 P4732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr19:40408647 G>C maps to NM_003890.2 P1397P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-PJ-A5Z9-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:157776892 G>A maps to NM_052938.4 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:157667659 G>A maps to NM_052939.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:157559027 T>C maps to NM_031282.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr11:111749724 A>G maps to ENST00000428306 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:72862363 G>A maps to ENST00000442102 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:4792819 C>A maps to NM_018708.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr8:124989659 C>T maps to NM_001039112.2 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:95603625 A>G maps to NM_018351.3 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr12:4554424 G>A maps to NM_020996.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr8:38314949 C>T maps to NM_001174067.1 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:167435949 C>A maps to NM_007045.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr4:1803583 C>A maps to NM_000142.4 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr4:1803748 C>T maps to NM_000142.4 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr5:176520384 A>G maps to NM_022963.2 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr5:176522538 C>T maps to NM_213647.1 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr4:155526042 T>C maps to ENST00000407946 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr1:60139805 G>C did not map to a codon.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:241661271 T>G did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:241663811 G>A maps to NM_000143.3 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:38463362 G>T maps to NM_004468.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr6:97051596 A>G maps to NM_020482.4 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr3:99648840 A>G maps to NM_001042459.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr4:54266006 G>C did not map to a codon.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr4:54244013 C>T maps to NM_030917.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr9:115973832 A>G maps to ENST00000446284 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:45603574 G>A maps to NM_002013.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:2909577 T>G maps to NM_002014.3 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:2909051 A>G maps to NM_002014.3 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:47259237 G>A maps to NM_024301.4 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr1:152279671 C>A maps to NM_002016.1 G2564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr17:18149934 G>A maps to NM_002018.2 F1008F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr8:142480801 G>A maps to NM_207414.2 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr8:142486195 G>A maps to NM_207414.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:71379996 C>G did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr9:84608131 G>A maps to NM_001001670.2 W916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr9:84605891 G>A maps to NM_001001670.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr23:153592961 C>G did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr23:153588775 G>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:58089734 C>T maps to NM_001164317.1 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:63885634 G>A maps to NM_013280.4 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr13:29001982 G>A maps to NM_002019.4 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr5:180048229 C>T maps to NM_182925.4 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr5:180050942 T>A maps to NM_182925.4 K514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr1:240371138 C>T maps to ENST00000406993 P1152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:240371138 C>T maps to ENST00000406993 P1152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:240371660 A>C maps to ENST00000406993 G1326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr1:240256170 G>A maps to ENST00000406993 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr1:240371516 T>A maps to ENST00000406993 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:240255570 C>G maps to ENST00000406993 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:153471510 T>A maps to NM_052905.3 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr23:147011650 T>A did not map to a codon.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:216271072 C>T maps to NM_212482.1 R958R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:94009755 G>A maps to ENST00000370253 Q414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr11:47745664 A>G maps to NM_015308.2 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr11:47788807 A>G maps to NM_015308.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr3:172025191 C>G maps to NM_022763.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:159756555 G>A did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr4:159825695 A>G maps to ENST00000379346 *1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr5:72743506 G>A maps to NM_004472.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr9:70177821 T>C maps to NM_001126334.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr1:42744041 T>A maps to NM_001198850.1 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr17:80559302 C>A maps to NM_004514.3 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr17:80525989 C>T maps to NM_004514.3 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr23:70316473 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr7:114299728 G>A did not map to a codon.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr19:52327624 T>A maps to NM_002030.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr9:14824064 T>G maps to ENST00000380880 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr9:14770685 G>T maps to ENST00000380880 S1662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr13:39452996 C>G maps to NM_207361.4 T2963T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:39422802 C>G maps to NM_207361.4 S2125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr4:190874220 A>G did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr10:135439106 C>T maps to ENST00000443774 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:131219748 T>C did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr23:12708336 G>T did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:100214267 A>G maps to NM_001013660.2 Y19Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr13:32841387 C>A maps to NM_023037.2 A2676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:48536645 A>G maps to NM_015030.1 S2207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr14:44974804 A>G maps to NM_032135.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr14:44975260 C>T maps to NM_032135.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:79496378 G>A maps to NM_001077182.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr17:79495865 G>A maps to NM_001077182.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr17:79504051 C>A maps to NM_001077182.2 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:4306031 C>T maps to NM_024333.2 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr2:49190327 G>A maps to NM_000145.3 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr15:40056079 C>T maps to NM_152597.4 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr2:186671592 C>T maps to NM_173651.2 Q5943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:186671551 C>G maps to NM_173651.2 S5929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr2:186671399 T>C maps to NM_173651.2 D5878D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:120122158 A>G maps to NM_007085.4 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr4:162307105 T>A maps to NM_020116.3 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr21:47571510 G>T maps to ENST00000397748 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr5:121187825 G>T maps to NM_177478.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr6:37442388 A>G maps to NM_015050.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:78444625 G>A maps to ENST00000436586 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:78414968 A>G maps to ENST00000436586 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr15:91419098 G>A maps to NM_002569.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr3:46000086 G>C maps to NM_024513.2 Y1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr3:46009967 C>T maps to NM_024513.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr3:197501075 T>C maps to NM_032288.6 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr7:90894983 G>T maps to NM_003505.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr2:202900341 C>G maps to NM_003507.1 Y324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr19:3527658 C>A maps to NM_001136198.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr19:3525915 G>A maps to NM_001136198.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr14:31081504 G>A maps to NM_017769.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:76570829 A>T maps to NM_203505.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr11:77934563 G>A maps to NM_080491.2 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:77991911 G>A maps to NM_080491.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr23:153908428 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr5:161281259 G>A maps to NM_001127648.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr4:46312217 A>T maps to ENST00000507069 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:161116040 T>C maps to NM_000811.2 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr4:47427722 C>G maps to NM_000812.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr5:160753380 C>G maps to NM_021911.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr15:26793189 G>C maps to NM_021912.4 S391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:46043271 C>T did not map to a codon.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:171687569 C>T maps to NM_000817.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr16:88889079 G>A maps to NM_000512.4 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr5:153755928 C>T maps to NM_198321.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr1:230372158 C>T maps to NM_004481.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr12:51758020 G>C maps to NM_007210.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:174225145 G>A did not map to a codon.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr12:132834319 G>A maps to NM_001122636.1 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr12:6645957 T>C did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr19:36029206 A>C did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr19:36033312 T>C did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr9:89560845 C>G maps to NM_002048.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr17:34077158 G>C maps to NM_139285.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:9846495 G>A maps to NM_201433.1 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr23:48652220 C>T did not map to a codon.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr20:61050058 G>T maps to NM_080473.4 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr7:92078079 T>A maps to NM_021167.3 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr7:92083892 A>G maps to NM_021167.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr22:30685453 C>T maps to NM_001037666.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr7:56046041 G>C did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr10:104120010 T>C maps to NM_004193.2 N416N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:89528890 G>T maps to NM_002053.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr4:72620173 G>A maps to ENST00000504199 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:109109238 C>T maps to NM_181453.3 T1480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr14:55310764 C>T maps to NM_001024024.1 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr12:120599293 C>T maps to NM_006836.1 E812E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr12:120582189 G>T maps to NM_006836.1 I1805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr12:120572148 G>C maps to NM_006836.1 A2421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:74838061 A>G maps to ENST00000238018 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:18499105 A>G maps to NM_004864.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:18499141 C>A maps to NM_004864.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr2:20870530 G>A maps to NM_182828.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:20871055 C>T maps to NM_182828.2 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr10:5855179 C>A maps to NM_001494.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr11:76944147 G>C maps to ENST00000376217 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr8:95262645 G>A maps to NM_181702.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:39008787 C>T maps to NM_024775.9 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:17955657 C>T maps to NM_001130009.1 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:74026106 G>T maps to NM_032380.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr5:179751867 G>A maps to NM_005110.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr20:3641541 G>A maps to NM_145762.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr20:3641290 A>C maps to NM_145762.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr20:3641541 G>A maps to NM_145762.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:73237523 G>T maps to NM_138619.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:34934556 C>T maps to NM_024835.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr20:23967128 C>T maps to NM_178311.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr17:61995167 G>T maps to NM_000515.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:40344971 C>T maps to NM_032484.4 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr7:100279775 C>T maps to NM_022574.4 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:233681743 T>A did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:233659497 T>A maps to ENST00000373566 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr2:233671360 T>A maps to ENST00000373566 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr7:150325337 G>A maps to ENST00000438845 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:27902917 T>C did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr23:70444363 C>T did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr1:35223632 C>T maps to NM_005268.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr15:35044906 C>T maps to NM_020660.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr10:35896875 C>A maps to NM_153368.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr2:69207169 A>G maps to NM_019617.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr11:134241358 A>G maps to NM_138342.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr9:6536186 C>A maps to NM_000170.2 V905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr16:74640707 A>C maps to NM_012201.5 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:121746537 C>T maps to NM_005270.4 D1016D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:53995547 C>T maps to NM_147193.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr1:92712095 C>G maps to NM_053274.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:14599356 C>G did not map to a codon.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr12:56865333 A>G maps to NM_013267.2 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr3:52731771 G>T maps to NM_018446.2 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:48205551 C>T maps to NM_015711.3 P1521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr19:48183659 G>A maps to NM_015711.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr19:48183986 G>T maps to NM_015711.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr23:120182119 C>T did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr23:120182435 A>G did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr23:120182119 C>T did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr23:120183025 T>G did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr23:120183025 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:120182122 A>T did not map to a codon.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr23:120182804 T>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr23:120182435 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:120182479 A>G did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr3:49760822 A>C did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr19:3110144 A>C did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr7:79842141 A>G maps to NM_002069.5 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr18:11689822 G>A maps to NM_182978.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:52446238 C>T maps to NM_016194.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:54578751 A>C did not map to a codon.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:131028576 G>A maps to NM_004486.4 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr9:131021445 C>T maps to NM_004486.4 Q672Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr12:133359034 C>T maps to NM_005895.3 E1104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr3:37369906 A>G maps to NM_001172713.1 K2002K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:121386443 G>A maps to ENST00000393667 Q3150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr3:121415216 G>A maps to ENST00000393667 Q1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr1:150634374 A>T maps to ENST00000369003 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr1:204183025 G>T maps to NM_198447.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:155723184 G>A maps to ENST00000368331 Y1884Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr1:155726781 C>T maps to ENST00000368331 R1828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr10:113913351 G>A maps to NM_020918.4 R815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr5:56542172 T>A maps to NM_001127236.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:46124747 A>G maps to NM_021639.4 H4H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:132437059 A>C did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:50503241 C>G maps to NM_005276.2 Y330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:157367410 C>T maps to NM_000408.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:48979067 G>A did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr12:110902938 T>C maps to NM_001164373.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:207040929 G>A maps to NM_005279.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr23:135431433 A>C did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:26532907 C>A maps to NM_001145168.1 V1048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr13:27332980 C>T maps to NM_005288.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr6:142691577 C>T maps to NM_198569.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr6:142741041 C>T maps to NM_198569.2 F1040F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr12:131590406 C>A maps to NM_198827.3 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:72368138 C>A maps to ENST00000440684 P1226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr3:154055934 A>G maps to NM_001038705.1 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr5:94957232 A>C maps to NM_199243.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr17:4937585 G>T maps to NM_017986.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr17:4937402 G>T maps to NM_017986.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr13:95271584 G>A did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr12:57389790 C>G maps to NM_007264.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:57389325 G>A maps to NM_007264.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr7:107115464 T>A maps to NM_005295.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:51273913 G>C maps to NM_001506.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr23:41555434 T>A did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr7:124405026 G>A maps to NM_005302.2 R2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:202097356 C>T maps to NM_004767.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:105858581 C>G maps to NM_007227.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:150348664 G>A did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr23:19026232 C>G did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:54080606 A>G maps to NM_006794.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:54756648 G>A maps to NM_020370.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr5:89971180 C>T maps to NM_032119.3 I1744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr5:89989973 A>T maps to NM_032119.3 T2467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:89979467 T>C maps to NM_032119.3 D1910D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr23:101910682 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr23:101908966 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr23:101910062 T>A did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:101971024 G>C did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:19884047 G>A maps to NM_016235.1 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr17:72428209 C>G maps to NM_022036.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr17:72436052 T>A maps to NM_022036.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr11:123448254 G>A maps to ENST00000456860 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:40367066 C>T maps to NM_004810.2 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr12:52401015 C>A maps to NM_181711.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr7:50742287 G>A maps to NM_005311.4 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr11:105623881 A>T maps to NM_000829.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr10:87484286 T>G maps to NM_017551.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:120745882 C>T maps to NM_014619.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:1003373 G>A maps to NM_138690.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr8:145066936 G>A maps to NM_001009184.1 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:14559361 G>A maps to ENST00000507975 C456C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr23:48840221 C>T did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr10:121212788 G>A did not map to a codon.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr6:34059741 C>T maps to NM_000841.1 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr5:148730493 C>T maps to NM_152407.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr5:148730748 C>T maps to NM_152407.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr22:19137289 G>A maps to NM_005315.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:119642254 G>T maps to NM_002093.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr9:124074614 A>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:67352041 G>C did not map to a codon.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr13:28367052 C>T maps to NM_145657.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:30877828 C>T maps to NM_001517.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr16:27549610 C>T maps to NM_001520.3 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr2:27565919 G>T maps to NM_001521.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr10:1043229 G>A maps to NM_012341.2 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr12:54857069 A>G maps to NM_144594.2 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr12:54856510 T>A did not map to a codon.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:14772232 A>C maps to NM_004963.3 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:7919109 G>A maps to NM_000180.3 L998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr4:44692822 G>A maps to NM_021927.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr23:2772025 T>A did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr19:49485592 A>G maps to NM_002103.4 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr12:31944971 A>G maps to NM_001013699.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr1:9305535 C>T maps to NM_004285.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr16:1869996 A>G maps to NM_005326.4 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr4:174449978 C>T maps to NM_021973.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:39887799 G>A maps to ENST00000310778 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr1:156593854 C>T maps to NM_021817.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr19:19371724 G>A maps to NM_023002.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:46637367 C>A maps to NM_173811.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr5:156482503 A>C maps to NM_001173393.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr5:45461991 G>A maps to NM_021072.2 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr15:73660575 G>C maps to NM_005477.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr22:50684493 A>G maps to NM_032019.5 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr3:13525051 T>G maps to NM_024827.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:114264644 A>C maps to ENST00000398283 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:141007713 C>A maps to NM_003883.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:239988462 A>T maps to NM_006037.3 I981I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr23:48676772 A>G did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr23:48682179 G>A did not map to a codon.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr23:71681921 G>C did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr7:18625058 C>T maps to NM_178425.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:18975516 C>T maps to NM_178425.2 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr23:7023837 T>G did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr18:44662720 T>C maps to NM_032124.4 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr18:44639348 A>T maps to NM_032124.4 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:242196032 T>C maps to NM_005336.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:242173342 G>A maps to NM_005336.3 D1060D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr16:50104087 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr2:37280724 C>A maps to NM_019024.1 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:58156269 A>G maps to NM_022070.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr6:138727186 C>A maps to NM_014320.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr1:45476718 G>A maps to NM_024602.5 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr7:43581575 T>A maps to NM_015052.3 V1409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr4:84342847 A>G maps to NM_133636.2 F939F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr17:65074430 G>A maps to NM_014877.3 L1922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:65162706 T>C maps to NM_014877.3 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr23:65423313 A>C did not map to a codon.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr23:65390504 C>T did not map to a codon.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:64021463 C>T maps to ENST00000261887 W1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr4:89575197 G>T maps to NM_014606.1 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr4:89410408 C>G maps to NM_016323.2 V685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr4:89408217 A>G did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr7:35707132 A>G maps to NM_022373.4 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:80382346 T>C maps to NM_173620.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr14:100119114 C>G maps to NM_001127258.1 Y270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr1:222715412 G>A maps to NM_024746.3 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr7:27582615 C>G maps to NM_152740.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:130500844 G>T maps to NM_005340.5 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr7:75183808 C>T maps to NM_005338.4 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:139258059 C>A maps to NM_022740.4 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr11:33374882 T>C maps to NM_005734.3 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr6:26056095 T>C maps to NM_005319.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:27775402 C>T maps to NM_003519.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr6:26021007 C>T maps to NM_003529.2 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:26104204 C>G maps to NM_003542.3 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr6:12123739 T>C maps to NM_002114.2 L1238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr1:41976754 G>C maps to NM_024503.3 P2196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:42048584 A>T maps to NM_024503.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr2:234749355 G>C maps to NM_018410.3 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr10:71128299 G>A maps to ENST00000439900 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr6:31323370 T>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:31324627 G>A maps to ENST00000428231 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:32714065 C>T maps to NM_020056.4 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:32489852 A>G maps to NM_002125.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr6:30459404 T>C maps to NM_005516.5 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr6:29692859 C>T maps to NM_001098479.1 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr6:29692865 G>A maps to NM_001098479.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr6:29797246 C>T maps to ENST00000376828 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:29797393 G>A maps to ENST00000376828 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:29797252 G>A maps to ENST00000376828 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr6:29797246 C>T maps to ENST00000376828 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr6:29797252 G>A maps to ENST00000376828 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr1:186083138 G>A maps to NM_031935.2 Q3720Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:185984289 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr1:186072769 A>G maps to NM_031935.2 G3580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:186024753 T>A maps to NM_031935.2 V2364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:77759507 C>A maps to NM_018200.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr15:77750832 C>G maps to NM_018200.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:34210571 G>A maps to NM_145899.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr13:31036767 C>T maps to NM_002128.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr1:24151845 A>G maps to NM_000191.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr6:79918283 G>T maps to NM_004242.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr19:1082888 G>T maps to NM_012292.2 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:4557883 G>T maps to NM_001127205.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr16:4557976 C>T maps to NM_001127205.1 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr12:121437342 C>T maps to NM_000545.5 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:36099581 T>C maps to NM_000458.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr5:137088930 G>A maps to NM_006805.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:177632983 G>A maps to NM_031266.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr9:86587098 G>T maps to NM_031262.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:86585224 T>A maps to NM_031262.2 K405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:41807609 G>C did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr11:62489599 C>A maps to NM_001079559.1 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr19:12875720 C>T maps to NM_013312.2 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:150689612 C>T did not map to a codon.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr7:27211694 C>T maps to NM_018951.3 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr7:27169875 C>A maps to NM_002141.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr16:72110799 G>A maps to ENST00000228226 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr10:100177416 G>A maps to NM_000195.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr4:84243393 G>A maps to NM_006665.5 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr10:100481442 C>T maps to NM_021828.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr8:21974549 C>T maps to NM_005144.4 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr18:22048830 C>T maps to NM_021624.