1628 NP_705833 K971T not found in SNVbox database
2338 NP_705833 G785S not found in SNVbox database
4046 NP_705833 D947N not found in SNVbox database
4700 NP_705833 N425S not found in SNVbox database
4721 NP_705833 G713W not found in SNVbox database
4993 NP_705833 N698K not found in SNVbox database
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr16:7629852 G>A maps to NM_145891.2 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:7743325 C>T maps to NM_145893.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:9243029 C>A maps to NM_000014.4 E840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr12:9265979 G>A maps to NM_000014.4 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:8995758 T>C maps to NM_144670.3 Y426Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:9001386 G>A maps to NM_144670.3 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:9007407 C>T maps to NM_144670.3 S915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr3:151545932 T>G maps to NM_001086.2 Y391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:12779664 C>T maps to NM_001103170.1 H62H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr1:12726160 C>T maps to NM_001013630.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:69769765 G>A maps to NM_014911.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr4:57244558 G>A maps to NM_181806.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:105950318 G>A maps to NM_015423.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:121733114 C>A maps to NM_005763.3 E585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:121773615 G>A maps to NM_005763.3 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:107553306 G>A maps to NM_005502.3 C1941C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr9:107584853 A>G maps to NM_005502.3 D917D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr17:67149982 G>A maps to NM_080282.3 L1318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:67151175 G>T maps to NM_080282.3 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:67152062 G>T maps to NM_080282.3 I1153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr17:67215768 G>T maps to NM_080282.3 Y149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr17:67149483 C>T maps to NM_080282.3 P1366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:215876209 A>C maps to NM_173076.2 L762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:215809801 C>T maps to NM_173076.2 P2422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:215821457 C>T maps to NM_173076.2 A2054A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:215823776 A>C maps to NM_173076.2 Y1970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:215875165 G>A maps to NM_173076.2 D787D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:48431625 G>A maps to NM_152701.3 P3921P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AG-A002-01A-01W-A00K-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr7:48312292 A>T maps to NM_152701.3 A1010A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr7:48285545 T>C maps to NM_152701.3 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:2336750 G>T maps to NM_001089.2 V1074V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:2369686 G>A maps to NM_001089.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:2347504 G>A maps to NM_001089.2 D696D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr1:94476935 C>T maps to NM_000350.2 L1822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr1:94474420 G>A maps to NM_000350.2 A1907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:94543388 C>A maps to NM_000350.2 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr1:94512602 G>A maps to NM_000350.2 C930C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:67248005 G>A maps to ENST00000392677 R1474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr17:67079366 C>A maps to NM_080284.2 V1487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:67119399 G>A maps to NM_080284.2 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr17:67079027 A>G maps to NM_080284.2 A1534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr19:1047522 C>T maps to NM_019112.3 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:66880486 A>G maps to NM_007168.2 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:66883512 G>A maps to NM_007168.2 F1053F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:66887689 C>T maps to NM_007168.2 W988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:66978728 G>T maps to NM_080283.3 S1565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:87150173 C>A maps to NM_000927.3 E902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:87041324 G>T maps to NM_018849.2 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:87035804 G>A maps to NM_018849.2 L1102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:87082276 G>T maps to NM_018849.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:220079116 G>A maps to NM_005689.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:74288916 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:74282175 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr7:150742297 T>C maps to ENST00000297504 A690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr16:16232298 G>A maps to ENST00000399408 T1467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr16:48244911 C>A maps to NM_032583.3 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr16:48234336 C>A maps to NM_032583.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:48174609 G>T maps to NM_033226.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr10:101567922 C>T maps to NM_000392.3 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr3:183670904 C>T maps to NM_005688.2 W879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:183705646 G>A maps to NM_005688.2 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:17426075 G>T maps to ENST00000302539 Y1181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:17415270 G>A maps to ENST00000302539 F1528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr11:17417397 C>T did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr11:17429961 G>A maps to ENST00000302539 R934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:21962851 T>G maps to NM_005691.2 R1417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:22078906 G>A maps to NM_005691.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr12:39979966 A>G maps to NM_005164.3 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr12:39979966 A>G maps to NM_005164.3 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr12:39980005 C>T maps to NM_005164.3 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:94943852 G>A maps to ENST00000454898 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:30558399 C>T maps to NM_001025091.1 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr7:150921027 A>G maps to NM_005692.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr3:183909025 G>T maps to NM_018358.2 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:43716282 C>T maps to NM_004915.3 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:89042907 C>A maps to NM_004827.2 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr4:89039395 G>A maps to NM_004827.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:44040323 T>G maps to NM_022436.2 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr2:44051052 C>A maps to NM_022436.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr13:108882234 A>G maps to NM_032859.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:19239216 G>A maps to NM_138340.4 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:43743999 G>T maps to NM_016006.4 G143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:27048110 G>A maps to NM_005470.3 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr10:27066140 T>C maps to NM_005470.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:133729568 C>T maps to NM_007313.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:179087821 C>A maps to NM_007314.3 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr1:179084016 T>C maps to NM_007314.3 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr1:179078142 T>C maps to NM_007314.3 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:116232815 C>A maps to ENST00000277895 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:116304802 A>G maps to ENST00000277895 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr9:136131337 C>T maps to NM_020469.2 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:150553723 C>T maps to ENST00000416793 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr7:150554580 C>T maps to ENST00000416793 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr17:1028682 G>A maps to NM_021962.2 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:38167343 G>A maps to NM_001607.3 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:38168130 C>T maps to NM_001607.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr17:35564695 G>A maps to NM_198834.1 N1242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr17:35536341 C>T maps to NM_198834.1 L1646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr17:35454824 G>A maps to NM_198834.1 A2220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:35609841 C>T maps to NM_198834.1 W649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:109679059 G>T maps to NM_001093.3 E1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:112167697 C>T maps to NM_001136538.1 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:132347191 G>T maps to NM_032169.4 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr3:128627863 G>A maps to NM_014049.4 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:76226905 C>T maps to ENST00000370834 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr1:76205780 A>G maps to ENST00000370834 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:121164910 G>A maps to NM_000017.2 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr15:89381984 C>T maps to NM_013227.3 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:7250450 C>T maps to NM_014716.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:7251306 G>T maps to NM_014716.3 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:7252363 C>T maps to NM_014716.3 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr17:31350985 G>T maps to NM_183377.1 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr17:31618779 C>T maps to NM_183377.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr17:31352989 A>T maps to NM_183377.1 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr2:220396777 G>A maps to NM_018674.4 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr2:220396732 G>A maps to NM_018674.4 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr11:44104785 A>T maps to NM_032592.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:15596328 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:15609835 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:15609912 C>A did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:15593882 G>A did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:23532746 C>A maps to NM_014977.3 E937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr17:40063715 G>A maps to ENST00000401700 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr9:32407367 G>A maps to NM_002197.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:80655778 G>A maps to NM_130767.2 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr1:6393598 G>A maps to NM_007274.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:23751330 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:8401375 G>A maps to NM_003501.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:47267286 C>T maps to NM_001610.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:132051044 C>T maps to NM_001134194.1 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:132086645 G>T maps to NM_001134194.1 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:6755660 G>T maps to NM_032489.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:70823979 T>C did not map to a codon.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:70824009 T>C did not map to a codon.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr23:70824009 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:6187385 T>C maps to NM_030924.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr2:223783819 C>A maps to NM_203372.1 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr2:223786007 T>A maps to NM_203372.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr16:20702393 T>C maps to NM_052956.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr16:20781478 C>T maps to NM_005622.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:7475016 T>C maps to NM_001080454.1 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:7479624 G>A maps to NM_001080454.1 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:90700995 G>A maps to NM_001141945.1 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:56778459 G>A maps to NM_001017992.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:179305756 G>T maps to NM_004301.3 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr1:236902651 C>T maps to NM_001103.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr1:236850014 C>G maps to NM_001103.2 Y14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:66319056 T>G maps to NM_001104.1 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:66330555 C>T maps to NM_001104.1 A866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr19:39212268 C>T maps to NM_004924.3 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr19:39198786 G>C maps to NM_004924.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:98275430 C>T maps to NM_005735.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:65467087 G>T maps to NM_001005386.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:152522208 T>C did not map to a codon.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr12:100617605 G>A maps to NM_022496.3 E368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:53907081 G>A maps to NM_022899.4 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:127185238 T>C did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr23:127185563 T>A did not map to a codon.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr12:52370256 C>T maps to NM_020328.3 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:158397680 G>T maps to NM_145259.2 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:148672870 G>T maps to NM_001616.3 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:148684828 G>T maps to NM_001616.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr3:38523729 A>G maps to NM_001106.3 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr4:123301394 G>A maps to NM_139243.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:123317450 G>T maps to NM_139243.3 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:58925523 G>T maps to NM_001110.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr10:127753557 C>A maps to NM_003474.4 G479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:155030607 C>T maps to NM_207197.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:9666361 G>A maps to NM_003183.4 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr2:9633047 G>A maps to NM_003183.4 F687F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr8:39581382 G>T maps to NM_014237.2 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr8:39613369 T>C maps to NM_001464.3 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr8:39645653 C>T maps to NM_001464.3 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:70926282 T>C maps to NM_003813.2 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr7:87810861 C>T maps to NM_021723.3 D817D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:24187505 C>T maps to NM_014265.4 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:120438356 G>A maps to NM_021794.2 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr8:39079178 C>T maps to NM_145004.5 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr8:24359064 C>A maps to ENST00000380789 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:24342813 G>A maps to ENST00000380789 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr10:135086832 G>T maps to NM_001109.4 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:38948859 G>T maps to NM_003816.2 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr21:28210257 A>G maps to NM_006988.3 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr21:28214927 C>T maps to NM_006988.3 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:8661279 G>A maps to NM_030957.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr19:8665922 T>C maps to NM_030957.2 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:33577193 G>A maps to NM_030955.2 C979C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:33662085 C>T maps to NM_030955.2 Q325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr5:33588802 C>T maps to NM_030955.2 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr5:33549335 C>T maps to NM_030955.2 A1426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr5:33577193 G>A maps to NM_030955.2 C979C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr5:33643572 G>A maps to NM_030955.2 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr9:136321302 C>T maps to NM_139025.3 L1227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr10:72462144 C>T maps to NM_139155.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:72493709 G>A maps to NM_139155.2 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr11:130343259 T>C maps to NM_139055.2 Y799Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:5303845 G>A maps to NM_139056.2 K1051K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr16:77334229 T>G maps to NM_199355.2 P868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr16:77326990 G>A maps to NM_199355.2 V1057V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:77401379 G>A maps to NM_199355.2 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr16:77465416 C>T maps to NM_199355.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:129030516 C>T maps to NM_133638.3 R969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr5:178579247 G>A maps to NM_014244.4 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:43825185 A>G maps to ENST00000389420 S1070S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:43777453 T>C maps to ENST00000389420 E1568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr12:43847819 C>T maps to ENST00000389420 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:43821125 G>A maps to ENST00000389420 Y1364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:73161477 G>T maps to NM_014243.1 C872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:73185067 C>A maps to NM_014243.1 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr4:73205405 C>T maps to NM_014243.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr4:73179471 G>T maps to NM_014243.1 S556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:161168327 C>T maps to NM_005099.4 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr21:28338137 G>A maps to NM_007038.3 H191H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:64466506 G>T maps to NM_197941.2 R1061R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr5:64625278 A>G maps to NM_197941.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr15:79058550 C>T maps to ENST00000258883 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr11:130275578 G>A maps to NM_007037.4 C848C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr3:64589753 A>T maps to NM_182920.1 T1197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr9:18474256 T>A maps to NM_001040272.4 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:84694130 T>C maps to NM_207517.2 P1533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:84539656 C>T maps to NM_207517.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:84651188 C>T maps to NM_207517.2 R937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:154574712 G>T maps to ENST00000292205 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr1:154570423 G>C maps to ENST00000292205 S648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:1313258 G>A maps to NM_018702.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr14:78285425 C>T maps to NM_020421.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr8:145618210 C>T maps to NM_174922.3 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:45662326 C>T maps to NM_021116.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr5:7802362 C>T maps to NM_020546.2 C887C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr5:7766869 C>G maps to NM_020546.2 S722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:25141364 C>T maps to NM_004036.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr2:25141304 G>T maps to NM_004036.3 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr14:24793330 T>C maps to NM_139247.3 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:123044305 C>A maps to NM_183357.2 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:123038661 G>A maps to NM_183357.2 N705N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:50343496 C>T maps to NM_001114.3 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr8:132051813 G>A maps to NM_001115.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr8:131848608 C>A maps to NM_001115.2 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr8:131916236 G>A maps to NM_001115.2 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:131792791 G>A maps to NM_001115.2 V1200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:131921958 G>A maps to NM_001115.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:132051898 G>A maps to NM_001115.2 C227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:4164269 C>A maps to NM_001116.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:31123783 G>A maps to ENST00000409489 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr10:111883965 T>C maps to NM_016824.3 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:100232765 G>A maps to NM_000668.4 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:100234998 G>T maps to NM_000668.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr4:99997943 T>A maps to NM_000671.3 K159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr4:100349245 G>A maps to NM_000673.4 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:67372615 C>T maps to NM_144650.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr2:3504620 G>A maps to NM_018269.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:202911344 G>A maps to NM_015999.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:76074454 C>T maps to NM_006721.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr22:50921163 A>C maps to NM_024866.4 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:49508541 G>T maps to NM_181442.1 I903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:49509855 G>A maps to NM_181442.1 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr18:77895440 G>A maps to NM_014913.3 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr1:203134703 C>T maps to NM_001048230.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr22:24836655 C>T maps to NM_000675.4 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:36558046 C>A maps to NM_017825.2 Y242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr8:26722323 G>A maps to ENST00000356368 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:159344472 G>A maps to NM_000679.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:96781138 C>T maps to NM_000682.5 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:96780979 C>T maps to NM_000682.5 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr2:96781428 G>A maps to NM_000682.5 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr11:67052394 C>A maps to NM_001619.3 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr22:26091118 G>A maps to NM_005160.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr1:244587340 G>A maps to NM_001126.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:44153268 G>A maps to NM_001129.3 P962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr5:148679891 C>T maps to NM_152406.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr10:116075426 G>A maps to NM_001001936.1 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:88052955 C>A maps to NM_001166693.1 S1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:88047376 C>T maps to NM_001166693.1 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:148038083 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:147743544 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:147891437 C>A did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:147744067 C>A did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:148037365 T>C did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:148068984 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:100343546 C>T maps to NM_001025108.1 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:100623207 C>T maps to NM_001025108.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr2:100168046 G>A maps to NM_001025108.1 N1215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:132232836 G>A maps to NM_014423.3 N495N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr5:132270222 A>G maps to NM_014423.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:74354424 C>A maps to NM_001133.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr4:74351751 C>T maps to NM_001133.2 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:64779346 G>T maps to ENST00000422803 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:64819126 G>A maps to ENST00000422803 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr2:237029021 A>G maps to NM_001037131.1 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:88768131 G>A maps to NM_133447.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:88768825 G>T maps to NM_133447.1 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr12:58121195 G>A maps to NM_001122772.1 R1009R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:47698867 A>C maps to ENST00000357610 L701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:47701596 G>A maps to ENST00000357610 I648I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:47707498 G>A maps to ENST00000357610 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr2:27292469 G>A maps to NM_021831.5 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr5:76355532 T>A maps to NM_018046.4 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr7:141333741 A>G maps to NM_018238.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr7:141315311 A>G maps to NM_018238.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr7:141321597 C>A maps to NM_018238.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:100379158 C>T maps to ENST00000311030 S1343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr1:100349685 A>G maps to ENST00000311030 E774E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr1:100343239 C>T maps to ENST00000311030 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:15909864 C>A maps to NM_024758.3 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr21:45391326 G>A maps to NM_001037553.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:161587402 G>T maps to NM_020133.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:41467285 C>T maps to NM_178819.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr2:178402820 A>G maps to NM_003659.3 Q625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:178357913 G>A maps to NM_003659.3 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr1:230841701 G>A maps to NM_000029.3 N367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:88162070 C>A maps to ENST00000395847 E1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr9:88247985 G>A maps to ENST00000395847 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:148459236 C>T maps to NM_032049.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:115304580 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:115303996 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:115303592 C>T did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:115304582 G>A did not map to a codon.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr5:35014170 G>A maps to NM_031900.3 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:135679299 A>C maps to NM_017651.4 P1045P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr6:135644339 T>C maps to NM_017651.4 G1096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr6:135787316 C>T maps to NM_017651.4 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:62286252 G>A maps to NM_001620.1 V5212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:62286993 G>A maps to NM_001620.1 I4965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:62297649 G>A maps to NM_001620.1 V1413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr11:62288673 G>A maps to NM_001620.1 V4405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr11:62298735 T>C maps to NM_001620.1 K1051K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr11:62299722 C>T maps to NM_001620.1 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:105411169 C>A maps to NM_138420.2 E3540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:105412943 G>A maps to NM_138420.2 V2948V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr14:105408335 G>A maps to NM_138420.2 V4484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr14:105423027 T>C did not map to a codon.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr1:222846663 A>G maps to NM_022831.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:129273793 C>A did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:129283520 T>C did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr23:129271122 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:106967177 C>T maps to NM_001624.2 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:106968527 G>T maps to NM_001624.2 E741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr21:45705993 C>T maps to NM_000383.2 H35H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:4834525 C>T maps to NM_018836.3 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr9:4719197 A>G maps to NM_016282.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr14:96924523 C>T maps to NM_152327.2 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr17:19839688 T>C maps to NM_007202.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:151673521 C>T maps to NM_005100.3 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:86270341 G>T maps to NM_006738.4 E2294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr15:86124043 G>C maps to NM_006738.4 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:4737262 G>A maps to NM_006422.2 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:4736320 C>A maps to NM_006422.2 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:4737700 C>A maps to NM_006422.2 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr12:4725012 G>T maps to NM_006422.2 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr23:49958223 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:49961559 C>A did not map to a codon.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr23:49958477 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:49957287 C>T did not map to a codon.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr23:49957692 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:33292122 G>T maps to NM_004274.4 E1702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr14:33147591 C>T maps to NM_004274.4 Q936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:91631397 G>T maps to NM_005751.4 E723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:91709402 C>A maps to NM_005751.4 G2652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr7:91726505 A>G maps to NM_005751.4 K3411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr7:91718760 T>G maps to NM_005751.4 S3092S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr7:91711951 T>C maps to NM_005751.4 A2712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr6:109854525 T>C maps to NM_001145128.2 E1166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr9:117139204 T>C maps to NM_030767.4 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:117138748 G>A maps to NM_030767.4 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:117139239 C>A maps to NM_030767.4 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr9:117099534 C>T maps to NM_030767.4 P1373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:109366199 C>A maps to NM_152763.3 E683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr7:134136460 G>A maps to NM_001628.2 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr7:134221873 G>A maps to NM_020299.4 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:5043728 C>A maps to NM_001354.4 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:5149673 T>C maps to NM_003739.4 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr1:19633530 G>A maps to NM_003689.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr19:50373290 G>A maps to ENST00000391835 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr3:52236598 G>A maps to ENST00000441729 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:55042054 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:55043971 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:74275167 C>T maps to NM_000477.5 C193C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CI-6620-01A-11D-1826-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr10:97387286 T>G maps to NM_002860.3 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr15:58257941 A>G maps to NM_003888.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:101448682 G>T maps to NM_000693.2 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr3:125872376 G>A maps to ENST00000273450 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:105431885 G>A maps to NM_001034173.3 R714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr12:112229926 G>T maps to NM_000690.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr11:67786315 T>C maps to NM_001161473.1 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:67434114 G>A maps to NM_001031615.1 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr6:135260507 C>T maps to NM_022568.3 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:165649906 G>T maps to NM_000696.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr13:52593264 A>G maps to NM_001004127.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr23:110987998 T>A did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:110987995 A>T did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr3:183963059 C>T maps to NM_005787.5 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:37524128 G>A maps to NM_013338.4 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:77815465 C>A maps to NM_024079.4 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr11:77815450 C>G maps to NM_024079.4 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr2:29519892 A>G maps to NM_004304.3 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr2:29443591 G>A maps to NM_004304.3 R1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr2:29450509 G>T maps to NM_004304.3 P948P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:29416200 G>A maps to NM_004304.3 Y1584Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:29606604 G>A maps to NM_004304.3 C425C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:29606678 G>A maps to NM_004304.3 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr2:3730542 C>T maps to ENST00000403787 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:3743374 G>T maps to ENST00000403787 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr2:3745026 T>C maps to ENST00000403787 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:73717162 G>T maps to NM_015120.4 E2692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:73679173 G>A maps to NM_015120.4 K1839K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:73718419 G>T maps to NM_015120.4 E3111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:73677073 C>A maps to NM_015120.4 T1139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr17:6913445 G>A did not map to a codon.
Multiple mappings detected for codon TCGA-AG-A002-01A-01W-A00K-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr17:7978911 C>A did not map to a codon.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr2:233321911 C>T maps to NM_001631.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3578-01A-01W-0831-10 chr4:113303596 G>A maps to NM_025144.3 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:56171303 C>A maps to NM_052947.3 E2036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:56204918 C>A maps to NM_052947.3 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr15:85402522 C>A maps to NM_020778.4 S1491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr2:202590170 T>C maps to NM_020919.3 G1085G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:202352459 C>A maps to NM_001168221.1 E1780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:202466488 G>A maps to NM_001168221.1 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr2:202208955 T>C maps to NM_139163.2 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:202172322 G>A maps to NM_139163.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr2:203846817 C>T maps to NM_024744.14 Y571Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr23:11316977 T>C did not map to a codon.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr16:56397906 G>A maps to NM_001144.4 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:47471879 G>A maps to NM_001143668.1 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr2:128627061 T>C maps to NM_031445.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr12:31841956 T>C maps to NM_001113402.1 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr23:112022803 G>A did not map to a codon.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr23:112022296 C>G did not map to a codon.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr1:115216604 A>G maps to NM_000036.2 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:10527314 C>T maps to NM_000480.2 R739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr4:71388494 C>T maps to NM_212557.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr1:104160212 G>T maps to NM_000699.2 G51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:104160194 C>T maps to NM_000699.2 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr17:66250662 T>C maps to NM_016627.4 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:112638396 C>T maps to NM_022662.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr9:140082198 G>A maps to NM_013366.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr4:25379129 C>T maps to ENST00000510092 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr12:121766192 C>T maps to NM_016237.4 W410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr12:121789948 C>T maps to NM_016237.4 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr12:110811951 C>T maps to NM_016238.2 Q599Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr8:108509612 C>A maps to NM_001146.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:6372269 G>C maps to NM_001147.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr20:858964 G>A maps to NM_015985.2 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:853725 G>A maps to NM_015985.2 N463N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:870987 G>T maps to NM_015985.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:63068013 G>A maps to NM_014495.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:8436305 C>T maps to NM_139314.1 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr8:41530173 G>A maps to ENST00000415018 H1598H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:41547810 C>T maps to ENST00000415018 A1346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr8:41545719 C>T maps to ENST00000415018 E1404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr4:114267165 G>A maps to NM_001148.4 P1453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr4:114279169 C>T maps to NM_001148.4 F3132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:114238866 C>T maps to NM_001148.4 R900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:114275275 C>A maps to NM_001148.4 S1834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr4:114262918 C>T maps to NM_001148.4 C1323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr4:114204003 A>G maps to NM_001148.4 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr10:61832652 G>A maps to NM_020987.2 A2662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr2:190592781 C>T maps to NM_144708.3 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:190584460 G>A maps to NM_144708.3 E796E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:190603400 C>A maps to NM_144708.3 V1231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:65239796 C>T maps to NM_182703.3 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:65242155 C>T maps to NM_182703.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr15:65239625 C>T maps to NM_182703.3 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:54554940 C>A maps to NM_153228.2 I625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:14713762 C>T maps to NM_054027.4 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:139838783 G>T maps to ENST00000253810 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:139909016 G>A maps to ENST00000253810 T2162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:91936789 C>A maps to NM_019004.1 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr2:241463531 C>G maps to ENST00000401804 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr7:16666719 T>G maps to NM_020319.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr13:111545495 G>A maps to NM_017664.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr16:89349028 G>A maps to NM_013275.4 S1307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:89347486 G>A maps to NM_013275.4 Y1821Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr18:9275529 C>A maps to NM_015208.3 L1924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:9257186 C>T maps to NM_015208.3 R1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr18:9254260 C>T maps to NM_015208.3 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:110461907 C>T maps to NM_033121.1 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:5922266 G>A maps to NM_001009941.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr4:74019690 C>T maps to NM_032217.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:74005397 C>A maps to NM_032217.3 E979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr10:90582736 T>C maps to NM_144590.2 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:27328954 C>A maps to NM_014915.2 E772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr10:27311603 G>A maps to NM_014915.2 L1366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:33137442 C>A maps to NM_032139.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr3:15727738 C>A maps to NM_015199.3 G651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr3:15727736 T>C maps to NM_015199.3 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr3:15711977 T>C maps to NM_015199.3 S987S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr10:37431114 C>T maps to ENST00000374660 C374C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr10:37508551 C>T maps to ENST00000374660 N1367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:37419197 C>T maps to ENST00000374660 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:37431190 G>T maps to ENST00000374660 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr18:14752563 G>A did not map to a codon.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr5:94022410 T>C maps to NM_032290.3 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:79855106 G>A maps to NM_001004441.2 H244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:186320759 C>T maps to NM_181726.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr11:82936043 T>A maps to ENST00000260047 L509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr2:197990135 G>A maps to NM_001195144.1 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:197948208 C>T maps to NM_001195144.1 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr2:197866499 G>T maps to NM_001195144.1 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:10025098 C>T maps to NM_198798.1 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:10030098 C>T maps to NM_198798.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr20:10032526 A>G maps to NM_198798.1 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:125592876 G>A maps to NM_020337.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr4:125592727 T>C maps to NM_020337.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:90315787 C>T maps to ENST00000339746 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:100169437 C>T maps to NM_152788.3 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:99145258 G>A maps to NM_152788.3 F1182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr9:101552641 C>T maps to ENST00000375018 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:70017143 C>T maps to NM_018043.5 I783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:43596802 G>A maps to NM_018075.3 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr3:43618187 T>C maps to NM_018075.3 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:26621242 C>A maps to NM_031418.2 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:26619918 C>A maps to NM_031418.2 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:101490407 C>T maps to ENST00000392977 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:22242677 C>T maps to NM_213599.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr11:22294384 T>C maps to NM_213599.2 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:45823009 C>A maps to NM_001025356.2 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:90348344 G>A maps to NM_001150.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr2:69409752 T>G maps to NM_032208.2 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr4:80992750 C>T maps to NM_001145794.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:81923334 G>A maps to NM_145869.1 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr15:60690088 A>G maps to NM_001002858.2 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:36671658 G>T maps to NM_001177506.1 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr17:41004706 G>A maps to NM_003734.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:41004493 A>G maps to NM_003734.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:41004706 G>A maps to NM_003734.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr2:201527646 T>C maps to NM_001159.3 A1166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:71807246 C>T maps to ENST00000423132 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr16:71808375 G>T maps to ENST00000423132 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr19:16338425 C>T maps to NM_001130524.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr19:50303388 C>T maps to NM_014203.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:985549 C>T maps to ENST00000332231 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:33954700 C>T maps to NM_001030006.1 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr17:33951543 C>T maps to NM_001030006.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:77334941 G>A maps to NM_003664.3 R912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:115205725 A>T maps to NM_001284.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:51289576 G>T maps to NM_007347.3 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr9:72047481 G>A maps to NM_001163.3 I804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:72131361 G>A maps to NM_001163.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr9:72131034 G>A maps to NM_001163.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:26789769 C>T maps to NM_019043.3 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr4:40892391 G>A maps to NM_004307.1 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr5:112175695 C>T maps to NM_001127510.2 Q1469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr5:112175327 C>G maps to NM_001127510.2 S1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr5:112173428 C>G maps to NM_001127510.2 S713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr5:112173345 G>A maps to NM_001127510.2 W685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr5:112175256 A>G maps to NM_001127510.2 E1322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr5:112175170 C>T maps to NM_001127510.2 Q1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr5:112163700 C>T maps to NM_001127510.2 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr5:112175270 C>A maps to NM_001127510.2 S1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr5:112175479 G>T maps to NM_001127510.2 E1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr5:112174743 A>G maps to NM_001127510.2 E1151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr5:112173957 A>G maps to NM_001127510.2 K889K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr5:112175059 G>T maps to NM_001127510.2 E1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr5:112164615 C>T maps to NM_001127510.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr5:112136974 G>A did not map to a codon.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr5:112174861 C>T maps to NM_001127510.2 Q1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3584-01A-01W-0831-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr5:112173599 C>A maps to NM_001127510.2 S770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr5:112175206 G>T maps to NM_001127510.2 E1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr5:112175347 G>T maps to NM_001127510.2 E1353*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AG-3598-01A-01W-0833-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr5:112128190 C>T maps to NM_001127510.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr5:112163651 C>A maps to NM_001127510.2 C525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr5:112137035 C>T maps to NM_001127510.2 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr5:112175234 C>A maps to NM_001127510.2 S1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr5:112175327 C>G maps to NM_001127510.2 S1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr5:112175422 C>T maps to NM_001127510.2 Q1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr5:112174839 T>A maps to NM_001127510.2 Y1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr5:112175389 C>T maps to NM_001127510.2 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr5:112164624 G>T maps to NM_001127510.2 G567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr5:112175506 C>T maps to NM_001127510.2 Q1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr5:112173289 C>T maps to NM_001127510.2 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr5:112175135 C>G maps to NM_001127510.2 S1282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr5:112175173 G>T maps to NM_001127510.2 E1295*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AG-3731-01A-11D-1733-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr5:112170691 A>G maps to NM_001127510.2 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr5:112170690 C>G maps to NM_001127510.2 S596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr5:112175389 C>T maps to NM_001127510.2 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr5:112151203 C>T maps to NM_001127510.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr5:112175409 T>C maps to NM_001127510.2 P1373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr5:112175943 A>G maps to NM_001127510.2 K1551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr5:112175068 C>T maps to NM_001127510.2 Q1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr5:112175357 C>G maps to NM_001127510.2 S1356*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AG-3894-01A-01W-1073-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr5:112173703 C>T maps to NM_001127510.2 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr5:112175152 G>T maps to NM_001127510.2 G1288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr5:112116522 G>T maps to NM_001127510.2 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr5:112174883 C>G maps to NM_001127510.2 S1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr5:112175272 C>T maps to NM_001127510.2 Q1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr5:112175425 G>T maps to NM_001127510.2 E1379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr5:112175418 T>A maps to NM_001127510.2 Y1376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:112175896 G>T maps to NM_001127510.2 E1536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr5:112174543 A>T maps to NM_001127510.2 K1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr5:112174915 G>T maps to NM_001127510.2 E1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr5:112175479 G>T maps to NM_001127510.2 E1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr5:112173298 A>T maps to NM_001127510.2 K670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr5:112175506 C>T maps to NM_001127510.2 Q1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr5:112174915 G>T maps to NM_001127510.2 E1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr5:112175146 G>T maps to NM_001127510.2 E1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr5:112175170 C>T maps to NM_001127510.2 Q1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr5:112175100 T>A maps to NM_001127510.2 C1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:112128190 C>T maps to NM_001127510.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr5:112175215 G>T maps to NM_001127510.2 E1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr5:112151260 C>T maps to NM_001127510.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr5:112175254 G>T maps to NM_001127510.2 E1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr5:112151260 C>T maps to NM_001127510.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr5:112175506 C>T maps to NM_001127510.2 Q1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr5:112175679 A>G maps to NM_001127510.2 R1463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr5:112175154 A>G maps to NM_001127510.2 G1288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr5:112151203 C>T maps to NM_001127510.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr5:112175506 C>T maps to NM_001127510.2 Q1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr5:112175357 C>G maps to NM_001127510.2 S1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr5:112154868 G>A maps to NM_001127510.2 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr5:112175347 G>T maps to NM_001127510.2 E1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr5:112175422 C>T maps to NM_001127510.2 Q1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr5:112175247 T>C maps to NM_001127510.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr5:112175479 G>T maps to NM_001127510.2 E1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr5:112175106 A>G maps to NM_001127510.2 S1272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr5:112174632 A>G maps to NM_001127510.2 R1114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr5:112175270 C>A maps to NM_001127510.2 S1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr5:112175575 C>T maps to NM_001127510.2 Q1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr5:112175241 A>G maps to NM_001127510.2 E1317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr5:112175323 G>T maps to NM_001127510.2 E1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr5:112175304 G>A maps to NM_001127510.2 Q1338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr5:112177788 A>G maps to NM_001127510.2 R2166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr5:112151203 C>T maps to NM_001127510.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr5:112154722 C>T maps to NM_001127510.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr5:112164587 A>G maps to NM_001127510.2 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr5:112175148 A>G maps to NM_001127510.2 E1286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr5:112164615 C>A maps to NM_001127510.2 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr5:112173800 C>A maps to NM_001127510.2 S837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr5:112175212 A>T maps to NM_001127510.2 K1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr5:112175307 T>C maps to NM_001127510.2 G1339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr5:112175479 G>T maps to NM_001127510.2 E1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr5:112175575 C>T maps to NM_001127510.2 Q1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr5:112170651 C>A maps to NM_001127510.2 S583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr5:112175241 A>G maps to NM_001127510.2 E1317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr5:112128144 A>G maps to NM_001127510.2 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr5:112175302 C>T maps to NM_001127510.2 Q1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr5:112175214 A>G maps to NM_001127510.2 K1308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr5:112175135 C>A maps to NM_001127510.2 S1282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr5:112174224 A>G maps to NM_001127510.2 Q978Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr5:112175215 G>T maps to NM_001127510.2 E1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr5:112174423 C>T maps to NM_001127510.2 Q1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr5:112174783 A>T maps to NM_001127510.2 K1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr5:112175206 G>T maps to NM_001127510.2 E1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr5:112175302 C>T maps to NM_001127510.2 Q1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr5:112175422 C>T maps to NM_001127510.2 Q1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr5:112175307 T>C maps to NM_001127510.2 G1339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr5:112175347 G>T maps to NM_001127510.2 E1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr5:112176816 A>G maps to NM_001127510.2 S1842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr19:1462029 G>A maps to NM_005883.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr20:57036436 G>A maps to NM_153360.1 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr23:55033486 C>T did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:55029488 C>T did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr11:43343565 T>C maps to NM_001142930.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr2:68740773 T>G maps to NM_173545.2 L195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr11:57003485 G>A maps to NM_005161.4 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr19:36362572 G>A maps to NM_001024807.1 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr2:21238335 G>A maps to NM_000384.2 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr2:21227305 C>T maps to NM_000384.2 A3974A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:21228261 C>T maps to NM_000384.2 T3826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:21233604 G>T maps to NM_000384.2 A2045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:21234123 G>A maps to NM_000384.2 I1872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:21236250 G>A maps to NM_000384.2 R1333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:21251355 G>A maps to NM_000384.2 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr2:21231333 T>C maps to NM_000384.2 E2802E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr22:39411747 C>T maps to ENST00000396762 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:39421628 C>T maps to NM_152426.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:39477044 C>A maps to NM_021822.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr22:39497387 C>T maps to NM_001166003.1 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:64208283 C>T maps to NM_000042.2 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:64216738 C>T maps to NM_000042.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:36627417 C>T maps to ENST00000451256 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:36122297 T>C maps to NM_030642.1 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:27327991 G>A maps to NM_000484.3 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:58539194 G>T maps to NM_006380.2 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:57302509 G>T maps to NM_012096.2 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:105593256 C>A maps to NM_018171.3 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:33443767 G>T maps to NM_004925.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr9:33447423 C>G maps to NM_004925.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:25232798 G>A maps to NM_001169.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr15:58467219 C>T maps to NM_020980.3 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr15:58467168 A>G maps to NM_020980.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:35152272 A>G maps to NM_014691.2 H1371H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:35240484 C>A maps to NM_014691.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr15:35166924 A>G maps to NM_014691.2 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:66765184 A>T did not map to a codon.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:66765187 A>T did not map to a codon.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr23:66942700 T>C did not map to a codon.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr23:66905929 G>A did not map to a codon.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr23:66765575 A>C did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:66765031 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:47424487 T>C did not map to a codon.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr11:72423598 C>T maps to NM_001040118.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr11:72437882 A>G maps to NM_001040118.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:36189181 C>T maps to NM_015230.2 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:36121306 C>A maps to NM_015230.2 E1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:141039453 C>G maps to NM_022481.5 R1053R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:47193019 G>A maps to NM_032389.3 R300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:68178265 C>A maps to NM_006421.3 E700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:68179399 C>A maps to NM_006421.3 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:47645143 C>T maps to NM_006420.2 R1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr20:62338072 C>T maps to NM_003224.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:131894433 G>A maps to ENST00000356962 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:68117553 G>T maps to NM_001172.3 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr4:148944514 A>G maps to NM_024605.3 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:148787882 G>A maps to NM_024605.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:148796272 C>T maps to NM_024605.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:32925186 C>T maps to NM_014783.3 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr15:32908528 C>T maps to NM_014783.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:30922925 T>A maps to NM_001039841.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:32132486 C>A maps to NM_018287.5 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr16:24942330 A>G maps to NM_001006634.1 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr11:110477338 G>A maps to NM_020809.2 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:110462841 G>T maps to NM_020809.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:24886892 C>A maps to NM_020824.3 E1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr10:49658680 C>T maps to ENST00000417912 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:49659109 C>T maps to ENST00000417912 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:86893266 G>A maps to NM_001025616.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr2:69049779 C>T maps to NM_001007231.2 Y503Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:69049680 C>T maps to NM_001007231.2 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:43481983 G>A maps to ENST00000428638 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:6882237 G>T maps to ENST00000400091 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr1:161018479 T>C maps to NM_001025598.1 Q777Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:161018731 C>T maps to NM_001025598.1 G693G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:119102035 C>A maps to NM_020754.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:128844370 C>T maps to NM_001142685.1 P893P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:130218327 C>T did not map to a codon.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr23:130217769 C>T did not map to a codon.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr23:130220335 C>T did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:130215772 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:11160377 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:11162359 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:11206943 G>T did not map to a codon.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr19:42396741 C>T maps to NM_199002.1 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr8:1905020 T>C maps to ENST00000398564 A1234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:1842704 C>T maps to ENST00000398564 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:156918166 C>T maps to NM_198236.1 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:8218582 G>A maps to NM_173728.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:73073161 C>T maps to NM_014786.3 Y1524Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:7518467 C>T maps to NM_001130955.1 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr1:155920266 G>A maps to NM_001162383.1 R904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr23:135862980 T>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:135751651 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:135757192 C>T did not map to a codon.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr13:111926251 C>T maps to NM_001113511.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:62885870 C>T did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:62885785 G>T did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:62898438 C>G did not map to a codon.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr1:27105551 A>G maps to NM_006015.4 R1721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr1:27087879 C>T maps to NM_006015.4 Q723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr1:27088758 C>T maps to NM_006015.4 Q790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr1:27105552 C>T maps to NM_006015.4 R1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr1:27056180 C>T maps to NM_006015.4 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr1:27101397 T>C maps to NM_006015.4 P1560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3575-01A-01W-0831-10 chr6:157528656 C>T maps to ENST00000367148 R2168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr12:46244263 C>T maps to NM_152641.2 G786G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:46215239 G>A maps to NM_152641.2 W225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:46231285 G>T maps to NM_152641.2 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr12:46123633 G>A maps to NM_152641.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:34627854 C>A maps to NM_001017363.1 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:34622065 G>A maps to NM_001017363.1 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr14:58794999 C>T maps to NM_002892.3 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr14:58831428 A>G maps to NM_002892.3 G874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr10:63850715 A>G maps to NM_032199.2 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr10:63852512 T>C maps to NM_032199.2 A1097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:101796695 C>T maps to NM_001177.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr3:93755532 G>A maps to NM_182896.2 Q208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr3:160395154 A>G maps to NM_025047.2 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr16:57286133 C>A maps to NM_012106.3 C149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:152663434 C>A maps to NM_012097.3 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:18804690 C>A maps to NM_015161.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr16:18804648 G>T maps to NM_015161.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:23250824 C>T maps to NM_173081.3 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:23292193 G>T maps to NM_173081.3 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:100808742 A>G did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr23:100911495 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:100880062 A>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:150789890 T>G maps to NM_001668.3 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:150812071 C>A maps to NM_001668.3 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:13395672 G>T maps to ENST00000403290 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:13397238 C>T maps to ENST00000403290 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:27543125 C>A maps to NM_020183.3 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr7:98985758 G>A maps to NM_005720.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr9:127637256 C>T maps to NM_030978.1 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:169485980 C>A maps to NM_032487.4 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:35780945 C>T maps to ENST00000458225 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:4621593 C>T maps to ENST00000412477 H241H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:90669529 G>A maps to NM_020801.2 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr5:90678753 T>C maps to NM_020801.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr23:3019146 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:3019147 G>A did not map to a codon.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr23:2945414 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:17915087 G>A maps to NM_004315.4 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr11:122953915 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:131073085 G>T maps to NM_018482.2 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:131124415 G>A maps to NM_018482.2 F775F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr8:131127885 A>G maps to NM_018482.2 D720D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:9528649 G>A maps to NM_003887.2 P786P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:23765718 G>A maps to NM_017707.3 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr7:150878271 G>A maps to ENST00000422024 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:15333667 C>T did not map to a codon.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:63444778 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:63445503 C>A did not map to a codon.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr23:63444306 G>A did not map to a codon.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr23:63445157 G>C did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr1:76397609 G>A maps to NM_080868.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:94417348 C>T maps to ENST00000434324 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr14:94420822 C>T maps to ENST00000434324 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:132400296 G>A maps to NM_017873.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:101169897 C>T maps to NM_198243.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr12:48543493 G>A maps to NM_024095.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr6:101248258 G>A maps to NM_006828.2 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr12:108169039 G>A maps to NM_203436.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:155450062 T>C maps to ENST00000368346 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:155340670 G>A maps to ENST00000368346 R2151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:155348172 G>A maps to ENST00000368346 Y2082Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr7:97482428 T>C maps to NM_183356.3 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr17:3402306 C>T maps to NM_000049.2 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr8:62430094 G>A maps to NM_004318.3 N706N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr1:197111701 G>A maps to NM_018136.4 N560N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr9:133346258 G>A maps to NM_000050.4 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:130743297 G>A maps to ENST00000514044 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:130743677 G>T maps to ENST00000514044 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:96795837 C>T maps to NM_001002036.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:96798408 C>T maps to NM_001002036.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:96799216 C>T maps to NM_001002036.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr1:176838002 T>C maps to ENST00000281881 R1216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr1:176833479 C>T maps to ENST00000281881 T1283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr1:176845694 C>T maps to ENST00000281881 V1155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr1:176998806 A>G maps to ENST00000281881 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr9:119413827 G>A maps to ENST00000313400 I1017I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr20:31023472 C>T maps to ENST00000375687 N986N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr20:31024480 G>A maps to ENST00000375687 P1322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:31016149 G>A maps to ENST00000375687 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr20:31024480 G>A maps to ENST00000375687 P1322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr20:31023709 G>A maps to ENST00000375687 W1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr2:25982385 G>A maps to NM_018263.4 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr18:31324230 C>A maps to NM_030632.1 V1473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:31326216 C>A maps to NM_030632.1 T2135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr7:117008722 G>A maps to NM_130768.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:124348639 C>A maps to NM_014109.3 E1062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:124357186 A>T maps to NM_014109.3 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:24046130 C>A maps to NM_017552.1 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr1:1417635 C>T maps to NM_031921.4 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:29161836 A>G maps to NM_024857.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:29221099 C>T maps to NM_024857.3 N1743N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:3913845 C>T maps to NM_033064.4 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr6:32088832 C>T maps to NM_004381.4 W211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr12:53931207 C>T maps to NM_001130059.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:14589104 C>T maps to NM_018179.3 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr16:10524821 G>A maps to NM_024997.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr11:64674882 C>T maps to ENST00000421419 S892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr11:64677562 G>C maps to ENST00000421419 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr11:64681703 C>A maps to ENST00000421419 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:96798892 G>T maps to NM_018036.5 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:112260668 T>G maps to NM_022488.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:107369365 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:106727583 C>A maps to NM_004849.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:220087384 G>T maps to NM_024085.3 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:150720252 G>A maps to NM_173681.5 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr2:216177302 C>T maps to NM_004044.6 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:51027014 G>A maps to ENST00000358385 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:38540385 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:63403806 C>A did not map to a codon.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr11:108115599 C>T maps to NM_000051.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr11:108117711 G>A maps to NM_000051.3 W308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr11:108106550 A>G maps to NM_000051.3 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:108151822 C>T maps to NM_000051.3 C1168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:108160487 C>T maps to NM_000051.3 R1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:108163372 A>G maps to NM_000051.3 L1488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:108172384 C>T maps to NM_000051.3 R1730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr11:108216546 T>C maps to NM_000051.3 R2832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr11:108199839 A>T maps to NM_000051.3 S2394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr11:108117838 A>G maps to NM_000051.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr11:108188128 T>C maps to NM_000051.3 I2076I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr11:108142043 T>C maps to NM_000051.3 H996H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr11:108180982 A>G maps to NM_000051.3 T1953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr11:108200956 C>T maps to NM_000051.3 Q2442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr11:108178711 G>T did not map to a codon.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr15:25966897 G>T maps to NM_024490.3 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr15:26026186 C>A maps to NM_024490.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr15:25924610 C>A maps to NM_024490.3 T1459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr15:25947068 G>T maps to NM_024490.3 T918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:26026171 C>T maps to NM_024490.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr15:25926043 G>A maps to NM_024490.3 N1197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr15:25947098 G>A maps to NM_024490.3 H908H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr15:25972334 G>A maps to NM_024490.3 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr15:25940053 G>A maps to NM_024490.3 S1000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr15:26026186 C>A maps to NM_024490.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr15:25959223 G>A maps to NM_024490.3 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:47560084 T>G maps to NM_020453.3 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:113527933 C>T maps to NM_032189.3 I1035I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:182585194 G>T maps to NM_014616.1 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr3:182584054 G>C did not map to a codon.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr23:138908950 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:138884447 G>T did not map to a codon.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr23:138871553 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:138825741 G>T did not map to a codon.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr23:138832228 T>C did not map to a codon.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr23:138886722 G>T did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:138813813 T>A did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:138864755 A>C did not map to a codon.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr13:25281180 C>T maps to NM_001185085.1 T736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:25263462 G>T maps to NM_001185085.1 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:25266634 G>T maps to NM_001185085.1 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:17314833 G>A maps to NM_022089.2 C915C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:17323635 C>T maps to NM_022089.2 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:116943801 C>T maps to NM_000701.7 F923F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:160105638 C>A maps to NM_000702.3 I765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:160109745 A>G maps to NM_000702.3 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr19:42492204 G>C maps to ENST00000441343 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:42482425 G>A maps to ENST00000441343 F561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:160134054 C>T maps to NM_144699.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:160141111 C>A maps to NM_144699.3 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr16:28912086 T>C maps to NM_173201.3 D650D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:110778763 G>T maps to NM_170665.3 E688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:110783823 C>A maps to NM_170665.3 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:3846738 G>A maps to NM_174953.1 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:10443973 G>A maps to NM_001001331.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr3:10452332 G>A maps to NM_001001331.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:152825353 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:203672837 C>T maps to NM_001001396.1 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr16:84456273 G>T maps to ENST00000416219 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr16:84402274 G>C maps to ENST00000416219 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:114307232 G>A maps to NM_000705.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr18:43669869 T>C maps to NM_001001937.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:7841768 G>T maps to NM_001001973.1 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:54063038 G>A maps to NM_005176.5 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:50792366 A>C maps to NM_001003803.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:153662731 T>C did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr5:81613866 C>T maps to NM_001017971.1 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:40464995 C>T did not map to a codon.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr12:124239010 C>T maps to NM_012463.3 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:67478506 G>A maps to NM_004691.4 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:113517214 C>T maps to NM_001690.3 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr23:77284879 G>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:52549226 G>C maps to NM_000053.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:42551063 T>G maps to NM_006095.2 R540R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:26402263 C>T maps to NM_016529.4 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr18:55322535 G>A maps to NM_005603.4 R941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:55317639 G>A maps to NM_005603.4 R1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:55336711 G>T maps to NM_005603.4 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr18:55338740 G>A maps to NM_005603.4 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr20:50310552 C>T maps to NM_006045.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:142218532 C>T maps to NM_001184.3 T1772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr3:142211988 A>G maps to NM_001184.3 I2021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr3:142176489 T>C maps to NM_001184.3 E2537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr3:142176503 G>A maps to NM_001184.3 R2533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr3:142176501 T>C maps to NM_001184.3 R2533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr10:117228802 G>A maps to NM_207303.2 V1206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr10:117061474 C>T maps to NM_207303.2 R914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr10:117059716 T>C maps to NM_207303.2 C863C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr23:76937491 C>T did not map to a codon.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr23:76814175 T>C did not map to a codon.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr23:76888870 A>G did not map to a codon.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr6:16327143 G>A maps to NM_000332.3 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:16328136 G>T maps to NM_000332.3 Y135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:16327461 G>A maps to NM_000332.3 H360H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr23:13337038 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:13337600 G>T did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:13337616 G>A did not map to a codon.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr23:13337615 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:63981252 G>A maps to NM_001177387.1 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr20:54958084 C>T maps to NM_198437.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr19:57744833 G>T maps to NM_001015878.1 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:57743430 C>T maps to NM_001015878.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr7:70239027 C>T maps to NM_015570.2 I615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:32593349 C>T maps to NM_015060.1 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr12:63544208 A>G maps to NM_000706.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr12:63541336 G>T maps to NM_000706.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr1:206230985 G>A maps to NM_000707.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:69455607 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:69261786 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:69263345 C>A did not map to a codon.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr23:69262937 G>A did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:63545762 G>A maps to NM_004655.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr17:79176092 C>T maps to ENST00000269392 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr1:193150026 A>G maps to NM_003783.3 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:41033163 G>A maps to NM_033172.1 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:17922924 C>T maps to NM_014256.3 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr2:232262678 C>T maps to NM_145236.2 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr11:372699 G>C maps to NM_178537.4 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr11:379597 A>G maps to NM_178537.4 E795E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr3:118948709 A>T maps to NM_212543.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr6:90660039 C>T maps to NM_001170794.1 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr9:33264429 G>A maps to NM_004323.5 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:104026639 C>A maps to NM_001015049.2 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:104026333 G>A maps to NM_001015049.2 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr17:79428600 C>T maps to ENST00000436173 A2304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr15:40751658 C>T maps to NM_014952.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr8:143614742 C>T maps to NM_001702.2 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr6:70098767 T>C maps to NM_001704.2 F1518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:69666021 C>T maps to NM_001704.2 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:97949420 C>T maps to NM_018842.4 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:28971075 C>T maps to NM_012342.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:65771216 C>T maps to NM_003860.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:102946431 G>T maps to NM_017935.4 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr4:102946614 C>T maps to NM_017935.4 R515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:102751343 C>T maps to NM_017935.4 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:88014703 G>T maps to NM_001173543.1 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:215645738 C>A maps to NM_000465.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:129321107 G>A maps to NM_003658.4 E217E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:31508300 C>T maps to ENST00000417556 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr6:31600023 C>T maps to NM_080686.2 L1192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:171510544 C>T maps to ENST00000392078 R1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr1:171526587 T>C maps to ENST00000392078 V1779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr14:35295262 A>G maps to NM_013448.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr7:72891393 T>C maps to NM_032408.3 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr11:66299433 C>T maps to NM_024649.4 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:123663571 T>C maps to NM_152618.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:56519561 C>A maps to NM_031885.3 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:122749339 C>A maps to NM_176824.1 E659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:122770017 G>A maps to NM_176824.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr7:33380539 C>T maps to NM_198428.2 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr7:33217165 C>T maps to NM_198428.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:107491948 C>T maps to NM_001142568.1 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:107492286 A>G maps to NM_001142568.1 K573K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:156622064 G>A maps to NM_021948.3 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:59112098 C>T maps to ENST00000407086 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr10:127515179 A>G maps to NM_016567.3 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:50232725 C>A maps to NM_181708.2 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr16:31121792 G>A maps to NM_005881.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr2:60689479 T>C maps to NM_022893.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr14:99642455 G>A maps to NM_138576.2 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:99697796 G>A maps to NM_138576.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:80263049 C>A maps to NM_004049.3 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:114424442 G>T maps to NM_001010922.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr19:45262730 C>A maps to NM_005178.4 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:6930823 C>T maps to NM_181844.3 C442C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr1:147086224 G>T did not map to a codon.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr1:147091809 C>T maps to NM_004326.2 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr11:118772692 G>A maps to NM_182557.2 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr11:118771915 G>A maps to NM_182557.2 Q846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr11:118771330 G>A maps to NM_182557.2 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr6:136599121 T>C maps to NM_014739.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:136589370 C>A maps to NM_014739.2 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr23:39913168 C>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:39914627 G>T did not map to a codon.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr23:129150015 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:104003288 G>A maps to NM_020139.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:96707027 C>T maps to NM_000623.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:70751775 T>G maps to NM_018429.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:70759923 G>A maps to NM_018429.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:40968061 C>A maps to NM_003766.3 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr6:107391650 G>A maps to NM_001080450.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr4:42145871 G>A maps to NM_207406.3 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:56879959 G>T maps to NM_152731.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:13538823 C>T maps to ENST00000396900 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr10:13481450 C>T maps to ENST00000396900 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr19:12866267 C>T maps to NM_017682.2 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr23:102318189 C>A did not map to a codon.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr23:102564881 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:17505515 C>A maps to NM_001195.3 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr20:17475195 G>A maps to NM_001195.3 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr23:152771508 C>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:152771345 T>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:78423680 C>A maps to NM_001713.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr5:78376647 C>T maps to NM_017614.4 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:78376541 C>T maps to NM_017614.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:78378751 G>T maps to NM_017614.4 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr5:78365613 T>C maps to NM_017614.4 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr10:60588614 T>A maps to NM_001080512.1 Y963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:60546738 C>T maps to NM_001080512.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:32369293 C>A maps to NM_001714.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr12:32481092 G>C maps to NM_001714.2 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:18220848 G>T maps to NM_197966.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr2:127809920 G>A maps to NM_139343.1 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:102201749 G>T maps to NM_182962.1 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr2:32654232 C>T maps to NM_016252.3 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:32702498 G>T maps to NM_016252.3 E2306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:32640363 G>T maps to NM_016252.3 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:32750028 G>T maps to NM_016252.3 E3900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:32770896 A>G maps to NM_016252.3 R4260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr8:11420486 G>A did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr10:97983656 G>T maps to NM_013314.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr7:43832379 T>C maps to NM_000712.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:169347744 C>T maps to NM_003666.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr8:22049653 G>T maps to NM_006129.4 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr2:69093667 G>A maps to NM_014482.1 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:79772085 A>G maps to NM_198892.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:79782574 G>A maps to NM_198892.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr4:96035969 T>C maps to ENST00000440890 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr4:96051101 C>T maps to ENST00000440890 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr23:15527455 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:83932835 G>A maps to NM_001717.3 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr9:16436675 G>A maps to NM_017637.5 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr9:16419343 G>A maps to NM_017637.5 D981D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr3:112969432 G>A maps to ENST00000273395 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr5:173036349 T>C maps to NM_138369.2 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:13604736 C>A maps to NM_148894.2 E1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:13606584 C>A maps to NM_148894.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:74362772 C>A maps to NM_212552.2 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:36932651 G>A maps to NM_001725.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:36954707 C>A maps to NM_001725.2 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr20:36965561 C>T maps to NM_001725.2 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:32831741 G>T maps to NM_174932.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:32841834 C>A maps to NM_174932.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr22:32853313 G>A maps to NM_174932.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:65890192 G>T maps to ENST00000321892 E945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:65907076 C>A maps to ENST00000321892 S1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr7:140500172 C>T maps to NM_004333.4 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr7:140453104 A>G maps to NM_004333.4 F610F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr7:140449172 G>A maps to NM_004333.4 Q636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr7:140482871 T>C maps to NM_004333.4 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr7:140453170 G>A maps to NM_004333.4 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr7:140481427 T>C maps to NM_004333.4 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:41197781 T>C maps to ENST00000471181 R1857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr13:32913405 A>G maps to NM_000059.3 K1638K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:32893290 G>T maps to NM_000059.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr13:32911878 G>A maps to NM_000059.3 Q1129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr13:32911251 C>T maps to NM_000059.3 P920P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr13:32912505 C>T maps to NM_000059.3 G1338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr13:32968952 A>G maps to NM_000059.3 R3128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr13:32914503 A>G maps to NM_000059.3 E2004E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:15355562 C>T maps to NM_058243.2 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr19:15376428 C>A maps to NM_058243.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:137488268 C>A maps to NM_139199.1 E920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:889243 C>T maps to NM_001009877.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:92433777 G>T maps to ENST00000347608 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr1:92445133 C>T maps to ENST00000347608 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr7:97920545 C>T maps to NM_015379.4 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr17:59886066 G>A maps to NM_032043.2 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:34923287 C>T maps to NM_018321.3 H204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:36182071 C>T maps to NM_015695.2 I966I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:135570622 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:135574340 G>T did not map to a codon.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr19:55815066 C>T maps to NM_032430.1 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr11:1466583 G>A maps to NM_003957.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:40587275 C>T maps to NM_018963.3 A1224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:79945492 A>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:79948459 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:79984251 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:80001173 A>G did not map to a codon.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr23:79945322 G>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:79999688 G>A did not map to a codon.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr3:49690303 G>A maps to NM_003458.3 P1105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr3:49698673 T>C maps to NM_003458.3 F3132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr1:55472903 C>T maps to NM_057176.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:17514560 G>A maps to NM_004335.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr11:122848536 G>A maps to NM_001098169.1 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:93754332 G>T maps to NM_003972.2 E1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:93786933 A>G maps to NM_003972.2 E1761E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:3640611 G>A maps to NM_032444.2 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:3641292 G>A maps to NM_032444.2 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:124049511 C>T maps to ENST00000368994 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr1:203274814 G>A maps to NM_006763.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr11:111365922 A>T maps to NM_017589.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:111369407 C>A maps to NM_017589.2 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:100608289 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:100612497 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:100613404 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:100629580 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:26502085 C>A maps to NM_001732.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:26409842 C>T maps to NM_007048.5 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:180475110 G>A maps to NM_152547.4 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:103310476 C>T maps to NM_033637.2 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:111406832 C>T maps to NM_004336.3 K775K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:105581443 A>C maps to NM_007073.4 Y3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:105564708 A>C maps to NM_007073.4 L228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:16714052 C>T maps to NM_014038.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr10:121596416 T>C maps to NM_024834.2 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:98744000 C>T maps to NM_015652.2 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr10:124459192 A>T maps to NM_001010912.1 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:5789269 G>T maps to NM_017782.4 E1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:82191768 G>T maps to NM_032333.4 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:50315816 G>A maps to NM_001031746.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:105883567 G>T maps to ENST00000336358 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr10:105920863 T>C maps to ENST00000389588 E1158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr10:128114640 C>T maps to NM_001004298.2 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:128153271 G>A maps to NM_001004298.2 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr10:128193072 G>T maps to NM_001004298.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:8942862 C>A maps to NM_020643.2 *468Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:68030060 C>T maps to NM_022338.3 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr11:76169373 A>G maps to ENST00000393457 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:76162981 G>T maps to ENST00000393457 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:4598999 G>T maps to NM_144663.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:33628361 C>T maps to ENST00000389726 N1394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:33564419 C>A maps to ENST00000389726 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:33564563 C>A maps to ENST00000389726 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr11:33581341 C>T maps to ENST00000389726 V1010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr11:33689561 G>A maps to ENST00000389726 S1810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:122775091 G>A maps to NM_024806.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:82643395 T>G maps to NM_145018.3 L339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr11:64707209 G>A maps to NM_001037225.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr11:109294679 C>T maps to NM_207645.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:111385658 C>T maps to NM_207430.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:111386828 C>T maps to NM_207430.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr11:111404520 A>G maps to NM_207430.2 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:61539073 C>T maps to NM_001127392.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr11:61539373 T>C maps to NM_001127392.1 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr12:27064183 A>G maps to NM_018164.2 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr12:91348042 C>T maps to NM_152638.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:82796815 C>T maps to NM_032230.2 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:82871103 G>T maps to NM_032230.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:88439528 G>T maps to NM_001009894.2 G198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr12:21681995 G>A maps to NM_030572.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:49048752 C>A maps to NM_017822.3 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:102558230 A>C maps to NM_017915.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:112654695 G>A maps to NM_001109662.2 I2250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr12:112617046 G>C maps to NM_001109662.2 G3542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:64746796 C>A maps to NM_001170633.1 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr13:39587387 A>G maps to NM_025138.3 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr13:39587546 A>G maps to NM_025138.3 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr13:31540435 C>T maps to NM_152325.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr13:113052450 A>G maps to NM_145248.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:73305522 T>C maps to ENST00000377815 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr13:103346827 G>A maps to NM_001010977.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:90769220 C>T maps to NM_017970.2 W418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:50092759 C>A maps to NM_018139.2 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr14:76644339 A>G maps to NM_017926.2 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:76639929 C>T maps to NM_017926.2 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:76668170 G>T maps to NM_017926.2 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:60581926 G>T maps to ENST00000404681 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:80993287 A>T maps to NM_152446.3 Y999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr14:59942586 C>T maps to NM_144581.1 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:52460479 C>T maps to NM_016039.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr14:77844696 T>C maps to NM_001010860.1 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:76455319 G>A maps to NM_052873.2 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:50550392 G>T maps to NM_001014830.1 C317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr14:58604741 A>C maps to ENST00000438670 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr14:60903653 G>T maps to NM_174978.2 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:77491801 G>A maps to NM_024496.2 G778G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:74516683 G>T maps to NM_025057.2 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr14:95921950 T>C maps to NM_152592.3 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr14:23465437 G>A maps to NM_021944.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr15:24921535 C>T maps to NM_018958.2 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:24921208 C>T maps to NM_018958.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:24923329 C>A maps to NM_018958.2 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr15:24921751 C>T maps to NM_018958.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:81428867 C>T maps to ENST00000458088 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:49869033 G>A maps to NM_152647.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:36950044 G>A maps to NM_001130010.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr15:65899640 C>T maps to ENST00000420799 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr15:34648026 C>G maps to ENST00000438749 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr15:40544942 A>G maps to NM_001039905.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:40849511 G>A maps to NM_001080791.1 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:19628081 G>A maps to NM_020314.5 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr16:89782979 A>G maps to NM_004913.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr16:4797374 C>T maps to NM_139170.2 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr16:58147931 T>C maps to NM_013242.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr16:30035137 C>G maps to NM_001109660.1 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr16:30770989 A>G maps to NM_001014979.