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:20818845 C>T maps to NM_022460.3 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:87570376 T>C maps to NM_012262.3 *357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr16:26147415 G>A maps to NM_006040.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:132091224 G>C did not map to a codon.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr11:43837919 T>C maps to NM_016142.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr6:33172820 C>T maps to NM_014234.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr16:84158327 A>C maps to NM_031463.4 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:56565508 G>A maps to NM_001080439.1 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr14:102548765 G>A maps to NM_001017963.2 R713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr6:31779707 G>A maps to NM_005527.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr6:31778273 G>T maps to NM_005527.3 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:65008124 G>A maps to NM_021979.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr5:132425376 T>C maps to NM_002154.3 D456D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr9:128001453 A>G maps to NM_005347.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:161495203 G>A maps to NM_002155.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr2:198365880 A>G maps to NM_002157.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr1:22190694 G>A maps to NM_005529.5 P1546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr23:135594032 A>T did not map to a codon.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr5:63257392 G>A maps to NM_000524.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr3:183756413 T>A did not map to a codon.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr7:154862731 G>T maps to NM_024012.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr4:3201561 C>T maps to NM_002111.6 S1824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr4:3124640 T>C maps to NM_002111.6 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:3076695 T>G maps to NM_002111.6 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr23:53589173 C>T did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr23:53607788 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr23:53564648 C>T did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr23:53584382 A>G did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:53641558 C>T did not map to a codon.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr23:53563130 A>G did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr3:50357590 C>T maps to NM_033158.4 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:71127827 G>A maps to NM_032821.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:10444568 T>A maps to NM_002162.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr15:90634782 A>G did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr20:2639398 A>C maps to NM_006899.2 *386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr8:39862888 T>C maps to NM_194294.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:6649693 A>G maps to NM_001193457.1 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:18288014 C>T maps to NM_006332.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr10:91177426 A>G maps to NM_012420.2 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr21:34725062 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr21:34799206 A>T maps to ENST00000381995 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr2:27704120 A>G maps to NM_015662.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr12:110565895 C>T maps to NM_014055.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr13:21163993 T>C maps to NM_175605.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr15:65628244 A>G maps to NM_004884.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr15:65684504 T>A maps to NM_020962.1 K697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:217541548 C>G maps to NM_000599.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:201166404 C>T maps to NM_001164586.1 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:51831096 C>A maps to NM_001101372.1 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr11:18738380 A>G maps to NM_173588.3 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:117122272 G>A maps to NM_001542.2 D1045D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr11:133814178 C>A maps to NM_014987.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr11:133805657 C>T did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:81517937 A>G maps to NM_172217.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr13:21295993 C>T maps to NM_138284.1 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr22:17566095 C>A maps to NM_014339.5 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:53891718 T>C did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:9959172 C>T maps to NM_153461.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr3:57136552 C>T maps to NM_017563.3 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr2:113540316 G>T maps to NM_000575.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr23:29973428 A>C did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:102849532 C>T maps to NM_003854.2 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:27459982 G>T maps to NM_181079.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr5:55212821 T>C maps to NM_139017.4 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:50397530 G>C maps to NM_172374.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr19:50393784 C>T maps to NM_172374.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr16:27374875 C>T maps to NM_000418.2 Q735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr16:27374133 G>A maps to NM_000418.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr23:155232600 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr23:155239601 G>A did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr19:15227274 G>T maps to NM_006844.3 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr7:111127298 T>A maps to NM_032549.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr7:111161446 G>A maps to NM_032549.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:86371414 T>G maps to NM_006839.2 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:76660532 G>A maps to NM_001563.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:76660635 G>A maps to NM_001563.2 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr6:76640749 G>A maps to NM_001563.2 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr1:62550316 C>T maps to NM_176877.2 P1458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr12:6760400 C>T did not map to a codon.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr2:220437359 C>G maps to NM_002191.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr12:57828749 A>C maps to NM_005538.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr2:206921630 G>A maps to NM_017759.4 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr4:143159033 A>G maps to NM_003866.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:38338747 G>A maps to ENST00000373026 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr2:234102515 G>T maps to ENST00000359570 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr17:1400004 G>C maps to NM_016532.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:71948602 A>G maps to NM_001567.3 P1105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:36005047 C>T maps to NM_032594.3 C530C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BQ-7059-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:156821561 G>A maps to NM_014215.2 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:156823724 G>A maps to NM_014215.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:156818723 G>A maps to NM_014215.2 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr1:153736637 A>G maps to ENST00000428986 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:153740252 G>T maps to ENST00000428986 E733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:62417116 A>G maps to NM_030628.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr8:95884141 A>G maps to NM_017864.2 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr4:128608919 T>C maps to NM_015693.3 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:154521108 C>G maps to NM_001130700.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr13:98667794 A>T maps to NM_002271.4 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:30790087 C>G maps to NM_006390.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr2:237272539 C>T maps to ENST00000457693 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr5:75888709 G>A maps to NM_006633.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr3:12957105 C>T maps to ENST00000429247 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr23:53268432 C>G did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr12:275006 G>A maps to NM_001170738.1 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr15:78758792 A>T maps to NM_004136.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:46388581 G>A maps to NM_015649.1 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:234744250 G>T maps to NM_182972.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr1:234744214 G>A maps to NM_182972.2 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:234743059 G>A maps to NM_182972.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:209974722 G>A maps to NM_006147.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr23:107977150 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr23:107978242 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:55360381 G>A maps to NM_024335.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:50683583 G>T did not map to a codon.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr19:55966663 G>A maps to NM_024710.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr5:52366068 C>G maps to NM_002203.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr17:42449791 C>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:15688932 G>A maps to NM_003638.1 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr16:31371299 G>A maps to NM_000887.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:31383748 G>A maps to NM_000887.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr16:31373394 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr10:33208865 A>G maps to ENST00000374956 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:73746315 G>A maps to NM_001005619.1 W1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:73749999 C>G maps to NM_000213.3 G1421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr12:53587038 G>A maps to NM_000889.1 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr23:54777528 G>A did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr13:48833063 A>G maps to NM_021999.4 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:231741582 G>C maps to NM_030926.4 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr14:93408016 C>T maps to NM_014216.4 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr19:41223384 A>T maps to NM_025194.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr3:4685827 A>T maps to ENST00000356617 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr12:26553126 G>A maps to NM_002223.2 T2488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr2:24469666 A>G maps to NM_006277.2 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr1:152883241 T>G maps to NM_005547.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr1:152883268 A>G maps to NM_005547.2 Q332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr20:10621488 C>A maps to NM_000214.2 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr20:10653489 A>C maps to NM_000214.2 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr9:5126751 T>C maps to NM_004972.3 A1120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr4:6066675 C>T maps to NM_001099433.1 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr5:147010973 A>G did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr14:59965597 G>C maps to ENST00000356057 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:59965573 T>C maps to ENST00000356057 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr10:64968539 A>G maps to NM_032776.1 F963F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr8:75227664 G>A maps to NM_020647.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr14:23444253 G>A maps to NM_032876.4 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:75678299 A>T maps to NM_001130089.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr3:20187857 C>T maps to NM_003884.4 Y685Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:65480306 T>A did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr15:65369366 C>T maps to NM_001101362.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr3:42727130 G>A maps to NM_152393.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr13:41766947 A>T maps to NM_032138.4 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr13:41767952 G>A maps to NM_032138.4 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr11:30032893 T>C maps to NM_002233.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr20:48098852 C>G maps to NM_004975.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr12:75436983 G>T maps to NM_139137.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr1:110774915 G>A maps to NM_004978.4 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:110774882 T>C maps to NM_004978.4 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:112524715 C>T maps to ENST00000315987 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr21:35743146 T>C maps to NM_172201.1 *124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr18:77659161 G>A maps to NM_012283.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr17:61623067 A>G maps to NM_030779.2 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr17:61623122 C>T maps to NM_030779.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr17:61616009 C>G maps to NM_030779.2 V647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr3:19389245 G>A maps to NM_144633.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:95976176 C>T maps to NM_013434.4 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr17:21319583 C>T maps to NM_021012.4 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:233633227 A>T maps to NM_002242.4 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr22:38822919 A>C maps to NM_152868.1 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr6:39159333 G>A maps to NM_003740.3 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr1:154841687 G>A maps to NM_002249.4 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:154744542 C>T maps to NM_002249.4 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr11:2798239 C>G maps to NM_000218.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr11:2466534 G>T maps to NM_000218.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr20:62078165 G>C maps to NM_172107.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:62070958 G>A maps to NM_172107.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr8:99441266 G>T maps to NM_020697.2 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr9:138594139 C>G maps to ENST00000298480 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr8:36698473 C>A maps to NM_001031836.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr9:2718278 C>T maps to NM_133497.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr12:109889449 G>T maps to NM_031954.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr17:7256620 C>T maps to NM_001002914.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr13:77460121 C>G maps to NM_138444.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr13:45768534 G>A maps to NM_198404.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:44450333 A>T maps to NM_198353.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr22:38877224 G>A maps to NM_016657.1 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:23380288 G>A maps to NM_001009999.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr12:121947831 C>T maps to ENST00000377071 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:137715372 T>C maps to NM_016604.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:5131902 G>C maps to NM_015015.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr1:202701001 A>C maps to ENST00000367264 Y1361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:53239615 G>T did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr23:53245083 T>C did not map to a codon.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr24:21901509 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr23:44949020 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr23:44733230 A>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:44870204 G>C did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr17:7748925 C>A maps to NM_001080424.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr17:7755371 T>G maps to NM_001080424.1 A1423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr17:7750210 A>C maps to NM_001080424.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr19:10610565 G>T maps to NM_203500.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:10610177 G>A maps to NM_203500.1 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr7:142640922 C>T maps to NM_000420.2 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr19:6420476 G>C maps to NM_003685.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr1:19545820 C>T maps to NM_015047.1 K986K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr17:26948414 A>G did not map to a codon.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr16:85706124 C>T maps to NM_014615.2 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:85689999 C>T maps to NM_014615.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr17:73487467 G>T maps to ENST00000375248 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr3:197408101 G>A maps to NM_014687.1 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:6860176 G>A maps to NM_014743.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr19:34832920 G>A maps to NM_014686.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr14:35593086 T>C maps to NM_014672.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr20:36612010 T>A maps to NM_014657.1 P1039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:22623803 C>T maps to ENST00000446597 Q800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr12:22646272 T>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr13:42273323 G>A maps to NM_015058.1 F1149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr11:46666906 C>T maps to NM_001142673.1 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr17:6531559 G>A maps to NM_014804.2 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:39880151 A>T maps to NM_015038.1 V1405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr18:8813134 C>T maps to ENST00000456698 N1240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr19:19431718 G>C maps to NM_015329.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr19:19454739 G>A maps to NM_015329.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr7:36396612 G>A maps to NM_001100425.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:155903552 C>G maps to NM_014949.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr4:154542028 C>A maps to NM_001131007.1 S1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr18:29496395 C>T maps to NM_014939.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:79748656 C>T maps to NM_015206.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:105527568 C>G maps to NM_015275.1 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr4:123156096 G>T maps to NM_015312.3 E1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr4:123264652 C>G maps to NM_015312.3 G4147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr7:141365047 A>T maps to NM_001080392.1 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr15:81181039 A>T did not map to a codon.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr23:118219439 T>G did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr23:118223093 A>G did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr10:24835171 T>C maps to NM_019590.3 H1917H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr10:70775349 G>A maps to NM_015634.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr3:113684199 G>A maps to NM_020817.1 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr8:95503872 T>C maps to NM_015496.3 S1691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr18:59888684 C>T maps to NM_020854.3 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr9:100128908 C>T maps to ENST00000375206 C1361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr4:1369833 G>A maps to NM_020894.2 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr7:138602634 C>T maps to NM_001164665.1 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr14:77580237 C>T maps to NM_033426.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr20:36870193 C>T maps to NM_001029864.1 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr9:20758139 G>A maps to NM_017794.3 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr3:113376112 C>T maps to NM_001009899.2 Q1472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr3:113376112 C>T maps to NM_001009899.2 Q1472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr3:113376679 G>T maps to NM_001009899.2 G1283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr3:113377558 T>C maps to NM_001009899.2 S990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:113376121 C>T maps to NM_001009899.2 Q1469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:113376127 C>T maps to NM_001009899.2 Q1467Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr23:73961091 C>T did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr8:28991586 C>T maps to NM_015254.3 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr8:29037679 G>A maps to NM_015254.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr20:16359621 G>A maps to NM_024704.4 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr17:43009570 C>T maps to ENST00000438933 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr17:72340926 C>A maps to NM_153209.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:10352149 A>G maps to ENST00000377086 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr17:4908296 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr1:200973947 C>A maps to NM_017596.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:86485504 T>A maps to NM_017576.1 K896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr17:51901647 C>T maps to NM_032559.4 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr23:69637855 T>C did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr23:69595070 G>A did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr5:154395500 G>A maps to NM_001099293.1 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr12:57965900 C>T maps to NM_004984.2 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr10:32320042 A>G maps to NM_004521.2 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:149835495 C>T maps to NM_004522.1 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:149850957 G>C maps to NM_004522.1 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr2:149799206 G>A maps to NM_004522.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr16:57806197 T>C maps to NM_005550.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr10:7811177 C>T did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:36353425 A>G maps to NM_199180.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr4:55570035 C>G maps to NM_000222.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr4:39435919 G>T maps to NM_175737.3 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:39435930 G>T maps to NM_175737.3 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr6:43042367 G>T maps to NM_201523.1 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr1:44595404 C>G maps to NM_173484.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:87764192 T>C maps to NM_017566.3 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:87760466 C>T maps to NM_017566.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr22:50987533 T>C maps to NM_138433.3 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:205306598 G>T maps to NM_018203.1 C327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:202866047 G>A maps to NM_021633.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr22:20796431 G>C maps to NM_032775.3 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr5:136963989 G>A maps to NM_017415.2 N529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr23:21675433 A>G did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr23:86773062 C>G did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr23:86887409 A>G did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:51518765 G>T maps to NM_001077500.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr19:51584904 G>T maps to NM_022046.4 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr12:9754097 T>C maps to NM_002258.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr7:139164444 C>T maps to NM_198508.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:10541381 G>A maps to NM_007360.3 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:160249254 A>G maps to NM_002268.3 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr17:45727755 G>A maps to NM_002265.4 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr12:75895545 T>C maps to NM_007043.6 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr17:38978228 G>A maps to NM_000421.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr17:39658759 G>A maps to NM_153490.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr17:39658843 T>C maps to NM_153490.2 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr17:39092458 C>G did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:38926070 C>A maps to NM_181539.4 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:52913573 G>T maps to NM_000424.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr12:53097169 G>T maps to NM_175078.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr12:53225245 C>A maps to NM_175834.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr17:39191010 G>C maps to NM_030966.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr17:39183128 A>G maps to NM_031957.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr21:45959196 G>A maps to NM_198691.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr21:46057372 C>T maps to NM_181688.1 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr21:46117130 C>T maps to NM_198699.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr21:45978022 G>A maps to NM_198696.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr21:45978007 G>A maps to NM_198696.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr21:31709824 G>A maps to NM_001077711.1 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:39274237 A>G maps to NM_033059.3 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:39324103 A>G maps to NM_033187.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr17:39305509 G>A maps to NM_033188.3 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:39261741 C>T maps to NM_001146041.1 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:1643278 C>T maps to ENST00000359229 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr11:1651126 C>T maps to NM_001001480.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:118293233 T>C maps to ENST00000339824 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:56079009 C>A maps to NM_001079521.1 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr14:56107680 C>T maps to NM_001079521.1 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:134323199 C>A maps to NM_178554.4 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr14:50713787 T>C maps to NM_024884.2 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr22:41621937 G>A maps to NM_031488.4 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr19:54872526 C>A maps to NM_002287.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr18:6992668 G>A maps to NM_005559.2 L1687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr18:7025997 A>G maps to NM_005559.2 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:129766959 C>T maps to NM_000426.3 A2141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:21451429 G>T maps to ENST00000416669 V1603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr18:21508089 T>C maps to ENST00000416669 F2729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:112454682 G>C maps to NM_001105206.1 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:112457350 G>A maps to NM_001105206.1 Q1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr20:60908163 G>A maps to NM_005560.3 I1088I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:60891784 C>T maps to NM_005560.3 L2566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr3:49158998 C>T maps to NM_002292.3 Q1709Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr9:133914284 G>A maps to ENST00000355048 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr13:113964010 C>T maps to NM_005561.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr23:119581841 G>A did not map to a codon.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr22:33679189 G>A maps to NM_133642.3 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr12:50869376 G>C maps to ENST00000429001 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:50847397 T>C maps to ENST00000429001 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr10:858886 A>G maps to NM_015155.1 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr15:71128825 T>C maps to NM_018357.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr4:113578402 T>C maps to ENST00000509061 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr23:64749563 C>A did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr1:150940936 C>T maps to NM_181746.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:150005369 G>T maps to NM_004690.2 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr6:149997826 C>G maps to NM_004690.2 G880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr20:36989401 T>G maps to NM_004139.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr6:80197554 C>T maps to NM_181714.3 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr1:152777876 G>A maps to NM_178351.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:152552160 G>A maps to NM_032563.1 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:136555629 T>G maps to NM_002299.2 R1649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:226075313 G>A maps to ENST00000419724 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:226075305 G>T maps to ENST00000419724 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:226127229 G>A maps to NM_003240.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr3:189711952 A>G maps to NM_018192.3 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr1:65895650 C>A maps to NM_017526.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr12:51450185 G>A maps to ENST00000448283 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr11:63273899 G>C maps to NM_001142535.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr17:20355184 G>A maps to ENST00000324290 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr10:95549894 T>C maps to NM_005097.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:27402258 C>G did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:206785683 C>T maps to NM_006893.2 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:9547648 G>A did not map to a codon.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr9:139091692 C>T maps to NM_014564.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:113909128 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:113901231 T>C maps to NM_022363.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr19:54822786 A>C maps to NM_021250.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:55144005 C>A maps to ENST00000427581 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:54783676 C>T maps to ENST00000391747 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr19:54725772 T>C maps to NM_001081450.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:54721051 G>T maps to NM_001081450.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr7:73535229 G>A maps to NM_002314.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr9:27950498 G>A maps to NM_152570.1 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:2290212 C>T maps to NM_001101391.1 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:42907052 G>A maps to NM_005357.2 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr21:15579136 T>C maps to NM_198996.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr21:15561569 G>A maps to NM_198996.2 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr21:15554118 C>T maps to NM_198996.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr5:96443095 C>A maps to NM_153234.4 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr17:73565070 C>A maps to NM_001031803.1 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:66522753 G>A maps to NM_032338.3 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr1:156105084 C>T maps to NM_170707.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr1:156107473 A>C maps to NM_170707.