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:32904629 C>T maps to NM_207454.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:72947703 G>A maps to NM_030630.2 Y776Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:56621429 G>A maps to NM_001038704.1 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr17:6919185 A>G maps to NM_001142798.1 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr17:45438837 T>C maps to NM_152347.4 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:45425208 C>T maps to NM_152347.4 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr17:34191814 G>A maps to NM_152781.2 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr17:79514033 C>A maps to NM_025161.5 G692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:57289008 C>T maps to NM_018149.6 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr17:7329757 C>T maps to NM_175734.4 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:7329355 G>A maps to NM_175734.4 W61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:71231872 C>T maps to NM_017941.4 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:30803113 G>A maps to NM_001105528.1 R630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr18:30806810 T>C maps to NM_001105528.1 E534E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr19:58469997 G>T maps to NM_152474.4 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr19:30502056 A>G maps to NM_003796.2 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:30496604 C>T maps to NM_003796.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:30499947 G>A maps to NM_003796.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr19:30502020 G>A maps to NM_003796.2 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr19:30477314 C>A maps to NM_003796.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:758400 G>A maps to NM_173481.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr19:1234737 G>A maps to ENST00000382477 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr19:3547268 C>T did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:3557197 G>T maps to NM_021731.2 A68A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AG-3999-01A-01W-1073-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:16612251 G>T maps to NM_032207.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr19:36498128 G>A maps to ENST00000455847 N285N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr19:55673653 T>C maps to ENST00000301249 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr19:50983929 C>T maps to ENST00000376920 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr19:10202906 C>T maps to NM_018381.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr19:51770668 G>A maps to NM_173635.1 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr1:22987485 C>T maps to NM_000491.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr10:16562532 G>A maps to NM_001010908.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:7173870 G>A maps to NM_001734.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr1:244780889 C>T maps to NM_001130957.1 Y850Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:111490844 C>T maps to NM_018372.3 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:169771775 C>T maps to NM_018186.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:169773342 T>G maps to NM_018186.2 L147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:169388387 G>A maps to ENST00000367806 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:179460807 C>T maps to NM_144696.4 R743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:11017788 G>A maps to NM_001170754.1 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:170940962 G>A maps to NM_001163629.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:170955787 C>T maps to NM_001163629.1 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:182909615 C>T maps to ENST00000287709 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr1:19949995 T>A maps to ENST00000433528 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr1:112020639 C>T maps to NM_174896.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:57257861 G>A maps to NM_001004303.4 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr1:75139185 G>A maps to NM_001002912.4 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:75036860 C>T maps to NM_001002912.4 Q1511Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:55307312 C>T maps to NM_152607.2 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:24687482 C>T maps to ENST00000374409 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr1:162351810 G>T maps to NM_001135240.1 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:185175835 T>G maps to NM_001105518.1 L638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr1:25571715 A>C maps to NM_020317.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:172558076 G>A maps to ENST00000367723 E764E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr1:34666526 T>C maps to NM_001134734.1 C388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:34666508 G>A maps to NM_001134734.1 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:31905144 C>A maps to ENST00000437789 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr20:31040746 A>G maps to NM_080616.3 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr20:31889043 G>A maps to NM_033197.2 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr20:35743617 G>A maps to ENST00000343811 T857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:35740791 C>A maps to ENST00000343811 E943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr20:62493444 C>T maps to NM_080622.3 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:58519763 G>T maps to NM_022106.2 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr20:31652530 C>T maps to NM_182658.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr20:31660529 G>A maps to NM_182658.1 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:5844087 G>A maps to NM_152504.2 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr20:55088411 T>C maps to ENST00000357348 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:45947240 G>A maps to ENST00000443468 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr21:45924703 G>T maps to ENST00000443468 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:33876260 G>A maps to NM_058187.3 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr21:19190536 G>A maps to NM_001100420.1 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr22:38343396 C>T maps to NM_032561.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr11:73820133 C>T maps to ENST00000334126 W636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:73789535 G>A maps to ENST00000334126 I1409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:73850696 A>G maps to ENST00000334126 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr2:27804574 T>C maps to NM_032266.3 S1712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr2:26624928 G>A maps to NM_145038.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:20939874 G>A maps to ENST00000381090 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr2:24261803 A>G maps to NM_025203.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:105959410 C>T maps to NM_024093.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:88828790 C>T maps to NM_152670.2 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:27360720 G>A maps to NM_178553.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr2:241835378 G>A maps to NM_001085437.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr2:74789457 C>T maps to NM_138804.3 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:210888873 A>C maps to NM_152519.2 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:29293988 G>A maps to NM_001029883.1 R1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr2:29294301 A>G maps to NM_001029883.1 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr2:170502569 T>C maps to NM_001085447.1 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:170531498 C>A maps to NM_001085447.1 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:63664614 C>T maps to NM_015910.4 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:6712605 G>A maps to NM_000064.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr12:8211803 G>A maps to NM_004054.2 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:14724417 C>A maps to NM_032137.4 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr3:118865608 C>T maps to NM_152539.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:11885643 G>A maps to ENST00000444133 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:155481611 G>T maps to ENST00000340171 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:37476597 G>T maps to NM_178339.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr3:129023620 C>A maps to NM_001006109.1 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:143704465 G>T maps to NM_173552.3 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:143708551 G>T maps to NM_173552.3 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:49314044 C>T maps to NM_198562.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:56681149 G>A maps to ENST00000447900 R539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:56680556 C>T maps to ENST00000447900 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:184800808 C>A maps to NM_001025266.1 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr3:138668422 C>T maps to NM_001040061.2 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:207318053 G>T maps to NM_000715.3 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr1:207318001 T>A maps to NM_000715.3 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr4:100443846 G>A maps to NM_032149.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr4:113538776 G>A maps to NM_018392.4 G807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr4:113462249 G>A maps to NM_018392.4 Q1925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr4:76489342 G>A maps to NM_178497.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr4:170663194 G>A maps to NM_017867.2 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr4:170663134 G>A maps to NM_017867.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:128951770 C>T maps to ENST00000454347 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:121957421 A>G maps to NM_024574.3 C568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:121966824 G>T maps to NM_024574.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:99055574 C>A maps to NM_174952.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr9:123792765 C>A did not map to a codon.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr5:31538630 T>C maps to NM_018356.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:32789653 G>T maps to NM_024563.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr5:102611998 C>T maps to NM_033211.2 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:37183287 C>T maps to NM_023073.3 S1665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:37180182 C>T maps to NM_023073.3 E1891E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:37187932 C>A maps to NM_023073.3 E1275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr5:37198854 T>C maps to NM_023073.3 V1207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:64960392 C>T maps to NM_001093755.1 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:179264843 G>A maps to NM_016175.3 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr5:7835500 G>A maps to NM_001089584.1 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:159821897 G>A maps to NM_022090.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr5:159822059 G>A maps to NM_022090.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr5:41153984 A>G maps to NM_001115131.1 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:32317570 C>A maps to ENST00000447241 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:11735841 T>C maps to NM_001143948.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr6:34574604 C>A maps to NM_024294.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:165723057 C>T maps to NM_144980.3 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:33669151 G>A maps to NM_032340.2 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr6:54067032 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:4069219 C>A maps to NM_173563.1 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:74135014 C>A maps to NM_138441.2 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:42993033 A>G maps to NM_033112.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:88049911 G>T maps to NM_020425.4 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:88123614 C>T maps to NM_001031743.2 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:88170750 T>C maps to NM_001031743.2 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:97715855 C>T maps to NM_198468.2 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:121577397 C>T maps to ENST00000275159 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:121600355 A>G maps to ENST00000275159 H548H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:121576484 T>C maps to ENST00000275159 E669E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:121624816 C>T maps to ENST00000275159 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:107361042 C>T maps to NM_001142470.1 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr6:118786675 A>G maps to NM_001042475.2 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:74073441 G>A maps to NM_001017361.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr6:36293093 T>C maps to NM_001010903.4 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr6:36298050 T>C maps to NM_001010903.4 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr6:31691922 C>T maps to NM_138272.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr6:31734090 G>T maps to NM_025258.2 S752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:40936570 G>T maps to NM_000587.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:40962229 G>T maps to NM_000587.2 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:40981527 G>A maps to NM_000587.2 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr7:40228167 C>T maps to NM_001193311.1 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:42949773 G>T maps to NM_001099858.1 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr7:5940193 C>T maps to NM_015622.5 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr7:66406935 C>T maps to NM_017994.4 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr7:66409967 G>A maps to NM_017994.4 W55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr7:99752696 C>A maps to NM_018275.3 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:120767206 G>T maps to NM_024913.4 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr7:120629708 C>T maps to NM_024913.4 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:89929333 G>T maps to NM_001039706.2 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:92161753 C>T maps to NM_032120.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr7:108524117 G>C maps to NM_001024607.1 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:33369963 A>G maps to NM_001102401.1 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:33361279 C>T maps to NM_001102401.1 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr9:131589351 C>A maps to NM_016390.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:35045409 C>A maps to NM_203299.2 V928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr9:100672272 G>A maps to NM_016481.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:89763752 C>T maps to NM_001001709.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:89771576 C>T maps to NM_001001709.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr9:135374837 C>T maps to NM_207417.1 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr9:77631257 A>T maps to NM_152420.1 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr9:116185754 G>A maps to ENST00000451722 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr9:86559712 G>A maps to NM_032307.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr9:4661997 A>G maps to ENST00000454239 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:4617926 C>A maps to ENST00000454239 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr9:90500812 C>T maps to NM_178828.4 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:15784545 G>T maps to NM_173550.2 E1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:49731051 C>A maps to NM_001082534.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:66886691 C>T maps to NM_005182.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:231655639 C>T maps to NM_001130850.1 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:49933953 C>T maps to NM_001079670.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:49957000 C>A maps to NM_001079670.1 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr22:24466812 C>T maps to NM_012295.3 N765N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr22:24561507 C>T maps to NM_012295.3 R1641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:67225906 C>T maps to NM_145200.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:13365980 G>A maps to NM_023035.2 F1565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:13339557 G>T maps to NM_001127221.1 P1861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:13470494 G>A maps to NM_023035.2 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:13476146 G>A maps to NM_023035.2 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr19:13409401 C>A maps to NM_023035.2 G1019G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr9:141010122 C>T maps to ENST00000277549 G1924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr9:140952515 C>T maps to ENST00000277549 S1375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:2692028 G>A maps to NM_199460.2 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:2676927 C>T maps to NM_199460.2 C621C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr3:53756424 C>T maps to NM_001128840.1 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:53845189 G>A maps to NM_001128840.1 V2081V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:181453005 G>A maps to ENST00000357570 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:181453095 C>T maps to ENST00000357570 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:181759604 G>T maps to ENST00000357570 S1937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr1:181727108 C>T maps to ENST00000357570 S1452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr23:49086833 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:49083496 T>C did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:49074242 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:48693688 C>A maps to NM_018896.3 V1655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr17:48687291 G>A maps to NM_018896.3 A1585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr16:1260599 C>T maps to NM_021098.2 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr16:1254136 G>A maps to NM_021098.2 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:201063113 C>T maps to NM_000069.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:201046241 G>A maps to NM_000069.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:81667422 G>T maps to NM_000722.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr7:81601175 G>A maps to NM_000722.2 N686N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr7:81596484 G>A maps to NM_000722.2 D834D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr3:50417406 G>A maps to ENST00000435965 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:50416555 G>A maps to ENST00000435965 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:54872645 G>T maps to NM_018398.2 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:54922005 G>T maps to NM_018398.2 E693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:54933866 G>A maps to NM_018398.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:55052287 C>A maps to NM_018398.2 V977V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr3:54603873 C>T maps to NM_018398.2 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr3:54537562 C>T maps to NM_018398.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr3:54914865 C>T maps to NM_018398.2 R630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr3:54661842 C>T maps to NM_018398.2 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr2:152830188 C>T maps to NM_001005747.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:36962444 G>A maps to NM_006078.3 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:37098605 G>A maps to NM_006078.3 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr16:24366208 C>T maps to NM_006539.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr16:24372803 G>T maps to NM_006539.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:24268257 G>T maps to NM_006539.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr17:64880888 G>A maps to NM_014404.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr19:54515328 C>T maps to NM_145814.1 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr19:54485409 G>A maps to NM_031895.5 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:174979149 C>T maps to NM_014412.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:27465747 C>T maps to NM_004341.3 F2129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr2:27458138 G>A maps to NM_004341.3 L1271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:115049433 G>A maps to NM_014333.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:85961685 A>G maps to NM_153184.3 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:159169595 C>T maps to NM_021189.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:62451122 G>A maps to ENST00000383709 F1190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr3:62499311 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:7374036 C>A maps to NM_001170692.1 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr16:71417307 G>A maps to NM_001740.4 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr7:93116297 G>C maps to NM_001164737.1 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr7:93055879 G>A maps to NM_001164737.1 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:93090147 G>A maps to NM_001164737.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr7:93055793 C>T maps to NM_001164737.1 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:134618821 G>A maps to NM_033138.3 K434K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:134632378 C>T maps to NM_033138.3 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr10:105209515 G>A maps to NM_015916.4 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr2:47397888 A>G maps to ENST00000456319 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr10:5541182 C>T maps to NM_017422.4 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:71275378 G>T maps to NM_031468.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:71488746 G>A maps to NM_031468.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr19:13051136 G>C maps to NM_004343.3 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:16601325 C>T maps to NM_145046.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr19:16594824 G>A maps to NM_145046.3 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:12595254 G>T maps to NM_153498.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr10:12856298 C>T maps to NM_153498.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:209778898 C>A maps to NM_020439.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:209782393 C>A maps to NM_020439.2 Y235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr5:149602709 C>T maps to NM_015981.3 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:200776523 C>T maps to ENST00000236925 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr1:7792592 A>G maps to NM_015215.2 K1000K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:67691630 A>G maps to NM_018448.3 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr12:67692813 C>T maps to NM_018448.3 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr1:40536641 C>A maps to NM_001105530.1 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:17539540 C>A maps to NM_006366.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:17541336 A>G maps to NM_006366.2 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:241528854 C>T maps to NM_023083.3 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:44148341 C>A maps to NM_007058.3 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:30955361 G>A maps to ENST00000295055 V623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:223934749 C>T maps to NM_001748.4 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:42682158 G>A maps to NM_000070.2 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr15:42689036 C>T maps to NM_000070.2 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr23:110496396 T>G did not map to a codon.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr23:110489889 C>G did not map to a codon.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr23:110489921 G>A did not map to a codon.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr23:110494228 T>C did not map to a codon.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr3:15282119 C>T maps to NM_014296.2 D516D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:30882055 T>G maps to NM_001002259.1 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:30887962 C>A maps to NM_001002259.1 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:116528222 G>T maps to NM_006136.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:116556134 G>T maps to NM_006136.2 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr7:2984151 G>A maps to NM_032415.4 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr7:2962845 G>A maps to NM_032415.4 R688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr13:111277574 C>T maps to NM_018210.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:111290840 T>G maps to NM_018210.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr11:3041470 G>A maps to NM_001014437.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:25297394 G>A maps to NM_018272.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:44620946 G>A maps to NM_138423.3 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:40939243 C>T maps to NM_170589.3 I2048I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr23:41446233 C>A did not map to a codon.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr11:104899869 A>G maps to NM_033292.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:202073853 G>A maps to NM_032977.3 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:104820489 C>T maps to NM_001225.3 A187A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AG-A002-01A-01W-A00K-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:110610628 C>A maps to NM_001226.3 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:160168501 C>T maps to NM_001231.4 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:116275577 C>A maps to NM_001232.3 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:121981045 G>A maps to NM_001178065.1 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr20:55012467 G>A maps to NM_020356.3 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr1:10720132 G>A maps to NM_001079843.1 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:10709167 G>A maps to NM_001079843.1 G1039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:34477736 C>T maps to NM_001752.3 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr11:34489851 G>C maps to NM_001752.3 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:43925014 C>T maps to NM_172095.1 E432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr1:26527919 G>T maps to NM_198137.1 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:92189395 C>A maps to NM_024764.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr19:38851274 C>T maps to NM_021185.4 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr11:119148967 T>C maps to NM_005188.2 C396C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr11:119148922 T>C maps to NM_005188.2 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr21:44478972 G>A maps to ENST00000398168 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:77757737 C>T maps to NM_005189.2 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr17:77808885 G>A maps to NM_003655.2 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr22:39262246 A>C maps to NM_014292.3 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr22:39530442 G>A maps to NM_175709.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:15518270 C>T maps to NM_001080522.2 D347D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr4:15517530 G>A maps to NM_001080522.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr4:15560805 C>T maps to NM_001080522.2 R950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr10:97791677 A>G maps to NM_001159747.1 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:97787005 C>T maps to NM_001159747.1 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:42979013 C>A maps to NM_213607.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:219892514 G>A maps to NM_194302.2 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr4:186382304 C>T maps to NM_152775.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:114611748 C>A maps to NM_001040440.2 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr16:58312465 C>T maps to NM_014157.3 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:48801291 C>T maps to NM_144577.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr19:48800265 C>T maps to NM_144577.3 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:44434059 A>G maps to NM_144974.3 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr19:33372822 G>A maps to NM_032816.3 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr19:33424369 C>T maps to NM_032816.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr19:33424434 C>A maps to NM_032816.3 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr7:23682718 G>A maps to NM_138771.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:42205911 G>T maps to NM_024821.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr16:57741448 C>T maps to NM_032269.5 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:128441289 G>T maps to NM_022742.3 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179701906 C>A maps to NM_173648.3 E1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179732884 C>T maps to NM_173648.3 P814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:16615031 G>T maps to NM_014695.1 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:16638084 G>T maps to NM_014695.1 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:18486810 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:18528712 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:76916809 C>A maps to NM_020879.2 I777I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:106118307 G>T maps to NM_001008723.1 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr11:124847417 A>G maps to NM_025004.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr19:49912497 G>T maps to NM_144688.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:133379806 A>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:133379234 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:133379514 G>T did not map to a codon.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr23:133379030 T>C did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr1:93680444 T>C maps to NM_206886.2 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:159846359 G>A maps to NM_012337.2 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:159847189 G>A maps to NM_012337.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:26603763 G>T maps to NM_022778.2 E757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr1:3683864 C>T maps to NM_152492.2 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:43032077 C>T maps to NM_001080850.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:43076720 G>T maps to NM_001080850.2 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:126152013 C>A maps to ENST00000505024 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:126137554 C>T maps to ENST00000505024 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr12:96300224 G>A maps to NM_182496.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:180337120 C>A maps to NM_181426.1 E731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:78023757 C>T maps to NM_017950.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:94805516 C>A maps to NM_001042399.1 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:62522264 G>T maps to NM_138363.1 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:191075805 G>A maps to NM_178335.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr3:191093013 G>T maps to NM_178335.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:113169308 C>A maps to NM_144718.3 E733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:28511764 C>T maps to NM_032141.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr12:82747085 G>A maps to NM_014167.4 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr10:61552764 A>G maps to ENST00000395341 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr12:123281893 G>A maps to NM_201435.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr12:111342485 C>G maps to NM_152591.1 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr11:93148219 G>A maps to NM_181645.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr18:52575086 C>A maps to NM_025214.2 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:150578617 G>A maps to NM_015621.2 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr5:150585024 T>C maps to NM_015621.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr3:112356985 A>G maps to ENST00000447230 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr11:86126221 G>T maps to NM_001156474.1 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:85622350 G>T maps to NM_173556.3 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:85622350 G>T maps to NM_173556.3 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:118882957 C>T maps to NM_198489.1 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr11:66359382 C>A maps to NM_018219.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:55571635 G>A maps to ENST00000436346 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:55561837 G>A maps to ENST00000436346 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:91739786 G>A maps to NM_001080414.2 L1757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr12:28459709 A>G maps to NM_018318.3 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:28460624 T>C maps to NM_018318.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:118706916 C>A maps to NM_019044.4 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:7043264 G>A maps to NM_153376.2 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr4:26483532 G>A maps to NM_000730.2 Y338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr9:34709647 G>A maps to NM_002989.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr7:45108040 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:37007241 C>T maps to NM_003914.3 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr13:37011833 C>T maps to NM_003914.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:50053968 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:50052383 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:50052742 C>T did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:50037949 C>A did not map to a codon.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr23:50053207 T>C did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:50053620 G>C did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:50053207 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:43482295 C>T maps to NM_012142.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:30311679 G>A maps to NM_001238.1 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr5:162869133 T>C maps to NM_199246.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:97810173 C>T maps to NM_001134375.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr5:159680549 C>T maps to NM_024565.5 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr5:159682575 C>T maps to NM_024565.5 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:156867316 C>A maps to NM_020307.2 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr1:1322688 T>C maps to NM_030937.4 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr12:49087214 A>G maps to NM_001240.2 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr2:135711083 A>G maps to NM_058241.2 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:135710269 C>T maps to NM_058241.2 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:135710247 G>A maps to NM_058241.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:46307365 G>A maps to NM_178328.1 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr3:45943248 A>G maps to NM_031200.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr3:45943062 C>T maps to NM_031200.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr2:62099330 C>T maps to NM_006430.2 E459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:10262651 C>T maps to NM_012073.3 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:56126154 G>T maps to NM_001762.3 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr21:30445899 G>A maps to NM_006585.2 H4H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:117564583 G>T maps to NM_004258.3 E803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:117552700 C>T maps to NM_004258.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:74528221 A>G maps to NM_133493.3 E1341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr12:7637926 G>T maps to NM_004244.4 G848G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr12:7640084 T>C maps to NM_004244.4 K640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr12:7640084 T>C maps to NM_004244.4 K640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:7527939 G>A maps to ENST00000416109 Q990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:7559281 G>A maps to ENST00000416109 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr12:7531631 T>C maps to ENST00000416109 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr12:7586045 A>G maps to ENST00000416109 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:66478755 G>A maps to NM_005582.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:66479418 C>A maps to NM_005582.2 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:66479671 G>A maps to NM_005582.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr1:158226759 C>T maps to NM_001763.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr1:158227280 G>A maps to NM_001763.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:158261185 G>A maps to NM_001765.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:112666715 C>T maps to NM_138806.3 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr3:112546238 A>G maps to NM_001008784.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr2:71062832 G>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:35827038 G>A maps to NM_001771.3 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr19:35823642 C>T maps to NM_001771.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr11:66083289 C>T maps to NM_020404.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr6:47522494 C>T maps to NM_012120.2 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr17:72539112 T>C maps to NM_006678.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3575-01A-01W-0831-10 chr17:72613482 G>A maps to ENST00000426295 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:72610103 G>A maps to ENST00000426295 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:72522124 G>T maps to NM_174892.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:41934499 C>T maps to NM_145273.3 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:8367691 G>A maps to NM_016579.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:15850221 C>A maps to NM_001775.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr23:135730439 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:207958994 G>A maps to NM_172359.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:111439343 C>T maps to NM_000560.3 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr1:111437610 C>T maps to NM_000560.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr1:157804356 C>A maps to NM_005894.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr17:80274178 A>G maps to NM_006137.6 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:35616243 C>T maps to NM_001782.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr17:62009606 C>T maps to NM_001039933.1 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr6:14133925 G>A maps to NM_004233.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:23065794 G>A maps to NM_012072.3 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr20:23066685 C>T maps to NM_012072.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:14515304 C>T maps to NM_078481.2 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:2644307 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:49854746 C>A maps to NM_030911.3 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr10:12291611 A>G maps to NM_006023.2 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:115007714 C>T maps to NM_003903.3 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr13:115008807 G>A maps to NM_003903.3 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:137622890 G>A maps to NM_001790.3 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr17:45216209 A>G maps to NM_001114091.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr17:45216215 A>G maps to NM_001114091.1 Y537Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:45201280 C>A maps to NM_001114091.1 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr1:227279610 T>C maps to ENST00000366766 K777K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr11:64600209 C>T maps to NM_017525.2 P957P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:37873217 C>T maps to NM_006449.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:130726735 A>C maps to NM_020240.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr6:44387289 A>G maps to NM_001253.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr6:44387287 C>T maps to NM_001253.2 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr1:193094253 A>G maps to NM_024529.4 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr1:193094337 A>G maps to NM_024529.4 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:193094274 C>T maps to NM_024529.4 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:45153824 G>A maps to NM_022842.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr16:68844146 A>G maps to NM_004360.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr16:68857306 G>T maps to NM_004360.3 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr16:68846035 A>G did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr16:68835726 C>T maps to NM_004360.3 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr5:24537630 G>A maps to NM_006727.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:24487809 C>A maps to NM_006727.3 E777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr16:64984823 C>T maps to NM_001797.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr16:64981766 T>C maps to NM_001797.2 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr16:65005938 T>A maps to NM_001797.2 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr16:83817012 C>T maps to ENST00000268613 N690N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr16:83520244 G>A maps to ENST00000268613 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:19483581 G>T maps to NM_004934.3 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr5:19571824 G>T maps to NM_004934.3 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr5:19721513 A>G maps to NM_004934.3 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr5:19838900 T>C maps to NM_004934.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr18:64197180 C>G maps to NM_021153.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:64197180 C>T maps to NM_021153.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr18:25563000 T>C maps to NM_001792.3 E752E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr10:73491852 C>G maps to ENST00000398860 T1280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:73461951 C>T maps to ENST00000398860 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:73491942 C>T maps to ENST00000398860 N1310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr20:58574705 G>A maps to NM_177980.2 T695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:68729807 C>T maps to NM_001793.4 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:60503344 C>T maps to NM_001794.2 C623C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr20:60503416 C>T maps to NM_001794.2 Y647Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr20:60504709 C>T maps to NM_001794.2 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:63547836 G>T maps to NM_004361.2 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr18:63489413 A>G maps to NM_004361.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr16:61689491 G>C maps to NM_001796.2 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr16:61854859 C>T maps to NM_001796.2 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:26915804 G>T maps to NM_016279.3 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr5:176016082 C>T maps to NM_001171976.1 R970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:176016162 C>T maps to NM_001171976.1 D996D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr5:175995736 G>T maps to NM_001171976.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:105653317 G>T maps to NM_152750.4 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr3:49837195 C>A did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:49831424 G>A maps to NM_001007540.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr11:621657 C>T maps to NM_021924.4 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:621657 C>T maps to NM_021924.4 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr11:617419 A>G maps to NM_021924.4 D823D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:1636055 G>A maps to NM_024011.2 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:1572824 A>G maps to ENST00000401097 Y503Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr17:37676316 A>G maps to NM_016507.2 E1024E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:37665961 C>T maps to NM_016507.2 Q872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr17:37676316 A>G maps to NM_016507.2 E1024E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr17:37676314 G>T maps to NM_016507.2 E1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr7:90741855 G>T did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr7:90585054 C>T maps to NM_012395.2 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:47083884 C>T did not map to a codon.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr12:96688839 G>T maps to NM_002595.4 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr12:96688845 A>G maps to NM_002595.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:123165284 C>T maps to NM_018249.4 S1702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr9:123210311 C>T maps to NM_018249.4 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:46052897 G>T maps to NM_176096.1 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:20955686 G>A maps to NM_017774.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr6:21065365 T>C maps to NM_017774.3 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:18664126 A>G did not map to a codon.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:18606246 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:18622821 C>A did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:18664126 A>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:12871796 G>T maps to NM_004064.3 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr12:12870994 C>G maps to NM_004064.3 Y74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr9:21968227 T>C maps to NM_000077.4 *157W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr9:21974592 G>A maps to NM_058197.4 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr9:21970973 C>T maps to NM_001195132.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr9:21970943 T>C maps to NM_001195132.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:115146888 G>T maps to NM_001801.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:125864236 G>T maps to ENST00000392693 I864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr23:139865856 T>A did not map to a codon.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr23:139865903 C>T did not map to a codon.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr23:139866051 G>A did not map to a codon.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr23:139866523 C>A did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:139866321 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:22358681 G>A maps to NM_001802.1 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:15492479 C>A maps to ENST00000261644 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:85555011 C>T maps to NM_001263.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:85569736 G>A maps to NM_001263.3 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr6:31085066 C>A maps to NM_001264.4 G109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:4935845 C>T maps to ENST00000328908 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:4943785 C>T maps to ENST00000328908 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr16:80654808 C>T maps to NM_152342.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr19:51986277 C>T maps to NM_001080405.1 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr19:43098026 C>T maps to NM_001816.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr19:33792389 G>A maps to NM_004364.3 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:23588015 G>A maps to NM_001805.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:17670852 C>T maps to NM_017424.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr22:17663505 G>A maps to NM_017424.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr22:17672655 C>T maps to NM_017424.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:17976596 C>T maps to ENST00000400579 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr22:18028279 G>A maps to ENST00000400579 P1080P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:109808787 C>T maps to NM_001408.2 F1991F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr1:109816154 C>T maps to NM_001408.2 S2869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr3:48696749 G>T maps to NM_001407.2 I1106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr4:104067000 T>C maps to NM_001813.2 K1466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:104070360 C>A maps to NM_001813.2 E1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:104072461 C>A maps to NM_001813.2 E1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr4:104065687 A>G maps to NM_001813.2 L1649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr1:214825153 A>G maps to NM_016343.3 E2695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:214826269 G>T maps to NM_016343.3 E2754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:214830462 G>A maps to NM_016343.3 Q2891Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:214816318 G>A maps to NM_016343.3 A1546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:214830331 G>T maps to NM_016343.3 E2848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr1:214795473 A>G maps to NM_016343.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:68490516 C>T maps to NM_022909.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:25457388 C>A maps to NM_018451.3 E1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:25473703 G>A maps to NM_018451.3 F948F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr13:25480369 T>C maps to NM_018451.3 E602E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:126667415 G>A maps to ENST00000368325 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr9:123877468 A>G maps to NM_007018.4 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr9:123924137 A>T maps to NM_007018.4 L1698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:122714085 T>A maps to NM_153223.3 K714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr4:56830454 C>T maps to NM_025009.3 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:56878139 G>T maps to NM_025009.3 E931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:49048557 C>A maps to NM_001194998.1 E963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:49030778 T>C maps to NM_001194998.1 E1600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:49037156 C>A maps to NM_001194998.1 E1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:49089911 C>T maps to NM_001194998.1 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:243363930 C>A maps to NM_014812.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:13071154 G>A maps to NM_032142.3 S1764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr18:13029759 T>C maps to NM_032142.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr20:34099298 C>T maps to NM_007186.3 L2391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:34065890 G>T maps to NM_007186.3 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:88465128 C>A maps to NM_025114.3 E1985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:88512328 C>A maps to NM_025114.3 E548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr12:88474159 G>A maps to NM_025114.3 N1675N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:179966251 C>T maps to NM_014810.4 N320N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr1:180012240 A>G maps to NM_014810.4 G1471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:180010310 G>A maps to NM_014810.4 L1383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:95279476 C>T maps to NM_018131.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:95562477 C>T maps to NM_014679.3 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr3:138216927 G>A maps to NM_024491.2 H559H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:12691449 G>A maps to NM_024899.2 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr2:182402916 T>C maps to NM_001030311.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr16:55857577 G>A maps to NM_001025195.1 H141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr16:66995284 A>G maps to NM_024922.5 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:55883536 G>A maps to NM_001143685.1 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr16:55880569 A>G maps to NM_001143685.1 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:196695702 C>T maps to NM_000186.3 C659C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:196716338 G>T maps to NM_000186.3 E1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:196857309 C>T maps to NM_006684.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr1:196953227 G>T maps to ENST00000367414 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr1:196963366 T>G maps to ENST00000367414 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:110682703 G>A maps to ENST00000394635 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:47485783 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:117282580 C>T maps to NM_000492.3 I1269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:117267578 C>T maps to NM_000492.3 R1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr15:57730904 C>T maps to NM_032866.3 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr21:37766862 G>A maps to NM_005441.2 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:50859977 G>A maps to NM_020549.4 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:50873014 C>T maps to NM_020549.4 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr10:50822316 A>C maps to NM_020549.4 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr3:126676390 C>T maps to ENST00000508789 H234H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:146736082 C>T maps to NM_004284.3 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr17:7810507 A>G maps to NM_001005271.2 E1636E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr12:6704570 G>A maps to ENST00000309577 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr12:6692268 G>A maps to ENST00000309577 D1385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr12:6696612 G>A maps to ENST00000309577 G1272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr12:6690893 C>T maps to ENST00000309577 G1562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:6212507 G>A maps to NM_015557.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr1:6181180 C>T maps to NM_015557.2 P1632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr20:40141529 A>G maps to NM_032221.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr20:40033808 G>A maps to NM_032221.3 G2524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr20:40081513 G>A maps to NM_032221.3 D1063D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr20:40083355 T>C maps to NM_032221.3 G1010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:61693774 G>T maps to NM_017780.2 E628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:61735154 C>T maps to NM_017780.2 G1017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr14:21870223 T>C maps to NM_001170629.1 E1318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr16:53272296 T>C maps to ENST00000219084 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:53342702 C>T maps to ENST00000219084 R2387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr16:53301837 G>T did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr11:125503112 T>C maps to NM_001274.4 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:111773481 C>T maps to NM_004000.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:111854962 C>T maps to NM_201653.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:203192282 G>A maps to NM_003465.2 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr11:67842204 G>A maps to NM_001277.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:85149240 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:85156153 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:87294955 G>A maps to NM_014043.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:24680976 C>T maps to NM_014169.3 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr20:32439956 C>T maps to NM_176812.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr7:29539489 A>G maps to NM_004067.2 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr2:220405094 C>T maps to NM_024536.5 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr2:220404218 C>T maps to NM_024536.5 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr23:109922586 T>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:109924836 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:110002959 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:109931906 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:110035399 T>G did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:109964646 C>T did not map to a codon.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr11:74424488 C>T maps to NM_015424.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:74429788 G>T maps to NM_015424.3 Y57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr11:62678245 G>A maps to NM_000738.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr7:136700136 G>A maps to NM_001006628.1 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr7:136699683 G>T maps to NM_001006628.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:34355301 T>C maps to NM_012125.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr15:34356327 G>A maps to NM_012125.3 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:27321065 C>T maps to NM_000742.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:27324846 G>A maps to NM_000742.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr15:78893714 A>G maps to NM_000743.4 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr15:78893714 A>G maps to NM_000743.4 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr20:61981475 G>T maps to NM_000744.5 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr4:40356302 C>T maps to NM_017581.2 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:40356518 C>A maps to NM_017581.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:154544156 C>T maps to NM_000748.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:154544279 C>T maps to NM_000748.2 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:42586935 C>T maps to NM_000749.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:42586824 C>T maps to NM_000749.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr2:233409533 T>A maps to NM_005199.4 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr11:45672344 G>A maps to NM_003654.4 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr2:101014520 G>T maps to NM_004854.3 C92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr12:105150989 C>T maps to NM_018413.5 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:2473317 C>T maps to NM_018641.3 D348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr7:2472318 G>A maps to NM_018641.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr10:125780810 G>A maps to NM_015892.3 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:142840584 C>T maps to NM_004267.3 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr16:71571444 C>T maps to NM_001166395.1 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr16:75513567 C>T maps to NM_021615.4 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr5:129243803 C>T maps to NM_175856.4 N279N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr5:129521022 C>A maps to NM_175856.4 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr10:101980419 T>C maps to NM_001278.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:24776618 C>T maps to NM_014430.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:65490079 G>A maps to NM_003613.3 G848G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr15:65496627 G>A maps to NM_003613.3 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr15:65496663 G>A maps to NM_003613.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr15:65496693 G>A maps to NM_003613.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr15:65496702 G>A maps to NM_003613.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr15:65496852 G>A maps to NM_003613.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:130931779 G>A maps to NM_012127.2 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:113498582 C>T maps to NM_152515.3 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:113509977 T>A maps to NM_152515.3 R490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr19:45821106 A>G maps to NM_001824.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr19:45815032 G>A maps to NM_001824.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr5:80559398 C>T maps to NM_001825.2 Y368Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:122120866 G>A maps to NM_015282.2 R1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr3:33725897 T>C maps to ENST00000359576 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr3:33725929 A>G maps to ENST00000359576 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr3:33725897 T>C maps to ENST00000359576 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:86939206 C>T maps to NM_001285.3 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr7:143047529 G>A maps to NM_000083.2 Q823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:143028406 C>T maps to NM_000083.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:10176599 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:10188804 C>T did not map to a codon.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr23:10176318 C>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:10188907 C>T did not map to a codon.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr23:10182006 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:49851223 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:49854842 C>T did not map to a codon.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr23:49851178 A>G did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:49851178 A>G did not map to a codon.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr23:49851218 C>T did not map to a codon.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr1:11889345 G>A maps to ENST00000376496 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:1505227 C>T maps to ENST00000382745 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:43200780 G>A maps to NM_148960.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:106171672 G>A did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:106171823 A>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr21:31588224 C>A maps to NM_199328.2 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:98240147 C>A maps to NM_001040182.1 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr14:38724288 G>A maps to NM_175060.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:38724495 A>G maps to NM_175060.1 C244C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr16:11214598 G>A maps to ENST00000409790 V748V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:11118740 C>T maps to ENST00000409790 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:11272333 C>T maps to ENST00000409790 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr16:11214595 A>G maps to ENST00000409790 G747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:14706089 G>T maps to ENST00000417570 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr12:10233935 G>T maps to NM_016511.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr12:10010126 G>T maps to NM_005127.2 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:7894041 G>A maps to NM_130441.2 C70C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr2:71043819 G>A maps to NM_173535.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr2:71043807 C>T maps to NM_173535.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:7794347 C>T maps to NM_198492.3 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:7831058 C>A maps to NM_014257.4 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr23:154528112 G>C did not map to a codon.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr1:25167304 A>G maps to NM_013943.2 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:157241237 C>A maps to NM_001195555.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:29383295 C>A maps to ENST00000379543 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr5:178030719 C>A maps to NM_020666.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:95670248 C>T maps to NM_024734.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:95670572 C>T maps to NM_024734.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr4:10560058 G>A maps to NM_052964.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:1334415 G>A maps to NM_030782.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:17528702 T>G maps to NM_001079827.2 *233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:36226480 G>T maps to NM_022111.3 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr1:36228829 A>G maps to NM_022111.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr3:140277685 C>T maps to NM_022131.2 D676D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:140185521 C>T maps to NM_022131.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:7288881 G>T maps to NM_014718.3 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr9:36191148 T>C maps to NM_007096.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:57758368 G>T maps to NM_004859.3 E1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:19175075 G>T maps to NM_007098.3 L1533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:19217447 G>A maps to NM_007098.3 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:27457479 G>A maps to NM_001831.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:3569973 C>T maps to NM_015041.1 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr8:62370876 T>C maps to NM_173519.2 H251H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr16:66611098 C>T maps to NM_052999.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr16:66620925 T>C maps to NM_144673.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:79031061 A>G maps to NM_153610.3 Q2158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:79034298 T>G maps to NM_153610.3 Y3237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:79029954 G>A maps to NM_153610.3 K1789K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:79035046 G>T maps to NM_153610.3 E3487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:88365982 G>A maps to NM_173538.2 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr8:88364007 C>T maps to NM_173538.2 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr18:72185801 C>T maps to NM_018235.2 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:47953445 C>A maps to NM_001142564.1 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:150911719 C>T did not map to a codon.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr23:150908118 C>T did not map to a codon.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr23:150908070 A>G did not map to a codon.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr2:98996643 G>A maps to NM_001298.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr2:99013468 C>T maps to NM_001298.2 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr2:99012712 C>A maps to NM_001298.2 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:6261485 C>T maps to NM_001037329.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr16:57953078 G>A maps to NM_001297.4 C627C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:87656093 G>A maps to NM_019098.4 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:87666268 T>A maps to NM_019098.4 K292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:87683199 G>T maps to NM_019098.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:66050205 C>T maps to NM_182553.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr23:21534688 C>G did not map to a codon.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr23:21627279 G>A did not map to a codon.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr23:21488901 A>G did not map to a codon.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr23:21627702 G>T did not map to a codon.
Sequencing variant TCGA-AG-3584-01A-01W-0831-10 chr19:11660519 C>T maps to NM_001299.4 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:1036151 C>T maps to NM_004368.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr10:104679742 C>T maps to NM_017649.3 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr19:54651929 T>G maps to NM_014516.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:78663366 G>T maps to ENST00000512485 S274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr7:99722183 C>T maps to NM_152755.1 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:88854249 G>A maps to NM_016083.4 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:34552807 G>A maps to NM_147164.1 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:41327266 A>G maps to NM_001843.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:41374825 G>A maps to NM_001843.2 Q640Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:205028275 C>T maps to NM_005076.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr3:74419062 T>C maps to NM_020872.1 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:3080650 C>T maps to NM_175607.1 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:3097903 A>G maps to NM_175607.1 *1027W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:99827691 G>A maps to NM_014361.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr11:99786792 A>G maps to NM_014361.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:1424808 G>T maps to NM_014461.2 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr3:1444039 T>C maps to NM_014461.2 I952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr3:1424681 G>C maps to NM_014461.2 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:40843518 C>T maps to NM_003632.2 C778C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:146829506 T>C maps to NM_014141.5 N418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:147675052 C>T maps to NM_014141.5 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr7:147926772 C>T maps to NM_014141.5 R1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:76555987 C>A maps to NM_033401.3 I862I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:125521350 T>C maps to NM_130773.2 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr2:125521263 C>A maps to NM_130773.2 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:125204384 C>A maps to NM_130773.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:125521708 C>T maps to NM_130773.2 R839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr2:125405503 C>T maps to NM_130773.2 H681H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr2:125175153 C>T maps to NM_130773.2 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr7:51095858 C>T maps to ENST00000395542 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:165552274 C>A maps to ENST00000392717 E619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr2:165552242 G>A maps to ENST00000392717 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:31349679 C>T maps to NM_004086.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr1:230827216 T>C maps to NM_007357.2 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:46050388 G>T maps to NM_031431.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:107053041 C>A maps to NM_006348.3 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr13:40297567 A>G maps to ENST00000255468 K594K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:23415068 G>A maps to NM_153603.3 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:103491078 C>A maps to NM_080629.2 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr6:75912478 G>A maps to ENST00000322507 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr6:75887463 T>C maps to ENST00000322507 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:75866075 C>T maps to ENST00000322507 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:75875406 G>A maps to ENST00000322507 R933R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr6:75884982 C>T maps to ENST00000322507 T827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr6:75833986 T>C maps to ENST00000322507 K2236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:75890796 C>T maps to ENST00000322507 E674E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr10:71700760 C>T maps to ENST00000356340 D621D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:121215984 C>A maps to NM_021110.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:121216099 G>T maps to NM_021110.1 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:121282316 A>G maps to NM_021110.1 G1039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr8:121322276 C>A maps to NM_021110.1 G1477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr8:121210068 T>C maps to NM_021110.1 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr8:121309823 C>A maps to NM_021110.1 G1437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:101832134 C>T maps to NM_001855.3 I1378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:101748144 G>A maps to NM_001855.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:101759253 A>G maps to NM_001855.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:101804385 A>G maps to NM_001855.3 E857E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr1:32119209 G>A maps to NM_001856.3 P1534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr21:46931119 C>T maps to ENST00000359759 D1678D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:70847623 A>G maps to NM_001858.4 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:48262895 G>A maps to NM_000088.3 F1454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:48263785 G>A maps to NM_000088.3 C1299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:94041405 C>T maps to NM_000089.3 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:55923978 A>G maps to NM_030820.3 G890G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr6:56029247 C>T maps to NM_030820.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:139845355 G>A maps to NM_152888.1 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr8:139606407 C>T maps to NM_152888.1 P1489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr8:139675947 C>T maps to NM_152888.1 P1062P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr1:86252102 A>G maps to NM_152890.5 A1331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr4:109773433 A>G maps to ENST00000333642 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr9:117063735 T>A maps to NM_032888.2 G1601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr9:117062384 A>T maps to NM_032888.2 A1540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:117012942 G>T maps to NM_032888.2 E1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr7:7413178 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:48371107 C>A maps to NM_001844.4 E1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:48393714 G>A maps to NM_001844.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:189854842 C>T maps to NM_000090.3 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr2:189875582 A>G maps to NM_000090.3 K1407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr13:111138050 G>T maps to NM_001846.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr13:111077127 A>C maps to NM_001846.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr13:111143589 A>G maps to NM_001846.2 G1119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr13:111102775 G>C maps to NM_001846.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr2:228128655 G>A maps to NM_000091.4 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr5:74676951 T>C maps to NM_001130105.1 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr5:74676951 T>C maps to NM_001130105.1 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:227907846 C>A maps to ENST00000396625 G1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr23:107936014 G>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:107824240 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:107910363 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:107938087 G>A did not map to a codon.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr23:107911594 C>T did not map to a codon.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr23:107846222 G>T did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:107898653 G>A did not map to a codon.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr23:107402852 G>T did not map to a codon.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr9:137622200 G>A maps to NM_000093.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr9:137712035 C>A maps to NM_000093.3 G1507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:137623484 G>A maps to NM_000093.3 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr9:137591755 G>A maps to NM_000093.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr9:137623960 G>A maps to NM_000093.3 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:189923246 G>A maps to NM_000393.3 R713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr2:189898825 G>A maps to NM_000393.3 G1490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr19:10090069 C>T maps to NM_015719.3 P912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:10112445 C>A maps to NM_015719.3 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr21:47552084 G>A maps to NM_001849.3 P893P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr21:47545811 G>T maps to NM_001849.3 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr2:238275459 C>T maps to NM_004369.3 A1790A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr2:238277701 G>A maps to NM_004369.3 I1468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr2:238253584 G>A maps to NM_004369.3 Y2391Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr2:238249122 G>A maps to NM_004369.3 F2812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:238244916 C>T maps to NM_004369.3 A2942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:238245102 C>T maps to NM_004369.3 T2880T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:238296671 C>A maps to NM_004369.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr2:238249185 G>A maps to NM_004369.3 N2791N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:130188077 C>A maps to ENST00000312481 I2410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr3:130345384 C>A maps to NM_001102608.1 G1645G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:130282332 C>A maps to NM_001102608.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:130287047 C>T maps to NM_001102608.1 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:130293040 C>A maps to NM_001102608.1 I1073I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:130293362 G>T maps to NM_001102608.1 E1181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:130361684 G>T maps to NM_001102608.1 G1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:130368039 C>T maps to NM_001102608.1 V1789V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr3:130282098 C>T maps to NM_001102608.1 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr3:130300561 T>C maps to NM_001102608.1 T1235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:48619918 C>A maps to NM_000094.3 G1531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:48630045 G>A maps to NM_000094.3 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:48631005 G>T maps to NM_000094.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr20:61461026 C>T maps to NM_001853.3 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr18:335078 G>T maps to NM_130386.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:128984447 G>A maps to NM_016128.3 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:17165396 C>T maps to NM_003653.3 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:83971075 G>T maps to ENST00000503682 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr2:198318328 G>A maps to NM_025147.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:109042425 G>A maps to ENST00000420959 C473C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:109042527 G>T maps to ENST00000420959 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:100890957 G>T maps to NM_052820.3 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr17:27946078 T>A maps to ENST00000345068 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:84600555 G>A maps to NM_021149.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:101487298 C>T maps to NM_078470.4 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:73923971 G>A maps to NM_173827.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr3:148894088 G>A maps to NM_000096.3 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:148927156 C>A maps to NM_000096.3 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr7:130023568 C>T maps to NM_001868.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:17040036 G>T maps to ENST00000443236 I1010I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr19:17014403 C>T maps to ENST00000443236 V1536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr19:17038951 G>A maps to ENST00000443236 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr5:173316924 T>C maps to NM_030627.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:173372100 C>T maps to NM_030627.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr4:780336 G>A maps to NM_006651.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:101802225 C>T maps to NM_001308.2 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr16:57144698 C>T maps to NM_152727.5 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:87544748 G>T maps to NM_003909.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr6:36714184 G>A maps to NM_020939.1 H396H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr2:207827158 C>T maps to NM_173077.2 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr2:207827151 A>G maps to NM_173077.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr3:98304421 C>T maps to NM_000097.5 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr16:12758910 G>A maps to NM_018340.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:211469885 G>T maps to NM_001122633.1 E639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:211473150 C>T maps to NM_001122633.1 V759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:211518790 G>T maps to NM_001122633.1 E1181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr8:145625386 G>A maps to NM_013291.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr23:88008495 T>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:88009304 G>T did not map to a codon.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr23:88009102 C>T did not map to a codon.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr20:2775015 G>A maps to NM_019609.4 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr4:8603129 C>T maps to NM_001014447.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:207741232 C>A maps to NM_000651.4 V1339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:207791443 C>T maps to NM_000651.4 N2306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr1:207646450 T>C maps to NM_001006658.2 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr15:78640276 C>T maps to NM_004378.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:94072801 G>A maps to NM_003805.3 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:197404376 C>A maps to NM_201253.2 I1128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr1:197396917 G>A maps to NM_201253.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:3215803 C>A maps to NM_016302.3 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr11:46321514 G>A maps to ENST00000288400 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr19:4171674 C>T maps to NM_032607.1 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr16:3779386 T>C maps to NM_004380.2 S1887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:3900774 C>T maps to NM_004380.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:3820702 A>G maps to NM_004380.2 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr16:3789725 C>T did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr16:3786782 T>A maps to NM_004380.2 P1476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr16:3801730 G>A maps to NM_004380.2 Q1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:43884431 C>T maps to NM_001145146.1 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr7:30693201 C>T maps to ENST00000348438 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:30694687 G>A maps to ENST00000348438 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:36740789 T>C maps to NM_016441.2 D624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr4:1388973 T>C maps to NM_175918.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr6:49819776 G>A maps to NM_001131.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr6:49663582 G>A maps to ENST00000211238 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr8:75928887 G>A maps to NM_031461.5 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr8:75941677 T>G maps to NM_031461.5 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:84900570 G>T maps to NM_031476.3 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:21288474 G>A maps to NM_005207.3 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:29111437 C>A maps to NM_015986.3 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:5830233 G>A maps to NM_001014809.1 R595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr4:5862768 G>A maps to NM_001014809.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr20:20018118 G>A maps to NM_016652.4 R743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr1:17281853 C>T maps to NM_014675.3 D1171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr7:86986889 G>A maps to NM_001143935.1 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:99640120 G>A maps to NM_018058.4 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:99683050 G>A maps to NM_018058.4 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:153925091 G>A maps to NM_181715.2 N219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr15:91169106 G>T maps to NM_022769.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr12:107386773 G>A maps to NM_004075.3 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr12:107393836 T>C maps to NM_004075.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:107393757 G>A maps to NM_004075.3 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr21:44592182 C>T maps to NM_000394.2 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:27579132 G>A maps to NM_005208.4 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr22:25625449 C>T maps to NM_000496.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr2:209010728 G>A maps to NM_005210.3 Y7Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr2:208994332 C>T maps to NM_020989.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:186257211 C>A maps to NM_017541.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:75185050 A>C maps to NM_001889.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr12:56668623 A>G maps to NM_004077.2 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr12:10862554 C>T maps to NM_003651.4 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr20:47711484 C>T maps to NM_001316.2 T937T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr20:47682748 A>G maps to NM_001316.2 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr5:149450118 G>A maps to NM_005211.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:1428403 C>A did not map to a codon.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr23:1407723 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:1401669 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:1407441 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:1428337 G>A did not map to a codon.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr22:37331393 G>C maps to ENST00000262825 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr22:37328933 G>A maps to ENST00000262825 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr1:36937229 T>C maps to NM_156039.3 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr8:19363228 G>A maps to NM_018371.4 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:43651250 C>T maps to NM_018590.3 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr17:61972613 G>A maps to NM_022640.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr17:61972820 C>T maps to NM_022640.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr17:61972613 G>A maps to NM_022640.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:61949542 G>A maps to NM_020991.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr17:61950622 G>T maps to NM_020991.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:3047449 C>T maps to NM_033225.5 T1794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr8:3224668 G>A maps to NM_033225.5 T1000T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:2887014 C>A maps to NM_033225.5 E2561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:3855476 C>A maps to NM_033225.5 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr8:3263695 G>A maps to NM_033225.5 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr8:2964062 G>C maps to NM_033225.5 L2312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr8:3245154 G>A maps to NM_033225.5 N881N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr1:33992804 G>A maps to ENST00000373381 Q3369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr1:34102146 C>T maps to ENST00000373381 P1554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr1:34164353 G>A maps to ENST00000373381 V1268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr1:34209046 A>G maps to ENST00000373381 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr8:113358401 G>T maps to NM_198123.1 I2122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr8:113277691 G>T maps to NM_198123.1 I3212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr8:113331117 C>G maps to NM_198123.1 T2436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr8:113569061 G>A maps to NM_198123.1 H1388H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:113249458 G>A maps to NM_198123.1 N3529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:113651099 A>G maps to NM_198123.1 H1117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:113933928 G>A maps to NM_198123.1 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:114290925 C>A maps to NM_198123.1 G137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr8:114290848 A>G maps to NM_198123.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr8:114290848 A>G maps to NM_198123.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr8:113314166 A>G maps to NM_198123.1 P2765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr8:113529389 T>C maps to NM_198123.1 G1543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:71115073 A>G maps to NM_005212.2 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr13:37678496 C>T maps to NM_145203.5 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:37678625 G>A maps to NM_145203.5 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:38694790 G>A maps to NM_001894.4 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr15:64506101 C>T maps to NM_022048.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr15:75982274 T>C maps to NM_001897.4 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr8:68007880 T>C maps to ENST00000389042 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr8:68102915 A>G maps to ENST00000389042 E1114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr8:68102915 A>G maps to ENST00000389042 E1114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr2:166536037 C>T maps to ENST00000409420 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr20:18143315 C>T maps to NM_020536.4 Y466Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr20:18165309 C>T maps to NM_020536.4 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr20:23805933 G>A maps to NM_001322.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:23616001 G>A maps to NM_000099.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr20:23667835 G>A maps to NM_001899.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:122056404 G>A maps to NM_005213.3 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr20:54970682 C>T maps to NM_001033522.1 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:23424575 G>A maps to NM_138283.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:153881591 G>A did not map to a codon.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr10:126715113 A>G maps to NM_022802.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr1:85039954 G>A maps to NM_004388.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr2:204736158 G>A maps to NM_005214.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:80801396 T>C maps to ENST00000402739 Y617Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr2:80101317 C>T maps to ENST00000402739 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr10:68940230 T>C maps to NM_013266.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:67748509 C>A maps to NM_013266.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr3:41266137 T>C maps to NM_001904.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr3:41266113 T>C maps to NM_001904.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr3:41266158 T>C maps to NM_001904.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr3:41266877 T>C maps to NM_001904.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr3:41266113 T>C maps to NM_001904.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr3:41266134 T>C maps to NM_001904.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr20:36470760 G>A maps to NM_030877.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:57563200 G>A maps to NM_001085458.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:11411650 C>A maps to NM_001332.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:11412149 G>A maps to NM_001332.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr5:11384789 C>T maps to NM_001332.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr11:10778347 C>T maps to NM_014633.3 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr1:206320204 G>T maps to ENST00000361052 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr14:25043994 G>A maps to NM_001911.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr9:90342637 C>T maps to NM_145918.2 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr9:90343678 T>C maps to NM_145918.2 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:70265867 C>T maps to NM_001184740.1 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:70277322 G>A maps to NM_001184740.1 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:117431350 C>T maps to NM_033427.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr7:117432607 G>T maps to NM_033427.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr1:112999694 T>C maps to NM_018704.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr10:16992024 G>A maps to NM_001081.3 G1685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:16975161 G>A maps to NM_001081.3 T2016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr10:16990489 G>A maps to NM_001081.3 T1732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr17:55945532 T>A maps to NM_017949.1 K338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:55950156 C>T maps to NM_017949.1 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr7:148451113 C>T maps to NM_003592.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:148496425 C>T maps to NM_003592.2 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:113897298 C>T maps to NM_001008895.1 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:119708409 G>A did not map to a codon.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr10:101502946 A>G maps to NM_015960.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:101925169 C>T maps to NM_001913.2 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr7:101837148 G>A maps to ENST00000360264 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr12:111729258 C>T maps to NM_015267.3 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:111742013 C>T maps to NM_015267.3 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:124598704 G>T maps to NM_022034.4 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr10:124598698 G>A maps to NM_022034.4 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:107300047 C>A maps to NM_152434.2 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr21:18924179 G>A maps to NM_001338.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:76924788 G>A maps to NM_002416.1 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr2:218999856 C>A maps to NM_001168298.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr23:70836932 A>G did not map to a codon.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr2:237489512 C>T maps to NM_020311.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr2:237489125 C>T maps to NM_020311.2 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr23:30578216 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:30577582 C>A did not map to a codon.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:35988901 T>C did not map to a codon.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:35993861 C>T did not map to a codon.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr23:35984743 G>C did not map to a codon.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr23:35985860 T>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:35993964 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:35993924 C>T did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:35971784 G>A did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:19971167 T>C did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:45017021 C>T did not map to a codon.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr23:40496388 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:105875932 T>G did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:105855766 G>A did not map to a codon.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr23:105868475 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:23956727 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:23953381 C>T did not map to a codon.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr23:23945401 G>A did not map to a codon.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr23:36116959 C>T did not map to a codon.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr23:36091287 G>A did not map to a codon.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr23:139040346 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:139038776 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:110038433 C>T maps to NM_001134400.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:7690471 G>A maps to NM_016229.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:54644917 G>A maps to NM_001031672.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:37651245 C>T did not map to a codon.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:37663244 A>C did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr15:22963841 C>A maps to NM_014608.2 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr5:156786107 G>A maps to ENST00000442283 Q948Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:156766138 C>T maps to ENST00000442283 F845F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:156786059 C>T maps to ENST00000442283 F932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:156816393 C>T maps to ENST00000442283 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr23:83128981 A>G did not map to a codon.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr23:83128112 A>G did not map to a codon.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr23:83129126 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:83128165 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:83129043 C>A did not map to a codon.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr23:83128790 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:83126528 G>T did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:83129019 A>T did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:83128418 T>C did not map to a codon.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr9:105767413 T>C maps to NM_001340.3 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr9:105767110 C>T maps to NM_001340.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:50783747 G>T maps to ENST00000311559 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr16:50820849 A>G maps to ENST00000311559 E678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr15:74631640 G>A maps to NM_000781.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr8:143957760 G>A maps to ENST00000377675 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr8:143996552 G>A maps to NM_000498.3 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:75042426 C>T maps to NM_000761.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:38298076 C>A maps to NM_000104.3 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:94837057 C>A maps to NM_000783.3 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr2:72359496 C>T maps to NM_019885.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr19:41597791 C>G maps to NM_000766.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr19:41386147 G>A maps to NM_000764.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr10:96796959 G>A maps to NM_000770.3 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:135350580 G>T maps to NM_000773.3 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr1:60377921 T>C maps to NM_000775.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr4:108853209 C>T maps to NM_183075.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:46620168 C>A maps to NM_016593.3 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr7:99381644 C>T maps to NM_017460.3 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:99319923 G>T maps to ENST00000292414 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr1:47407090 C>G maps to ENST00000371904 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr1:47280903 C>T maps to NM_001099772.1 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr1:47282755 C>T maps to NM_001099772.1 C370C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:15794312 G>T maps to NM_023944.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr19:15789138 G>T maps to NM_023944.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr19:15661489 C>A maps to NM_173483.3 Y447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr19:15770101 C>T maps to NM_000896.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:187120129 C>T maps to NM_207352.3 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:47515095 C>A maps to NM_178033.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:47583599 T>G maps to NM_178134.2 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:59409434 G>A maps to NM_000780.3 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr8:65509288 A>G maps to NM_004820.3 D477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr13:49281252 A>G maps to NM_020377.2 R100R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DY-A1H8-01A-21D-A152-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr22:37678615 C>T maps to NM_013385.3 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:27840831 G>A maps to ENST00000435845 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:57535046 C>A maps to ENST00000371231 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr1:57602311 G>A maps to ENST00000371231 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:57480580 A>C maps to ENST00000371231 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:39376884 C>T maps to NM_001343.2 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:39383130 C>T maps to NM_001343.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr5:39382914 A>G maps to NM_001343.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr9:124528808 G>A maps to ENST00000408936 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr13:72063260 T>C maps to ENST00000359684 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr23:86069705 G>A did not map to a codon.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr23:85769337 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:86069730 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:85403760 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:85969624 G>T did not map to a codon.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr23:86069704 C>T did not map to a codon.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr7:6476075 G>A maps to NM_139179.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr13:106142253 G>T maps to NM_172370.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:90315113 C>T maps to NM_004938.2 R945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr9:90301541 G>A maps to NM_004938.2 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:173797500 C>T maps to NM_018122.4 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr9:121971142 G>T maps to NM_014618.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:121930275 G>A maps to NM_014618.2 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr9:121930132 G>A maps to NM_014618.2 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr9:121930147 G>A maps to NM_014618.2 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr7:87536886 G>A maps to NM_006716.3 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr5:176884463 T>C maps to ENST00000393565 E686E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:20180779 G>A maps to ENST00000227256 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr12:45410112 C>A maps to NM_001004329.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:125298617 C>T did not map to a codon.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr23:125299058 G>A did not map to a codon.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr23:125299669 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:125299655 G>A did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr23:125298990 C>A did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:125299498 G>A did not map to a codon.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr8:88885716 C>T maps to NM_152418.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:88885806 G>T maps to NM_152418.3 C131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:88886082 G>A maps to NM_152418.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:167962639 G>T maps to ENST00000367840 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:27999203 C>T did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:27998264 A>G did not map to a codon.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:27765437 G>A did not map to a codon.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr23:27765529 A>G did not map to a codon.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr6:117859998 G>T did not map to a codon.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr3:98518392 T>A maps to ENST00000326857 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr18:50734110 T>C maps to NM_005215.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr18:51025777 C>T maps to NM_005215.3 R1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr6:24278379 G>A maps to NM_016356.