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr7:123302917 T>C maps to NM_207163.1 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr3:69169079 T>C maps to NM_198271.3 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr4:54362297 G>A maps to NM_001126328.1 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr4:54343068 T>C maps to NM_001126328.1 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr13:28143268 G>A maps to NM_153371.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr16:22545905 C>T maps to NM_001135865.1 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr1:13183398 A>G maps to NM_001136561.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr19:11350387 C>T maps to ENST00000252453 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:20851090 C>T maps to NM_030941.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr16:48286155 G>A maps to NM_031490.2 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr16:48385616 T>C maps to NM_031490.2 F821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr23:118109100 G>T did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr23:118151558 G>A did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr5:121409740 G>T maps to NM_002317.5 Y334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:121413455 G>C maps to NM_002317.5 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr2:74761482 G>A maps to NM_032603.2 H633H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr23:78011380 C>T did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr23:78010715 C>A did not map to a codon.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr5:1488542 A>T maps to NM_024830.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr12:7125632 C>T maps to NM_005768.5 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr4:62542579 T>G maps to ENST00000506720 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr2:11925179 C>T maps to ENST00000396099 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:11960559 A>G maps to ENST00000396099 V853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr8:19811709 C>T maps to NM_000237.2 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr4:151827109 A>T maps to NM_006726.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr4:151829519 G>A maps to NM_006726.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr11:66627367 T>A maps to NM_024036.4 L537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr14:42360767 C>T maps to NM_152447.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:66460689 C>A maps to NM_015541.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:113657325 C>A maps to NM_014813.1 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr12:59274492 G>A maps to NM_153377.3 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr2:141607701 G>A maps to NM_018557.2 N1636N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr2:170012841 G>T maps to NM_004525.2 V4031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:170055305 A>G maps to NM_004525.2 P2856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr2:170072852 A>G maps to NM_004525.2 T1912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:170136008 T>A maps to NM_004525.2 K480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:68197136 C>T maps to NM_002335.2 L1244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr12:12274104 A>G maps to NM_002336.2 H1599H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr12:12303826 G>C maps to NM_002336.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:12302075 C>T maps to NM_002336.2 V1002V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr1:53723083 T>G maps to NM_004631.3 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr4:3519767 A>G maps to NM_002337.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr2:44207046 A>G maps to NM_133259.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr2:44203319 T>A maps to NM_133259.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr8:145745729 A>G maps to NM_014665.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:7023219 A>C maps to NM_006992.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:196387839 C>T maps to NM_198565.1 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:62855781 A>T maps to NM_199340.2 I1494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr1:46751889 T>G maps to ENST00000254454 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr12:122669245 T>C maps to NM_001098519.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:150033985 C>G maps to NM_023942.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr9:131670919 G>T maps to NM_001127244.1 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr1:90048544 A>G maps to NM_015350.2 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:90179187 T>C maps to NM_032270.4 Y353Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr19:7964009 T>G maps to NM_025061.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr8:86057650 G>T maps to NM_033402.4 E1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr12:85449851 G>T maps to NM_001079910.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr15:101529602 A>G maps to NM_024652.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:40758850 A>G maps to NM_198578.3 L2463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:42117588 C>T maps to ENST00000411445 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:34710314 T>G maps to NM_001114093.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr19:34710314 T>G maps to NM_001114093.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr19:35757259 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:35758027 C>A maps to NM_205834.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr21:47626683 T>G did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr14:74970232 G>A maps to NM_000428.2 C1553C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr14:75019016 C>G maps to NM_000428.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr11:65319016 A>T did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:41129531 C>T maps to ENST00000308370 R1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr3:46492032 A>G maps to NM_002343.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr15:41798199 G>T maps to NM_002344.5 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr23:114541170 T>A did not map to a codon.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:31675741 G>A maps to ENST00000375834 W159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr6:5260905 T>A maps to NM_001164840.1 K21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr1:235884163 G>A maps to NM_000081.2 L3119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:20107304 G>A maps to NM_021020.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr12:9096394 A>G did not map to a codon.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr1:39908527 C>G maps to ENST00000361689 S4357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:39888511 C>T maps to ENST00000361689 A3301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr23:151870044 G>A did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr23:30260476 G>C did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:30261229 C>A did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr23:54841946 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr3:65425596 C>T maps to NM_001033057.1 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr7:78131030 C>A maps to NM_012301.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr12:10766046 G>T maps to NM_018048.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr23:77150837 C>A did not map to a codon.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:110873285 G>A maps to NM_005434.4 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:139748711 C>T maps to ENST00000392881 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:179160184 C>T maps to NM_014757.4 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:179192886 G>A maps to NM_014757.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr5:179201052 G>A maps to NM_014757.4 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr5:179193184 G>T maps to NM_014757.4 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:95825430 T>C maps to NM_032427.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr11:95825430 T>C maps to NM_032427.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr11:95825220 C>T maps to NM_032427.1 Q658Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:95825247 C>T maps to NM_032427.1 Q649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr11:95825355 T>C maps to NM_032427.1 Q613Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr11:95825394 C>T maps to NM_032427.1 Q600Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:95825430 T>C maps to NM_032427.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr11:95825361 C>T maps to NM_032427.1 Q611Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:95825430 T>C maps to NM_032427.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr4:140811125 C>T maps to ENST00000509479 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr4:140811128 T>C maps to ENST00000509479 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr4:140811101 C>T maps to ENST00000509479 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:12483848 G>T maps to NM_018050.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:43590944 A>C did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr23:43515618 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr23:43702914 C>G did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:43655116 C>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:71495627 C>G maps to NM_005909.3 S2149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr19:17837416 G>A maps to NM_018174.4 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:12016634 T>C maps to ENST00000415385 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr17:11998977 C>T maps to ENST00000415385 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:7976337 A>G maps to ENST00000425613 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr5:56177036 T>A maps to NM_005921.1 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr5:56170959 G>T maps to NM_005921.1 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr3:185191374 G>A maps to NM_004721.3 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:185146746 C>T maps to NM_004721.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr6:161470013 C>A maps to NM_005922.2 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr6:161413040 G>A maps to NM_005922.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr6:137113271 G>A maps to NM_005923.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:91226400 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:39526943 T>C did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:102493543 C>A maps to NM_145686.2 I1043I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:102493591 C>G maps to NM_145686.2 V1059V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:36642064 G>A maps to NM_018067.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr23:135312675 A>G did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr23:135314168 T>C did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr6:36040749 C>A maps to NM_139012.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr8:144801160 A>T did not map to a codon.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr16:1815159 G>A maps to NM_015133.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr3:50685440 C>G maps to NM_004635.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:27248499 C>T maps to NM_012326.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr17:44101443 C>G maps to NM_001123066.3 V746V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr19:8503276 C>T maps to NM_016496.4 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:58149445 C>T maps to NM_138396.4 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr11:63671475 C>G maps to NM_001039469.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr12:57894253 G>C maps to NM_004990.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:46290208 T>C maps to NM_015112.2 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr5:66432457 C>G maps to NM_001164664.1 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr8:99019719 C>T maps to ENST00000254898 C488C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr20:43927152 G>A maps to ENST00000372754 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr18:47800702 C>T maps to ENST00000424334 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:149248039 A>C maps to ENST00000404807 P1613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:57918526 C>A maps to NM_052897.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:152163261 C>T maps to NM_021038.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:131540268 T>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr18:74700844 C>T maps to NM_001025101.1 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr16:84094305 G>C maps to NM_003791.2 V895V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr18:13826447 G>A maps to NM_005913.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr11:119182660 T>A did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr11:119185944 C>T maps to NM_006500.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:103349336 C>T did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:112458402 A>T maps to NM_001085377.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr23:138684575 C>T did not map to a codon.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr13:113728834 G>A maps to NM_001112732.1 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr3:183013204 G>A maps to NM_015078.2 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:150551616 C>T maps to NM_021960.4 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr7:99690936 C>A maps to NM_005916.3 G646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:119245293 T>C did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:85491699 A>G maps to NM_018298.9 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:85491893 G>C maps to NM_018298.9 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:6302562 T>C maps to NM_024596.3 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr15:94841733 C>T maps to NM_018349.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr6:37622224 G>T maps to ENST00000297153 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:63826355 C>G maps to NM_005917.3 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr12:68696604 T>A maps to NM_017440.4 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr6:90402312 G>C maps to NM_014611.1 S3479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr6:90459293 G>A maps to NM_014611.1 Q1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr17:37579983 A>T maps to NM_004774.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr23:70349197 G>T did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr3:150877785 C>T maps to NM_053002.4 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr12:116428912 C>T maps to NM_015335.4 G1282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr23:40586007 T>C did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr22:20920815 G>A maps to NM_001003891.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:38182476 C>T maps to NM_014815.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr17:38187789 C>G did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr9:134889752 A>G maps to NM_004269.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr5:126705694 G>T did not map to a codon.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr22:42191443 C>A maps to NM_152513.3 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr22:42154471 A>C maps to NM_152513.3 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr9:36583633 A>G maps to NM_014791.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr7:15725808 G>A maps to NM_005924.4 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:15725799 G>A maps to NM_005924.4 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr7:15725799 G>A maps to NM_005924.4 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:81282036 G>A maps to NM_015154.1 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr15:90321561 C>T maps to NM_001039958.1 Y397Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr12:95867963 T>G maps to NM_006838.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:95867963 T>G maps to NM_006838.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:95867963 T>G maps to NM_006838.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:58165806 G>A maps to ENST00000408972 Y45Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr10:126477650 A>G maps to NM_212554.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:60501295 A>G maps to NM_181725.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr2:170677783 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr16:21611191 C>G maps to NM_016025.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr19:1555891 G>A maps to NM_001174118.1 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:44105506 C>T maps to NM_005926.2 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr15:44109599 T>G maps to NM_005926.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:8655001 C>A did not map to a codon.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:179094913 T>G maps to NM_033540.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr17:74738355 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:74772620 C>T maps to NM_024311.2 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr12:53647797 C>T maps to NM_001170790.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr15:42057123 C>T maps to ENST00000219905 N2644N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:141759732 A>G maps to ENST00000475668 K1342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr7:141731532 T>G maps to ENST00000475668 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr10:103552625 A>G maps to NM_012215.3 Y715Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr10:103563516 A>G maps to NM_012215.3 N337N. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr11:12225945 G>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:12316189 C>T maps to NM_032867.2 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr7:1477989 C>G did not map to a codon.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr23:38664367 G>T did not map to a codon.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr1:67394624 T>C maps to NM_020948.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:67423740 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:12089879 C>T maps to NM_021933.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr3:97673273 G>T maps to NM_153182.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:4800539 T>G maps to NM_153827.4 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr22:50926722 G>T maps to NM_017584.5 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr3:69928531 A>T maps to ENST00000448226 K118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr22:40813488 G>A maps to NM_020831.3 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:75516129 T>A maps to NM_001040108.1 K77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr16:74716658 G>T maps to NM_152649.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr12:49445197 A>G maps to NM_003482.3 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr12:49425838 G>A maps to NM_003482.3 Q4217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr12:49426525 G>A maps to NM_003482.3 Q3988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr12:49431829 A>T maps to NM_003482.3 A3103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr12:49433379 C>G maps to NM_003482.3 L2689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr7:151945348 T>A maps to ENST00000355193 K724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:151884404 A>T maps to ENST00000355193 T1650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr7:151879015 G>A maps to ENST00000355193 Q1977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr7:151921113 A>T maps to ENST00000355193 C1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr19:36229180 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr7:104750954 G>T maps to NM_182931.2 P1292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr6:168276026 A>C maps to ENST00000400822 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr13:49796386 C>G maps to NM_001507.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr16:2258564 C>T maps to NM_022372.4 G271G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DZ-6134-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr17:40720855 T>C maps to NM_170607.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr12:122616845 C>T maps to NM_014938.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:154855892 T>A maps to NM_007289.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr3:154858035 A>G maps to NM_007289.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr1:2540841 C>T maps to NM_033467.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:58074477 C>A maps to NM_002428.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:102713446 G>T maps to NM_002422.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr10:88703694 G>A maps to NM_024756.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr10:99222419 C>T maps to ENST00000422291 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr14:61434958 T>C maps to NM_002431.3 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:61434985 T>C maps to NM_002431.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:49946455 G>A maps to NM_032355.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr23:106201625 A>G did not map to a codon.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr1:220971316 G>A maps to NM_022746.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr1:220960438 G>T maps to NM_022746.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr1:220964856 G>A maps to NM_022746.3 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr9:13183482 A>G maps to ENST00000319217 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:58978385 A>T maps to NM_001039396.1 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:56355332 C>T maps to ENST00000340482 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr23:154033609 G>T did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr14:67787026 T>C maps to NM_022474.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr17:17080726 G>A did not map to a codon.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr17:60766322 T>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:60753773 C>A maps to NM_006039.3 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr11:18195247 C>T maps to NM_054032.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr11:18195096 C>T maps to NM_054032.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:13875776 C>T maps to NM_001031727.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr18:48331526 A>G maps to NM_001127176.1 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr16:1822946 C>G maps to ENST00000432952 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:1822946 C>G maps to ENST00000432952 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:10647665 C>G maps to NM_001098579.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr5:80037367 G>C did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr5:80040401 G>A maps to NM_002439.3 K577K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr23:64936757 G>C did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr8:16021616 A>G maps to ENST00000445506 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr8:9912061 C>T maps to NM_012331.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:38288351 G>T maps to NM_005955.2 S403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr15:65295423 A>C maps to NM_139242.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:86565820 G>A maps to NM_001159377.1 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:55473594 G>A maps to NM_002453.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr15:31251263 G>C maps to NM_017762.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr22:30413917 G>T maps to NM_021090.3 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr22:30416248 C>T maps to NM_021090.3 C867C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:11273602 G>C maps to NM_004958.3 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:11270888 G>A maps to NM_004958.3 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr5:7878201 G>T maps to NM_024010.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr5:7878350 A>C maps to NM_024010.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr3:124632010 A>G maps to NM_033049.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr19:9077785 G>T maps to NM_024690.2 I3220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr19:9085837 C>A maps to NM_024690.2 E1993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr19:9088826 T>C maps to NM_024690.2 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:9058715 G>C maps to NM_024690.2 S9577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr7:100692246 G>A maps to NM_001040105.1 T4219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:100675713 G>C maps to NM_001040105.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr7:100681164 T>C maps to NM_001040105.1 Y2156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr11:1093325 C>A maps to ENST00000441003 G1715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:1092812 C>T maps to ENST00000441003 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:1093409 C>A maps to ENST00000441003 T1743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:1092812 C>T maps to ENST00000441003 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:1093391 C>T maps to ENST00000441003 T1737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:1092812 C>T maps to ENST00000441003 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:1093115 C>T maps to ENST00000441003 T1645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr11:1093253 C>T maps to ENST00000441003 T1691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr11:1092965 C>A maps to ENST00000441003 T1595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr11:1092812 C>T maps to ENST00000441003 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:1099776 T>C maps to ENST00000441003 P2458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:1098667 G>A maps to ENST00000441003 V2346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr11:1092629 T>C maps to ENST00000441003 T1483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr6:30954812 T>C maps to NM_001010909.2 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr6:30954602 G>A maps to NM_001010909.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr11:1268537 G>A maps to ENST00000447027 S3479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:1281624 T>G did not map to a codon.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr11:1253367 C>A maps to ENST00000447027 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr11:1264091 C>T maps to ENST00000447027 R1997R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:1027278 G>A maps to NM_005961.2 N740N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr23:3238718 A>G did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr17:4451583 C>T maps to NM_001105538.1 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:67477039 T>A maps to NM_001080416.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr20:42328635 C>T maps to NM_002466.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr12:102046969 G>T maps to NM_002465.2 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr19:50939281 G>T maps to NM_004533.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr17:48600412 A>T maps to NM_032133.4 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr2:16082257 A>G maps to NM_005378.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr3:38180514 C>T maps to NM_001172567.1 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:8424547 G>A maps to ENST00000360416 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr17:8416921 C>T maps to ENST00000360416 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr17:10258305 C>G maps to NM_003802.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:10267724 C>T maps to NM_003802.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:10227378 A>T maps to NM_003802.2 L965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr19:50783388 C>T maps to NM_001145809.1 H1376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:108110609 G>A maps to NM_014981.1 S1829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr17:10433385 G>A maps to NM_017534.5 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr17:10426830 G>A maps to NM_017534.5 I1818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr17:10554907 G>A maps to NM_002470.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr17:10366487 G>A maps to NM_017533.2 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr14:23898981 A>G did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr20:33577861 C>T maps to NM_020884.3 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr17:10312635 A>T maps to NM_002472.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr17:10300167 A>T maps to NM_002472.2 S1438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr22:36702091 G>T maps to NM_002473.4 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr20:35177591 C>T maps to NM_006097.3 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr16:46766186 C>T maps to NM_182493.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr5:16764478 G>T maps to NM_012334.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:16701575 G>A maps to NM_012334.2 C976C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:16877716 C>G did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr13:109793008 C>T maps to NM_015011.1 H1461H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr13:109793008 C>T maps to NM_015011.1 H1461H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr17:27437603 G>T maps to NM_078471.3 G979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr22:26423001 C>G maps to ENST00000407587 L2356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr22:26400726 C>T maps to ENST00000407587 Q2128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:26422671 C>T maps to ENST00000407587 P2246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr12:57440665 G>A maps to NM_005379.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr17:1370771 A>C did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr15:59515312 C>G maps to NM_004998.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:59501014 G>A maps to NM_004998.2 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr15:52606370 T>C maps to ENST00000358212 P1813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr18:47500736 C>T maps to NM_001080467.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr15:52500780 G>T maps to NM_018728.3 L1452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr11:76890089 G>T did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:76867020 C>T maps to NM_000260.3 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr11:76891502 G>A maps to NM_000260.3 K890K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr11:76903187 C>T maps to NM_000260.3 N1339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr15:72190907 A>G maps to ENST00000424560 P1312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr15:72192124 T>G maps to ENST00000424560 R1125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr19:17322845 G>A maps to NM_004145.3 T2067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr1:171605340 G>C maps to NM_000261.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr19:46394099 C>T maps to NM_001012643.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:59125679 A>G maps to NM_001085487.1 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr20:62851190 C>T maps to NM_004535.2 D699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:1805512 T>C maps to ENST00000399161 E1077E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:59082639 G>A maps to NM_198055.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:48576973 G>A maps to NM_153029.3 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:33095587 T>C did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr13:21306118 T>C maps to NM_174928.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr23:153198017 C>T did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:64813974 G>A maps to ENST00000340252 Y592Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr12:57485519 T>G maps to NM_005967.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:59668190 C>T maps to NM_199290.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:59668145 A>G maps to NM_199290.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr16:66857504 T>C did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr4:164050120 G>A maps to NM_138386.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr4:164061508 T>C maps to NM_138386.