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr4:155156338 G>A maps to NM_017639.3 A2700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr4:155156596 C>T maps to NM_017639.3 P2614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:155219827 C>A maps to NM_017639.3 E1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr4:155180708 A>T maps to NM_017639.3 A1804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr4:155241579 G>A maps to NM_017639.3 S1202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr13:36686074 G>A maps to NM_004734.4 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr4:151160898 T>C maps to NM_001040261.4 C541C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr3:36779762 C>A maps to NM_033403.1 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr3:36779796 G>A maps to NM_033403.1 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:115609267 C>T maps to NM_014881.3 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr12:91552211 T>C maps to NM_133503.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:2062037 G>A maps to NM_152640.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr12:2102454 A>G maps to NM_152640.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:112336789 G>T maps to NM_152624.4 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:155015220 T>G maps to NM_152494.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:95092216 G>A maps to NM_001129889.1 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr13:95112464 C>A maps to NM_001129889.1 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr13:95114391 A>G maps to NM_001129889.1 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr3:182681754 A>G maps to NM_020640.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:110653357 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:110653450 C>T did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:110653619 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:31696519 G>A maps to NM_013974.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:61089809 G>A maps to NM_001923.3 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:47259488 C>T maps to NM_000107.2 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr7:50605569 T>C maps to NM_000790.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:53529664 G>A maps to NM_001160148.1 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:38091915 A>G maps to NM_001164232.1 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3584-01A-01W-0831-10 chr12:57910759 C>T maps to NM_001195056.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr12:57910756 A>G maps to NM_001195056.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr12:57910756 A>G maps to NM_001195056.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:101108892 G>A maps to NM_145244.3 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr1:20980729 C>T maps to NM_005216.4 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr1:20978949 G>A maps to NM_005216.4 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:20981190 G>A maps to NM_005216.4 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:162731038 C>A maps to NM_006182.2 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:162724617 C>T maps to NM_006182.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr2:15760411 T>C maps to NM_004939.1 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr2:15742717 A>G maps to NM_004939.1 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:108593862 G>T maps to NM_004398.2 E547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:31247734 C>T maps to NM_030653.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr22:38891909 G>A maps to NM_001098504.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr2:118579561 T>C maps to NM_006773.3 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:70399021 C>T maps to NM_018332.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:94521490 G>A maps to NM_020414.3 R677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:125786920 C>T maps to NM_013264.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr23:134713963 G>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:135521322 G>A maps to NM_022779.7 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr23:41203508 A>G did not map to a codon.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr5:55056043 T>C maps to NM_024415.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr5:55056043 T>C maps to NM_024415.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr5:55111251 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:61886997 C>T maps to NM_203499.1 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:134154651 G>T maps to ENST00000452510 E979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:70706227 C>T maps to NM_024045.1 R686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:132624674 G>A maps to NM_175066.3 D581D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:35984403 C>A maps to NM_007010.3 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr12:124093311 C>T maps to NM_020936.1 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:32466352 C>A maps to NM_014314.3 E758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr1:200635456 G>A maps to NM_001031725.4 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:200635469 C>T maps to NM_001031725.4 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr1:200619723 A>G maps to NM_001031725.4 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr1:200619723 A>G maps to NM_001031725.4 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr11:118627888 T>C maps to NM_004397.4 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:169158485 A>G maps to NM_017631.5 S1454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:169294924 G>A maps to NM_001012967.1 L1556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:169300924 C>T maps to NM_001012967.1 E1391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:169336824 G>T maps to NM_001012967.1 S951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr4:169321987 T>A maps to NM_001012967.1 T1160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:688018 C>A maps to NM_021008.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:42703604 C>T maps to NM_133328.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr16:90030714 C>T maps to NM_207514.1 C441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr6:50016274 T>C maps to NM_001037498.1 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:126220143 G>A maps to NM_020946.1 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr9:126143788 G>A maps to NM_020946.1 D984D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:6475302 G>A maps to NM_024898.2 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:6467847 T>C maps to NM_024898.2 E691E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:140246736 G>T maps to NM_015689.3 I680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:140266969 G>A maps to NM_015689.3 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:140285475 G>A maps to NM_015689.3 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr7:140287513 C>T maps to NM_015689.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:115166143 G>T maps to ENST00000393274 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:65982885 G>T maps to ENST00000443035 S1349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr15:65964190 G>C maps to ENST00000443035 S1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr15:66044812 C>T maps to ENST00000443035 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr1:153905204 A>G maps to NM_014856.2 P1224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr12:31540607 G>A maps to NM_144973.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:31577525 G>A maps to NM_144973.3 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:123253327 G>T maps to ENST00000455982 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr12:100649876 G>A maps to ENST00000422147 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr22:32162609 C>T maps to NM_001136029.1 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:32188762 C>T maps to NM_001136029.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:32215143 C>T maps to NM_001136029.1 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr2:234296985 A>G maps to NM_152879.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:234343073 G>T maps to NM_152879.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr2:234363414 T>C maps to NM_152879.2 Y757Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr2:234346054 C>A maps to NM_152879.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:54939585 C>T maps to NM_003647.2 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr3:185986589 C>T maps to NM_001346.2 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:186015889 C>T maps to NM_001346.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr3:186024719 A>G maps to NM_001346.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:50114797 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:50121638 G>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:50144115 G>A did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:50111944 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:49488037 G>T maps to NM_021044.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr17:27225674 G>A maps to NM_144683.3 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:24113358 T>C maps to NM_182908.4 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr14:24423017 A>T maps to NM_021004.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:24520092 C>T maps to NM_001082488.1 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr14:24505825 C>T maps to NM_001082488.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr14:24459528 T>C maps to NM_198083.3 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:2139177 C>A did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:12131130 G>A maps to NM_018706.5 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:54558598 C>T maps to NM_019030.2 G1229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:54581677 C>A maps to NM_019030.2 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:47891173 C>A maps to NM_138615.2 S1082S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:127540945 C>A maps to NM_018180.2 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:127555590 G>A maps to NM_018180.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:37632400 G>T maps to NM_021931.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr3:154032849 C>T maps to NM_020865.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:154002754 C>A maps to NM_020865.2 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr3:154022660 G>A maps to NM_020865.2 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr12:125441654 G>A maps to NM_032656.3 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:72130867 G>A maps to NM_014003.3 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:72138440 G>A maps to NM_014003.3 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:40257052 C>A maps to NM_024119.2 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:182852427 C>T maps to NM_001357.4 H1023H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr23:96502814 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:96213130 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:96684687 C>T did not map to a codon.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr23:96502830 A>G did not map to a codon.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr13:60413499 G>T maps to NM_001042517.1 P940P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr13:60584788 T>C maps to NM_001042517.1 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr13:60407363 C>A maps to NM_001042517.1 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr20:61542511 G>A maps to NM_033081.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:61524261 G>A maps to NM_033081.2 R1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr20:61513407 A>G maps to NM_033081.2 A1300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr20:61527956 A>G maps to NM_033081.2 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr5:61694693 T>C maps to NM_014473.2 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr1:54371957 C>T maps to NM_000792.5 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:80669238 C>T maps to NM_001007023.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:80669433 C>T maps to NM_001007023.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr12:51127943 T>G maps to NM_173602.2 T1336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:51126252 C>T maps to NM_173602.2 I1305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:461733 G>A maps to NM_014974.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:122564616 C>T maps to NM_032839.2 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr13:73336149 A>G maps to NM_014953.3 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:111844960 C>A maps to NM_001037954.2 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:154003540 C>T did not map to a codon.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr11:11988506 G>A maps to ENST00000450094 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:49868899 C>T maps to NM_014419.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr8:12957274 G>A maps to NM_182643.2 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr8:12948825 C>T did not map to a codon.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr8:13356869 T>C maps to NM_182643.2 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:12957490 T>G maps to NM_182643.2 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:13356683 A>G maps to NM_182643.2 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:13251147 G>A maps to NM_182643.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:13357259 T>C maps to NM_182643.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr8:12957208 G>A maps to NM_182643.2 Y879Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr8:13259110 T>C maps to NM_182643.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr8:13259110 T>C maps to NM_182643.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr8:12957787 C>T maps to NM_182643.2 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:38103774 C>T maps to NM_007335.2 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:38125713 G>A maps to NM_007335.2 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr3:38134330 C>T maps to NM_007335.2 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr23:69711974 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:69669295 A>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:69712392 C>T did not map to a codon.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr10:79579710 C>T maps to NM_004747.3 S1156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr18:3879897 G>A maps to NM_004746.2 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr18:3582067 G>T maps to NM_004746.2 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr1:35370069 C>T maps to NM_001080418.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr14:55636178 G>A maps to NM_014750.4 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:55625285 G>A maps to NM_014750.4 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:170597465 G>A maps to NM_005618.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr2:172966864 A>G did not map to a codon.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr7:96653611 G>A maps to NM_005221.5 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:96650233 G>C maps to NM_005221.5 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:96653797 G>A maps to NM_005221.5 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr7:96653815 A>G maps to NM_005221.5 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:124384802 A>C maps to ENST00000368915 I1873I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr10:124402856 C>T maps to ENST00000368915 V2524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr23:32456458 G>A did not map to a codon.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr23:32563360 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:32361362 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:32662381 G>T did not map to a codon.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr23:32867867 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:31947776 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:32361386 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:32430295 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:32613884 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:32834696 G>T did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr23:32381008 A>G did not map to a codon.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr23:31986497 C>T did not map to a codon.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr23:32360314 C>T did not map to a codon.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr23:32827652 G>A did not map to a codon.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr23:32486673 G>T did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:31165490 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:78326676 G>T maps to NM_013391.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr19:35996855 A>G maps to NM_033317.4 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:88583910 G>A maps to NM_004407.3 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr1:53927245 C>T maps to NM_033067.1 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:46289814 G>A maps to NM_004943.1 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr19:46289502 C>T maps to NM_004943.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:118469656 G>T maps to NM_005509.4 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr15:51839563 C>T maps to NM_001174116.1 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:51806662 C>A maps to NM_001174116.1 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr3:52420859 G>A maps to ENST00000273600 K2998K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr12:124352060 T>C maps to NM_207437.3 Y2287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr12:124297817 T>C maps to NM_207437.3 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr12:124272482 G>T maps to NM_207437.3 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:124416235 G>T maps to NM_207437.3 E4206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:124337883 C>A maps to NM_207437.3 S2023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr12:124398917 G>A maps to NM_207437.3 K3347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr12:124297817 T>C maps to NM_207437.3 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:21641065 G>T maps to NM_003777.3 E1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:21646159 C>T maps to NM_003777.3 D1255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:21654842 G>T maps to NM_003777.3 E1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:21727070 C>A maps to NM_003777.3 I1957I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:21813409 T>G maps to NM_003777.3 L3050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:21856161 C>T maps to NM_003777.3 N3477N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr7:21765556 T>C maps to NM_003777.3 A2472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr7:21781774 C>T maps to NM_003777.3 N2722N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr7:21778448 C>T maps to NM_003777.3 H2599H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr7:21847576 G>A maps to NM_003777.3 T3421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr3:57458290 G>T maps to NM_178504.4 I586I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CI-6620-01A-11D-1826-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr17:76506522 G>A maps to ENST00000389840 Y1389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:76497339 G>A maps to ENST00000389840 C1789C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr17:7702524 C>T maps to NM_020877.2 I2888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:7626991 G>A maps to NM_020877.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:20975761 T>C maps to NM_017539.1 K3148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:20999095 C>T maps to NM_017539.1 S2267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:21128593 C>A maps to NM_017539.1 E582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr5:13754366 T>C maps to NM_001369.2 K3500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr5:13717497 C>A maps to NM_001369.2 E4211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr5:13894786 A>G maps to NM_001369.2 A801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:13721198 C>A maps to NM_001369.2 G4063G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:13777393 C>A maps to NM_001369.2 G3008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:13807782 C>A maps to NM_001369.2 G2602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr5:13885212 G>A maps to NM_001369.2 R956R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr5:13792153 C>A maps to NM_001369.2 R2799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr5:13809284 C>T maps to NM_001369.2 T2540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:84804496 G>T maps to NM_001370.1 E681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:196605507 A>C maps to NM_018897.2 L3950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:196636560 G>A maps to NM_018897.2 V3752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:196636524 G>A maps to NM_018897.2 F3764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:196737057 G>A maps to NM_018897.2 F2183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:196774762 T>C maps to NM_018897.2 G1364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:196791206 A>G maps to NM_018897.2 C1185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:196912112 G>A maps to NM_018897.2 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:38919246 A>G maps to ENST00000327475 G4122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr6:38939411 C>T maps to ENST00000327475 R4154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:38754598 C>T maps to ENST00000327475 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:38758141 C>T maps to ENST00000327475 V902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:38831812 G>T maps to ENST00000327475 E2147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr6:38980050 G>T maps to ENST00000327475 E4466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr6:38840415 C>T maps to ENST00000327475 C2353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr17:11725300 A>G maps to NM_001372.3 E2924E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr17:11872711 C>T maps to NM_001372.3 R4443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr17:11648154 G>C maps to NM_001372.3 L2051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr17:72295953 G>A maps to NM_023036.4 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:4491407 C>T maps to NM_005147.4 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr10:74103214 C>T maps to NM_017626.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:100827711 G>A maps to NM_001031723.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:22217460 A>C maps to NM_022365.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr10:69571293 G>A maps to NM_021800.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:132192015 C>T maps to NM_015268.3 R746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:132172152 G>A maps to NM_015268.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:56221643 C>A maps to NM_032364.5 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:15873341 G>A maps to NM_015291.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:138755805 C>T maps to NM_152686.3 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr5:138760696 A>G maps to NM_152686.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:102957317 T>C maps to NM_014377.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr5:34945130 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr21:34861072 C>A maps to NM_001040192.1 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:66963833 G>T maps to NM_033105.4 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr23:153633877 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:58186822 G>A maps to NM_004944.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr19:12989211 G>A maps to NM_001375.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr2:230456483 C>A maps to NM_139072.3 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:230271990 G>A maps to NM_139072.3 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:6568739 C>T maps to NM_144666.2 R2191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:10939860 C>T maps to NM_001005361.2 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:172001593 G>A maps to ENST00000359070 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr19:10250807 C>G maps to NM_001130823.1 P1240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:25458667 C>T maps to NM_175629.1 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:25462056 C>A maps to NM_175629.1 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:31384644 C>A maps to NM_006892.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr2:220250688 C>T did not map to a codon.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr20:44424048 G>A maps to NM_052951.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:129046279 C>T maps to ENST00000398025 F997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr10:128824641 C>T maps to ENST00000398025 N505N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr10:128830402 C>T maps to ENST00000398025 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr10:129055678 C>T maps to ENST00000398025 N1055N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:225796381 C>A maps to NM_014689.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr23:117815032 T>C did not map to a codon.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr23:117739299 G>A did not map to a codon.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr23:117695436 C>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:117777427 T>G did not map to a codon.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr23:117744320 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:117733154 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:117783027 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:117809973 C>A did not map to a codon.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr5:169145672 A>G maps to NM_004946.2 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr5:169461456 C>T maps to NM_004946.2 F1174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr5:169423159 G>T maps to NM_004946.2 E1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:169122928 C>A maps to NM_004946.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:169477279 C>T maps to NM_004946.2 R1364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:51251553 T>C maps to NM_004947.4 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:51196712 C>T maps to NM_004947.4 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:51418779 C>T maps to NM_004947.4 C1961C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:111508203 C>A maps to ENST00000428084 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:62960061 G>A maps to ENST00000371140 R1701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:63018422 G>A maps to ENST00000371140 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr13:99554619 C>T maps to ENST00000428223 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:67365721 C>A maps to NM_152721.5 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr4:3495128 C>T maps to ENST00000389653 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:83847933 C>T maps to NM_015018.2 I1391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr6:83843970 A>T maps to NM_015018.2 I945I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:37661102 C>A maps to NM_005128.2 S2116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr6:30918664 T>C maps to NM_080870.3 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr16:68021777 G>T maps to NM_022355.2 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr16:68021796 G>T maps to NM_022355.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:101487278 C>A maps to NM_015958.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr2:116520176 C>T maps to NM_020868.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:116594285 G>T maps to NM_020868.3 E716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr2:116497364 A>C maps to NM_020868.3 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr2:116572434 T>A maps to NM_020868.3 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr15:65773926 T>G maps to NM_197960.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr15:65771244 G>A maps to NM_197960.2 R493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr1:168698172 C>T maps to NM_001937.4 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr19:32959704 G>A maps to NM_001172774.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr8:95746942 A>G maps to NM_181787.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:97564143 G>T maps to NM_000110.3 I889I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:97544683 C>A maps to NM_000110.3 E976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:97770899 G>T maps to NM_000110.3 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr8:105459695 T>C maps to NM_001385.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:146795308 G>A maps to NM_001197294.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:134006167 C>T maps to NM_006426.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:74746691 G>T maps to NM_133637.2 Y599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:113858436 G>A maps to NM_000796.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr3:113878600 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:9785071 G>A maps to NM_000798.4 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr4:9783955 C>T maps to NM_000798.4 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:100515080 T>C did not map to a codon.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr23:100515537 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:100497322 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:100503512 G>A did not map to a codon.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr23:100509466 C>T did not map to a codon.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr23:100492612 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr18:28714672 C>A maps to NM_024421.2 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr21:41450656 G>A maps to NM_001389.3 C1556C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:41447045 G>A maps to NM_001389.3 I1602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:41450635 G>A maps to NM_001389.3 F1563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr21:41684281 C>T maps to NM_001389.3 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr21:41559866 A>G maps to NM_001389.3 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr21:41385059 T>C maps to NM_001389.3 G1980G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr11:117332232 C>T maps to NM_020693.2 P1175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr11:117374605 G>A maps to NM_020693.2 N831N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:117389391 G>A maps to NM_020693.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr8:120865286 C>T maps to NM_024094.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:38610882 C>A maps to NM_006052.1 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:39427067 C>A maps to NM_005867.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:116720487 C>T maps to NM_013352.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr18:65180783 A>G maps to NM_032160.2 N364N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:28906913 C>T maps to NM_001942.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:28934567 C>T maps to NM_001942.2 F803F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr18:29121186 C>T maps to NM_001943.3 C637C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:28968332 C>T maps to NM_001134453.1 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr18:28983529 G>A maps to NM_001134453.1 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr4:88533323 C>G maps to NM_014208.3 S40*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AG-3885-01A-01W-0899-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AG-3885-01A-01W-0899-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AH-6643-01A-11D-1826-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DC-5337-01A-01D-1657-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DC-6155-01A-11D-1657-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr4:88535011 G>T maps to NM_014208.3 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:56357098 G>A maps to ENST00000361203 R6684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:56417039 G>T maps to ENST00000361203 S5306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:56417395 G>A maps to ENST00000361203 F5187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:56443633 C>T maps to ENST00000361203 K4124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:56480712 G>A maps to ENST00000281662 R3082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:56499631 C>T maps to ENST00000361203 P891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:18608840 G>A maps to NM_080820.4 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr2:25875496 G>A maps to NM_021907.3 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr15:49917517 C>T maps to NM_001144955.1 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr15:45454505 C>T maps to NM_175940.1 T1393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:45436369 C>T maps to NM_175940.1 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr17:80017881 C>T maps to NM_022156.3 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:76854631 G>A maps to ENST00000356369 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3584-01A-01W-0831-10 chr12:12630317 G>A maps to NM_030640.2 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr2:183960265 T>C maps to NM_080876.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr6:348818 A>G maps to ENST00000457386 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr8:33451177 G>A maps to NM_024025.1 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:167097349 C>T maps to NM_001080426.1 H994H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:52088013 G>T maps to NM_001947.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:57666740 C>A did not map to a codon.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr3:183884307 G>A maps to NM_004423.3 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr3:183884626 G>T maps to NM_004423.3 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:102470911 C>T maps to NM_001376.4 V1647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:102481635 T>C maps to NM_001376.4 D2403D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr11:103157019 G>T maps to NM_001080463.1 E3650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:102985943 G>T maps to NM_001080463.1 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:103019292 G>T maps to NM_001080463.1 E965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:80577223 G>T maps to NM_130897.1 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr12:4705884 G>T maps to NM_003845.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr2:71795139 G>A maps to NM_001130987.1 W875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr2:71896833 C>T maps to NM_001130987.1 F1914F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr2:71753471 G>A maps to NM_001130987.1 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr2:71766337 G>A maps to NM_001130987.1 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr2:71892300 G>A maps to NM_001130987.1 P1728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr2:71801459 A>T maps to NM_001130987.1 K1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:96246323 C>T maps to NM_198968.2 Q518Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:96239898 C>T maps to NM_198968.2 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:96264406 G>A maps to NM_198968.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:96282323 G>A maps to NM_198968.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr13:96239829 G>A maps to NM_198968.2 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr13:96277048 T>C maps to NM_198968.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr13:96277050 A>G maps to NM_198968.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr3:108391418 A>G maps to NM_014648.3 E835E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr16:67228641 C>T maps to NM_001950.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr12:77449721 G>A maps to NM_203394.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:77427748 G>T maps to NM_203394.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr11:19251429 C>T maps to NM_024680.2 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr11:19252184 G>A maps to NM_024680.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:19259670 G>T maps to NM_024680.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr5:158139267 A>G maps to NM_024007.3 Y481Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr8:25718590 G>C maps to NM_022659.2 S439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr10:131646711 G>A maps to ENST00000355311 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:48382320 G>T did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:48382319 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:74897826 C>A maps to NM_001135752.1 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:21599381 G>A maps to NM_001397.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr1:21599258 G>A maps to NM_001397.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr3:183995776 C>T maps to NM_014693.3 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr2:233347829 C>T maps to NM_004826.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:233349231 C>T maps to NM_004826.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr2:233344868 C>A maps to NM_004826.2 V774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr2:233348872 C>A maps to NM_004826.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr1:150483553 A>G maps to ENST00000369049 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:139210148 G>T maps to NM_001195037.2 E799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:139223643 G>A maps to NM_001195037.2 K865K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:68836509 G>T did not map to a codon.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr23:69176976 C>T did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:69247709 A>G did not map to a codon.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr16:67916938 C>T maps to NM_014329.3 A1236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:184675861 G>A maps to NM_025191.3 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr5:83433095 C>T maps to NM_005711.3 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:57876615 G>A maps to NM_207034.1 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:78474008 G>A maps to ENST00000377211 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr11:85967511 C>T maps to ENST00000351625 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:207027211 G>T did not map to a codon.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr8:144663456 G>A maps to NM_032378.4 H443H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr8:144671243 C>A maps to NM_032378.4 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr3:127983521 G>T maps to NM_021937.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:127981060 C>A maps to NM_021937.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:44031027 G>A maps to NM_022785.3 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:44074009 G>A maps to NM_022785.3 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:44083428 C>T maps to NM_022785.3 W355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:44107476 T>C maps to NM_022785.3 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:44131803 G>A maps to NM_022785.3 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr22:43950937 C>T maps to NM_022785.3 P1153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:52303218 G>T maps to NM_018100.3 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:52318994 C>T maps to NM_018100.3 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:44094667 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:44037697 C>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:106763001 G>A maps to NM_001962.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:132982783 C>T maps to NM_015137.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr8:132999935 A>G maps to NM_015137.3 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr8:132958828 A>G maps to NM_015137.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr15:82533622 T>C maps to NM_024580.5 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr15:82443977 C>T maps to NM_024580.5 E939E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:42964103 G>A maps to NM_004247.3 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:13636107 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:13645186 G>A did not map to a codon.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr7:55259521 A>G maps to NM_005228.3 K860K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr7:55249086 C>T maps to NM_005228.3 F795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr7:55242428 A>G maps to NM_005228.3 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr7:55242473 A>G maps to NM_005228.3 R748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr7:55249095 C>T maps to NM_005228.3 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr7:55269456 T>G maps to NM_005228.3 A1048A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr7:55241636 T>C maps to NM_005228.3 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr10:64573434 C>T maps to NM_001136178.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr2:73518869 C>T maps to NM_001965.3 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:42192923 G>A maps to NM_139265.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr3:184910745 C>T maps to NM_001966.3 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr3:184910847 A>G maps to NM_001966.3 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:40318188 C>T maps to NM_001013703.2 F1467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr3:183859764 G>A maps to NM_003907.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:36385201 C>T maps to NM_012199.2 F856F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr1:36316528 G>C maps to NM_017629.2 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:36282547 C>T maps to NM_017629.2 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr23:24082407 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:120810096 C>T maps to NM_003750.2 R803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr8:109240602 A>G maps to NM_001568.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr8:109240602 A>G maps to NM_001568.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr11:8013379 C>T maps to ENST00000449102 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:8013364 C>A maps to ENST00000449102 C149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr1:32691859 C>T maps to NM_003757.2 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:44843087 C>T maps to NM_003758.2 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr3:186503977 T>C maps to ENST00000440191 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:53412778 C>T maps to ENST00000438209 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:184035242 C>A maps to NM_001194947.1 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:184044406 C>A maps to NM_001194947.1 P1112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:21191647 G>T maps to NM_001198801.1 V890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:21212818 C>A maps to NM_001198801.1 E747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:21268769 G>A maps to NM_001198801.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr7:73609164 T>C maps to NM_022170.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr14:103807328 G>A maps to NM_183004.3 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:100006293 T>C maps to NM_015904.3 I795I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr1:50666846 C>A maps to NM_021952.3 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:139981755 C>T maps to ENST00000379550 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:139993091 C>A maps to ENST00000379550 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr1:201982404 G>T maps to NM_004433.4 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr23:129205112 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:129200946 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:129205131 C>A did not map to a codon.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr23:129200875 G>A did not map to a codon.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr23:129205129 T>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:18556071 G>A maps to NM_006532.3 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr7:37382249 C>T maps to NM_014800.9 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:33739746 T>G maps to ENST00000442325 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr8:28047217 G>A maps to NM_018091.5 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:153608712 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:101063296 C>T maps to ENST00000397927 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr18:2885078 C>T maps to NM_032048.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:2891315 C>T maps to NM_032048.2 C397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr18:2891252 G>T maps to NM_032048.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr20:39991143 A>G maps to NM_052846.1 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr20:39991170 G>A maps to NM_052846.1 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:100363622 C>T maps to NM_001008707.1 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:46116873 A>G maps to NM_001193268.1 H784H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:89082537 G>A maps to ENST00000380664 R1949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:89163194 G>A maps to ENST00000380664 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:10631920 C>T maps to NM_001424.4 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:14772865 G>A maps to NM_032571.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:225686081 C>A maps to ENST00000284563 E795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:71509134 C>A maps to NM_031889.2 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr4:71508195 A>G maps to NM_031889.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr11:94861650 T>G maps to NM_015036.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr12:48111364 G>T maps to NM_001172439.1 C106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:77076343 C>T maps to NM_001042573.1 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr10:25273711 G>A maps to NM_145010.2 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:4856136 G>T maps to NM_053013.3 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:43810868 G>T maps to NM_001127615.1 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:129771325 G>A did not map to a codon.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr4:111412298 A>G maps to NM_001977.3 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:132207857 C>T maps to NM_006208.2 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:132179886 C>T maps to NM_006208.2 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3584-01A-01W-0831-10 chr6:132006579 C>T maps to NM_005021.3 Y399Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr4:185138882 C>A maps to NM_153343.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:40231925 G>A maps to NM_152512.3 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr14:74439697 C>A maps to NM_001249.2 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:25201874 T>C maps to NM_001247.2 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr22:41573424 C>T maps to NM_001429.3 Q1904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr22:41513645 C>T maps to NM_001429.3 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr22:41523525 C>T maps to NM_001429.3 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr22:41548250 A>G maps to NM_001429.3 E1013E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr22:41564511 C>T maps to NM_001429.3 R1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr12:132445289 C>T maps to ENST00000333577 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:132471279 A>G maps to ENST00000333577 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:34765944 C>T maps to NM_012156.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:5428394 G>A maps to NM_012307.2 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:5478332 G>T maps to NM_012307.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr18:5410582 C>T maps to NM_012307.2 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr18:5395106 G>A maps to NM_012307.2 R1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:111576501 G>A maps to NM_022140.3 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:111600632 C>A maps to NM_022140.3 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:21927801 C>T maps to ENST00000265800 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr7:37988627 G>A maps to NM_017549.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr7:143096855 G>A maps to NM_005232.4 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr7:143095524 C>G maps to NM_005232.4 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:143095467 G>A maps to NM_005232.4 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr1:38227113 G>A maps to NM_001099439.1 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr3:89391121 G>T maps to NM_005233.5 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr3:89259542 T>C maps to NM_005233.5 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:222365808 C>A maps to NM_004438.3 G303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr4:66213861 A>G maps to NM_004439.5 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:66280128 A>C maps to NM_004439.5 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr4:66361109 G>A maps to NM_004439.5 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr4:66217172 G>T maps to NM_004439.5 C814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr4:66230762 G>A maps to NM_004439.5 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:97439160 C>T maps to NM_001080448.2 F947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr3:96706661 T>C maps to NM_001080448.2 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr3:96706205 T>C maps to NM_001080448.2 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:93956552 G>A maps to NM_004440.3 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr6:94066482 G>T maps to NM_004440.3 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr3:134884858 G>A maps to NM_004441.4 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr3:134920411 C>A maps to NM_004441.4 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr3:134670616 T>C maps to NM_004441.4 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr3:184298231 T>C maps to NM_004443.3 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:100405105 G>A maps to NM_004444.4 R739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr7:100417811 G>A maps to NM_004444.4 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr7:142566365 C>A maps to NM_004445.3 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr17:48614237 G>A maps to NM_017957.2 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:51871632 C>A maps to NM_001981.2 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr12:15818786 G>A maps to NM_004447.5 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr11:720196 C>T maps to NM_022772.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr11:720174 G>C maps to NM_022772.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:96136648 G>T maps to NM_016442.3 C193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:48688027 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:37866081 G>A maps to NM_004448.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr5:65288659 G>A maps to ENST00000506030 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr12:56477658 A>G maps to NM_001982.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr12:56481923 A>G maps to NM_001982.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:212251836 T>C maps to NM_005235.2 E1074E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:212288963 C>A maps to NM_005235.2 E928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:1137558 G>T maps to NM_178040.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:55768861 C>T maps to ENST00000460849 T883T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr3:55922426 G>A maps to ENST00000460849 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:14024595 G>A maps to NM_005236.2 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr16:14041759 C>T maps to NM_005236.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr13:103518116 G>C maps to NM_000123.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:50666881 T>C maps to NM_000124.2 K1487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:71427102 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:71427572 C>A did not map to a codon.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr23:71425228 C>T did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:71427619 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:60200627 A>G maps to NM_000082.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:42754574 G>A maps to NM_006494.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:42754535 G>A maps to NM_006494.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr5:172324071 A>C maps to NM_001031711.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr5:172341768 C>T maps to NM_001031711.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr5:172324047 G>T maps to NM_001031711.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr5:172336687 C>T maps to NM_001031711.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr20:34136261 G>A maps to ENST00000447986 K154K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AG-3599-01A-02W-0833-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr9:5801199 C>T maps to NM_024896.2 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr9:102784446 C>T maps to NM_015051.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:102861077 G>T maps to NM_015051.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr9:102768906 G>A maps to NM_015051.1 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:11105314 G>A maps to NM_207582.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr6:11105462 T>C maps to NM_207582.2 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr6:11105006 A>G maps to NM_207582.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr18:19144170 A>T maps to NM_052911.2 L605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr12:53683295 T>C maps to NM_012291.4 F1677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr2:239040030 C>T maps to NM_194312.2 H892H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:95704958 C>T maps to NM_017697.3 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr16:68266360 G>C maps to NM_024939.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:68265748 G>A maps to NM_024939.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:103498875 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:56537080 C>A maps to NM_001184796.1 S1073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr3:138187693 C>T maps to NM_031913.3 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:67631730 C>A maps to NM_019002.3 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr12:22811989 A>G maps to NM_018638.4 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:204109169 C>T maps to NM_018208.2 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr1:204115852 G>A maps to NM_018208.2 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:128391832 G>T maps to NM_005238.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr11:128354816 G>A maps to NM_001143820.1 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr3:185783740 C>T maps to NM_004454.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr4:5667310 C>A maps to NM_147127.4 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:29632027 A>C maps to NM_006495.3 Y200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr1:93070950 T>C maps to NM_005665.4 E645E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr17:74005244 C>T maps to NM_001988.2 A1347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr17:74014585 A>G maps to NM_001988.2 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:176948314 C>A maps to NM_001080458.1 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr2:176948351 C>T maps to NM_001080458.1 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr15:41476617 T>C maps to NM_152596.2 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:69695624 C>A maps to NM_001193363.1 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:133041121 G>T maps to NM_021807.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr14:57676673 A>C maps to ENST00000340918 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:94675519 G>A maps to NM_019053.4 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr1:11139839 C>T maps to NM_001001998.1 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:45030717 C>A maps to NM_015004.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr13:37578693 C>T maps to NM_181503.2 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr11:108381958 A>G maps to NM_015065.2 S1425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr8:119122508 G>A maps to NM_000127.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr8:28573809 C>T maps to NM_001440.2 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:28574616 C>T maps to NM_001440.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:45633580 A>G maps to ENST00000360649 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:45717938 G>A maps to ENST00000360649 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr20:45801435 C>A maps to ENST00000360649 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:133827282 G>T maps to ENST00000452339 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr6:65612336 G>A maps to ENST00000370616 Q900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:40864380 G>A maps to ENST00000264646 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr7:148523588 T>C maps to NM_004456.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:148523603 C>T maps to NM_004456.3 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr13:113803788 G>A maps to NM_000504.3 K475K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:113803326 C>T maps to NM_000504.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:160970813 G>T maps to NM_016946.4 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr5:76129106 C>A maps to NM_005242.4 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:169521893 G>A maps to ENST00000367796 Y399Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:169526042 C>A maps to ENST00000367796 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr1:169483637 G>T maps to ENST00000367796 I2201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:154157961 G>T did not map to a codon.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr23:154159113 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:154158355 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:154088800 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:154157348 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:154159391 C>A did not map to a codon.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr23:154158722 C>T did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:154157706 A>G did not map to a codon.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr23:154159622 T>C did not map to a codon.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr23:138623282 A>G did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:57358059 C>A did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:57319014 T>C did not map to a codon.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr4:120241983 C>T maps to NM_000134.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:82371561 G>A maps to NM_001080526.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:80465479 G>A maps to NM_000137.1 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr16:1877619 G>T maps to NM_001018104.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr2:97749738 T>C maps to NM_199336.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr2:97751496 T>C maps to NM_199336.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:207085259 A>C maps to NM_005449.4 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr23:55187582 C>T did not map to a codon.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr10:14563960 T>C maps to NM_031453.2 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr19:1881394 T>C maps to NM_031213.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr20:825677 T>C maps to NM_031424.4 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:59059478 C>T maps to NM_147189.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:58919839 C>A maps to NM_198847.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:58920754 T>C maps to NM_198847.2 F538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr12:47629679 G>A maps to NM_138371.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:47628896 C>T maps to NM_138371.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:57627403 G>A maps to NM_152678.2 R370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:96291858 G>A maps to ENST00000333936 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:170626642 A>T maps to NM_032448.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:170667321 G>A maps to NM_032448.1 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr23:54106712 T>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:133923268 C>A did not map to a codon.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr13:25744386 C>T maps to NM_152704.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr13:25745583 C>T maps to NM_152704.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3584-01A-01W-0831-10 chr23:63411245 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:63411545 T>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:63412117 C>T did not map to a codon.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr23:63411290 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:63411707 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:63411947 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:63412492 C>A did not map to a codon.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr23:63411782 C>A did not map to a codon.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr23:63412094 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:63412870 A>G did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:63412109 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:63412931 T>C did not map to a codon.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr2:131521630 C>T maps to NM_001105195.1 H662H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr2:131519854 G>A maps to NM_001105195.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr2:225266121 G>A maps to NM_001122779.1 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:17534603 C>A maps to NM_138401.2 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr9:129154393 G>A maps to NM_033446.1 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:23000876 C>A maps to NM_032581.3 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr7:22999941 A>C maps to NM_032581.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr2:201846544 T>C maps to NM_173822.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:17664140 G>A maps to ENST00000335393 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:143054020 G>A maps to NM_001031690.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr1:16385030 G>A maps to NM_182623.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr23:92964842 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:92965095 G>A did not map to a codon.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr5:16478971 T>C maps to NM_001034850.1 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:139158254 C>A maps to NM_015912.3 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:139165313 G>A maps to NM_015912.3 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:139380193 C>T maps to NM_015912.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:139180282 C>T maps to NM_015912.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:137354050 C>A maps to NM_016603.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr10:61062599 C>T maps to ENST00000442566 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:187086608 C>T maps to ENST00000356371 R676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr13:107823114 T>A maps to NM_001080396.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr1:53108594 C>T maps to NM_001042693.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:116602891 C>T maps to NM_020940.3 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:62067352 G>A maps to ENST00000404929 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:62067076 T>A maps to ENST00000404929 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr9:136444470 C>T maps to NM_001080515.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr8:79610709 A>G maps to NM_016010.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr1:32713033 G>C maps to NM_032648.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr2:187627012 G>A maps to NM_177454.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr2:187618690 C>T maps to NM_177454.3 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:126519949 A>G maps to NM_032182.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr2:29221081 G>T maps to NM_199280.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr2:29259555 C>G maps to NM_199280.2 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:45513966 G>T maps to ENST00000361462 E1350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr14:45535819 C>T maps to ENST00000361462 V1533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:94394675 C>T maps to NM_138344.3 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:94395494 C>A maps to NM_138344.3 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:119332523 C>A maps to NM_024581.4 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:119301400 C>A maps to NM_024581.4 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr6:119324730 T>C maps to NM_024581.4 E624E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr6:119301434 C>T maps to NM_024581.4 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr6:119399305 C>T maps to NM_024581.4 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr6:119301419 C>A maps to NM_024581.4 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:30830902 G>A maps to NM_032222.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:71992597 G>A maps to NM_001127608.1 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:18700944 A>G maps to NM_016078.4 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:2648549 C>T maps to ENST00000324666 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr4:2698259 C>T maps to ENST00000324666 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr3:150403600 C>T maps to NM_152394.3 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:128973612 G>A maps to NM_001039762.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr7:99145376 G>A maps to NM_145111.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:47922314 C>T maps to NM_018232.1 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr9:99694094 C>T maps to NM_001170741.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr18:10677754 T>C maps to NM_022068.2 S2577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:110587642 G>A maps to NM_033088.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr3:194408703 A>G maps to NM_153690.4 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr6:82461681 A>C maps to ENST00000369756 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:79698169 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:79698516 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:79699081 T>G did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:79698871 G>T did not map to a codon.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr23:79698262 C>T did not map to a codon.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:34148721 C>T did not map to a codon.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr23:34148935 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:34150199 C>T did not map to a codon.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr23:34149086 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:34148397 G>A did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:34148876 C>G did not map to a codon.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr23:34148376 T>G did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:34150180 C>T did not map to a codon.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr23:34961582 G>A did not map to a codon.
Sequencing variant TCGA-AG-3578-01A-01W-0831-10 chr23:34961787 G>A did not map to a codon.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr23:34962541 C>T did not map to a codon.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr23:34961581 C>T did not map to a codon.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr23:34962200 G>A did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:34961531 C>T did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:34961412 C>T did not map to a codon.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr23:37026703 A>G did not map to a codon.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr23:37026938 G>A did not map to a codon.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr23:37028774 G>A did not map to a codon.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr23:37027596 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:37027490 G>T did not map to a codon.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr23:37028880 C>T did not map to a codon.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr23:37027368 C>T did not map to a codon.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr23:37028939 C>T did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:37027471 T>C did not map to a codon.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr23:37028323 G>A did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:37028522 G>A did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:37028940 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:37599554 C>A maps to NM_001014286.2 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr23:24382404 G>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:130867924 G>A maps to NM_016623.3 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:153674895 A>G did not map to a codon.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr1:26156307 C>T maps to NM_001099626.1 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:114441971 G>T maps to NM_001077639.1 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr18:29867437 G>A maps to ENST00000269209 Y374Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:29848073 G>A maps to ENST00000269209 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:177250108 G>A maps to NM_021165.2 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr1:190067894 G>A maps to NM_199051.1 D518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr1:190067929 G>A maps to NM_199051.1 R507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:150974948 C>A maps to NM_001163258.1 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr16:67578877 T>G maps to NM_001193523.1 S983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr20:49225050 C>T maps to NM_080829.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:119394744 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:119438237 T>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:119410865 G>A did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:212799706 G>A maps to NM_153606.3 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr1:212799670 C>T maps to NM_153606.3 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:156590198 C>T maps to NM_130899.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr5:156589769 G>A maps to NM_130899.2 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr5:156593119 C>T maps to NM_130899.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr14:67669809 G>A did not map to a codon.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr7:128359088 G>A maps to NM_032599.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr9:40701735 C>T maps to NM_001083124.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:94749804 C>T maps to NM_152548.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:94782292 C>T maps to NM_152548.2 Y307Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr6:54735194 C>T maps to NM_001010872.1 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr20:33875029 G>A maps to NM_178468.4 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr20:37581027 G>A maps to NM_030919.2 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr22:40415323 T>G maps to NM_138435.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr17:18875007 G>A maps to NM_001039999.2 D712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr11:71498590 C>G maps to NM_018172.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:124786340 G>T maps to NM_144963.2 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:94713526 C>T maps to ENST00000452913 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr2:33810659 C>T maps to ENST00000395190 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:38765779 A>G maps to NM_173611.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:38897588 C>T maps to NM_174905.3 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:8766198 T>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:8997409 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:8997355 C>A did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:14882749 C>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:10076387 G>T maps to NM_033084.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr3:10084271 G>T maps to NM_033084.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:35075281 C>A maps to NM_004629.1 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:58388665 G>A maps to NM_001114636.1 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:45618081 G>T maps to NM_020937.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:127668863 G>T maps to ENST00000368692 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:127677131 G>A maps to ENST00000368692 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr2:163055366 T>A maps to NM_004460.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr2:163055300 G>A maps to NM_004460.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:13733356 T>C did not map to a codon.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr13:99020389 T>G maps to NM_005766.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr13:99061751 G>A maps to NM_005766.2 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:99099065 C>T maps to NM_005766.2 F1017F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:242407589 C>T maps to NM_014808.2 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:90767571 T>C maps to NM_000043.3 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr17:80044288 G>A maps to NM_004104.4 N1191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr2:170417201 G>A maps to NM_024622.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:207638987 C>T maps to NM_014929.3 R432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr2:207652841 C>T maps to NM_014929.3 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr5:7867092 A>G maps to NM_024091.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:7866829 G>T maps to NM_024091.3 S456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr20:3127925 G>A maps to NM_021826.4 N597N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr4:187535390 C>T maps to ENST00000260147 T3064T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr4:187630477 G>A maps to ENST00000260147 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:187518149 C>A maps to ENST00000260147 G4185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:187542150 C>T maps to ENST00000260147 A1866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr4:187539012 G>A maps to ENST00000260147 T2912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:150911475 G>T maps to NM_001447.2 S3161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:150923292 C>A maps to NM_001447.2 V2465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:150923555 C>A maps to NM_001447.2 E2378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:150947934 G>T maps to NM_001447.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr5:150925223 G>A maps to NM_001447.2 L1822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr5:150922758 G>T maps to NM_001447.2 V2643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr5:150946371 A>G maps to NM_001447.2 I707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr5:150921909 C>T maps to NM_001447.2 A2926A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr5:150901014 T>G maps to NM_001447.2 S3713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:92085331 C>A maps to ENST00000298047 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:92086976 C>T maps to ENST00000298047 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:92498145 C>T maps to ENST00000298047 F1362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:92531060 G>T maps to ENST00000298047 E1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr11:92086534 C>T maps to ENST00000298047 Y419Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr11:92534750 C>T maps to ENST00000298047 Q2858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr4:126355454 T>C maps to NM_024582.4 N2358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr4:126411431 G>A maps to NM_024582.4 A4485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:126389778 G>A maps to NM_024582.4 T4004T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr4:126412295 G>T maps to NM_024582.4 P4773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:126238810 G>A maps to NM_024582.4 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:126367513 C>T maps to NM_024582.4 S2420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr4:126411848 C>T maps to NM_024582.4 N4624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr4:126238183 C>A maps to NM_024582.4 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr4:126238750 C>T maps to NM_024582.4 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:16103736 C>T maps to NM_017556.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:45931215 T>C maps to ENST00000348697 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr3:13671425 G>A maps to NM_001165035.1 A983A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr3:13678032 C>T maps to NM_001165035.1 F1101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr15:48782243 G>A maps to NM_000138.4 Y962Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:48707950 G>A maps to NM_000138.4 C2611C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:48776108 G>T maps to NM_000138.4 I1248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:127636560 G>T maps to NM_001999.3 S2038S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:127668691 G>A maps to NM_001999.3 C1378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:127671686 G>A maps to NM_001999.3 G1239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:8183823 A>G maps to NM_032447.3 C1098C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:8171112 G>A maps to NM_032447.3 I1564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:8154510 G>A maps to NM_032447.3 G2098G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:102523813 G>A maps to NM_145032.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr3:33420181 C>T maps to NM_012157.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:77589658 C>T maps to NM_012158.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:99323497 C>A maps to NM_012160.3 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr5:15616098 C>A maps to NM_012304.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:382884 G>T did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr8:401362 T>C maps to NM_183421.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr14:55818418 A>G maps to NM_152231.1 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr5:147820738 G>A maps to NM_205836.1 R1109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr5:147806905 C>T maps to NM_205836.1 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:147790242 C>A maps to NM_205836.1 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr5:147796630 C>A maps to NM_205836.1 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:121340648 T>C maps to NM_016298.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:101154373 C>T maps to NM_001029860.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:37118235 G>T maps to NM_001008777.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:153296105 G>A maps to NM_012177.3 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr22:32875252 C>T maps to NM_012179.3 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:32894279 C>T maps to NM_012179.3 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr4:175158654 G>A maps to NM_012180.2 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr4:175183937 C>T maps to NM_012180.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr17:18653068 C>T maps to ENST00000395665 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr9:139837341 G>T maps to NM_018998.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr4:153247366 G>A maps to NM_033632.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr4:153251900 C>A maps to NM_033632.2 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr4:153271205 G>C maps to NM_033632.2 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr4:153258968 T>C maps to NM_033632.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:153244184 G>A maps to NM_033632.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:153273870 C>T maps to NM_018315.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr4:153251904 T>C maps to NM_033632.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr4:153244184 G>A maps to NM_033632.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr4:153332916 T>C maps to NM_033632.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr4:153332661 T>C maps to NM_033632.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr4:153249382 A>G maps to NM_033632.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr4:153245444 C>T maps to NM_033632.2 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr4:153249382 A>G maps to NM_033632.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr4:153244077 T>C maps to NM_033632.2 E693E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr4:153245444 C>T maps to NM_033632.2 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr4:153251904 T>C maps to NM_033632.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr4:153253823 T>C maps to NM_033632.2 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr4:153332918 G>A maps to NM_033632.2 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:207135886 G>T maps to NM_001170631.1 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr19:55396780 C>T maps to NM_002000.2 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr19:40420086 G>A maps to NM_003890.2 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:40366250 G>T maps to NM_003890.2 S4661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:40430319 C>T maps to NM_003890.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr19:40433292 C>A maps to NM_003890.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr19:40408806 G>A maps to NM_003890.2 N1344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr19:40368552 C>T maps to NM_003890.2 T4265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr1:161569550 C>T maps to NM_201563.4 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr19:50017732 G>A maps to NM_004107.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:72264390 G>T maps to NM_138782.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:72553793 C>A maps to ENST00000409314 E624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:72700016 G>A maps to ENST00000409314 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:137804954 C>A maps to NM_002003.3 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr1:157737123 G>T maps to NM_030764.3 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:157665844 G>A maps to NM_052939.3 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:157508986 C>A maps to NM_031281.2 G431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:159784038 T>G maps to NM_001004310.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:4793083 C>T maps to NM_018708.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr5:114860763 C>T maps to NM_020177.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:108382852 T>C maps to NM_005246.2 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:125072829 C>T maps to NM_001039112.2 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr8:125131952 C>T maps to NM_001039112.2 I1832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr2:219848965 G>A maps to NM_017521.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:62355880 G>A maps to NM_018008.3 C419C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:62357279 G>A maps to NM_018008.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:35940828 G>A maps to NM_005306.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:35940981 G>A maps to NM_005306.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:35941524 C>G maps to NM_005306.2 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:54495269 G>A did not map to a codon.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr23:54496874 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:54481893 C>T did not map to a codon.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr23:54472703 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:14862557 G>A maps to NM_152536.3 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:95488459 C>A maps to NM_018351.3 E1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:95602979 C>A maps to NM_018351.3 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:191861893 C>T maps to NM_021032.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr23:137717736 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:137717684 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:103053932 C>A maps to NM_175929.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr8:21903638 G>A maps to NM_003867.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr5:170863254 C>T maps to NM_003862.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr11:69514272 G>A maps to NM_005117.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:81188188 G>T maps to NM_004464.3 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr12:4554550 G>A maps to NM_020996.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:38287254 G>A maps to NM_001174067.1 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:38287380 G>A maps to NM_001174067.1 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr8:38272132 C>T maps to NM_001174067.1 V695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:167447411 G>T maps to NM_007045.2 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr10:123274628 T>C did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr10:123279630 G>A maps to ENST00000351936 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr10:123258039 G>T maps to ENST00000351936 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr10:123279562 C>T maps to ENST00000351936 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr4:1018762 C>T maps to NM_021923.3 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:76826264 G>A maps to NM_006682.2 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:241669399 G>T maps to NM_000143.3 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:241675353 G>A maps to NM_000143.3 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr1:241665823 G>A maps to NM_000143.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:241663755 T>C maps to NM_000143.3 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:153864539 C>T maps to NM_033393.2 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:135288596 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:135288731 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:34174853 G>A maps to NM_025135.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:34205695 C>T maps to NM_025135.2 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr9:133787221 C>T maps to NM_001145106.1 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:15376293 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:15376223 G>T did not map to a codon.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr7:50514772 A>G maps to NM_022116.3 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr6:76023351 G>A maps to NM_015687.2 H732H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:76023072 C>T maps to NM_015687.2 R825R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:76023381 G>A maps to NM_015687.2 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr6:76023701 G>A maps to NM_015687.2 R616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr7:100884116 C>A maps to NM_016068.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr17:39977327 C>T maps to NM_021939.3 H462H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:49317627 G>A maps to NM_016594.2 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:30058685 G>A maps to NM_017946.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:33042433 G>T maps to NM_007270.3 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr1:152286281 G>A maps to NM_002016.1 H360H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr1:152279750 A>T maps to NM_002016.1 A2537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:152275589 G>T maps to NM_002016.1 T3924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:152280008 C>T maps to NM_002016.1 R2451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr1:152279804 G>A maps to NM_002016.1 N2519N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr1:152282660 C>A maps to NM_002016.1 R1567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr1:152282660 C>A maps to NM_002016.1 R1567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr1:152282996 G>A maps to NM_002016.1 H1455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr1:152328755 G>T maps to NM_001014342.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:152325188 T>C maps to NM_001014342.2 R1691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:152325884 G>A maps to NM_001014342.2 S1459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:152326847 G>T maps to NM_001014342.2 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr1:152328899 G>T maps to NM_001014342.2 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr11:128680651 G>A maps to NM_002017.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:142481239 G>A maps to NM_207414.2 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:142505581 G>T maps to NM_207414.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr9:84603894 C>T maps to NM_001001670.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr9:84606599 A>T maps to NM_001001670.2 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:153599407 G>A did not map to a codon.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:153592919 C>T did not map to a codon.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr23:153590614 C>T did not map to a codon.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr23:153577743 T>C did not map to a codon.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr23:153588463 G>C did not map to a codon.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:153593245 C>T did not map to a codon.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr23:153585988 A>G did not map to a codon.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr23:153590347 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:58067370 G>T maps to NM_001164317.1 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:128483555 C>T maps to NM_001458.4 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:128492796 C>A maps to NM_001458.4 R1999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr7:128484812 C>T maps to NM_001458.4 T1098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr7:128496862 C>T maps to NM_001458.4 N2483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:63883855 C>T maps to NM_013280.4 Y39Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:86089234 C>T maps to NM_013231.4 H459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr13:28903788 G>A maps to NM_002019.4 N890N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr13:28895698 C>A maps to NM_002019.4 A1025A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr13:28592644 G>A maps to NM_004119.2 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr5:180045830 G>A maps to NM_182925.4 V980V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:76101258 G>T maps to NM_017791.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:240286539 G>A maps to ENST00000406993 E702E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr1:240371483 A>T maps to ENST00000406993 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr1:240371303 T>C maps to ENST00000406993 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:153484971 C>T maps to NM_052905.3 I775I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:171236710 C>A maps to NM_002021.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:171076910 C>A maps to NM_006894.5 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr1:171083341 T>A maps to NM_006894.5 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:203316630 G>T maps to NM_002023.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr23:147024826 C>T did not map to a codon.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr23:147011727 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:147010318 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:147018984 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:147026496 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:147026506 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:147090222 C>A did not map to a codon.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr2:216251568 G>A maps to NM_212482.1 P1485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:216259431 A>G maps to NM_212482.1 G1205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:216240045 C>T maps to NM_212482.1 P2016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:216271900 C>A maps to NM_212482.1 E888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr1:94000446 C>T maps to ENST00000370253 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr6:159670204 C>T maps to NM_032532.2 R1609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr6:159660579 C>T maps to NM_032532.2 D1404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:49742799 C>A maps to NM_001079673.1 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr13:49772149 T>C maps to NM_001079673.1 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr3:172065126 T>A maps to NM_022763.3 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:172013250 C>T maps to NM_022763.3 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:171969254 C>T maps to NM_022763.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:33333803 G>T maps to ENST00000291421 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr1:109270589 G>A maps to NM_001144937.1 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr14:65520040 G>A maps to ENST00000448390 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:89407301 G>T maps to NM_153696.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:71932697 G>A maps to NM_001113536.1 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr11:71932637 C>T maps to NM_001113536.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr11:65661580 C>T maps to NM_005438.3 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr14:38061631 C>T maps to NM_004496.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:169535098 C>T maps to NM_012188.4 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr10:129537054 C>T maps to NM_207426.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:74136146 G>A maps to NM_001454.3 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:4780516 G>A maps to ENST00000450194 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr7:4801866 G>A maps to ENST00000450194 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:4794935 G>A maps to ENST00000450194 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr17:80545005 G>A maps to NM_004514.3 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr3:138664469 G>A maps to NM_023067.3 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:2968602 G>T maps to NM_202002.1 S536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:2981353 G>A maps to NM_202002.1 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:109719221 G>A maps to NM_213596.2 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:70316637 C>T did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:70320925 G>A did not map to a codon.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr7:114268632 C>T maps to NM_148898.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:79285131 C>T maps to NM_025074.6 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:79387384 C>T maps to NM_025074.6 I2351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:79442732 C>T maps to NM_025074.6 R3533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:14756378 A>G maps to ENST00000380880 F1803F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr9:14868885 G>A maps to ENST00000380880 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr13:39264108 C>T maps to NM_207361.4 H876H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr13:39343883 C>T maps to NM_207361.4 P1860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr13:39265930 C>T maps to NM_207361.4 Q1484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:39450480 G>T maps to NM_207361.4 E2836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:39453092 C>T maps to NM_207361.4 V2995V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr6:116263657 T>C maps to NM_002031.2 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr6:116264270 A>G maps to NM_002031.2 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr6:116325142 G>T maps to NM_002031.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:85950441 T>C maps to NM_174938.4 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:13743444 G>A maps to NM_018027.3 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr3:69244462 T>C maps to NM_015123.1 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr3:69244256 C>G maps to NM_015123.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr14:52174920 C>T maps to ENST00000344768 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:131212719 G>T did not map to a codon.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr9:37740789 C>G maps to NM_014907.2 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:37735604 C>T maps to NM_014907.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr9:37740285 C>T maps to NM_014907.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:12712555 G>A did not map to a codon.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:12734594 A>G did not map to a codon.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr23:12720003 T>C did not map to a codon.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr23:12734760 C>T did not map to a codon.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr23:12734766 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:12720126 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:12725709 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:12736203 C>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:12734434 G>T did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:12701705 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:32705848 G>T maps to NM_023037.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:32826037 A>G maps to NM_023037.2 V2398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:32721487 C>T maps to NM_023037.2 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:32745148 G>A maps to NM_023037.2 R631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:48502083 C>A maps to NM_015030.1 E2916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr4:48569286 C>T maps to NM_015030.1 A1049A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr14:44974060 T>C maps to NM_032135.3 E710E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr19:4307964 C>T maps to NM_024333.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr19:4318478 G>A maps to NM_024333.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:83455608 G>T maps to NM_001007122.2 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:30255341 G>T maps to NM_001018080.1 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr11:30255299 C>T maps to NM_001018080.1 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:49191104 G>A maps to NM_000145.3 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr2:49190039 C>A maps to NM_000145.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr5:52779466 A>G maps to NM_013409.1 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr5:132939652 G>A maps to NM_015082.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:162577527 C>T maps to NM_020116.3 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:162577628 G>A maps to NM_020116.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr5:121188026 C>T maps to NM_177478.1 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:71317987 A>G maps to NM_018348.5 C612C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:37430661 C>T maps to NM_015050.2 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:78433327 C>T maps to ENST00000436586 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:24180866 C>A maps to NM_000147.4 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:70513116 G>A maps to NM_145059.2 S988S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:33310893 C>T maps to ENST00000380081 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:33246540 G>A maps to ENST00000380081 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:66188689 G>T maps to NM_178155.1 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:96651687 G>A maps to NM_006581.3 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr3:180669153 A>G maps to NM_005087.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr3:180675610 A>G maps to NM_005087.3 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr17:7496123 G>C maps to NM_004860.3 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr5:39202864 G>T maps to ENST00000263405 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:46014656 G>T maps to NM_024513.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr6:112041167 G>T maps to NM_153047.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:130648737 C>T maps to NM_007197.3 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr17:42636399 C>T maps to NM_001466.3 D448D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:28385477 C>T maps to NM_017412.3 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr8:28385089 A>G maps to NM_017412.3 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:209849136 C>T maps to NM_015714.3 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:41063103 C>T maps to NM_000151.2 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:153760919 C>A did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:153760261 A>G did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr4:144359718 C>T maps to NM_207123.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr23:153940898 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:29574675 C>A maps to NM_001470.2 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:29577097 C>T maps to NM_001470.2 Q589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr6:29576461 G>A maps to NM_001470.2 G636G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr6:29589552 A>G maps to NM_001470.2 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:101068621 G>A maps to NM_005458.7 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr9:101340281 C>A maps to NM_005458.7 G132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr21:27136963 C>T maps to NM_002040.3 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:50578347 C>A maps to NM_005254.5 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:151532993 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:27126046 G>A maps to NM_000810.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:27128355 C>T maps to NM_000810.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr15:27182371 C>T maps to NM_000810.3 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr5:160757951 T>A maps to NM_021911.2 K339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:26792956 G>A maps to NM_021912.4 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:151131055 G>A did not map to a codon.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:151123284 T>C did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr23:151129760 A>G did not map to a codon.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr4:46053441 G>T maps to NM_173536.3 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:161530911 G>T maps to NM_198903.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:170238980 G>T maps to NM_014211.2 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:170222235 C>T maps to NM_014211.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr23:151815598 A>G did not map to a codon.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr23:151818309 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:89890094 G>A maps to NM_002042.3 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:89927008 G>T maps to NM_002042.3 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr6:89910947 C>T maps to NM_002042.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:26569983 T>C maps to NM_001134366.1 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr10:26518594 C>T maps to NM_001134366.1 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr23:49161342 G>A did not map to a codon.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr22:30953351 C>A maps to NM_004861.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:230415128 C>T maps to NM_004481.3 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:158157216 C>A maps to NM_014568.1 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr2:158156137 T>C maps to NM_014568.1 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:69808473 G>T maps to NM_020692.2 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr3:16216963 C>T maps to NM_054110.4 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr11:11454216 G>A maps to NM_198516.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:11292768 G>A maps to NM_198516.2 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr4:173734791 G>T maps to NM_001034845.2 G281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:74980804 G>T maps to NM_001480.3 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:81388122 G>A maps to NM_022041.3 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:81388327 C>T maps to NM_022041.3 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:81391483 C>T maps to NM_022041.3 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr11:62414062 C>T maps to NM_198335.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr3:115394916 A>T maps to NM_001130064.1 K66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:57790675 G>T maps to NM_152687.2 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:128099641 A>G maps to NM_015635.2 E910E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:128064673 T>C maps to NM_015635.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:128097500 G>T maps to NM_015635.2 E827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr9:130075822 T>C maps to NM_032293.4 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr9:130149569 G>A maps to NM_032293.4 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr21:34876604 T>C maps to NM_001136006.1 G953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr17:39872081 A>G maps to NM_000805.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:48652424 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:8115901 G>A maps to NM_001002295.1 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:8115749 C>A maps to NM_001002295.1 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr1:155209749 G>A maps to NM_001005742.