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:40695934 C>T maps to NM_000263.3 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr13:101881860 T>C maps to NM_052867.2 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr19:13988493 A>G maps to NM_001098622.1 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr23:92927723 C>T did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr7:102769016 C>T maps to ENST00000455523 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr8:144660317 G>T maps to ENST00000276844 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:80443513 C>T maps to ENST00000374611 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr8:18080419 T>C maps to NM_001160176.1 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr1:201781617 G>T maps to ENST00000367296 E1684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr11:19954836 G>A maps to ENST00000396087 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:78604233 C>T maps to NM_014903.4 C2343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr12:78574709 A>G maps to NM_014903.4 T1837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr12:78591181 G>C did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr2:15691632 A>G maps to NM_015909.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr13:35733739 A>C maps to ENST00000400445 T1144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr2:203972838 G>A maps to NM_001114132.1 W597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:47032942 G>T maps to NM_015175.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:148025785 G>A maps to ENST00000310701 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr21:22658661 A>T maps to NM_004540.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:19338432 A>C maps to NM_004386.2 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr12:6638742 C>A maps to NM_014865.3 R1213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:6637491 T>C maps to NM_014865.3 A1099A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr19:39687742 C>T maps to NM_001001414.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr2:24991158 C>T maps to NM_003743.4 L1409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr2:24930396 G>A maps to NM_003743.4 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:71126195 A>C maps to NM_006540.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr20:46254224 G>A maps to NM_181659.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr10:51585172 G>A maps to NM_001145260.1 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr10:51586275 A>T maps to NM_001145260.1 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr17:15971430 T>G maps to ENST00000395857 T1522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:15964733 A>G maps to ENST00000395857 S1969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:16089948 G>C maps to ENST00000395857 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr12:124887101 C>T maps to NM_006312.4 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr12:124829473 G>A maps to NM_006312.4 T1468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:124848290 A>G maps to NM_006312.4 N954N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr6:41303623 C>T maps to NM_004828.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:8350136 T>C maps to ENST00000402554 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr17:8370301 T>C maps to ENST00000402554 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr5:149921205 C>T maps to NM_001543.4 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr4:115767017 G>A maps to NM_022569.1 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:5897009 T>A did not map to a codon.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr19:5897009 T>A did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr15:41689068 G>A maps to NM_016013.2 H63H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr6:97344646 A>G maps to NM_014165.3 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:47002142 T>G did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:179322635 G>A maps to NM_002492.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr19:14677077 C>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:161183706 C>A maps to NM_004550.4 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr11:47605942 G>A maps to NM_004551.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr21:44317077 T>C maps to NM_021075.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:152397246 C>T maps to NM_001164507.1 L6917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr2:152372971 C>A did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:152512858 C>T maps to NM_001164507.1 E2101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr2:152390039 G>T maps to NM_001164508.1 A7111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr2:152382498 G>A maps to NM_001164507.1 V7378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr10:21309108 G>A maps to NM_213569.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr18:56056372 T>C maps to NM_001144967.1 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:29885428 T>C maps to NM_021076.3 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr8:24771575 C>T maps to NM_005382.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr4:178243704 C>G maps to NM_018248.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr14:75558058 G>A maps to NM_033116.4 R786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr2:233898966 C>T maps to NM_005383.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:182543428 C>A maps to NM_002500.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:31377934 G>A maps to NM_022728.2 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:29533388 G>A maps to NM_001042492.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr22:30069349 T>C maps to NM_181832.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr22:30000102 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr22:30038222 C>A maps to NM_181832.2 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr22:30050708 A>T maps to NM_181832.2 K171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:30051665 G>A did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr22:30057328 G>A did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr1:204985553 G>T maps to ENST00000367172 E1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:69727577 C>T maps to NM_138713.2 Q1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr1:61554263 T>C maps to NM_001145512.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr10:104156716 C>T maps to NM_001077494.1 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr14:35872503 A>G maps to NM_020529.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr11:129747270 G>A maps to NM_006165.3 D532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr17:47588005 G>T maps to NM_002507.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr3:25773884 A>T maps to NM_018297.3 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:25770622 C>T did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr5:177580731 G>T maps to NM_017838.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:49463423 C>G maps to NM_032316.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:236195869 A>G maps to NM_002508.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:51219340 T>A maps to NM_020921.3 T1615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr4:48037861 T>C maps to NM_207330.1 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr8:99215363 A>T maps to NM_024759.1 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr5:156899850 C>T maps to NM_001099287.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr9:107531255 T>A maps to NM_018376.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:52505968 C>T maps to NM_007184.3 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:23942483 G>A maps to NM_020345.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr20:21376575 G>T maps to NM_033176.1 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr5:172659919 C>G maps to NM_004387.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr5:172659919 C>G maps to NM_004387.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr4:13545663 G>A maps to NM_001189.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr23:70387071 C>T did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:70387443 G>C did not map to a codon.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr24:16952766 C>T did not map to a codon.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr24:16952766 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr24:16952766 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr24:16952766 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr17:26490599 A>G maps to NM_016231.4 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr16:3598163 T>C maps to ENST00000448023 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:247588674 C>T maps to NM_004895.4 Q644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr19:56539071 C>T maps to NM_153447.4 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr11:281107 G>C maps to NM_138329.1 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr19:55452314 C>T maps to ENST00000446217 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:55450842 G>A maps to ENST00000446217 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr19:56487642 C>T maps to NM_176811.2 N950N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr6:142396952 G>A maps to NM_002511.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr3:48336156 T>C maps to NM_005793.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:48338259 C>T maps to NM_005793.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:96121494 T>C maps to NM_022451.9 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr7:30492405 G>A maps to NM_006092.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:6610593 G>A maps to NM_024654.4 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr10:103917062 A>G maps to ENST00000405356 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr7:156742604 A>G maps to NM_138400.1 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:203155145 T>C maps to NM_015934.3 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr19:50063189 C>G did not map to a codon.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:139418247 G>A maps to NM_017617.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr1:120506374 G>T maps to NM_024408.2 C579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr19:15303026 G>T maps to NM_000435.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr6:32188965 G>A maps to NM_004557.3 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr6:32191690 T>C maps to NM_004557.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:32169042 C>T maps to NM_004557.3 R1330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:79913364 G>A maps to NM_178493.5 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:100099032 T>C did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:66191470 C>A maps to NM_178864.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:108032023 A>G maps to NM_002519.2 S1263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:79860377 A>G maps to NM_148896.3 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr20:57282246 A>C maps to NM_024663.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:45668144 A>G maps to NM_006310.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr17:45669356 A>T maps to NM_006310.3 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr4:73012853 C>G maps to NM_004885.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr3:132418234 A>T maps to ENST00000393156 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:5935028 G>A maps to NM_015102.2 A983A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr1:153651703 A>G maps to NM_000906.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr9:35792785 T>C maps to NM_003995.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr15:73884464 G>A maps to NM_012428.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:38253600 A>G maps to NM_021724.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr15:72104833 C>T maps to NM_014249.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr9:127262608 C>A maps to NM_004959.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr7:107808821 G>A maps to ENST00000379032 S1071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:52256296 C>A maps to NM_002525.2 E1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr21:16337669 A>G maps to NM_003489.3 D948D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr23:105167296 A>G did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr10:33543117 G>A maps to NM_003873.5 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr2:50574024 G>C maps to NM_138735.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr11:64428552 A>T maps to NM_015080.3 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr5:176696647 C>T maps to NM_022455.4 N1783N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr5:176637985 C>T maps to NM_022455.4 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr5:176639041 T>C maps to NM_022455.4 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr17:44806263 G>A maps to NM_006178.2 Q624Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr5:6600167 G>A maps to NM_017755.5 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr19:49167944 A>C maps to NM_145807.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr1:156843560 C>T maps to NM_002529.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:156851383 C>T maps to NM_002529.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr23:51075839 C>T did not map to a codon.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr23:51239273 G>A did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr1:229631731 G>T maps to NM_018230.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr11:47819409 A>C maps to NM_015231.1 A1070A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr11:47837536 A>G maps to NM_015231.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr9:131755474 G>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:135290918 A>G maps to NM_015135.2 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr7:135307640 C>T maps to NM_015135.2 R1483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:13399892 G>A maps to NM_024923.2 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:154033033 T>C maps to NM_207308.2 E944E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr9:134004847 G>T maps to ENST00000451030 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr22:45574341 A>G maps to NM_007172.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr19:50412017 C>T maps to NM_012346.4 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:50412995 C>T maps to NM_012346.4 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr16:56792501 T>C maps to NM_014669.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr15:41669494 C>T maps to NM_016359.3 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr1:224468832 G>A maps to NM_002533.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr23:102332663 C>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr23:102337710 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr23:101096013 T>A did not map to a codon.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr19:17571477 T>G maps to NM_138454.1 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr23:108780249 G>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:108779192 A>C did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr23:41333523 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr12:121465529 C>A maps to NM_003733.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr1:228467537 C>G maps to NM_001098623.1 L2471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr1:228473854 G>C maps to NM_001098623.1 R3027R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr1:228469851 G>T maps to NM_001098623.1 E2806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:220420910 G>A maps to NM_015311.2 A1480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:28090199 T>A did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr23:128678969 T>G did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr9:131256868 T>C maps to NM_153435.1 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr23:123637523 G>T did not map to a codon.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr23:123515036 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:123518586 G>C did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr23:123519704 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:123680888 T>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr4:183713662 C>T maps to NM_001080477.1 V1946V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr23:13754639 T>C did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr7:44747233 T>C maps to ENST00000444676 N965N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr16:56485679 T>C did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr23:70782730 C>T did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr9:127572162 C>T maps to NM_182487.2 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr1:161989777 C>G maps to ENST00000451379 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:67283720 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr23:153496171 C>A did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr7:128415146 C>T maps to NM_001708.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr6:47754338 C>A maps to ENST00000489301 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr10:13160993 C>T maps to NM_021980.4 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:158576302 C>T maps to NM_001004478.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr14:20666033 C>T maps to NM_001005503.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr9:35869822 C>T maps to NM_001004487.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr9:125391499 G>A maps to NM_001004450.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr9:125486285 T>C maps to NM_001005235.1 Y6Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr9:125315954 C>T maps to NM_001004457.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr11:6789369 G>T maps to NM_001004490.1 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:247694871 T>A maps to NM_198074.4 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr1:247751787 T>C maps to NM_001001915.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:248112584 G>A maps to NM_001001963.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:248309354 G>A maps to NM_001004690.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:248458379 G>A maps to NM_001004692.1 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:248059781 G>A maps to NM_001001957.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:49974075 C>A maps to NM_001001955.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr11:48347235 C>T maps to NM_001004702.1 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr15:102346641 G>T maps to NM_001005326.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr14:20345256 C>A maps to NM_001005501.1 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr11:55418711 C>T maps to NM_001004059.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr11:4929157 C>T maps to NM_001004749.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:4936272 G>A maps to NM_001005238.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr11:4904095 A>C maps to NM_001004759.1 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:6191109 G>A maps to NM_001004052.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr11:5068081 C>T maps to NM_001001916.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:6048448 A>G maps to NM_001001917.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr3:97852335 G>A maps to NM_001005338.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:158735809 G>A maps to NM_001005185.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:158517502 A>T maps to NM_001005189.1 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr19:14991894 G>A maps to NM_030901.1 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:124310918 C>T maps to NM_012378.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr11:124135726 C>T maps to ENST00000341493 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr11:124095996 C>A maps to NM_001007249.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:55904465 C>T maps to NM_001004064.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:142724165 C>G maps to NM_001001658.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:52849238 G>A maps to NM_004153.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr2:201790561 C>A maps to NM_006190.4 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr18:21819190 C>A maps to NM_080597.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr18:21914247 T>C maps to NM_080597.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr11:3143329 T>C did not map to a codon.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr2:179255927 G>A maps to ENST00000392505 K835K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr1:36915922 C>T maps to ENST00000356637 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:83994294 G>A maps to NM_013370.3 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr4:109571837 C>T maps to ENST00000512478 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr23:38260573 C>A did not map to a codon.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr17:72942795 G>A maps to NM_178233.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:20233030 T>C maps to NM_015207.1 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr15:31818595 G>A maps to ENST00000382902 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr2:42990998 C>A maps to NM_148962.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr8:107718928 T>C maps to NM_001198533.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr3:8809351 G>T maps to NM_000916.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr3:8809675 G>A maps to NM_000916.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:121648005 C>T maps to NM_002560.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr10:74810905 G>A maps to NM_000917.3 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr5:131546091 G>T maps to NM_001142599.1 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr8:101719225 C>G did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr13:25672006 A>G maps to NM_030979.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr13:25672006 A>G maps to NM_030979.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:40029529 C>T maps to NM_001135653.1 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr11:66008915 T>A maps to NM_018026.2 Y816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr14:105833602 C>T maps to ENST00000458164 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr1:17609567 G>A maps to NM_016233.2 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr23:110366493 G>A did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr4:169433374 G>A maps to NM_001166108.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr12:56720459 T>C maps to NM_001127460.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr11:93911575 C>G maps to NM_015368.3 Y121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr10:135193908 C>T maps to NM_152911.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:176525850 G>A maps to NM_020318.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr10:89501011 C>T maps to NM_001015880.1 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr20:49367022 T>C maps to NM_032521.2 *373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr6:162864431 C>T maps to NM_004562.2 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr4:75937686 G>C maps to NM_015393.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:14678280 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:122414351 G>A maps to NM_017554.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:122437695 A>G maps to NM_017554.2 T1566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr3:122436992 C>G maps to NM_017554.2 S1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr3:122354764 C>T maps to NM_001113523.1 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr13:25029239 T>C maps to NM_006437.3 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr13:25020899 C>T did not map to a codon.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr13:25067775 T>C maps to NM_006437.3 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr15:72552950 G>T maps to NM_020214.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr22:44564536 C>T maps to NM_001003828.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr23:150828199 G>T did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:223066672 C>T maps to NM_181459.3 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:113984804 G>A maps to NM_003466.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr3:52678739 A>G maps to ENST00000296302 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr3:52649429 T>A maps to ENST00000296302 K621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr3:52584608 A>T maps to ENST00000296302 Y1575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr3:52651554 C>T did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr1:154920115 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr11:66636399 C>A maps to NM_022172.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:66636375 G>T maps to NM_022172.2 Y321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:70314949 A>G maps to NM_006196.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr13:100925448 G>A did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:91456391 C>T did not map to a codon.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr23:91133624 C>A did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:91873699 C>T did not map to a codon.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr10:55617002 C>A maps to NM_001142763.1 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr10:55626410 G>A maps to NM_001142763.1 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:55583105 G>C maps to NM_001142763.1 L1467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:138450854 G>A maps to NM_019035.3 H796H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr23:99661615 G>C did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:140176264 C>A maps to NM_018905.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr5:140188709 C>T maps to NM_018907.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:140222315 G>C maps to NM_018911.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr5:140223200 G>A maps to NM_018911.2 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr5:140307712 A>G maps to NM_018898.3 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr5:140595248 T>C maps to NM_018933.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr5:140605206 G>C maps to NM_018934.2 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:140625664 T>C maps to NM_018935.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr5:140563806 C>A maps to NM_020957.1 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr5:140481177 T>C maps to NM_018937.2 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr5:140531289 C>T maps to NM_018939.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr5:140712437 A>G maps to NM_018912.2 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr5:140711927 G>A maps to NM_018912.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr5:140800832 G>A maps to NM_018914.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:140802437 G>C maps to NM_018914.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr5:140811804 G>A maps to NM_003735.2 E493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:140724209 A>T maps to NM_018916.3 K204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr5:140724919 G>T maps to NM_018916.3 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr5:140745639 C>T maps to NM_018918.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr5:140753887 C>T maps to NM_018919.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr5:140772926 C>T maps to NM_032088.1 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr5:140751664 G>A maps to NM_018924.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:140856909 G>A maps to NM_002588.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr5:140865324 C>G maps to NM_018928.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:82877723 A>G maps to NM_015885.3 K595K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr11:82879803 A>T maps to NM_015885.3 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr11:82877726 A>G maps to NM_015885.3 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr20:56140433 C>T maps to NM_002591.3 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:56140805 C>A maps to NM_002591.3 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr7:82784462 C>T maps to NM_033026.5 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr7:82763634 A>G maps to NM_033026.5 N1077N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr7:82532015 A>G maps to NM_033026.5 P4493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr3:142607734 T>G maps to NM_013363.3 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:101933521 G>A maps to NM_002570.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr15:101865151 A>G maps to NM_002570.3 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:117077796 G>A maps to NM_004716.2 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:117097975 C>A maps to NM_004716.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:195974372 G>A maps to NM_005017.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:79865646 A>G did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr6:170893453 C>T maps to NM_002598.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr19:34895340 G>T maps to NM_032346.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr10:112655818 A>G maps to NM_014456.4 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr9:125582791 G>A maps to NM_005388.4 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr2:178936707 G>A maps to NM_016953.3 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr7:31877506 C>T maps to NM_001191057.1 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr4:120486566 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr10:95400271 G>A maps to NM_006204.3 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr7:148702374 C>T maps to NM_004911.4 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr2:10927528 A>T maps to ENST00000381611 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:20376784 G>A maps to NM_174924.1 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:131602210 C>T maps to NM_003687.3 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr8:94934632 C>T maps to NM_001161778.1 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr16:15130100 C>A maps to NM_015027.2 S779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:31983431 C>G maps to NM_178140.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:32108144 G>A maps to NM_178140.2 L2808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr10:119044854 G>A maps to NM_173791.3 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:119134717 G>T maps to NM_173791.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:145761287 T>C maps to NM_002614.3 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr3:73673577 G>C maps to NM_015009.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr3:73673577 G>C maps to NM_015009.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr12:41585334 C>T maps to NM_001164595.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr1:160181402 C>A maps to ENST00000368075 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr6:4128066 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr1:32100868 T>C maps to NM_012392.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr1:32100954 C>A maps to NM_012392.3 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr17:4575450 T>C maps to ENST00000301396 E1089E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr17:4575081 C>T maps to ENST00000301396 E1212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:8047042 T>G maps to NM_002616.2 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:239184525 A>C maps to NM_022817.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr2:239162230 G>A maps to NM_022817.2 T811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr2:239186361 C>T maps to NM_022817.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr1:7845602 A>C maps to ENST00000377532 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:7854050 T>C maps to ENST00000377532 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:92151472 A>G maps to NM_000466.2 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:92119226 T>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:2341813 A>C maps to NM_153818.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr1:10678474 G>A did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr1:10535060 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr12:7362623 T>G maps to NM_001131023.1 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr3:48577176 C>A maps to NM_004567.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr3:48576037 G>T maps to NM_004567.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr21:45743722 C>T maps to NM_002626.4 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr12:48538848 C>A maps to NM_001166686.1 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr10:3172123 A>G maps to NM_002627.3 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr10:99192202 C>T maps to NM_002629.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr19:15587342 G>T maps to NM_052890.