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr10:104121551 G>A maps to NM_004193.2 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:104119977 C>T maps to NM_004193.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr1:89726431 G>A maps to NM_052942.3 H572H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:89732027 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:89598019 G>A maps to NM_207398.2 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:89637480 G>A maps to NM_207398.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:72631189 G>T maps to ENST00000504199 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr22:38212574 C>T maps to NM_001171690.1 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:127224308 G>A maps to NM_024523.5 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr2:109086274 T>C maps to NM_181453.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:109088434 G>T maps to NM_181453.3 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:109116157 G>A maps to NM_181453.3 T1644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:13007746 C>T maps to NM_000159.2 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:111844101 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:34134470 C>T maps to NM_016631.3 E269E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr21:34117132 T>C maps to NM_016631.3 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr21:34117132 T>C maps to NM_016631.3 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:44184794 G>A maps to NM_000162.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:10876731 G>A maps to NM_004752.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr6:10875151 T>C maps to NM_004752.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr12:120591163 G>A maps to NM_006836.1 N1305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr12:120602181 G>A maps to NM_006836.1 H602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:10529381 C>T maps to NM_145649.4 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:10529971 C>T maps to NM_145649.4 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:10556721 C>T maps to NM_001491.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr15:59910944 G>T maps to NM_004751.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:74842908 C>T maps to ENST00000238018 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr9:74860095 G>T maps to ENST00000238018 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:42893092 C>A maps to NM_024034.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr16:19522172 G>A maps to NM_016641.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:48413859 G>A maps to NM_016204.1 F336F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AG-A002-01A-01W-A00K-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr20:34025242 G>A maps to NM_000557.2 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:37815941 G>A maps to NM_001190468.1 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:69644907 A>C did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr12:58009798 C>T maps to NM_001111270.1 N512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:154311117 G>A maps to NM_015465.3 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr5:154278134 C>T maps to NM_015465.3 T1070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr5:154287313 C>T maps to NM_015465.3 K744K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr7:931980 G>A maps to NM_015949.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr7:926224 T>C maps to ENST00000457861 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr17:42985482 G>T maps to NM_002055.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:2035968 C>T maps to NM_005262.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr1:92944145 A>G maps to NM_005263.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr9:135865172 C>A maps to NM_004188.4 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:158378751 C>T maps to ENST00000264263 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:67709825 G>A maps to NM_030819.3 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr16:67709585 G>C maps to NM_030819.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:179729563 G>A maps to NM_005110.2 C621C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr5:179762828 G>A maps to NM_005110.2 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:117824002 G>T maps to NM_005264.4 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:117825110 C>T maps to NM_005264.4 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr5:137589744 C>T did not map to a codon.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr19:38877874 G>A maps to NM_152657.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:34935714 G>T maps to NM_024835.3 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:24622607 C>T maps to NM_001099781.1 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr22:24622042 C>T did not map to a codon.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr17:4461462 A>T maps to ENST00000414312 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr20:23966528 C>A maps to NM_178311.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr22:22989501 C>T maps to ENST00000215938 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:85903851 G>T maps to ENST00000436406 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr7:31008525 A>G maps to NM_000823.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:172166053 G>A maps to NM_198407.2 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr2:233671230 G>A maps to ENST00000373566 W579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:233704625 C>A maps to ENST00000373566 S967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr2:233681634 C>T maps to ENST00000373566 R777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:233697614 C>T maps to ENST00000373566 R882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:150269395 G>T maps to ENST00000430830 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr7:150325094 G>A maps to ENST00000438845 C267C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:102442550 C>A maps to NM_017676.2 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr5:102432329 G>T maps to NM_017676.2 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:85715219 G>T maps to NM_016095.2 Y91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:78585114 G>T maps to NM_017655.4 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:110377016 C>T maps to NM_057169.3 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:121768667 C>A maps to NM_000165.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:90605507 C>T maps to NM_032602.1 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:90604468 C>T maps to NM_032602.1 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr1:35260476 G>A maps to NM_002060.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:147380237 C>T maps to NM_005267.4 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr1:147380600 C>T maps to NM_005267.4 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:20797481 G>A maps to NM_001110221.2 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:100656740 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:8124632 C>A maps to NM_138426.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr16:74499591 G>A maps to NM_012201.5 V883V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr12:57865075 C>A maps to NM_005269.2 Y851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr2:121747299 C>A maps to NM_005270.4 C1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr2:121729539 C>T maps to NM_005270.4 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr2:121746705 G>A maps to NM_005270.4 A1072A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr7:42004759 G>T maps to NM_000168.5 S1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr7:42004785 G>A maps to NM_000168.5 F1295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr7:42064964 C>T maps to NM_000168.5 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:42007392 G>A maps to NM_000168.5 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:42017210 A>C maps to NM_000168.5 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr7:42064964 C>A maps to NM_000168.5 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr12:75816729 C>A maps to ENST00000378692 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr1:53975699 C>A maps to NM_147193.2 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:3856068 G>A maps to NM_001042413.1 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:92735332 G>A maps to NM_053274.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr6:39034025 C>T maps to NM_002062.3 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:9792802 C>T maps to NM_004246.1 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:9792898 G>A maps to NM_004246.1 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:14625261 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:102968539 C>T did not map to a codon.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr4:158065028 C>T maps to NM_001166060.1 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr4:158091816 A>T maps to NM_001166060.1 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:95158186 A>C maps to NM_002064.2 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:193065765 C>A maps to NM_016066.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr2:191819354 T>A maps to NM_014905.3 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:129431919 G>T maps to ENST00000442111 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:138516032 C>A maps to NM_182974.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:104408871 G>A maps to NM_031302.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr12:104413413 G>A maps to NM_031302.3 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr23:120181653 C>A did not map to a codon.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr23:120182922 C>T did not map to a codon.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr23:120182602 T>C did not map to a codon.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr23:120182713 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:58723382 C>A maps to NM_080661.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr2:70081985 A>G maps to NM_178439.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:1961100 T>A maps to NM_001500.2 K149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr20:62224376 G>A maps to NM_012384.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr19:19745479 G>A maps to NM_016573.2 Y640Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr8:143922588 C>T maps to NM_002066.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:3118948 G>A maps to NM_002067.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:63010572 A>G maps to NM_006572.4 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr19:3150214 G>A maps to NM_002068.2 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr7:79840383 C>T maps to NM_002069.5 Y230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:80336399 C>A maps to NM_002072.3 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr20:57415469 C>T maps to NM_016592.2 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr20:57415589 C>T maps to NM_016592.2 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr3:179134312 A>G maps to NM_021629.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr1:235715438 G>A maps to NM_004485.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:54559004 G>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr12:65115434 G>T maps to ENST00000418919 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr9:131030737 A>C maps to NM_004486.4 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:131036224 G>A maps to NM_004486.4 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr3:37365329 A>G maps to NM_001172713.1 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr3:37365329 A>G maps to NM_001172713.1 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:37368057 G>T maps to NM_001172713.1 E1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:121416426 T>C maps to ENST00000393667 E981E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:121412606 A>G maps to ENST00000393667 L2255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:121412681 C>A maps to ENST00000393667 E2230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:121412903 C>A maps to ENST00000393667 E2156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr3:121409534 T>C maps to ENST00000393667 Q2892Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:155722013 T>C maps to ENST00000368331 K2070K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:117884479 C>T maps to NM_020399.3 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:39139726 T>G maps to NM_031899.2 *441Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:101163355 C>A maps to NM_002079.2 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:58752150 C>T maps to NM_002080.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:194118501 C>T maps to NM_004488.2 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:33600678 G>T maps to NM_018025.2 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:33584410 C>A maps to NM_018025.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:132730610 G>T did not map to a codon.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr23:132887833 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:5539374 C>A maps to NM_019593.3 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:1131795 C>T maps to NM_001505.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:64702828 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:34890645 C>T maps to NM_000175.3 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:48979962 T>C did not map to a codon.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr23:48978805 A>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:24456736 C>T maps to NM_001503.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr7:23300195 C>G maps to ENST00000435486 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:23299725 C>T maps to ENST00000435486 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr23:136112714 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:136113724 C>T did not map to a codon.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr23:136113119 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:136113162 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:136113506 G>A did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr23:136113067 A>G did not map to a codon.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr12:123201275 C>T maps to NM_006018.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr6:46996731 C>T maps to ENST00000283297 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr6:46984470 A>G maps to ENST00000283297 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3578-01A-01W-0831-10 chr23:135482099 G>T did not map to a codon.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr23:135426909 G>T did not map to a codon.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr23:135431745 T>C did not map to a codon.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr23:135430848 A>G did not map to a codon.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr23:135427605 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:135428506 C>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:135429805 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:135405087 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:135432546 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:135487986 C>T did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr23:135427195 G>C did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:135427392 C>T did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:135427478 C>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:57601914 C>T maps to ENST00000349457 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr6:47682171 C>T maps to NM_153838.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr6:47682171 C>T maps to NM_153838.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr6:46849285 T>C maps to NM_015234.4 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:129519300 G>T did not map to a codon.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr10:134940769 C>A maps to ENST00000368577 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr4:22463423 G>A maps to NM_145290.2 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:142738464 C>A maps to NM_198569.2 V998V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:105517708 G>A maps to NM_013345.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:236368475 C>T maps to NM_003272.3 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:53066893 C>T maps to NM_001099652.1 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr7:37780300 G>A maps to NM_181791.1 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr7:37780909 T>C maps to NM_181791.1 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:9711654 T>C did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:1097945 C>T maps to NM_138445.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:154055622 G>T maps to NM_001038705.1 I687I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr3:154055523 A>G maps to NM_001038705.1 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr3:154146597 C>T maps to NM_001038705.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr11:67219091 C>T maps to NM_206997.1 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr11:67219262 C>T maps to NM_206997.1 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:175333666 A>G maps to NM_152529.5 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:119886769 G>A maps to NM_153002.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr1:9165616 C>T maps to NM_024980.4 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr10:25701342 C>T maps to NM_020752.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr10:25887863 C>T maps to NM_020752.2 N1103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:168065844 C>A maps to NM_153832.1 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:168065764 G>A maps to NM_153832.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:6936002 C>T maps to NM_019858.1 D467D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr23:78427339 G>T did not map to a codon.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr23:78426545 T>C did not map to a codon.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr23:78427422 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:36485802 C>A maps to ENST00000398597 E1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:36485719 G>A maps to ENST00000398597 C1245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:36486505 G>A maps to ENST00000398597 S983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:36493058 G>A maps to ENST00000398597 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr17:36483853 C>T maps to ENST00000398597 L1867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:99907894 G>A maps to NM_005292.3 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr13:99947988 T>G maps to NM_004951.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:107114855 C>T maps to NM_005295.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:167570743 G>T maps to NM_005299.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:41555213 C>T did not map to a codon.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr7:124387043 G>T maps to NM_005302.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr2:133174725 C>T maps to NM_001508.2 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr11:60620802 C>T maps to NM_004778.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr2:105858989 C>T maps to NM_007227.3 N225N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr2:105858360 C>T maps to NM_007227.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr6:110301319 G>A maps to ENST00000414000 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:51989778 C>T maps to NM_080865.3 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr6:97246934 G>A maps to NM_030784.2 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:19028797 C>A did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr23:19032030 T>G did not map to a codon.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr23:19039315 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:151012744 G>A maps to NM_023915.3 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr3:151012460 G>A maps to NM_023915.3 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr1:145765380 T>C maps to NM_001097612.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr5:90074422 G>A maps to NM_032119.3 Q4282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:90087049 C>T maps to NM_032119.3 R4802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:89914925 T>C maps to NM_032119.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:89939792 C>A maps to NM_032119.3 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:89971991 T>G maps to NM_032119.3 S1803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:90052804 G>T maps to NM_032119.3 E3923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr5:90040914 G>A maps to NM_032119.3 S3534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr5:90052962 A>G maps to NM_032119.3 E3975E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr5:90024538 A>C maps to NM_032119.3 R3405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr5:89940599 C>T maps to NM_032119.3 Q938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:101912764 C>A did not map to a codon.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr23:101912024 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:101969950 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:101970982 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:101971498 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:13103216 G>A maps to NM_018654.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr10:46999029 C>T maps to NM_014696.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:46999896 G>A maps to NM_014696.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:90169764 C>T maps to NM_198281.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:7217622 G>A maps to NM_004489.4 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr16:46958407 C>T maps to NM_133443.2 Y440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr16:46943597 G>T maps to NM_133443.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr5:125828620 A>G maps to NM_023927.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:47022794 C>T maps to NM_015124.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:50672998 G>A maps to NM_005311.4 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:165383582 C>A maps to NM_004490.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:11716644 C>A maps to NM_014668.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:11733112 C>T maps to NM_014668.3 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:10104083 G>A maps to NM_198182.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:102589727 G>A maps to NM_024915.3 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:158256989 G>A maps to NM_000826.3 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr4:158281127 C>T maps to NM_000826.3 A708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr23:122538639 G>T did not map to a codon.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr23:122598805 G>A did not map to a codon.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr23:122387323 G>T did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr23:122616761 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:105850444 C>A maps to NM_000829.3 V896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:87379700 G>A maps to NM_017551.2 I761I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr10:87484364 C>T maps to NM_017551.2 K534K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:94006398 G>A maps to NM_001510.2 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:94547442 C>T maps to NM_001510.2 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:101847236 T>G maps to NM_021956.4 Y28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:102516367 T>C maps to NM_021956.4 G903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:102074300 A>G maps to NM_021956.4 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr6:102483298 A>G maps to NM_021956.4 E723E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr6:102516286 A>G maps to NM_021956.4 K876K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:37346415 G>T maps to NM_000831.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:37291298 G>A maps to NM_000831.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:37346244 G>A maps to NM_000831.3 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr1:37346244 G>A maps to NM_000831.3 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:120823598 A>C maps to NM_014619.2 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr16:9858208 C>T maps to NM_000833.3 T1064T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr16:9857656 G>A maps to NM_000833.3 I1248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr16:10031859 G>A maps to NM_000833.3 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:9858097 G>A maps to NM_000833.3 V1101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:9858393 C>A maps to NM_000833.3 E1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:9916247 G>A maps to NM_000833.3 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr19:1004843 T>C maps to NM_138690.1 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr8:145066194 C>T maps to NM_001009184.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr8:145065645 A>C maps to NM_001009184.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:66935704 G>A maps to ENST00000359742 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr12:66849240 T>C maps to ENST00000359742 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:48847484 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:48847363 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:121140354 G>A maps to NM_005308.2 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:146350901 C>T maps to NM_000838.3 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:146720610 C>A maps to NM_000838.3 I812I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr6:146720508 C>T maps to NM_000838.3 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:146755712 C>T maps to NM_000838.3 D1122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr3:51749543 G>A maps to NM_000839.3 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr11:88337887 T>C maps to NM_001143831.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr11:88300543 G>A maps to NM_001143831.2 N769N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr5:178413955 G>A maps to NM_000843.3 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:178419042 G>A maps to NM_000843.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:178413301 G>A maps to NM_000843.3 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:6903440 C>T maps to NM_181874.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:126542724 G>A maps to NM_001127323.1 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:126746619 C>T maps to NM_001127323.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr7:126746619 C>T maps to NM_001127323.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr5:148730566 G>T maps to NM_152407.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:71693715 G>A maps to NM_002092.3 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:43032518 G>T maps to NM_001080476.2 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr4:43032467 C>T maps to NM_001080476.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:38130557 G>T maps to NM_178171.4 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr16:27840213 G>T maps to NM_001109763.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr19:42735002 C>T maps to NM_019884.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr20:33529526 G>A maps to NM_000178.2 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr6:52616422 G>A maps to NM_000846.4 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr4:106744147 A>G maps to NM_001031720.2 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:110279776 G>A maps to NM_000849.4 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr1:110201531 G>T did not map to a codon.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr2:48848420 C>A maps to NM_172311.2 S784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr2:48873703 A>G maps to NM_172311.2 V871V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr15:59931351 A>G maps to NM_004492.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr1:89325833 G>T maps to NM_001514.5 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:45781629 C>T maps to NM_004128.2 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:74212434 C>T maps to NM_173537.2 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr7:74211462 A>G maps to NM_173537.2 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr7:74564622 A>G maps to NM_001003795.2 K790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:27476024 C>A maps to NM_001520.3 E1830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr16:27549525 G>A maps to NM_001520.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr16:27509108 C>T maps to NM_001520.3 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr2:197639867 G>A maps to NM_012086.2 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr2:197639858 T>C maps to NM_012086.2 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:135553404 C>T maps to NM_012204.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr9:135554145 T>C maps to NM_012204.2 Y380Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:17450339 C>T maps to NM_133644.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:112715817 G>T maps to NM_014170.2 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:112718375 A>G maps to NM_014170.2 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:42355025 G>T maps to NM_176791.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:106810508 C>A maps to ENST00000282249 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:156632280 G>T maps to NM_001130684.1 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr4:156631751 C>T maps to NM_001130684.1 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr23:108691388 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:108673540 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:108638579 A>T did not map to a codon.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr23:108619325 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:189452662 T>G maps to NM_016315.2 L277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr7:65444799 C>A maps to NM_000181.3 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:73016725 G>A maps to NM_001080393.1 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:2777918 G>A did not map to a codon.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr11:45946115 G>C maps to NM_152312.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:49485576 C>A maps to NM_002103.4 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:21721868 G>A maps to NM_021957.3 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:21728966 C>A maps to NM_021957.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:25101152 G>A maps to ENST00000382542 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:134724633 G>A maps to NM_138610.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:103267810 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:105233164 A>G maps to NM_020771.3 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:15602372 T>C maps to NM_012260.2 *579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:108930968 C>T maps to ENST00000351726 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr2:26437988 T>C maps to NM_000182.4 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:26417501 T>C maps to NM_000182.4 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:26432730 C>A maps to NM_000182.4 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:26486263 G>A maps to NM_000183.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:96374439 G>A maps to NM_002108.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr12:96371737 G>A maps to NM_002108.2 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:35775855 C>T maps to NM_021175.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr4:174450035 G>A maps to NM_021973.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr4:174450095 G>A maps to NM_021973.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:7866188 G>T maps to NM_017545.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr20:7886842 T>G maps to NM_017545.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr5:82937440 G>A maps to NM_001884.3 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr19:19372261 G>A maps to NM_023002.2 H38H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr19:19371742 G>A maps to NM_023002.2 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr5:140073237 C>T maps to NM_012208.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:52222482 G>A maps to NM_001523.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:172821965 C>T maps to NM_003642.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr2:172844218 C>T maps to NM_003642.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr9:19063005 C>T maps to NM_017645.3 E543E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr9:19063007 C>A maps to NM_017645.3 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr23:152728109 G>A did not map to a codon.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr23:11139873 T>A did not map to a codon.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr23:11139859 G>A did not map to a codon.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr23:153218215 G>A did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:153220359 A>G did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:104487252 G>A maps to NM_013320.2 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr20:30689234 G>A maps to NM_002110.3 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr20:30681682 C>T maps to NM_002110.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:45303767 G>A maps to NM_021072.2 H517H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:45267196 G>A maps to NM_021072.2 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:45645648 C>A maps to NM_021072.2 G163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:73617476 C>T maps to NM_005477.2 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:55039579 C>T maps to NM_001526.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:55113599 G>T maps to NM_001526.3 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr3:13542267 G>A maps to NM_024827.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr6:114277792 G>A maps to ENST00000398283 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:240061475 G>A maps to NM_006037.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr2:240024514 C>T maps to NM_006037.3 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:240024583 G>A maps to NM_006037.3 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr17:42169091 G>T maps to NM_001015053.1 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:48661317 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:48681937 G>T did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:48676707 C>A did not map to a codon.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr7:18767219 G>A maps to NM_178425.2 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr7:18687499 G>A maps to NM_178425.2 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:18631235 C>T maps to NM_178425.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:18801809 G>T maps to NM_178425.2 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:50544659 C>T maps to NM_002112.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr15:50555517 G>A maps to NM_002112.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr15:50535200 A>G maps to NM_002112.3 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr15:83826708 G>A maps to NM_016073.2 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:7023670 C>T did not map to a codon.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr9:116136300 G>A maps to NM_031219.2 Q112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:83723903 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:83576991 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:83599312 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:83723655 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:83723826 C>A did not map to a codon.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr1:236723028 G>A maps to NM_018072.5 Y1585Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:50136319 G>T maps to NM_182922.2 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr16:50109492 C>T maps to NM_182922.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:73965777 G>A maps to ENST00000334988 R738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:31813173 G>T maps to ENST00000389961 I1046I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:31844093 C>A maps to ENST00000389961 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:31855691 C>A maps to ENST00000389961 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:37208730 G>A maps to NM_019024.1 R2040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:37268421 G>A maps to NM_019024.1 R904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr2:37234316 T>C maps to NM_019024.1 E1551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr2:37230721 A>G maps to NM_019024.1 A1671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:41000447 G>A maps to ENST00000296803 C1453C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:138734053 G>T maps to NM_014320.2 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr14:31675094 T>C maps to NM_015382.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr14:31582525 T>C maps to NM_015382.2 L2007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:45476351 G>A maps to NM_024602.5 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:43540369 C>A maps to NM_015052.3 V1170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:43580824 C>T maps to NM_015052.3 F1361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:43581489 G>T maps to NM_015052.3 E1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr7:43531696 A>G maps to NM_015052.3 R1086R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr7:43591928 C>A maps to NM_015052.3 R1502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr2:197171283 C>T maps to NM_020760.1 T914T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:197183693 G>A maps to NM_020760.1 C640C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr10:96353344 T>C maps to NM_018063.3 D687D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:84342783 G>A maps to NM_133636.2 R961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr17:65174932 C>T maps to NM_014877.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:100692499 C>A maps to NM_018437.3 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:100689697 C>A maps to NM_018437.3 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr7:92848753 C>T maps to ENST00000453812 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:65480092 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:65483519 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:65486345 G>T did not map to a codon.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr23:65418744 T>C did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:65427041 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:93800714 G>T maps to NM_001098672.1 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:93815697 G>T maps to NM_001098672.1 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:63928189 G>A maps to ENST00000261887 I4128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr15:64041864 A>G maps to ENST00000261887 H676H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr15:64048878 G>A maps to ENST00000261887 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr15:63952072 A>G maps to ENST00000261887 L3096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:28420711 G>A maps to NM_004667.4 I3259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:28460811 G>A maps to NM_004667.4 V2055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:28514474 C>T maps to NM_004667.4 Q455Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr15:28422161 G>A maps to NM_004667.4 T3122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:89575194 C>T maps to NM_014606.1 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr4:89591098 A>G maps to NM_014606.1 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:89400526 G>T maps to NM_016323.2 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:89407318 C>A maps to NM_016323.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:89334266 T>C maps to NM_017912.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:35678030 C>A maps to NM_022373.4 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:35712882 C>T maps to NM_022373.4 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr7:35674830 T>C maps to NM_022373.4 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr7:35674830 T>C maps to NM_022373.4 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr15:72638892 G>T maps to ENST00000457859 Y446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:43246602 G>A maps to NM_144608.1 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr8:80677422 T>G maps to NM_001040708.1 *309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:91818704 G>T maps to NM_001017975.3 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:91731610 C>A maps to NM_001017975.3 E1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr1:91781406 G>A maps to NM_001017975.3 D1035D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:81336624 G>A maps to NM_000601.4 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr8:43027509 C>T maps to ENST00000458501 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr1:210577848 G>A maps to NM_001170580.1 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:210796899 C>T maps to NM_001170580.1 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr14:100135192 C>T maps to NM_032425.4 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:222717147 G>A maps to NM_024746.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:100533592 C>T maps to NM_033055.2 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:62187160 G>T maps to ENST00000394997 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:46838170 C>T maps to NM_152795.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:126296097 C>A maps to NM_138571.4 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:75168732 C>A maps to NM_005338.4 E991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:75211409 C>A maps to NM_005338.4 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr1:114483238 T>C maps to ENST00000426820 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:33370112 T>C maps to NM_005734.3 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr19:40886844 C>T maps to NM_144685.3 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:40886832 G>T maps to NM_144685.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr6:27835016 C>T maps to NM_005322.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr6:27100949 C>T maps to NM_021064.4 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr6:26189064 C>T maps to NM_003539.3 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr1:149858596 C>T maps to NM_003517.2 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr1:228645871 T>C maps to NM_175055.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr6:143090730 G>A maps to NM_006734.3 T1715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:143091957 A>C maps to NM_006734.3 T1306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:143090994 C>T maps to NM_006734.3 T1627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr6:143090796 A>G maps to NM_006734.3 L1693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr1:42045587 G>A maps to NM_024503.3 Y1627Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:42041222 G>A maps to NM_024503.3 F1733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr1:42046814 C>T maps to NM_024503.3 R1218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr2:234749730 T>C maps to NM_018410.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:176315424 G>A maps to NM_002115.2 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr6:31323115 C>T maps to ENST00000428231 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:32906578 C>T maps to NM_002118.4 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr6:32975250 G>A maps to NM_002119.3 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr6:33037507 C>A maps to NM_033554.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:33048479 C>A maps to NM_002121.4 C44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:33048539 C>T maps to NM_002121.4 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr6:33052767 T>C maps to NM_002121.4 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:29796473 C>T maps to ENST00000376828 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr6:29797677 C>T maps to ENST00000376828 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr21:38309486 A>G maps to NM_000411.5 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr3:148792067 C>A maps to NM_003071.3 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:221055524 G>A maps to NM_021958.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr1:186113777 A>C maps to NM_031935.2 R4737R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:186023025 C>A maps to NM_031935.2 S2257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:186097327 C>A maps to NM_031935.2 S4270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr1:185984510 G>A maps to NM_031935.2 T1617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr1:186059938 T>C maps to NM_031935.2 L3259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr1:186121954 G>A maps to NM_031935.2 V4990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:31036767 C>T maps to NM_002128.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr4:174254767 G>T maps to NM_002129.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr23:150155625 G>A did not map to a codon.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr1:24143200 T>C maps to NM_000191.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr6:55443835 G>A maps to NM_019036.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:80370222 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:80370581 C>T did not map to a codon.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr23:80370222 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:35661202 C>T maps to NM_001003681.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr12:121431482 A>G maps to NM_000545.5 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr20:43034728 C>T maps to ENST00000338692 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:76471262 C>T maps to NM_004133.4 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr12:54675592 A>C maps to NM_031157.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr2:178080347 C>T maps to NM_194247.2 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr14:21681137 T>C maps to NM_031314.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:43882986 G>A maps to NM_001098204.1 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:100668017 G>T did not map to a codon.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr10:70101792 A>G maps to NM_012207.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr19:39329198 G>A maps to ENST00000221419 Y465Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr19:39330792 A>C maps to ENST00000221419 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:8553641 C>T maps to NM_005968.3 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr4:83349483 T>G maps to NM_031372.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr8:42814396 A>G maps to NM_032410.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:42761365 G>A maps to NM_032410.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:57514897 G>A maps to NM_032495.5 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:27237977 C>A maps to NM_000522.4 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:27141984 C>T maps to NM_006735.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:46607953 C>A maps to NM_002144.3 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:46670753 G>A maps to NM_002147.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:46685368 C>T maps to NM_004502.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr12:54404942 C>G maps to NM_022658.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr12:54394193 C>T maps to NM_006897.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr2:176981953 C>T maps to NM_002148.3 Y131Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:177036548 C>A maps to NM_006898.4 Y282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:176988294 C>T maps to NM_014213.3 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:10566859 C>A maps to NM_002149.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr1:40149641 G>T maps to NM_016257.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:35551572 C>T maps to NM_182983.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr19:35556184 C>T maps to NM_182983.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr16:72110328 G>A maps to ENST00000228226 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:133627614 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:26860707 G>A maps to NM_022081.4 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:18318407 C>A maps to NM_181507.1 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr11:18305411 C>T maps to NM_181507.1 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:192980823 C>T maps to NM_020386.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr3:186389445 G>A maps to NM_000412.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr3:186389430 T>C maps to NM_000412.2 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr3:11301061 G>A maps to NM_001098211.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:22057075 G>A maps to NM_021624.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr1:152193162 G>A maps to NM_001009931.1 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr1:152191577 G>A maps to NM_001009931.1 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr1:152192775 C>A maps to NM_001009931.1 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:87538642 C>T maps to NM_012262.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:22926877 G>T maps to NM_006043.1 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr17:13504317 G>A maps to NM_006042.1 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:114378561 G>A maps to NM_153612.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:114378705 G>T maps to NM_153612.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr13:97484896 G>T maps to NM_153456.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr13:97485094 C>T maps to NM_153456.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:53460775 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:43876281 C>T maps to NM_016142.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:82069064 C>T maps to NM_002153.2 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:82069254 G>T maps to NM_002153.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr1:162773312 G>A maps to NM_016371.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr1:162773312 G>T maps to NM_016371.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:33173616 C>A maps to NM_014234.3 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:120050164 C>T maps to ENST00000235547 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr21:44949837 T>C maps to NM_007031.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr21:45033772 G>T maps to NM_007031.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:102551262 C>A maps to NM_001017963.2 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr6:44219535 C>A maps to NM_007355.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:44221323 G>T maps to NM_007355.2 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:104336388 G>T maps to NM_003299.1 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr10:118441350 G>T maps to NM_025015.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr21:15750651 G>A maps to NM_006948.4 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:14894395 A>G maps to NM_016299.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:128719824 A>G maps to ENST00000438626 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr5:137906734 C>T maps to NM_004134.6 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:53751889 G>T maps to NM_006308.2 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:198353094 G>A maps to NM_199440.1 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr2:198362020 G>T maps to NM_199440.1 Y90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:22206926 G>A maps to NM_005529.5 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:20388725 G>T maps to NM_001098520.1 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr23:135579932 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:135584988 G>A did not map to a codon.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr4:70896509 T>A did not map to a codon.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr6:87725675 G>A maps to NM_000865.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:87725303 C>A maps to NM_000865.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:88040033 C>T maps to NM_000866.3 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:47469873 G>T maps to NM_000621.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:113965949 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:114141427 A>G did not map to a codon.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr11:113816849 C>T maps to NM_006028.3 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr11:113815340 T>G maps to NM_006028.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:147889583 C>A maps to NM_001040173.2 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr7:154863298 C>T maps to NM_024012.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:92508831 G>T maps to NM_019859.3 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:8305988 G>A maps to NM_053044.