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr1:153279660 G>C maps to NM_052891.1 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr11:74085549 G>A maps to NM_173582.3 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:118370496 C>T did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr6:13230365 C>A maps to NM_030948.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:144086446 G>C maps to NM_001100164.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr6:170117954 C>A maps to NM_018288.3 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr23:46918437 A>G did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr23:53966768 C>G did not map to a codon.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr23:71829513 C>T did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr23:71822084 T>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:71886082 G>A did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:71802351 G>A did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr23:18972369 A>G did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:18919657 C>A did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr12:76424936 T>C maps to NM_007350.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr17:47302351 G>T maps to NM_001143804.1 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr2:170557974 T>A maps to NM_001008489.3 L165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr4:41748006 T>G maps to NM_003924.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr10:60936660 C>A maps to NM_032439.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr4:25235820 C>A maps to NM_018323.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr22:21073054 G>A maps to NM_058004.2 S1666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr22:21119516 C>T maps to NM_058004.2 W757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr15:68479998 T>C maps to NM_016166.1 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr9:35089136 A>C maps to NM_032634.2 G1074G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr16:624547 C>T maps to NM_148920.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:207105905 C>A maps to NM_002644.3 G635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:207106512 T>C did not map to a codon.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr1:207105816 C>G maps to NM_002644.3 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:27121058 C>T maps to NM_017837.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:196675119 A>T maps to NM_025163.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:49950352 A>G maps to NM_017916.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:138456587 T>C maps to NM_006219.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:67576766 T>G maps to ENST00000396611 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr5:67588177 A>G maps to ENST00000396611 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr19:18279616 G>A maps to NM_005027.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr7:99972036 C>T maps to NM_013439.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr6:37139028 C>G maps to ENST00000373507 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:23003186 G>A maps to NM_005028.4 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr17:65665780 T>C did not map to a codon.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr11:67267650 G>A maps to NM_004910.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr11:67265786 G>A maps to NM_004910.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr12:123479958 C>T maps to NM_020845.2 Q677Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr17:6375989 C>T maps to NM_031220.3 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr11:94341804 C>T maps to NM_152431.2 D632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr23:68382202 G>A did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr16:2168071 G>A maps to NM_001009944.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr16:2153594 G>A maps to NM_001009944.2 D2821D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr16:2168404 G>A maps to NM_001009944.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr16:2142547 G>A maps to NM_001009944.2 Y3734Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr16:2168071 G>A maps to NM_001009944.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr22:46654193 G>A maps to NM_006071.1 Q1676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr6:51930864 A>G maps to NM_138694.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr6:51882413 G>A maps to NM_138694.3 F1798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr6:51889789 G>A maps to NM_138694.3 V1606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr8:110420392 G>C maps to ENST00000426474 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr8:110488891 C>G maps to ENST00000426474 Y2971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:110451258 G>A maps to ENST00000426474 K1298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:159490675 G>T maps to NM_003628.3 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr1:20304928 G>A maps to NM_001161728.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:20416293 G>A maps to NM_000929.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr9:26925950 C>A maps to NM_001031689.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr20:8608960 T>G maps to NM_015192.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr15:40594159 T>A maps to NM_004573.2 K194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:64034707 C>T maps to NM_000932.2 Q1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr10:95849075 A>G maps to NM_001165979.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:2426374 C>T maps to NM_014638.2 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:2415963 C>T maps to NM_014638.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:2418422 G>A maps to NM_014638.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr3:17053309 G>C maps to NM_001144382.1 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr3:111432756 C>T maps to ENST00000312791 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:171394618 G>A maps to NM_002662.3 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr3:171395428 G>A maps to NM_002662.3 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr8:145001216 C>T maps to NM_201380.2 A1428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr8:144998456 C>T maps to NM_201380.2 L2017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr8:144995792 C>T maps to NM_201380.2 A2869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr8:144997532 C>G maps to NM_201380.2 L2325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr7:30094388 T>C maps to ENST00000440706 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr5:163210 A>G maps to NM_052909.3 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:40821476 C>A maps to NM_024927.4 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr9:19126157 C>A maps to NM_001122.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:4511772 G>A maps to NM_001080400.1 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr20:21142792 T>A maps to NM_018474.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr4:128813595 T>C maps to NM_014264.4 Y705Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr3:145803002 A>T maps to NM_182943.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr4:155465647 T>C maps to NM_002669.2 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:155470081 T>C maps to NM_002669.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr23:114874763 A>G did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr23:114883785 G>C did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:146167109 C>T maps to ENST00000497985 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr20:44534918 G>A maps to NM_006227.2 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr20:44539885 C>T maps to NM_006227.2 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr23:153700939 C>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr23:153696320 G>A did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr3:48447206 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr3:48459372 C>A maps to NM_001130082.1 T1107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr22:50716443 T>C did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr23:153037077 G>C did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr23:153037466 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:129324249 C>G maps to NM_015103.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr3:129281630 A>G maps to NM_015103.2 L1608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr6:89859123 T>A maps to NM_001010853.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr20:56227615 C>T maps to NM_020182.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr1:156209391 A>C maps to NM_007221.3 *206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:74325642 G>A maps to NM_033238.2 K515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr15:74327952 G>A maps to NM_033239.2 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:152937047 G>C did not map to a codon.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr23:152937463 A>T did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr23:152938462 C>G did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:152938522 C>A did not map to a codon.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr10:118357346 T>C maps to NM_006229.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:26365720 C>T maps to NM_007257.5 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr23:152226010 A>G did not map to a codon.
Multiple mappings detected for codon TCGA-MH-A562-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr23:7868820 A>G did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:7615222 G>A maps to NM_001166111.1 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:7619509 G>A maps to NM_001166111.1 Q855Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:89793800 T>C maps to NM_006813.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:74981181 G>C maps to NM_001099271.1 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr19:14044011 G>A maps to NM_024825.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr7:131241088 C>T maps to NM_001018111.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr3:127379563 A>G maps to NM_015720.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr3:127379598 T>A maps to NM_015720.2 L243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:151381039 G>A maps to NM_015100.3 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:24744125 T>A did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr23:24906192 C>G did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr23:24750525 T>A did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr12:133235891 A>G maps to ENST00000455752 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr17:7404999 G>A maps to NM_000937.4 K767K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr4:57891053 A>G maps to NM_000938.1 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:57503975 G>A maps to NM_032940.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr11:840427 G>A maps to NM_021128.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr20:18448194 G>A maps to NM_006466.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr7:72416769 G>A maps to ENST00000434423 K1249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr14:77765101 G>A maps to NM_013382.5 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr8:99152323 G>T maps to NM_015029.2 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:75615289 T>C maps to NM_000941.2 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr22:16287579 G>T maps to NM_001136213.1 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr23:82764045 G>T did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr4:147561257 T>C maps to NM_004575.2 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr5:145719655 G>T maps to NM_002700.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr5:93076681 A>T maps to NM_153216.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:39446254 C>T maps to NM_007252.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr9:4662476 C>A maps to NM_203453.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr6:35392131 A>C maps to NM_006238.4 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:12447396 G>C maps to NM_015869.4 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr12:81661719 A>G maps to NM_003625.2 L1153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:203025586 C>A maps to ENST00000367238 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr12:27787952 T>C maps to NM_003622.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr15:64454354 T>C did not map to a codon.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr5:122359695 T>A maps to NM_000943.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:60749543 G>T maps to NM_177952.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr2:44457730 T>C maps to NM_002706.4 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr2:44429129 A>G maps to NM_002706.4 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr17:58740445 G>T maps to NM_003620.3 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr17:56833489 G>A maps to NM_014906.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr3:52282682 C>T maps to NM_144641.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:46002035 C>T maps to NM_001080401.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:204379051 A>G maps to NM_032833.3 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr1:204379182 C>A maps to NM_032833.3 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr20:37536821 G>T maps to NM_015568.2 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:135825107 T>C maps to NM_002718.4 A1091A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:102323021 G>A did not map to a codon.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr19:8563523 C>A maps to NM_032152.4 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:12854435 G>C maps to NM_023013.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr1:12835788 C>T maps to NM_001080830.1 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:13497725 A>C maps to NM_001045480.1 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:12919094 A>C maps to NM_023014.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:11420474 A>G maps to NM_006249.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr11:82560213 T>C maps to NM_199418.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr11:129817184 G>A maps to NM_020228.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr21:43298958 C>G maps to NM_022115.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr21:43241556 C>T maps to NM_022115.3 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:3334450 C>T maps to NM_022114.3 D917D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr16:90127012 C>A maps to NM_001098173.1 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr2:44566371 G>A maps to NM_001171603.1 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr2:44566450 A>G maps to NM_001171603.1 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr20:47271872 G>A maps to NM_020820.3 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr20:47258947 G>A maps to NM_020820.3 N1227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr20:47361657 G>A maps to NM_020820.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:72360283 G>A maps to NM_005041.4 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr20:62191641 T>C maps to NM_001037335.2 V2513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr20:62197378 G>A maps to NM_001037335.2 I932I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:42858292 G>A maps to NM_153026.2 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr6:57467162 G>C maps to NM_000947.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr1:84663464 T>C maps to NM_182948.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:71628288 G>A maps to NM_002732.3 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr9:71628294 G>A maps to NM_002732.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr7:151262971 C>T did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr17:66526490 G>A maps to NM_212472.1 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:106799966 T>A maps to NM_002736.2 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr16:23848698 C>T maps to NM_002738.6 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr3:53220040 A>T maps to NM_212539.1 K362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr3:170002333 T>C maps to NM_002740.5 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr19:11558372 A>G maps to ENST00000436195 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr1:2066776 C>T maps to NM_002744.4 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr8:48744422 G>T maps to NM_006904.6 L2738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:48826504 G>A maps to NM_006904.6 R913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr4:82061796 A>T maps to NM_006259.1 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr23:3544549 G>C did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr21:48083429 G>A maps to NM_206962.1 W411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:107599741 C>T maps to NM_018137.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr16:68386312 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr20:33762616 A>T maps to NM_006404.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr3:93646099 C>T maps to NM_000313.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr14:45579917 A>G maps to NM_017922.3 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr20:62648173 T>C maps to NM_012469.3 H541H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr20:62642771 G>C maps to NM_012469.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr12:49690228 C>T maps to ENST00000451891 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:12840842 C>G did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:50097990 G>C maps to NM_020719.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr16:30666136 G>A maps to NM_024031.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr19:42814765 C>T maps to NM_199285.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr16:863366 C>T maps to NM_001013638.1 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr23:150869295 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr3:9989479 G>C maps to NM_207351.3 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr4:119273491 A>T maps to NM_003619.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr9:33796656 C>T maps to NM_007343.3 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr6:84233612 C>T maps to NM_153362.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr16:31098020 C>T maps to NM_001039503.2 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr8:10390472 G>A maps to NM_198464.3 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:841047 C>T maps to NM_002777.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr9:79325025 G>A maps to NM_015225.2 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr5:139193772 T>C maps to NM_032289.2 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:139197068 C>T maps to NM_032289.2 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr19:43585216 A>T maps to ENST00000449000 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr19:43237191 G>T maps to NM_021016.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:43689068 C>A maps to ENST00000270059 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr19:43773526 C>A maps to NM_002784.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr11:14536020 C>A maps to NM_148976.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:151372077 G>A maps to NM_002796.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:151372468 G>A maps to NM_002796.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr17:40726132 G>T maps to NM_016556.2 C107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr19:40486338 T>C maps to NM_006503.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr19:40478460 A>G maps to NM_006503.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr17:65362548 G>C maps to NM_002816.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:162227814 T>C maps to NM_005805.4 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr3:184019769 C>T maps to NM_002808.3 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr3:184019769 C>T maps to NM_002808.3 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:123591453 T>C maps to NM_005047.2 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr3:64004273 C>A did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr14:24613238 C>T did not map to a codon.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr2:54176407 A>G maps to NM_014614.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr10:124740204 A>G maps to NM_153336.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr15:77328194 A>G maps to NM_003978.3 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr1:28477259 G>A maps to NM_001164721.1 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:99022429 G>A maps to NM_001198879.1 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:99022813 G>A maps to NM_001198879.1 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr23:23411324 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr1:11562883 G>T maps to NM_020780.1 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr10:89624274 C>T maps to NM_000314.4 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:78959186 G>A maps to NM_000959.3 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:114332439 A>G maps to NM_001146108.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr3:46939562 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:141745381 C>T maps to NM_005607.4 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr6:43044270 T>G maps to NM_002821.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:43112986 G>A maps to NM_002821.3 E819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:87691258 C>T maps to NM_080685.2 V1575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:214556992 G>A maps to NM_005401.4 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr1:114402064 A>G maps to NM_015967.5 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr9:112185014 A>G maps to NM_002829.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr20:2998528 C>T maps to NM_002836.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr20:3016488 G>T maps to NM_002836.3 V700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr12:71002987 G>A maps to NM_001109754.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:198704381 G>A did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:198678921 C>T maps to ENST00000271610 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr9:8507426 C>G maps to NM_002839.3 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr10:129859260 C>A maps to NM_006504.4 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:44063473 C>T maps to NM_002840.3 V623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:44063521 C>T maps to NM_002840.3 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:44083551 C>T maps to NM_002840.3 V1447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr18:8379244 G>A maps to NM_001105244.1 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr18:8378411 G>T maps to NM_001105244.1 R1204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr18:8314789 C>T maps to NM_001105244.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:220164915 A>G maps to NM_002846.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:157414138 G>A maps to NM_002847.3 C753C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:5220166 T>A did not map to a codon.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:5214699 G>T maps to NM_002850.3 R1456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr20:40710578 G>A maps to ENST00000373198 D1427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr20:41100969 G>A maps to ENST00000373198 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr20:40730778 G>A maps to ENST00000373198 N1255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr7:121651530 C>T maps to NM_002851.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr7:121681009 G>A maps to NM_002851.2 V1926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr7:121652843 T>C maps to NM_002851.2 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:130476384 C>T maps to NM_001002913.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr8:144898884 G>A maps to NM_078480.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr8:144902838 T>C maps to NM_078480.1 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:45162148 C>T maps to NM_006505.3 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:45381870 T>C maps to NM_002856.2 Y478Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:110830988 G>A maps to NM_015480.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:161049404 C>T maps to NM_030916.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr5:159520918 G>A maps to NM_001130864.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr10:134218415 C>T maps to NM_138499.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:120653398 G>A maps to NM_001080855.1 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr11:64522810 G>A maps to NM_005609.2 Y263Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:158912062 T>G maps to NM_152501.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr17:74288034 G>A maps to NM_032134.1 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr11:32954929 C>A maps to NM_001076786.1 S580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:113795753 A>G maps to ENST00000485050 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:57674167 T>C maps to ENST00000438036 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:37729418 C>A maps to NM_001002814.2 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr16:570231 C>T maps to NM_014700.3 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr16:568987 G>A maps to NM_014700.3 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:238494740 C>A maps to NM_022449.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr15:55516127 T>A maps to NM_183235.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr11:87908438 G>A maps to NM_022337.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr23:69502406 G>T did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:130738209 G>A maps to NM_032144.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr19:42461227 G>T maps to NM_006423.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr9:125751641 C>T maps to NM_012197.3 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr14:24734892 C>T maps to NM_182836.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:114391750 G>A maps to ENST00000409875 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr5:131953818 A>G maps to NM_005732.3 A1074A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:131976366 T>C maps to NM_005732.3 L1208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:51667681 C>T maps to NM_015106.2 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:51697405 C>T maps to NM_015106.2 D1458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:110969391 A>G maps to NM_152442.3 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr7:4841356 G>A maps to NM_018059.4 G923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr6:150342041 T>A maps to NM_130900.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr5:34757667 C>T maps to NM_001145521.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr23:17819165 T>G did not map to a codon.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr14:36143778 A>C maps to NM_194301.2 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:20491912 A>T maps to NM_020343.3 L1638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr16:67840334 C>T maps to NM_020850.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr2:109392303 T>C maps to NM_006267.4 I2803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr2:109379712 T>C maps to NM_006267.4 N906N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr1:21936723 G>C maps to NM_001145658.1 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:21952820 G>T maps to NM_001145658.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr9:134505711 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr2:204305854 C>T maps to ENST00000374493 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:47469614 C>A maps to NM_005055.3 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:167937679 G>T maps to NM_002887.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr9:85624581 A>T maps to NM_152573.2 Y311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:79264260 G>A maps to NM_002891.4 R1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr8:53570006 C>T maps to NM_014781.4 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr8:53569321 G>A maps to NM_014781.4 Q1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr23:16864058 A>G did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr18:20562276 G>A maps to ENST00000360790 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr8:94747483 A>G maps to NM_203390.2 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:110882977 T>C maps to NM_022768.4 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:114385204 G>A maps to NM_016196.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:23374813 C>G did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr13:79945131 C>T maps to ENST00000438737 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr23:48434993 T>G did not map to a codon.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr23:48434951 T>G did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:36128156 G>A maps to NM_024321.3 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:238722325 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:178977554 C>T maps to ENST00000456670 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr11:66444484 G>A maps to NM_031492.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr3:50147867 T>C maps to NM_005778.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr3:50155813 T>A maps to NM_005778.2 Y791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr22:36206006 A>G maps to NM_001082578.1 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr23:135960072 C>T did not map to a codon.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr23:129546640 A>T did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr4:26426304 C>T maps to NM_005349.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr20:43940943 C>T maps to NM_014276.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr13:50115836 G>A maps to NM_018191.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr13:50134122 G>C maps to NM_018191.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr15:91500667 G>A maps to NM_033544.2 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr11:66613412 A>C maps to NM_005133.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr4:76439475 T>C maps to NM_015436.2 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:31922208 T>C maps to ENST00000375425 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr14:68157016 G>A maps to NM_016026.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr14:68191258 C>T maps to NM_152443.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:56118169 A>T maps to NM_002905.3 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr19:10132217 C>A maps to NM_015725.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:65423174 A>G maps to NM_021975.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr7:103234872 G>C maps to ENST00000428762 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr7:103159948 T>C maps to ENST00000428762 L2561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:153200790 G>T did not map to a codon.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr7:150069171 C>A maps to NM_001099695.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:139235872 G>T maps to ENST00000367663 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr1:8415615 G>T maps to NM_012102.3 P1510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr6:111701284 C>A maps to NM_002912.3 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr4:39325031 C>T maps to ENST00000381897 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr12:118462709 C>A maps to NM_007370.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr3:53126087 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr1:175914296 A>G maps to NM_022457.5 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:175996825 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:107154994 T>A maps to ENST00000357881 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr6:117241540 T>C maps to NM_173560.3 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr3:101284213 C>T maps to NM_017819.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr4:100478513 C>T maps to NM_001134666.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:109695056 A>T did not map to a codon.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr23:109694571 T>C did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr23:109695934 T>G did not map to a codon.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr23:71351212 T>C did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr22:24041047 A>T maps to ENST00000382833 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr5:73136426 T>C maps to NM_001080479.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr5:73161822 C>T maps to NM_001080479.2 Q713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr9:35751269 G>A maps to ENST00000456972 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:107032392 G>A maps to ENST00000304514 L1659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:107073431 G>A maps to ENST00000304514 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr4:3441323 T>C maps to NM_198229.2 P1419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr5:176798988 C>T maps to ENST00000398128 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr6:153332801 A>T maps to NM_012419.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:192128418 C>T maps to NM_130782.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr8:54764572 T>C maps to NM_170587.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr8:101054050 G>A maps to NM_015668.3 Y639Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr22:29656764 C>A maps to NM_012265.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr17:30632399 C>T maps to NM_138328.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:25628089 G>A maps to ENST00000357542 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr10:62637690 G>A maps to NM_014836.4 C567C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr1:113244308 C>G maps to NM_175744.4 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr11:208889 G>T maps to NM_021932.4 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr5:38954923 A>C maps to ENST00000296782 Y883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:130892348 A>C maps to NM_015347.4 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:130919338 G>A maps to NM_015347.4 D714D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:41107441 C>T maps to NM_014747.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr20:19956189 C>T maps to ENST00000255006 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr20:19955385 C>T maps to ENST00000255006 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr14:24805464 G>T maps to NM_006871.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr21:43166866 G>C maps to ENST00000352483 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr6:84563844 C>T maps to NM_001009994.1 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr23:73811840 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:73811736 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:73811738 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr23:73811736 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr23:73811738 A>G did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr23:73811994 G>T did not map to a codon.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr16:67683207 C>T maps to NM_001013838.1 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:151751271 C>T did not map to a codon.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:86947924 G>A maps to NM_022780.3 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr2:86832537 A>C maps to NM_005667.3 Y162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr23:106031217 T>C did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:105970390 T>G did not map to a codon.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr23:106034464 G>A did not map to a codon.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr3:149678839 C>T maps to NM_007282.4 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr8:125487508 C>T maps to NM_007218.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:74158076 C>A maps to NM_052916.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:88765420 C>A maps to NM_178841.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:196214404 G>T maps to NM_152617.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr13:25352541 T>C maps to ENST00000381927 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr1:185060811 T>C maps to NM_007212.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:78293015 C>G maps to NM_020914.4 A1025A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr17:78321575 C>T maps to NM_020914.4 R3196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr17:78355390 C>G maps to NM_020914.4 G4663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:5781126 G>C maps to NM_207111.2 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr2:219536684 C>G maps to NM_022453.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:90342857 A>C maps to NM_001031709.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr2:241516156 C>T maps to NM_018226.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:78685207 G>A maps to NM_002941.3 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr11:124765530 G>A maps to NM_019055.5 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr6:117706857 T>A maps to NM_002944.2 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr8:55534828 A>G maps to NM_006269.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr8:10470572 C>T maps to NM_178857.5 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr23:46713305 C>G did not map to a codon.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr23:46696622 G>T did not map to a codon.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr7:33136130 G>A maps to NM_203288.1 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr23:96139634 G>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:38145450 T>C did not map to a codon.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr14:21793035 C>T maps to NM_020366.3 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:21769355 C>G maps to NM_020366.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr14:21769307 C>T maps to NM_020366.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr23:153627910 G>A did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr6:35436590 C>T maps to NM_007104.4 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr9:130213581 G>A maps to NM_000976.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr19:49118704 C>T did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:6246872 A>T maps to NM_000983.3 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr3:101404667 T>C maps to NM_000986.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:52027875 G>T maps to NM_000992.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:52029444 G>A maps to NM_000992.2 N11N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr22:39711371 A>C did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:217364691 T>A maps to NM_000998.4 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:1995883 C>T maps to NM_005061.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr9:136216908 T>A did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr9:136216908 T>A did not map to a codon.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr18:33606994 C>T maps to NM_018170.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr1:150415710 T>C maps to NM_015203.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr1:150390093 T>C maps to NM_015203.3 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr2:154334998 C>T maps to NM_019845.2 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr17:45056016 C>T maps to NM_203400.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:26873741 G>A maps to NM_001006665.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr23:20206636 T>C did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr23:20194423 C>T did not map to a codon.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr23:20195137 T>C did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr23:20222170 G>A did not map to a codon.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr1:213244384 T>C did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr1:152128053 T>C maps to NM_001122965.1 Q507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:78858926 C>T maps to NM_020761.2 D654D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr23:55744772 G>A did not map to a codon.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr6:7246993 C>T maps to NM_001003699.3 G1437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr10:99116858 G>A maps to NM_015179.3 R1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr21:45107949 C>G maps to NM_015056.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr22:42910735 C>T maps to NM_015703.4 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr3:51968674 G>A maps to NM_004704.3 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:48559511 C>A maps to NM_018346.1 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr1:15987647 T>C maps to NM_006511.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr11:77412779 T>C maps to NM_016578.3 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:46317978 G>A maps to NM_030785.3 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr8:108970371 T>C maps to NM_178565.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:74668861 G>T maps to NM_001015055.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr2:218954704 C>T maps to NM_198483.3 C548C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:155292769 A>C maps to NM_001105203.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr9:35560974 G>A maps to NM_001135999.1 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:155912174 G>A maps to NM_181885.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr9:137300035 C>T maps to NM_002957.4 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:39039029 T>C maps to NM_000540.2 R4084R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:39058442 C>T maps to NM_000540.2 P4515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr19:38948846 C>G maps to NM_000540.2 Y694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr15:33954437 C>T maps to NM_001036.3 C1569C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr15:34152845 C>T maps to NM_001036.3 R4784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr19:3179455 C>T maps to NM_003775.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:134990741 A>G did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr16:51172850 A>G maps to ENST00000251020 H1094H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr20:50405585 G>A maps to NM_020436.3 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr6:147830099 G>A maps to NM_001030060.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr7:92763421 G>A maps to NM_152703.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr19:55752902 A>T maps to ENST00000443936 L379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:55743011 T>G maps to ENST00000443936 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:68377389 T>A maps to NM_001164160.1 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:148808751 C>G maps to NM_015278.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:100572513 A>C maps to NM_194292.1 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr7:66456177 G>C maps to NM_016038.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr19:1132139 G>A maps to NM_001100122.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:1924168 G>A maps to NM_079834.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr3:47456624 C>T maps to NM_012235.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr15:77087750 A>T maps to ENST00000324767 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr8:27516083 C>T maps to NM_016240.2 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:83557888 G>C maps to NM_001037582.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr15:51993376 A>G maps to NM_013243.3 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr6:25701538 T>C maps to NM_006998.3 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr3:159606613 A>T maps to NM_001197113.1 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:239006932 C>T maps to NM_016510.4 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:41503103 G>A maps to NM_001031694.2 H526H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:166915108 C>T maps to NM_001165963.1 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:166153544 A>T maps to NM_001040142.1 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:166201261 C>G maps to NM_001040142.1 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr2:165947166 G>C maps to NM_006922.3 V1832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:166012355 G>T maps to NM_006922.3 Y363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr17:62045581 C>T maps to NM_000334.4 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr17:62045584 C>T maps to NM_000334.4 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:167060899 C>T maps to ENST00000303354 K1492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:23360138 C>G maps to ENST00000307331 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr17:45918191 A>G maps to NM_138355.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr6:35213119 G>A maps to ENST00000394681 K855K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr6:35182248 C>T maps to ENST00000394681 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr11:65305493 G>A maps to NM_020680.3 W696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr12:100731224 C>T maps to NM_017988.4 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:169824949 A>T maps to NM_181093.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr4:76877178 C>T maps to NM_018115.2 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:31347252 G>T maps to NM_014654.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr14:50256252 C>T maps to NM_004713.3 Q886Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:243419489 G>A maps to NM_006642.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr7:4056808 C>T maps to NM_152744.3 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr5:134002686 G>A did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr4:119666216 T>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr3:127774578 C>T maps to ENST00000464451 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:169706124 C>T maps to NM_003262.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr6:108227976 A>G maps to NM_007214.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr15:49293278 A>C maps to NM_001193489.1 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:49304925 A>T maps to NM_001193489.1 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:13868445 G>T maps to NM_025229.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr22:50649113 C>T maps to NM_031454.1 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:83739848 G>A maps to NM_006080.2 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr7:83023611 C>G did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr9:92007356 A>T maps to NM_006378.3 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr10:102732886 G>A maps to NM_017893.2 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr5:9226980 C>T maps to NM_003966.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr5:9119219 A>T maps to NM_003966.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr5:115822557 G>A maps to ENST00000257414 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:151109385 C>T maps to NM_001178061.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:151112137 T>C maps to NM_001178061.1 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr17:7470322 G>A did not map to a codon.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr22:19710007 C>T did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr22:19709429 C>T maps to NM_002688.5 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr23:118797594 T>A did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr7:35912376 G>A did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr6:122777746 A>G maps to NM_020755.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr14:94756789 C>T maps to NM_001100607.1 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr23:105280774 A>G did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr6:2948771 C>A maps to ENST00000316782 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr6:2955760 G>C maps to ENST00000316782 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr22:21140327 G>A maps to NM_000185.3 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:100780345 G>C maps to NM_000602.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:1673259 C>A maps to NM_002615.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr3:167170763 G>A maps to NM_006217.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr18:42281355 C>T maps to NM_015559.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr18:42533243 C>T maps to NM_015559.2 D1313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr3:47098859 C>T maps to NM_014159.6 Q2138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr3:47061275 T>A maps to NM_014159.6 K2469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:47143046 T>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr3:47164504 G>T maps to NM_014159.6 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr14:99929880 C>T maps to NM_032233.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr21:37418116 T>C maps to NM_017438.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr21:37408417 G>C maps to NM_017438.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr3:9512541 T>C maps to ENST00000407969 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr22:26702083 G>A maps to NM_021115.4 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr19:2248400 G>A maps to NM_007165.4 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr2:198285206 T>C maps to NM_012433.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr11:65829381 C>A maps to NM_006842.2 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr16:70605580 G>A maps to NM_012426.4 V1173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:19420930 C>T maps to NM_172231.2 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr10:7214000 G>A maps to NM_001018039.1 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr10:99531062 T>C maps to NM_003015.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr17:56083836 G>T maps to NM_006924.4 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr21:33044134 A>G maps to NM_020706.2 N1007N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr21:33057762 A>G maps to NM_020706.2 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:45572383 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr23:1718089 A>T did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr23:1719997 C>T did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:46318585 T>A maps to NM_004719.2 P1277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:81702147 G>C maps to NM_003019.4 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:156186310 C>T maps to NM_000337.5 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr8:8235102 A>T maps to NM_001080826.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr15:77406688 G>A maps to NM_024776.2 L1684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr15:77472612 A>T maps to NM_024776.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr2:201438488 T>G maps to NM_152524.5 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr22:40800333 C>T maps to NM_015705.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr22:40804934 A>G did not map to a codon.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:111885275 G>A maps to NM_005475.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:80532506 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr22:38051327 C>A maps to NM_018957.3 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:15298470 G>A maps to NM_004844.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:249106347 G>C maps to NM_030645.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr23:19560044 C>A did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:19626145 G>T did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr4:170043336 A>G maps to NM_020870.3 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr4:170028337 A>G maps to NM_020870.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr4:8230106 C>T maps to NM_018986.3 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr1:154938021 A>C maps to NM_001130040.1 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr19:4290584 C>T maps to NM_020209.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr7:155596097 G>A maps to NM_000193.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr13:26625046 G>A maps to NM_001007538.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr13:26625046 G>A maps to NM_001007538.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr3:48510781 C>T maps to NM_016479.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr17:3514080 G>T maps to NM_013276.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr5:132161118 C>T maps to NM_001172700.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr23:9863547 C>T did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr23:50350751 T>C did not map to a codon.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr23:50350697 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr23:50350750 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr23:50350697 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr23:50350697 C>T did not map to a codon.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr11:111590500 C>T maps to NM_015191.1 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr15:75673956 T>A maps to NM_001145357.1 A1095A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr15:75692464 C>T maps to NM_001145357.1 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr15:75664532 G>A maps to NM_001145357.1 S1203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr15:75705129 G>A maps to NM_001145357.1 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:232649813 A>T maps to NM_020808.3 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr20:1615979 C>A maps to NM_018556.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:79870324 G>A maps to NM_016538.2 C390C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:105222012 C>T maps to NM_006427.3 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr13:21732195 A>G maps to NM_145061.5 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:46239836 C>G maps to NM_003726.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr7:26894414 A>G maps to NM_003930.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:2238152 G>A maps to NM_003036.3 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:127477531 T>A maps to NM_001046.2 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr16:56906658 A>G maps to NM_000339.2 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr20:44670174 C>T maps to NM_001134771.1 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr5:1064224 C>G maps to NM_006598.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr5:1094289 C>T maps to NM_006598.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr5:1093743 C>A maps to NM_006598.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:122765635 A>G maps to NM_022444.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr7:135370356 C>A maps to NM_012450.2 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:6597516 C>G did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr18:43319598 G>A maps to NM_001146037.1 W362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr1:113460276 G>A maps to NM_003051.3 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr17:6946082 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr17:6942203 C>G maps to NM_201566.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr2:230910734 G>A maps to NM_152527.4 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr17:66270211 C>A did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr17:66267172 A>G maps to NM_004694.4 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr6:25811998 C>T did not map to a codon.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr10:119003519 G>T maps to NM_003054.4 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:169446749 G>A maps to NM_006996.2 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr1:53555557 G>A maps to NM_006671.4 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr2:113418128 G>A maps to NM_005415.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr2:113404572 A>G maps to NM_005415.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:63065115 A>T maps to NM_001039752.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:38316202 T>C maps to NM_004256.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:38316609 C>A maps to NM_004256.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:110746233 C>A maps to NM_033125.2 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr6:160769795 C>T maps to ENST00000392145 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:131647951 A>C maps to NM_003059.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr5:131729503 G>A did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr6:43266248 G>A maps to ENST00000372585 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr15:65942808 A>G maps to NM_004727.2 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr20:19679324 G>C did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr22:19164389 G>A maps to NM_005984.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr7:95818644 C>T maps to NM_001160210.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr5:140683029 G>A maps to NM_031947.2 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr3:39431017 C>T maps to NM_017875.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr17:42399918 C>T maps to NM_001143780.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr23:118603719 T>G did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr4:983982 T>C maps to NM_213613.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr4:982689 A>G maps to NM_213613.2 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:149361288 T>C maps to NM_000112.3 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr7:103029856 G>A maps to ENST00000354356 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr7:103029510 A>G maps to ENST00000354356 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:103017285 G>T maps to ENST00000354356 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:48668740 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr6:35949920 C>T maps to NM_052961.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:50528291 G>A maps to NM_003645.3 *621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:85476452 G>A maps to NM_004213.3 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:43394676 G>T maps to NM_006516.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr22:24226510 C>T maps to NM_030807.3 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr20:62374340 T>C maps to NM_020062.3 *388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr4:42077745 T>C maps to NM_006345.3 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr20:37356312 C>T maps to NM_080552.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr23:48762074 G>A did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr5:139947278 T>A maps to NM_080670.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr17:47781477 T>A maps to ENST00000415270 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr6:8413925 T>C maps to NM_001142540.1 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:67519573 C>A maps to NM_015139.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr5:150660716 G>T maps to NM_001145017.1 Y375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr11:92917686 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:79220315 C>T maps to NM_001037984.1 Q800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr16:58713826 C>T maps to NM_018231.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr16:84063152 A>G maps to NM_001080442.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr12:56630208 C>G maps to NM_001135195.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr14:69866097 C>T maps to NM_018375.3 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr2:44547378 A>G maps to NM_000341.3 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr2:44508524 G>C did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:62648665 G>A maps to NM_001012661.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr11:57182148 G>A maps to ENST00000428603 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr1:95330397 T>A maps to NM_001114106.1 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr8:142238283 G>A maps to NM_001080431.1 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr13:29278213 A>G maps to NM_001135919.1 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr17:42335910 T>A maps to NM_000342.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr4:72429511 T>A maps to NM_001098484.2 S1034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr11:26725401 A>G maps to NM_178498.3 H206H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr21:35468405 C>G maps to NM_006933.4 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:27427729 G>C maps to NM_021095.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:108604762 T>A maps to NM_021815.2 L51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr12:101588896 C>T maps to NM_145913.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr23:115573955 G>A did not map to a codon.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr23:115568960 G>C did not map to a codon.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr12:85279277 A>G maps to NM_182767.4 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr5:1219217 C>T maps to NM_001003841.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr16:55705979 C>T maps to NM_001043.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr3:14508106 A>G maps to NM_001134367.1 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:152960546 C>T did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr23:152958792 T>C did not map to a codon.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr23:152956938 A>G did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:44467232 G>C maps to NM_201649.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr13:30096466 C>T maps to NM_003045.4 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr8:87226721 T>A maps to NM_138817.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr8:17419588 G>A maps to NM_001164771.1 Q587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:17401958 G>T did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr14:70527577 C>T maps to NM_183002.1 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:27428599 C>T maps to NM_003047.3 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr3:111983129 T>C maps to NM_183061.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr5:475167 G>A maps to NM_004174.2 P777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr17:72745285 A>T maps to NM_004252.3 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr23:135098842 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr23:46491074 A>T did not map to a codon.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr20:48431565 T>C maps to ENST00000417961 H16H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:133692537 G>C maps to NM_005630.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr11:74915492 C>T maps to NM_007256.4 F666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr20:61300282 G>A maps to NM_016354.3 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr5:101834203 C>A maps to NM_173488.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr5:101811426 G>A maps to NM_173488.3 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr17:33679779 G>A maps to NM_152270.3 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:33749974 C>A maps to NM_018042.3 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:33586029 T>G maps to NM_144975.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr4:20535254 T>A maps to ENST00000273739 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr23:144904632 G>C did not map to a codon.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr23:144904237 C>T did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr3:57743530 A>G maps to ENST00000428312 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr20:57611523 A>C did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr20:57611628 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr20:57613689 C>T did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr15:67473651 C>T maps to NM_005902.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:40839875 T>A maps to NM_022733.2 C28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr9:2110311 C>T maps to NM_003070.3 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr9:2039760 A>G maps to NM_003070.3 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr19:11144468 C>A maps to NM_001128849.1 G1267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr19:11134285 C>G maps to NM_001128849.1 V984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr4:144445523 C>T maps to NM_003601.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr2:217279801 C>G maps to NM_014140.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr12:56558429 A>C maps to NM_003075.3 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr23:53407984 A>T did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr23:53440301 C>G did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr10:112342363 A>G maps to NM_005445.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:160119802 T>C maps to NM_005496.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr18:2718193 C>T maps to NM_015295.2 Q767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:55844409 C>T maps to NM_001122964.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr16:18849888 A>G maps to ENST00000389467 N2356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr16:18864920 G>T maps to ENST00000389467 I1584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr16:18844470 G>A maps to ENST00000389467 F2861F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:109764876 A>G maps to NM_003080.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr22:31484746 G>C maps to ENST00000454496 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:48600832 C>T maps to NM_005985.3 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr9:139272474 G>T maps to NM_003086.2 A1268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr9:139273026 C>G maps to NM_003086.2 G1084G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr2:242026824 A>T maps to NM_001080437.1 R1380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr20:32026770 G>A maps to NM_003098.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr8:121587443 G>A maps to NM_021021.3 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr15:25207296 C>T maps to NM_022804.2 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr15:64426981 G>A maps to NM_003099.3 Q447Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr23:70280927 G>T did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr11:130785009 T>G maps to NM_014758.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr11:130785819 T>A maps to NM_014758.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr5:122154606 T>G maps to NM_003100.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr16:50707451 G>T maps to NM_182854.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr16:12618620 C>T maps to NM_001080530.2 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr14:35062275 A>T maps to NM_152233.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr6:158330821 T>G maps to NM_016224.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr17:36508825 C>A maps to NM_014598.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr2:39285903 C>T maps to NM_005633.3 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr2:39284008 T>C did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr22:38374015 C>T maps to NM_006941.3 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:231077476 T>G maps to NM_080424.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr7:21468914 G>A maps to NM_003112.3 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr7:21469334 T>C maps to NM_003112.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr2:171572791 G>A maps to NM_001003845.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr17:45925060 G>A maps to NM_199262.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr12:53722358 C>T maps to NM_001173467.1 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr7:20824952 G>C maps to NM_182700.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr7:20824955 C>G maps to NM_182700.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr8:7308687 G>T maps to NM_016512.3 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr17:4871030 A>C maps to NM_004890.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr17:49067111 G>T maps to ENST00000376407 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:32289268 C>G maps to NM_014946.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:217975147 G>T maps to NM_138796.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr17:48628384 G>A maps to NM_022827.2 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr7:101988945 G>A maps to NM_001146210.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr2:220338576 C>A maps to NM_005876.4 R1467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr2:220349150 C>T maps to NM_005876.4 S2322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:7324266 C>A maps to NM_199339.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:16258647 T>C maps to NM_015001.2 P1971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:16260462 T>G maps to NM_015001.2 V2576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr15:44951364 A>T maps to NM_025137.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr16:89613083 G>T maps to NM_003119.2 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:228860229 G>C maps to NM_001142644.1 S1543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr5:147661755 C>T maps to NM_001040129.2 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr15:41146020 C>T maps to NM_181642.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:38774303 G>T maps to NM_021102.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:136328173 G>A maps to NM_004598.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr11:14063069 C>T maps to NM_006108.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr2:139308571 A>G maps to NM_001001664.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:152957849 C>T maps to NM_005987.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:153004964 C>T maps to NM_003125.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr12:56862410 C>T maps to NM_207344.3 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:131339497 T>C maps to NM_001130438.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr9:131370208 G>T maps to NM_001130438.2 G1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:131386740 G>A maps to NM_001130438.2 K1989K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr2:54851999 C>T maps to NM_003128.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr2:54855277 G>C maps to NM_003128.2 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:41018831 A>G maps to NM_020971.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr19:41018831 A>G maps to NM_020971.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:41018831 A>G maps to NM_020971.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr15:42147763 G>A maps to ENST00000320955 S3067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr15:42143072 G>A maps to ENST00000320955 R3634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr9:94821489 G>A maps to NM_006415.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:94877625 A>T maps to NM_006415.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr5:179248067 C>T maps to NM_003900.4 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr2:45616664 G>C maps to NM_018079.4 G924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr16:30718523 G>T maps to NM_006662.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr16:30735226 A>C maps to NM_006662.2 A1494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr16:30734927 T>C maps to NM_006662.2 L1395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr16:30744760 A>G maps to NM_006662.2 E2096E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr12:64521383 C>G maps to NM_020762.2 S807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr23:99919924 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr16:2817458 T>C maps to NM_016333.3 S2310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr7:100485328 T>C maps to NM_015908.5 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr20:633660 A>G maps to NM_080725.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr1:54870253 C>T maps to NM_145716.2 W62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr1:54707863 G>T maps to NM_145716.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:182765432 T>C maps to NM_001130445.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr2:182780850 T>C maps to NM_001130445.1 T828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr12:26348667 C>G maps to NM_005086.4 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr7:149502568 C>A maps to NM_198455.2 G2795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr7:149518181 C>T maps to NM_198455.2 C4179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:57100281 C>A maps to NM_003146.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:65338204 C>T maps to NM_006396.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:1480324 C>T maps to NM_014188.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr23:48123288 G>A did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr23:48054485 G>T did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr8:53028900 C>T maps to NM_014682.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:113126669 T>C maps to NM_017744.4 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr10:17495607 C>T maps to NM_001004470.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:52554290 C>A maps to NM_015136.2 C1828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:104030937 G>C maps to NM_017564.9 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:37368583 C>T maps to NM_198993.3 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr17:37373421 G>A maps to NM_198993.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr23:123197833 C>A did not map to a codon.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr23:123185065 C>T did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr23:123176468 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr23:123200036 T>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:123202455 C>T did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr17:37817258 G>T maps to NM_006804.3 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr12:56742946 C>T maps to NM_005419.3 Q480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr20:47741018 T>A maps to NM_017453.2 K239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr8:74464270 A>G maps to NM_001164380.1 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:171471933 T>G maps to NM_005990.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr2:220470427 G>T maps to NM_052902.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr10:134036391 C>T maps to NM_173575.2 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr2:219556969 C>G maps to NM_015690.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr8:27099959 G>A maps to NM_030795.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr15:74281092 A>G maps to NM_004809.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr14:81744520 G>A maps to NM_033104.2 H378H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr16:732018 G>T did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr9:102730747 G>A maps to NM_017919.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr11:62592561 C>A maps to NM_003164.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr6:147637420 G>A maps to NM_001127715.1 E560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:84652538 C>T maps to NM_003849.3 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr22:39138451 G>A maps to ENST00000405018 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:21821860 C>T did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr17:27014485 G>T maps to NM_003170.3 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr22:24581139 C>A maps to NM_019601.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr1:223401080 C>G did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr12:102125408 T>C maps to ENST00000449403 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr23:47432307 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:12192766 C>T maps to NM_133625.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr14:64633997 G>A maps to NM_182914.2 L5551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr14:64519116 T>G maps to NM_182914.2 L2829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr6:158449968 A>T maps to NM_003898.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr6:158450004 C>T maps to NM_003898.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:99672332 G>T maps to ENST00000336292 V1255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr23:49050638 T>C did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr1:210267874 T>C maps to NM_001146261.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr14:62463093 A>C maps to NM_031914.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr23:99945080 T>C did not map to a codon.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:132859484 C>T maps to NM_175057.3 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr22:39814794 G>A maps to NM_006116.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr23:70618523 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:70643917 T>C did not map to a codon.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr9:32633309 G>A maps to NM_153809.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr18:23969873 T>C maps to ENST00000418698 R834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr7:99707630 G>A maps to ENST00000472509 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr2:160086334 C>A maps to NM_033394.2 P1466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr1:6639490 C>T maps to NM_138697.3 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr1:19166251 C>G maps to NM_152232.2 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:1269264 G>A maps to NM_152228.1 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr5:9629373 G>A maps to NM_019599.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:143175819 C>T maps to NM_176883.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr20:13561620 C>T maps to NM_017714.2 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr7:27856558 A>T maps to ENST00000409980 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:27856086 T>C maps to ENST00000409980 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr12:72288465 A>T maps to NM_022771.4 K237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:77915894 C>A maps to NM_019020.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr4:26585818 T>C maps to NM_018317.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr20:419912 G>T maps to ENST00000246077 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr22:47507401 A>G did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr16:2550435 G>T maps to ENST00000434757 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr17:18541948 A>G maps to NM_001039397.2 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr13:75923414 C>A maps to ENST00000431480 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr3:17550056 A>G maps to NM_001134381.1 Y2Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:101706725 G>C maps to NM_001102426.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:101670696 G>A maps to NM_001102426.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr23:106109169 G>A did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr4:141590819 G>T maps to NM_015130.2 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr4:141590873 G>A maps to NM_015130.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr4:141580760 G>C maps to NM_015130.2 Y634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr4:141600811 G>A maps to NM_015130.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:179326224 C>T maps to NM_198868.2 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:80885834 G>C maps to NM_005993.4 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr4:106967780 G>A maps to NM_001163436.1 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr4:107163638 G>A maps to NM_001163436.1 C386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:9683002 C>T did not map to a codon.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr23:79286335 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr17:59544912 G>C maps to ENST00000393853 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr12:114841565 G>A maps to NM_000192.3 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr17:37821722 G>A did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr23:102841990 A>G did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr23:102841928 A>T did not map to a codon.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr18:44560192 G>A maps to NM_016427.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr2:27373230 A>T maps to NM_175769.2 K155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr18:52921811 A>G maps to ENST00000398339 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:85361149 C>G maps to NM_031283.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr1:152082278 C>T maps to NM_007113.2 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:152059686 C>T maps to NM_001008536.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr11:59622264 A>G maps to NM_001062.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr6:35086063 T>G maps to NM_001093728.1 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr12:104378525 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr12:104359838 G>C did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr12:104378525 G>T did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:104378525 G>T did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr14:90429931 G>A maps to NM_018319.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:154493834 G>A maps to NM_001098475.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr13:61102843 T>C maps to NM_001146070.1 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr9:100227198 T>G maps to NM_014290.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr7:97847036 C>T maps to ENST00000379795 E1119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr14:102910131 G>A maps to NM_014844.3 P967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr17:6703553 C>A did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:36552573 C>T maps to NM_014466.2 N225N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr2:95540715 G>A maps to NM_144705.2 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr14:20840923 T>C maps to NM_007110.4 K2348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr14:20846266 G>C maps to NM_007110.4 A1879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr14:20845480 G>A maps to NM_007110.4 L2016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:106157460 G>T maps to ENST00000513237 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:74275020 C>T maps to ENST00000409262 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:74320720 G>T maps to ENST00000409262 G972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr23:69898663 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr8:30694448 T>C maps to NM_031271.3 Q2734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr23:48895569 G>C did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:48888985 G>A did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:41658861 G>A maps to ENST00000343317 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr7:100224940 C>A maps to NM_003227.3 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr15:43571976 C>A maps to NM_052955.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr15:43571976 C>A maps to NM_052955.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr15:39886355 C>A maps to NM_003246.2 Y1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr15:39882094 C>G maps to NM_003246.2 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr15:39880742 T>G maps to NM_003246.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:155175048 C>T maps to NM_007112.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:155172113 G>A maps to NM_007112.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr23:122756984 T>A did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr23:122755200 T>A did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr23:122770006 A>G did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr23:122801089 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:122757674 T>C did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr7:11675887 G>A maps to ENST00000423059 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr2:138400115 C>T maps to ENST00000272643 C1289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr2:39964199 C>G did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr21:32638550 G>A maps to NM_003253.2 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr6:155566797 G>A maps to ENST00000456144 A1195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:134785314 G>C maps to NM_001099221.1 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:90035226 G>T maps to NM_145715.2 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr23:48751201 T>C did not map to a codon.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr17:76921134 G>A maps to NM_003255.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:24709983 G>C maps to NM_001099274.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr1:168168188 G>A maps to NM_152902.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr15:30008819 A>G maps to NM_003257.3 S1399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr15:30019081 T>G maps to NM_003257.3 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:3730390 C>G maps to NM_014428.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr17:27052950 G>T maps to NM_138463.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr4:166996129 T>C maps to ENST00000507499 H786H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr9:35711015 C>T maps to NM_006289.3 K1361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:223286360 G>A maps to NM_003268.5 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr23:12906680 C>A did not map to a codon.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr2:74742181 C>G maps to NM_016170.4 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr5:170736389 G>A maps to NM_021025.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr20:30730876 C>T maps to NM_014742.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr12:66546146 T>C maps to ENST00000286424 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr9:75355126 T>C did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr19:54669260 G>T maps to NM_001145303.1 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr16:19073097 A>T did not map to a codon.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr16:19051690 C>A maps to NM_024847.3 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:76133811 C>T maps to NM_152468.4 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr17:76133426 T>G maps to NM_152468.4 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:140021511 G>A maps to ENST00000252100 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr1:93620446 T>A did not map to a codon.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr2:193056716 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr17:42089523 C>T maps to NM_032376.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr17:41365848 C>T maps to NM_145041.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:75617586 G>T maps to NM_031925.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:98413328 T>A maps to NM_015348.1 A997A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr12:130184818 C>G maps to NM_133448.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr19:36230749 G>C maps to NM_024660.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr2:85828226 G>T maps to NM_001031738.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr4:38990525 G>T maps to NM_024943.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr23:109352335 C>G did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:150500796 C>A maps to NM_018487.2 Y144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr7:1589782 G>A maps to NM_001097620.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr20:48713265 T>C maps to NM_199203.2 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr16:29982730 G>A maps to NM_194280.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr23:15682859 A>G did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr11:129724697 A>G maps to NM_138788.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:64174891 T>G maps to NM_014254.1 L88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr1:45120713 G>T maps to NM_024587.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr3:69072459 T>C maps to NM_007114.2 Q1050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:69096706 T>C maps to NM_007114.2 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:69101210 G>A maps to NM_007114.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr1:151146998 T>A maps to NM_013353.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:33135654 C>T maps to NM_001039770.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr4:68777128 C>T maps to NM_182606.3 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr4:68930402 C>A maps to NM_207407.2 G339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr21:19685346 T>G maps to NM_002772.2 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr19:2416796 G>A maps to NM_182973.1 Q635Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:2408352 G>A did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr19:2410352 G>A maps to NM_182973.1 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr12:29670367 A>G maps to NM_001193451.1 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr12:83290129 G>A maps to NM_152588.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr6:47254096 G>A maps to NM_014452.3 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr17:7464140 G>A maps to NM_003808.3 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr5:150444533 C>G maps to NM_006058.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:7287557 T>C maps to NM_003985.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:57076185 C>T maps to NM_033396.2 G1333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr16:11362954 G>A maps to NM_005425.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr5:72183031 T>G maps to NM_002270.3 L429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr7:5372498 C>T maps to NM_001080495.2 K1967K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr7:5415787 G>A maps to NM_001080495.2 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr7:5396873 G>A maps to NM_001080495.2 Q1623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr2:218712983 G>C maps to NM_022648.4 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr2:218713667 C>G maps to NM_022648.4 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:218678432 T>A maps to NM_022648.4 P1508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:218678510 C>G maps to NM_022648.4 P1482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr6:32052211 C>T maps to ENST00000375244 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr6:32016287 C>T maps to ENST00000375244 A3299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr17:18212207 A>G maps to NM_004618.3 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr3:133331388 C>T maps to NM_007027.3 L1293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr1:179815211 A>C maps to NM_145034.4 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr17:7579414 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr15:43724400 G>A maps to NM_001141980.1 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr15:43733776 A>G maps to NM_001141980.1 P1015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr15:43771710 T>C maps to NM_001141980.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr15:43748236 G>A maps to NM_001141980.1 Q857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:223984098 A>G maps to NM_001031685.2 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr3:189612035 G>C maps to NM_003722.4 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr12:113704161 G>T did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr12:6976717 C>T maps to NM_001159287.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr16:67424232 C>G maps to NM_016140.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:186324771 T>A maps to NM_003292.2 K673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:186316561 A>G maps to NM_003292.2 D935D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:65705942 C>G maps to NM_003596.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr9:139794875 C>G maps to ENST00000359662 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr1:211545689 C>A maps to ENST00000427925 Y451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr3:42218378 G>A maps to NM_001042646.1 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr2:202262966 G>A maps to NM_015049.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr3:36873054 C>T maps to NM_014831.2 L2629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr16:3712966 G>A maps to NM_016292.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr21:45502875 G>A maps to NM_003274.4 W644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr23:13732605 A>G did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr6:41129013 C>T maps to NM_018965.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr23:152710188 G>T did not map to a codon.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr8:110131437 G>A maps to NM_003301.4 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr2:12858615 C>A maps to NM_021643.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:5717509 C>T maps to NM_006074.4 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr7:138145433 G>A maps to NM_015905.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr11:119988940 G>A maps to NM_012101.3 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr11:6486811 C>T maps to NM_033278.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr5:114515695 G>A maps to NM_018700.3 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr6:25967010 G>C maps to NM_006355.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr3:140401753 G>A maps to NM_152616.4 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr11:89537574 G>C maps to NM_020358.2 Y21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr5:180687082 G>T maps to NM_032765.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:33625314 C>T maps to NM_018207.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr15:45048564 G>C did not map to a codon.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr3:32860207 C>T maps to NM_001039111.1 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:32932840 G>A maps to NM_001039111.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr7:75028468 A>G maps to ENST00000430211 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:75028468 A>G maps to ENST00000430211 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr10:104415048 G>A maps to NM_030912.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr10:104404880 C>T maps to NM_030912.2 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr5:908119 C>T maps to NM_004237.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr5:916036 C>T maps to NM_004237.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr15:64692968 T>C maps to NM_016213.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr7:100466247 C>T maps to NM_003302.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr23:54948718 T>G did not map to a codon.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr8:72958840 G>A maps to NM_007332.2 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:122853524 G>A maps to NM_001130698.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr13:38237840 G>T maps to NM_003306.1 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:33623073 A>C maps to NM_015638.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr20:33622950 G>T maps to NM_015638.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:135561910 T>A maps to NM_020389.2 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr21:45825793 C>T maps to ENST00000397932 I888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr19:49674875 C>T maps to NM_017636.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:49703679 G>T maps to NM_017636.3 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr19:49714006 G>T maps to NM_017636.3 T1123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr11:2432684 C>T maps to ENST00000452833 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:142606702 G>A maps to NM_019841.4 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr16:2122848 G>A did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:150128648 C>T maps to NM_014779.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:99720472 C>A maps to NM_025244.2 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr2:99689478 A>C did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr18:72999467 C>A maps to NM_005786.4 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr1:115601515 G>A maps to NM_005725.4 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr7:128804349 C>A maps to NM_178562.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr23:53114043 C>A did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:54482520 G>A maps to NM_001003937.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr6:43226955 C>G maps to NM_032538.1 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr2:3483102 G>A maps to NM_016030.5 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr2:3392362 G>C maps to NM_016030.5 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr10:75037056 G>A maps to NM_145170.3 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:33002959 G>A maps to NM_017735.4 W564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:74718486 G>A maps to NM_022492.4 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr8:109462082 A>G maps to NM_014673.3 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr8:109489021 C>T maps to NM_014673.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr8:109462687 A>T maps to NM_014673.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr14:20774051 T>C maps to NM_138376.2 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr2:47300863 C>T maps to ENST00000394850 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr14:89338025 G>T maps to NM_144596.2 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:117633171 A>T maps to NM_003594.3 K839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr22:43442516 C>G maps to NM_012263.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr22:43569807 G>T maps to NM_015140.3 C418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr2:219612346 C>T maps to NM_014640.4 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:179411555 A>G maps to NM_133378.4 D28965D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:179449123 T>C maps to NM_133378.4 E19150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:179452052 C>T maps to NM_133378.4 G18727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:179575503 G>A maps to NM_133378.4 G8196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr2:179611916 T>C maps to ENST00000375038 L5072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:179433842 G>C maps to NM_133378.4 Y23104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:179419673 A>G maps to NM_133378.4 D26936D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:179425265 A>G maps to NM_133378.4 Y25963Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr2:179567315 C>A maps to NM_133378.4 E8856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:179599139 A>G maps to NM_133378.4 F3893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:179598481 C>A maps to NM_133378.4 G3968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr2:179615957 C>T maps to ENST00000375038 T3725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:54937847 A>G did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr7:2691877 T>C did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr12:49522586 G>A maps to NM_006082.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr2:132236968 G>A maps to NM_080386.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr20:57599036 G>A maps to NM_030773.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:40765684 C>T maps to NM_001070.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr1:151552138 A>G maps to NM_020127.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr7:19738025 T>C maps to NM_001002926.1 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr7:19738031 C>T maps to NM_001002926.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr7:19738031 C>T maps to NM_001002926.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr1:32646098 T>C maps to NM_175852.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr6:139563746 T>C maps to ENST00000358430 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:16804660 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr9:113013694 T>C maps to NM_003329.2 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr18:9887669 A>G maps to NM_001098529.1 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr6:7889003 A>C maps to NM_030810.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr22:19870862 A>T maps to NM_006440.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr15:41864762 G>A did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr15:41854917 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr15:41854917 T>G did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr10:71906009 C>G maps to NM_173555.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr7:66474574 C>T maps to NM_018264.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr15:70987422 C>T maps to NM_018003.2 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr15:70991968 G>A maps to NM_018003.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr23:47069021 T>G did not map to a codon.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr4:68534338 T>C maps to NM_018227.5 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:138839742 T>C maps to NM_016172.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr9:33960822 C>G did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:16285475 C>G maps to NM_018955.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr12:125397654 C>A maps to NM_021009.5 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:83728804 G>T maps to NM_198920.1 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr19:55913034 A>G maps to NM_014501.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr15:25615994 A>G maps to NM_000462.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr7:156963037 T>A maps to NM_014671.2 L79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr11:118250227 C>T maps to NM_004788.2 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:10177625 C>A maps to NM_001105562.2 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr1:11346094 G>C maps to NM_013319.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr20:3090942 G>A maps to NM_014948.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr15:43299482 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr6:42657390 G>A maps to NM_015255.2 E1703E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr8:103300467 T>C maps to NM_015902.4 G1580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:99327794 G>A maps to NM_024954.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr1:26608864 A>G maps to NM_183008.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr2:136505918 T>C maps to NM_014607.3 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr9:134404930 G>A maps to NM_031432.2 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:128918713 C>A maps to NM_020120.3 I899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr2:234637942 G>A maps to NM_019093.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr4:69816983 A>G maps to NM_024743.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr4:69978198 A>G maps to NM_001074.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:34825519 C>T maps to NM_017754.3 Y531Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr6:150290453 G>T maps to NM_025218.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr12:132405712 C>G maps to NM_003565.2 A1010A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr12:132395296 C>T maps to NM_003565.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr15:75132965 T>C maps to NM_001099436.1 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr15:75132622 C>T maps to NM_001099436.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr19:17767188 G>T maps to ENST00000428389 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr9:35243361 G>C did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr15:54557622 T>A maps to ENST00000260323 V1249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:73831765 G>T maps to ENST00000412096 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr5:176305474 G>A did not map to a codon.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr10:73055665 C>T maps to NM_170744.3 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr8:35541183 C>T maps to ENST00000416672 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:67763106 A>G maps to NM_030930.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr23:118977250 T>C did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr23:118985466 C>G did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:158971731 A>G maps to NM_001135098.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr1:229771820 G>A maps to NM_014777.2 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr11:17542426 G>T maps to NM_153676.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr11:17542435 T>G maps to NM_153676.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:215820885 G>T maps to ENST00000366943 I4923I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr19:17366409 G>A maps to NM_031941.3 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:84797743 G>A maps to NM_005153.2 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr23:47102997 T>C did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr3:179426710 C>A maps to NM_003940.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:62795033 T>A maps to ENST00000280377 T914T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr1:55612676 A>G maps to NM_015306.2 Y725Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr21:17138431 C>G maps to ENST00000285681 Y80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr23:132160220 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr11:113679908 G>T maps to NM_020886.2 Y680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr16:23083423 G>T maps to NM_020718.3 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:78194349 T>C maps to NM_015017.3 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr2:61454344 A>C maps to NM_014709.3 V2484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr2:61493233 C>T maps to NM_014709.3 K1834K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:85875074 T>G maps to NM_006590.2 L529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:49362338 T>C maps to NM_003363.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr6:99894084 T>C maps to NM_001080481.1 R521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:22073614 A>G maps to NM_032236.5 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr15:50835959 G>A maps to ENST00000456636 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr23:40999923 C>A did not map to a codon.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr23:41043809 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:41022127 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr24:14847583 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr24:14847618 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr23:129045743 C>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr13:52603704 G>C maps to NM_021645.5 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr5:72864378 T>A maps to NM_032175.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr1:116226630 C>A maps to NM_001172412.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:116226587 C>T maps to NM_001172412.1 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:31745373 C>T maps to NM_006295.2 L1264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:30883014 G>A did not map to a codon.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr16:4432542 A>C maps to NM_138440.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr16:4432671 T>C maps to NM_138440.2 C598C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr16:4432542 A>C maps to NM_138440.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr10:118893698 C>T maps to NM_001112704.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr5:82850837 G>A maps to NM_004385.4 W3239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:82786053 G>T maps to NM_004385.4 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr5:82815684 G>A maps to NM_004385.4 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr9:35062135 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:35061056 A>G maps to NM_007126.3 D438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr23:7811789 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:87017992 C>T maps to NM_016206.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:156268770 C>T maps to NM_001004319.2 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:17278344 T>G maps to NM_003380.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:42577628 C>T maps to NM_004624.3 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr7:158828653 T>C maps to ENST00000402066 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:53762786 C>T maps to NM_173856.2 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr19:53762719 T>C maps to NM_173856.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr3:51452312 T>G did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:51457621 C>G maps to ENST00000273612 R934R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr9:79955423 T>A maps to ENST00000376646 A2328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:62155702 C>A maps to NM_020821.2 E3630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr15:62219325 A>G maps to NM_020821.2 P2160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:12327037 T>C maps to NM_015378.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr1:12304649 T>C maps to NM_015378.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr11:134115447 C>T maps to NM_052875.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr15:42462023 G>T maps to ENST00000348544 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr18:61058288 T>C maps to NM_004869.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr2:64199371 T>A maps to NM_016516.2 K129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:184603939 C>T maps to ENST00000437079 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr12:118506353 T>C maps to NM_019086.5 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:118506350 C>T maps to NM_019086.5 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr23:65244922 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr14:68118140 C>T maps to NM_006370.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr2:98907041 G>A maps to NM_144992.4 Q1038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:49815192 C>T maps to NM_198570.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr7:49815180 C>T maps to NM_198570.3 H50H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:215440517 G>T maps to NM_001080500.2 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr11:61026691 C>A maps to NM_152718.2 E775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr12:6138618 G>A maps to NM_000552.3 H952H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:27739178 A>G maps to NM_006990.2 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr1:27736339 A>G maps to NM_006990.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:17010 T>C maps to NM_182905.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:14943405 A>G maps to NM_016312.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr7:73249147 A>C maps to NM_152559.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr4:85675020 T>C maps to NM_014991.4 Q1856Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr4:10099337 A>G maps to NM_017491.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr10:122622313 G>A maps to NM_018117.11 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr10:122664156 G>A did not map to a codon.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr23:48462760 G>A did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr17:9501595 C>A maps to NM_145054.4 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:991961 C>T maps to NM_024100.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr14:102675937 T>C maps to ENST00000454394 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr14:102689210 T>A maps to NM_181291.1 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:128526505 C>A did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr23:117526749 T>G did not map to a codon.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr5:140049031 T>C maps to NM_017706.4 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr1:241875145 T>C maps to NM_144625.4 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr12:122413566 T>C maps to NM_144668.4 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:37381725 C>T maps to NM_018034.2 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr17:1633710 G>A maps to NM_001163809.1 K1235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:707222 T>G did not map to a codon.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr16:707786 C>T maps to NM_145294.4 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr7:134873247 C>T maps to NM_014149.3 E606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:683831 C>A maps to NM_053284.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr4:6303093 C>T maps to NM_006005.3 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr17:38416824 G>A maps to NM_133264.4 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr17:38420805 A>G maps to NM_133264.4 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr17:66440667 C>T maps to NM_017983.5 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:988848 A>C maps to NM_018979.3 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr9:96055158 C>T maps to ENST00000297954 P1841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr23:54319392 A>T did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr17:44845985 C>T maps to NM_030753.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:6012934 C>G maps to NM_015253.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr4:184129217 C>T maps to ENST00000448232 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr23:10062248 A>T did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr23:10066561 A>C did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr23:123020209 G>T did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:168105758 G>A maps to NM_152381.5 R2619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr22:17280835 G>T maps to NM_175878.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:56435873 C>G maps to NM_052898.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:28290010 C>T maps to NM_018053.2 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr23:128895979 A>G did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:43541218 G>C maps to NM_020750.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr12:64808727 C>A maps to NM_007235.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr5:82406898 G>T maps to NM_022406.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr3:38404483 C>G maps to NM_005108.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr16:17202724 C>A maps to NM_022166.3 E903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:102100554 G>T maps to NM_001130145.2 G467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:43166451 G>A maps to NM_004559.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr14:75248110 G>A maps to NM_019589.2 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr4:69202907 C>T maps to NM_001031732.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr20:61833791 T>C maps to NM_017798.3 K500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr22:32352659 C>T maps to NM_003405.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:155630356 G>A maps to ENST00000368339 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr23:21875587 G>A did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr7:100344176 C>T maps to ENST00000349350 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr7:100349674 T>C maps to ENST00000349350 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr8:81412102 T>C maps to NM_001105539.1 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr11:62519738 G>A maps to NM_024784.3 Y516Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr23:119387345 C>T did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr9:129595384 G>T maps to NM_014007.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr20:62407207 G>A maps to NM_025224.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:4322598 C>A maps to NM_145291.3 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:203819760 C>T maps to NM_014827.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr16:88694028 G>C did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:88653022 G>T maps to ENST00000452588 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr16:88653084 C>T maps to ENST00000452588 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:144522451 G>T maps to NM_015117.2 P858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr2:113069432 G>A maps to NM_198581.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr5:132342535 T>G maps to ENST00000509437 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:52902540 G>T maps to NM_001009881.2 R1350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr10:81146145 G>A maps to NM_153367.3 C227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr23:77913358 G>A did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr5:80600584 G>A maps to NM_032280.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:207171573 G>A maps to NM_020923.1 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr1:27176924 G>A maps to NM_032283.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr16:85010784 G>A maps to NM_001145548.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr23:128963039 G>T did not map to a codon.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:145156026 G>A maps to NM_014795.3 F909F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr2:220072713 C>T maps to NM_138802.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr12:72017887 A>T maps to NM_144982.4 L1501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr16:72984697 G>A maps to NM_006885.3 G962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr16:72821092 G>T maps to NM_006885.3 T3694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:72992634 T>C maps to NM_006885.3 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:72992637 C>T maps to NM_006885.3 E469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr8:77616433 G>A maps to NM_024721.4 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr17:4995908 T>C maps to NM_153018.2 C370C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr19:39898402 T>C maps to NM_003407.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:69256348 C>G maps to NM_004926.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr20:50769884 C>T maps to NM_018197.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr11:58346867 G>A maps to NM_053023.4 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr5:32407028 A>T maps to NM_016107.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr24:2843188 G>C did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:68282658 C>A maps to NM_015346.3 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr14:68268850 G>T maps to NM_015346.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:62366739 T>A maps to NM_032527.4 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:147128793 G>T maps to NM_003412.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr3:147109012 C>A maps to NM_001168379.1 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr13:100623584 C>T maps to NM_033132.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:99621200 A>G maps to NM_003439.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr6:28333713 G>A maps to NM_024493.2 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:101152940 A>T did not map to a codon.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr3:178785386 C>A maps to NM_022470.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:81037037 C>G maps to NM_020338.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:44805817 C>G maps to NM_031449.3 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr1:40733504 A>G maps to NM_005857.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr1:40724032 G>C maps to NM_005857.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:35569919 G>C maps to NM_024772.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr23:70468026 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr13:20398871 T>C maps to NM_001142684.1 K585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr13:20398976 A>G maps to NM_001142684.1 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr13:20413048 G>T maps to NM_001142684.1 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:50379016 C>T maps to NM_015896.2 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr19:19789580 G>C maps to NM_033204.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:58945193 T>A maps to NM_003433.3 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr19:19822256 T>G maps to NM_021030.2 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:219509114 A>T maps to NM_001105537.1 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:219503379 G>T maps to NM_001105537.1 T1582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:9519249 T>G maps to NM_003442.5 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr3:44612086 T>C maps to NM_018651.2 Y495Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr9:97063237 C>T maps to NM_194320.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr19:35232371 A>G maps to ENST00000392232 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:44570871 C>T maps to NM_013361.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr19:44635910 A>C maps to NM_013362.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr19:44739324 A>T maps to NM_182490.1 K248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:5009511 A>G maps to NM_014519.2 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr19:44792843 T>C maps to NM_004234.4 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr18:74622685 C>T maps to NM_007345.3 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr18:74680293 G>T maps to NM_007345.3 *1846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr8:145947049 A>T maps to NM_138367.1 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr19:24309779 A>G maps to NM_203282.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:24310236 A>T maps to NM_203282.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:22271295 G>A maps to NM_033468.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:58724016 G>C maps to NM_133502.1 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr23:152613053 G>A did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr1:200376814 T>C maps to NM_012482.3 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:200378263 C>T maps to NM_012482.3 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr21:43413769 T>C maps to NM_020727.4 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr16:58031773 G>A maps to NM_020807.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr19:53385206 A>G maps to NM_207333.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr19:53384826 A>G maps to NM_207333.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr20:44578918 G>C maps to NM_022095.3 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr20:32376705 G>T maps to ENST00000375200 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr5:176471534 G>C did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:53643806 A>G maps to NM_001172674.1 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:53644103 G>C maps to NM_001172674.1 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:53644115 A>G maps to NM_001172674.1 C656C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:71739939 G>C maps to NM_152625.1 Y626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:71739708 C>T maps to NM_152625.1 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr12:54764719 T>C maps to NM_001130967.1 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:180308132 A>G maps to NM_152520.4 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:180309602 T>A maps to NM_152520.4 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr8:28209092 C>A maps to NM_018660.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:58084257 A>G maps to NM_017879.1 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr19:58084872 A>T maps to NM_017879.1 C133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr7:148800799 A>G maps to NM_001001661.2 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr1:23693622 G>A maps to NM_001077195.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:58991384 G>A maps to NM_017908.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:57037031 A>G maps to NM_020813.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr19:50550198 G>T maps to NM_015428.1 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:44112495 C>T maps to NM_145312.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr19:58867602 C>A maps to NM_198458.1 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:19905759 G>C maps to NM_001099269.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:32873420 T>A maps to NM_014910.4 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:27840356 A>G maps to NM_032434.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:14105674 T>C maps to NM_145287.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:22805628 G>C maps to NM_015461.2 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr19:7083598 T>C maps to NM_024341.2 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:7075687 C>G maps to NM_024341.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr19:2915554 C>T maps to NM_173480.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:38056036 G>A maps to NM_016536.3 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr19:52376954 A>G maps to NM_032679.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr16:2052643 C>T maps to ENST00000431526 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr19:35250174 C>A maps to NM_001007248.2 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr19:58490169 A>G maps to NM_025027.3 C626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:64966234 G>T maps to NM_015042.1 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr19:52496291 C>A maps to ENST00000354939 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:40553891 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr19:55993789 A>G maps to NM_033113.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:30794424 G>A maps to NM_001080417.1 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:71607374 T>C maps to NM_014497.3 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:91406115 G>A maps to NM_201269.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr1:91403568 G>T maps to NM_201269.1 S1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr16:31090722 G>A maps to NM_014699.3 E1026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr16:31092684 C>T maps to NM_014699.3 T1680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:31089678 T>C maps to NM_014699.3 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr19:11594520 G>A maps to NM_138783.3 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr3:88190086 A>T maps to NM_018293.2 R543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:99158260 C>T maps to NM_001083956.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:53668283 T>A maps to NM_024733.3 K487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:63720696 A>G maps to NM_153363.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:151259372 C>G maps to NM_020832.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr1:43317093 C>A maps to ENST00000442768 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr1:249150135 A>G maps to NM_001136036.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr4:437055 A>G maps to NM_133474.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr19:12088186 G>A maps to NM_001012753.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:30569337 G>T maps to NM_033410.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr7:149129442 C>T maps to ENST00000440594 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr16:89294016 C>T maps to NM_182531.2 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:12502557 C>T maps to NM_001080821.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:12502923 A>T maps to NM_001080821.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr19:12502159 G>T maps to NM_001080821.2 S351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr19:58805587 G>A maps to NM_021089.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:185801067 A>G maps to NM_194250.1 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr19:53057179 T>C maps to NM_001039886.3 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr19:58385872 T>C maps to NM_001144989.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:58384711 A>G maps to NM_001144989.1 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr19:53454064 G>A maps to NM_001031665.1 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:33288776 C>A maps to NM_052857.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:33289280 T>C maps to NM_052857.3 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr20:57769661 G>A maps to NM_178457.1 A1196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr19:52660095 G>A maps to NM_001102657.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr19:52659396 G>A maps to NM_001102657.1 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr19:52877550 G>A did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr22:29445938 C>G maps to NM_032173.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:238053764 A>T maps to NM_021186.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr23:15841259 C>G did not map to a codon.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr16:3142578 C>T maps to NM_032805.1 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr19:58596699 G>A maps to NM_001145542.1 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:33960784 C>T maps to NM_145238.3 I947I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr15:43653717 T>C maps to NM_152455.3 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr19:13919689 C>A maps to NM_023072.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr23:57618844 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:57618702 G>C did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr23:57619096 G>A did not map to a codon.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr23:57619096 G>A did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:57618714 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:53262038 T>C maps to NM_024646.2 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr17:3977516 C>T maps to NM_015113.3 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr17:3919675 C>A maps to NM_015113.3 G2696*. Only missense variants will be evaluated by CHASM.