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:3088672 G>T maps to NM_002111.6 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:3176737 G>A maps to NM_002111.6 T1437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr4:3231639 C>T maps to NM_002111.6 T2712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:33346965 C>T maps to NM_014586.1 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr7:48007442 A>G maps to NM_004507.2 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr6:656917 G>A maps to NM_148959.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr23:53642762 T>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:53561009 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:53574916 C>A did not map to a codon.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr23:53565405 C>T did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:53610678 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:53616546 G>C did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:50357872 C>A maps to NM_033158.4 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:123509052 C>A maps to NM_012269.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr16:70975667 G>A maps to NM_032821.2 Q2241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:70852465 G>A maps to NM_032821.2 R4812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:70884494 G>A maps to NM_032821.2 C4168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:70937661 G>T maps to NM_032821.2 V2904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:70942261 G>A maps to NM_032821.2 F2762F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:70942692 G>A maps to NM_032821.2 F2691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:71009118 G>A maps to NM_032821.2 V1563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:71220668 G>A maps to NM_032821.2 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr16:70891662 G>A maps to NM_032821.2 T4079T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr16:70894710 C>T maps to NM_032821.2 S3956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr16:70862200 C>A maps to NM_032821.2 L4747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr4:88732920 C>T maps to NM_004967.3 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr6:82891705 C>T maps to NM_015525.2 R1205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr6:82922422 C>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:8167695 G>T maps to ENST00000422063 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:203682155 C>T maps to NM_138468.4 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:10404498 G>T maps to NM_003259.3 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr6:52905983 G>A maps to NM_016513.4 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:94297212 G>A maps to NM_004969.3 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr15:90631878 T>C maps to NM_002168.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:78455866 T>G maps to NM_005530.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr10:1065498 G>A maps to NM_033261.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr8:39780139 G>A maps to NM_002164.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr1:159023462 G>A maps to ENST00000295809 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr14:94578075 A>G maps to ENST00000448882 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:79116170 A>T maps to NM_006417.4 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:79102805 C>A maps to NM_006820.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr9:21440947 C>T maps to NM_024013.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:21239628 C>T maps to NM_002172.2 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr9:21304925 A>G maps to NM_002169.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr9:21304925 A>G maps to NM_002169.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr21:34721522 C>G maps to NM_000629.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:34632959 C>A maps to NM_207585.1 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr9:21077535 A>G maps to NM_002176.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:34805068 C>A maps to ENST00000381995 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:27524856 G>T maps to NM_020124.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:112112835 C>T maps to NM_001007245.2 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr3:129183576 G>A maps to NM_052985.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:1633318 A>G maps to NM_014714.3 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:1568240 G>A maps to NM_014714.3 Y1386Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr16:1636256 G>A maps to NM_014714.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr16:1560953 G>A maps to NM_014714.3 D1460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:107884330 G>A maps to ENST00000457963 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:159997000 T>G maps to ENST00000483754 R777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr12:110581325 T>C maps to NM_014055.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:21265281 G>T maps to NM_175605.3 E824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:69385813 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:69366634 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:69353824 C>T did not map to a codon.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr15:65623922 G>T maps to NM_004884.3 S408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr15:65703613 T>A maps to NM_020962.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:102869448 G>A maps to NM_001111285.1 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:99440114 C>A maps to NM_000875.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:99482584 C>T maps to NM_000875.3 I1151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr15:99452111 C>T maps to NM_000875.3 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:160453695 C>T maps to NM_000876.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr7:45956871 G>A maps to NM_001013398.1 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr22:23915764 G>T maps to NM_020070.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr19:51827032 C>T maps to NM_001101372.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:130409617 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:130413157 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:130415812 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:130419170 G>A did not map to a codon.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr23:130408646 C>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:151156326 C>A maps to NM_178822.4 E2008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr3:151156168 G>A maps to NM_178822.4 C2060C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr3:118621492 G>T maps to NM_152538.2 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr1:18703367 C>T maps to NM_032880.4 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:18688675 G>A maps to NM_032880.4 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr1:18704792 C>T maps to NM_032880.4 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:18731033 G>A maps to NM_173588.3 I966I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:18735887 C>T maps to NM_173588.3 E578E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr11:18735519 G>A maps to NM_173588.3 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr11:18735959 C>T maps to NM_173588.3 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:117142914 G>A maps to NM_001542.2 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr1:117142867 C>T maps to NM_001542.2 W595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:206651574 C>T maps to NM_014002.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:50450340 C>T maps to NM_006060.3 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:37948974 T>C maps to NM_012481.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:117859200 G>T maps to NM_001558.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:34655473 C>T maps to ENST00000433395 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:158750221 G>T maps to NM_002187.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:117910395 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:114239864 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:114251823 G>A did not map to a codon.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr23:114249075 G>A did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:114245296 C>A did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:114239798 G>A did not map to a codon.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr10:6002513 A>G maps to NM_002189.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:81592201 C>A maps to NM_172217.3 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:81598383 C>T maps to NM_172217.3 R1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr15:81595963 A>G maps to NM_172217.3 G1131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr6:52101767 G>T maps to NM_052872.3 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr22:17590337 C>T maps to NM_014339.5 D743D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:57132038 G>A maps to NM_017563.3 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr22:50437750 C>T maps to NM_001001694.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr2:102984373 G>T maps to NM_003855.2 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:103068313 C>A maps to NM_003853.2 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:113818506 C>A maps to NM_173170.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr2:102641109 C>T maps to NM_004633.3 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:190363534 G>T maps to NM_002182.3 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:29301119 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:29414494 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:29935660 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:29973735 C>T did not map to a codon.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr23:29935624 G>T did not map to a codon.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr23:29972755 A>G did not map to a codon.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr23:29972783 A>G did not map to a codon.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr23:29938088 A>G did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:29938089 A>G did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:29973735 C>T did not map to a codon.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr23:104984640 C>T did not map to a codon.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr23:104984650 C>T did not map to a codon.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr23:104993062 A>C did not map to a codon.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr23:105011532 C>T did not map to a codon.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr23:104984641 C>T did not map to a codon.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr23:104984641 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:104999213 C>A did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:104440213 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:102849558 C>T maps to NM_003854.2 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:102851531 C>T maps to NM_003854.2 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:24465082 G>A maps to NM_021258.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr19:39760611 C>T maps to NM_172138.1 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:6063597 G>A maps to NM_000417.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:122658408 C>T maps to NM_001014336.1 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:1471017 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:50394667 C>T maps to NM_172374.1 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:131877811 G>A maps to NM_000879.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr3:3137078 A>G maps to NM_000564.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr7:22769161 T>G maps to NM_000600.3 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr1:154401729 G>A maps to NM_000565.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3575-01A-01W-0831-10 chr5:135228121 A>G maps to NM_000590.1 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr3:121725901 G>A maps to ENST00000344209 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:10799331 C>A maps to NM_017620.2 G847G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr11:6629428 T>C maps to NM_001014795.1 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr19:15226086 G>A maps to NM_006844.3 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:86371719 C>A maps to NM_006839.2 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:86389193 G>A maps to NM_006839.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr2:131103400 G>A maps to NM_033416.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr8:57878750 A>T maps to NM_017813.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:100963581 C>T maps to NM_016247.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:100948232 A>C maps to NM_016247.2 L1208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:100992505 A>C maps to NM_016247.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:101038553 C>A maps to NM_016247.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr3:101022987 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:62380321 G>T maps to NM_176877.2 E1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:62582287 C>A maps to NM_176877.2 I1580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr1:62321733 G>A maps to NM_176877.2 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr11:61897358 C>T maps to NM_001040694.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr13:111372024 C>T maps to NM_005537.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:41729664 C>T maps to NM_002192.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr7:41729982 C>T maps to NM_002192.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr2:121106897 C>T maps to NM_002193.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:30793368 G>T maps to NM_006774.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:30793497 G>A maps to NM_006774.4 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr2:74684547 G>T maps to ENST00000452361 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:206869646 G>T maps to NM_017759.4 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:99169413 C>T maps to NM_001134224.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr17:1416806 G>A maps to NM_016532.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:1401247 G>A maps to NM_016532.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:5185386 G>A maps to NM_007179.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:156816325 G>A maps to NM_014215.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr7:1522332 G>A maps to ENST00000389470 S1351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:1526650 G>A maps to ENST00000389470 C1059C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:1539937 G>A maps to ENST00000389470 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:59968948 C>T maps to NM_020748.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:59984935 C>T maps to NM_020748.2 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:51961530 C>T maps to NM_012141.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:95844296 G>A maps to NM_017864.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:95848807 C>A maps to NM_017864.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:28638403 G>A maps to NM_018250.3 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr9:103015294 C>T maps to NM_014425.2 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:9459656 A>G maps to NM_006391.2 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr11:9459624 A>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:46206617 G>A maps to NM_005897.2 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:121500703 C>T maps to NM_001023570.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr1:32673148 A>G maps to NM_001160042.1 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:51928986 C>T maps to NM_152397.2 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:51895691 C>T maps to NM_203424.1 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:67713869 G>A maps to NM_001031715.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:19838449 G>T maps to NM_153208.1 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr15:91026786 C>A maps to NM_003870.3 I1250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr5:75866403 G>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:75964613 C>T maps to NM_006633.2 R930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr5:75996930 A>G maps to NM_006633.2 G1466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr5:75996928 G>T maps to NM_006633.2 G1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr5:75996928 G>T maps to NM_006633.2 G1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr5:75996930 A>G maps to NM_006633.2 G1466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:156521880 G>A maps to NM_178229.4 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:156503577 G>A maps to NM_178229.4 I1321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:53283904 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:274616 G>A maps to NM_001170738.1 P909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:123136906 C>T maps to NM_178827.4 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr7:123152364 A>G maps to NM_178827.4 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr6:79595105 A>T maps to NM_001010844.1 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:78789593 G>T maps to NM_004136.2 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:407592 G>T maps to NM_002460.3 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr19:44223630 G>A maps to NM_019612.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr2:227662785 G>A maps to NM_005544.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:227660927 G>A maps to NM_005544.2 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr23:107979462 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:107977569 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:107977985 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:107978274 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:107978377 G>A did not map to a codon.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr23:107976411 A>T did not map to a codon.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr23:107978809 C>A did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:107979262 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:107976662 G>A did not map to a codon.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr5:3599403 G>A maps to NM_024337.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:54966651 C>T maps to NM_005853.5 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:55362816 C>T maps to NM_024335.2 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr16:55363056 C>T maps to NM_024335.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr15:74425862 C>T maps to NM_001130137.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr15:74426456 G>A maps to NM_001130137.1 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:13279838 G>A maps to NM_080826.1 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr20:13260507 C>T maps to NM_080826.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:77948668 G>A maps to NM_199296.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr22:35463235 A>T maps to NM_001008494.1 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr22:35481586 T>C maps to NM_001008494.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr3:128852985 T>C maps to ENST00000418265 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:52211304 A>C maps to NM_181501.1 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:52235743 G>A maps to NM_181501.1 S1085S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr1:145536013 A>G maps to NM_003637.3 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr15:68613808 C>T maps to ENST00000423218 E785E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr15:68661570 G>A maps to ENST00000423218 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:52366009 G>T maps to NM_002203.3 E719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr17:48155478 C>T maps to NM_002204.2 Q737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:54794764 G>A maps to NM_002205.2 G836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:54805672 G>T maps to NM_002205.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:173356031 G>A maps to ENST00000264106 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:56088240 C>T maps to ENST00000347027 E825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:56087080 C>T maps to ENST00000347027 S896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr12:56092681 C>T maps to ENST00000347027 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:15646221 G>A maps to NM_003638.1 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr3:37783235 C>A maps to NM_002207.2 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr16:31434698 G>C maps to ENST00000444228 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:3631412 C>A maps to NM_002208.4 E988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr16:30507467 C>T maps to NM_002209.2 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr16:30521752 T>A maps to NM_002209.2 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr16:30507512 C>T maps to NM_002209.2 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:30507762 G>T maps to NM_002209.2 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:30507878 C>T maps to NM_002209.2 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:31308848 C>T maps to NM_001145808.1 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:31308908 C>T maps to NM_001145808.1 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:187521023 C>T maps to NM_002210.3 R539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr2:187540407 C>A maps to NM_002210.3 Y928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr10:33209232 G>A maps to ENST00000374956 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3582-01A-01W-0831-10 chr23:70522362 G>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:3941107 C>T maps to NM_170678.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr21:46320233 C>T did not map to a codon.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr17:45384949 C>T maps to NM_000212.2 R750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:63919603 C>A maps to ENST00000371092 G196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr17:73747127 G>A maps to NM_001005619.1 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr10:7780596 C>T maps to NM_002216.2 Y657Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:7762889 C>T maps to NM_002216.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr10:7773949 G>A maps to NM_002216.2 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr3:52828866 C>T maps to NM_002217.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr10:7618863 C>T maps to ENST00000256861 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:54777504 G>T did not map to a codon.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr23:54785074 G>A did not map to a codon.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr23:54777770 G>A did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:54780086 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:156607996 C>T maps to NM_005546.3 N3N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:156638363 C>T maps to NM_005546.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:156668696 C>T maps to NM_005546.3 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr5:156649961 C>T maps to NM_005546.3 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr23:78618103 G>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:48830428 C>A maps to NM_021999.4 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:93460333 G>A maps to NM_014216.4 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:4722293 C>T maps to ENST00000356617 R1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr3:4704847 A>G maps to ENST00000356617 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:26811001 C>A maps to NM_002223.2 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:26648162 G>A maps to NM_002223.2 R1702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:26748459 C>A maps to NM_002223.2 E1440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:33658851 C>T maps to ENST00000374316 L2397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr6:33653285 G>T maps to ENST00000374316 E1820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:96992558 C>T maps to ENST00000420728 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:35140023 C>T maps to NM_003024.2 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:35154338 G>T maps to NM_003024.2 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:24498708 C>A maps to NM_006277.2 E652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:24521589 C>A maps to NM_006277.2 E480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr2:24438974 T>C maps to NM_006277.2 G1311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr2:24438974 T>C maps to NM_006277.2 G1311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr20:10622146 C>T maps to NM_000214.2 A959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:65321240 C>T maps to NM_002227.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:65312353 G>A maps to NM_002227.2 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:5064898 C>A maps to NM_004972.3 S358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr9:5072517 T>C maps to NM_004972.3 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr9:5070030 C>T maps to NM_004972.3 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr9:5070045 G>A maps to NM_004972.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr9:5022142 A>T maps to NM_004972.3 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr19:17945505 G>A maps to NM_000215.3 Q742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr4:6064098 G>A maps to NM_001099433.1 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:15452402 C>T maps to NM_004973.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:15497177 C>T maps to NM_004973.2 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr1:227922371 G>A maps to NM_023007.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr20:42788286 C>T maps to NM_020433.4 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr20:42788478 G>A maps to NM_020433.4 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr16:87723384 C>T maps to NM_020655.2 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr8:143746190 C>T maps to NM_003724.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr17:39913780 G>A maps to NM_021991.2 Y644Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr23:8553402 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:124193560 A>G maps to NM_001024660.3 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:124415013 T>C maps to NM_001024660.3 N2537N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:711609 C>T maps to NM_015158.2 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr19:11304014 C>T maps to NM_015493.6 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr16:75662508 A>G maps to NM_001130089.1 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:20187846 C>T maps to NM_003884.4 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr11:65482087 C>T maps to NM_182710.1 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:65482031 C>T maps to NM_182710.1 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:149916261 G>A maps to NM_007044.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:149922870 G>A maps to NM_007044.2 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr13:30857793 G>A maps to NM_032116.3 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:15392181 C>T maps to NM_201628.2 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:15428236 C>T maps to NM_201628.2 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:170367160 C>A maps to NM_006063.2 Y291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:127646658 C>T maps to NM_207335.2 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:105923756 A>G maps to NM_198439.2 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:105924349 G>A maps to NM_198439.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr3:42728219 C>T maps to NM_152393.2 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:41705090 G>A maps to NM_152903.4 C519C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr12:5021086 C>T maps to NM_000217.2 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr1:111060544 G>T maps to NM_005549.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr1:111061226 C>T maps to NM_005549.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr1:111060605 G>A maps to NM_005549.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr1:111146774 G>A maps to NM_004974.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr1:111216789 G>A maps to NM_002232.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:30033499 C>T maps to NM_002233.2 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:5154029 C>A maps to NM_002234.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:5154806 G>A maps to NM_002234.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr12:4919893 C>T maps to NM_002235.3 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr20:47991334 C>T maps to NM_004975.2 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr20:48098747 G>A maps to NM_004975.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr8:73480196 G>C maps to NM_004770.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:73480175 A>G maps to NM_004770.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr8:73848702 A>G maps to NM_004770.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr8:73848792 C>A maps to NM_004770.2 C401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr8:73849623 C>T maps to NM_004770.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:73848315 A>G maps to NM_004770.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr8:73848534 C>A maps to NM_004770.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr8:73848939 T>C maps to NM_004770.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:73480415 C>T maps to NM_004770.2 N149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr11:17757797 C>T maps to NM_001112741.1 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:17757863 C>A maps to NM_001112741.1 C105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:17757800 G>A maps to NM_001112741.1 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:75444658 G>A maps to NM_139137.2 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr12:75444892 A>G maps to NM_139137.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:110766274 T>C maps to NM_004978.4 C456C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:48826472 G>A did not map to a codon.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr23:48819900 T>C did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:48819869 G>T did not map to a codon.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr7:120385962 C>T maps to NM_012281.2 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:119915141 G>A maps to NM_012281.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr1:112524801 G>A maps to ENST00000315987 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr2:11053814 C>T maps to NM_002236.4 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:49626407 G>A maps to NM_002237.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr16:84270674 G>A maps to NM_172347.2 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:84256455 C>T maps to NM_172347.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:210857204 C>T maps to NM_172362.2 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:210857359 G>A maps to NM_172362.2 R745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:211093326 C>A maps to NM_172362.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr14:63473135 A>G maps to NM_139318.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:63468132 C>A maps to NM_139318.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:61623143 G>T maps to NM_030779.2 G956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr2:163228443 G>A maps to NM_033272.2 Y1162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:163291771 G>A maps to NM_033272.2 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr2:163250943 T>A maps to NM_033272.2 K889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:19498416 C>T maps to NM_144633.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:19575273 G>T maps to NM_144633.2 E1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr3:19436738 G>A maps to NM_144633.2 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr5:170162791 G>A maps to NM_001034837.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:170139861 C>T maps to NM_001034837.1 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:170148873 C>T maps to NM_001034837.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr5:170160887 G>T maps to NM_001034837.1 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr11:128709850 A>G maps to NM_000220.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr17:21319766 C>T maps to NM_021012.4 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:21319682 G>A maps to NM_021012.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr17:68129145 G>A maps to NM_018658.1 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:68129007 G>A maps to NM_018658.1 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr2:155555805 C>T maps to NM_002239.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:39086847 G>T maps to NM_002240.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr21:39086697 C>T maps to NM_002240.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:21918736 G>A maps to NM_004982.2 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:21918956 C>T maps to NM_004982.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:21919460 C>T maps to NM_004982.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr1:160057419 C>A maps to NM_004983.2 S332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:90650752 C>T maps to NM_022054.2 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:215342567 G>T maps to NM_001017425.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr2:26950589 C>T maps to NM_002246.2 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:26950925 C>T maps to NM_002246.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:64064726 C>T maps to ENST00000422670 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:64064979 G>A maps to ENST00000422670 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr3:178968640 T>C maps to NM_171828.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr5:113831788 C>T maps to NM_021614.2 H550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:113831647 C>T maps to NM_021614.2 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr1:154841978 C>A maps to NM_002249.4 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr1:154842329 T>C maps to NM_002249.4 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr20:62059775 C>T maps to NM_172107.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr20:62076009 A>G did not map to a codon.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr8:133141601 C>T maps to NM_004519.2 T842T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr8:133152332 G>A maps to NM_004519.2 R520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:41300695 C>T maps to NM_004700.3 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr9:138678149 C>T maps to ENST00000298480 G1095G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr9:138657013 C>T maps to ENST00000298480 N391N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr1:196398808 C>A maps to NM_198503.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:36768479 G>A maps to NM_001031836.2 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr18:24039634 C>T maps to NM_001142730.1 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr5:143586925 C>T maps to NM_020768.3 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:201357970 C>A maps to NM_152387.2 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:67333308 G>A maps to NM_001100915.1 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:77884837 G>A maps to NM_001029859.1 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:77885444 G>A maps to NM_001029859.1 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:215751366 G>T maps to NM_016121.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:215751366 G>T maps to NM_016121.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:103443319 G>A maps to NM_024089.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:6513836 G>T maps to NM_006854.3 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr1:23395123 C>T maps to NM_001009999.2 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:23381622 C>T maps to NM_001009999.2 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr2:86693887 T>C maps to NM_001146688.1 C467C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr1:44121266 T>C maps to NM_014663.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr1:44132641 A>G maps to NM_014663.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr19:5047542 C>T maps to NM_015015.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:430228 C>A maps to NM_001042603.1 E825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr1:202699083 T>C maps to ENST00000367264 R1452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:53223694 A>G did not map to a codon.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr23:53230859 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr24:21870161 G>T did not map to a codon.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr23:44942736 T>C did not map to a codon.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr23:44929212 T>C did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:44929023 A>G did not map to a codon.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr17:7749470 A>G maps to NM_001080424.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr4:55968136 G>A maps to NM_002253.2 D731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr4:55964965 G>A maps to NM_002253.2 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr4:55981158 G>A maps to NM_002253.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:61027000 C>A maps to NM_002035.2 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:142638473 C>T maps to NM_000420.2 Q688Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr7:142641481 A>G maps to NM_000420.2 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr1:32504196 A>G maps to NM_006559.1 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:32508134 C>T maps to NM_006559.1 D414D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:19549949 G>T maps to NM_015047.1 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:26961565 T>C maps to NM_014680.2 R1013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:141318236 C>T maps to NM_014773.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr16:71956516 C>A maps to NM_014761.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr16:85690940 G>A maps to NM_014615.2 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr17:73481571 C>T maps to ENST00000375248 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr8:126049482 A>G maps to ENST00000377985 N1064N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr8:126079938 G>T maps to ENST00000377985 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:6864664 G>A maps to NM_014743.2 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr4:6862993 A>G maps to NM_014743.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr14:105352894 C>T maps to ENST00000453495 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr9:114184266 C>T maps to NM_001080398.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:127770988 G>A maps to NM_014702.4 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr6:127768830 A>G maps to NM_014702.4 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr7:4827329 C>T maps to ENST00000450194 D1170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr16:15704937 A>T maps to NM_014647.3 T1215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:43895394 C>T maps to NM_015284.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:43896698 C>A maps to NM_015284.2 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr1:3662494 G>C did not map to a codon.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr12:22666293 A>G maps to ENST00000446597 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:27720168 G>A maps to NM_015202.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:3765181 G>A maps to NM_014704.3 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:42524078 C>T maps to NM_015058.1 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr13:42465570 G>T maps to NM_015058.1 Y212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr13:42263627 T>G maps to NM_015058.1 I1331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:42275563 C>A maps to NM_015058.1 E1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:42293872 A>G maps to NM_015058.1 F990F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:42335333 C>A maps to NM_015058.1 G786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:42524078 C>T maps to NM_015058.1 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr12:55356418 C>T maps to NM_001098815.1 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:55356688 C>T maps to NM_001098815.1 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr18:8824819 C>T maps to ENST00000456698 D1423D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:8813095 C>A maps to ENST00000456698 V1227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr18:8819106 G>A maps to ENST00000456698 P1321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr18:8825455 G>A maps to ENST00000456698 T1635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr1:155883953 T>C maps to NM_014949.2 Q601Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr10:75556555 G>T maps to NM_015037.2 E1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:154557595 C>T maps to NM_001131007.1 V1567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:154533545 C>T maps to NM_001131007.1 F1187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:154555409 C>T maps to NM_001131007.1 N1465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr4:154533464 G>A maps to NM_001131007.1 V1160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:5464036 C>T maps to NM_015325.1 F1530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr5:5461210 A>G maps to NM_015325.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr5:5464066 A>G maps to NM_015325.1 T1540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:84872917 G>A maps to NM_014895.2 F819F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:84936056 C>A maps to NM_014895.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr6:84913785 C>T maps to NM_014895.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:79749340 G>A maps to NM_015206.2 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:79750666 C>A maps to NM_015206.2 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr9:34977129 C>T maps to NM_015297.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:123147935 G>A maps to NM_015312.3 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:123170682 C>A maps to NM_015312.3 S1852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr4:123132180 A>G maps to NM_015312.3 E726E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:44795811 C>A maps to NM_020696.3 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:81173324 A>G maps to NM_018689.1 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:118220750 T>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:118238990 C>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:118284420 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:118220597 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:118239093 C>A did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:118220566 T>C did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr4:57181416 C>T maps to NM_020722.1 H583H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr10:24835174 T>C maps to NM_019590.3 T1918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr6:138640981 G>A maps to NM_020340.4 L1539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:72294539 G>T maps to NM_014431.2 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:86541519 T>C maps to NM_001142749.2 E679E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:86544124 C>A maps to NM_001142749.2 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:86554958 A>G maps to NM_001142749.2 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr7:86542400 C>T maps to NM_001142749.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr18:34647214 T>C maps to NM_020776.1 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:52876984 G>A maps to NM_019600.2 R1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr11:101832752 T>C maps to NM_020802.2 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:101833847 C>A maps to NM_020802.2 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:101815106 T>C maps to NM_020802.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr3:113697079 C>T maps to NM_020817.1 K853K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr3:113753851 T>C maps to NM_020817.1 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr14:94083505 C>G maps to ENST00000393153 L1382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr14:94060162 G>A maps to ENST00000393153 W1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:95539111 G>A maps to NM_015496.3 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr9:5743013 G>A did not map to a codon.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr10:30315077 C>T maps to NM_020848.2 P1333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:30318176 C>T maps to NM_020848.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr12:13208557 G>A maps to NM_020853.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:226273725 C>T maps to NM_020864.1 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:226378117 G>T maps to NM_020864.1 G85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:226446993 C>T maps to NM_020864.1 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr2:226447284 G>A maps to NM_020864.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:33236573 G>T maps to NM_020888.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:108301904 A>G maps to NM_020890.2 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:7670118 G>A maps to NM_001080429.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr7:138596009 C>A maps to NM_001164665.1 T1009T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:138566237 C>T maps to NM_001164665.1 A1375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:56918188 G>T maps to NM_020931.2 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:56918625 T>C maps to NM_020931.2 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr6:56918145 T>C maps to NM_020931.2 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:84531578 C>T maps to NM_020947.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:84529435 C>T maps to NM_020947.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr19:18377047 C>G maps to NM_001145304.1 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:176857127 C>A maps to NM_030650.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr20:36874450 G>A maps to NM_001029864.1 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr9:20929412 G>A maps to NM_017794.3 T1045T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr9:20953056 A>G maps to NM_017794.3 G1375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr9:20885120 T>C maps to NM_017794.3 F839F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr11:105880290 G>A maps to NM_032424.1 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr2:61361294 C>T maps to NM_032506.2 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:30653330 C>A maps to NM_133471.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr9:115422111 C>T maps to NM_133465.2 Y638Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr9:115422300 G>A maps to NM_133465.2 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr3:113376112 C>T maps to NM_001009899.2 Q1472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr3:113376118 C>T maps to NM_001009899.2 Q1470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:73959988 T>C did not map to a codon.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr23:73960926 G>C did not map to a codon.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr23:73960373 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:73963427 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:73963724 G>A did not map to a codon.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr23:73963618 C>A did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:73960070 C>T did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:73963105 A>G did not map to a codon.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr23:73963170 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:5920352 A>G maps to NM_001017969.2 S1881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr9:5988412 T>C maps to NM_001017969.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:8958875 T>C maps to NM_020738.2 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr2:8871761 G>A maps to NM_020738.2 N1468N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr10:94353173 G>A maps to NM_004523.3 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr6:17764877 C>T maps to NM_022113.4 T1627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:17856347 C>A maps to NM_022113.4 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:17834269 G>A maps to NM_022113.4 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr1:200524570 T>C maps to NM_014875.2 E1455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:200524572 C>A maps to NM_014875.2 E1455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr1:200529954 G>T maps to NM_014875.2 I1375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr1:200522806 A>G maps to NM_014875.2 P1552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:44841852 T>G maps to NM_020242.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr20:16360506 C>A maps to NM_024704.4 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:16506741 C>A maps to NM_024704.4 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr20:16474980 G>A maps to NM_024704.4 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:28104407 G>A maps to NM_031217.3 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr17:72342635 C>T maps to NM_153209.3 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:72338094 C>T maps to NM_153209.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr17:72350577 G>T maps to NM_153209.3 G862G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:10364221 C>T maps to NM_183416.3 D993D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:91497973 G>T maps to ENST00000416354 E1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:91498276 G>T maps to ENST00000416354 E1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:39726185 G>A maps to ENST00000395670 R961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr12:39713816 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:69718483 G>T maps to NM_138555.1 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:34290239 G>A maps to NM_194313.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:168440762 G>A maps to NM_030615.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:245530623 C>A maps to NM_018012.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:86518333 G>A maps to NM_017576.1 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr17:51901681 C>T maps to NM_032559.4 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr20:30898369 G>T maps to NM_004798.3 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr23:69573482 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:69518976 A>C did not map to a codon.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr23:69510410 G>A did not map to a codon.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr5:154395878 T>C maps to NM_001099293.1 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:32307308 C>A maps to NM_004521.2 E792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:32323683 C>A maps to NM_004521.2 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:149679725 C>T maps to NM_004522.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:149818508 C>A maps to NM_004522.1 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:149840213 C>A maps to NM_004522.1 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr6:39328284 G>A maps to NM_145027.4 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:33374421 T>C maps to NM_002263.3 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr16:57799529 A>G maps to NM_005550.3 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr19:55295141 C>T maps to ENST00000291633 C334C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr19:55258811 A>T maps to NM_015868.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr19:55344245 G>A maps to NM_012314.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr19:55333225 G>T maps to ENST00000355608 G288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:55341720 C>A maps to NM_013289.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr19:55365481 C>T maps to NM_006737.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr19:55237552 C>T maps to NM_153443.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr19:55239242 G>A maps to NM_153443.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr19:36348302 G>T maps to NM_199180.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:126299106 C>T maps to NM_032531.3 E591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr4:55592091 A>G maps to NM_000222.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:55561831 G>A maps to NM_000222.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:55602677 G>T maps to NM_000222.2 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr4:55599315 C>T maps to NM_000222.2 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr4:55561762 C>T maps to NM_000222.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr4:55593631 C>T maps to NM_000222.2 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr4:55593664 T>C maps to NM_000222.2 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr4:55599333 T>C maps to NM_000222.2 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr4:55594222 A>G maps to NM_000222.2 K642K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:88912554 G>T maps to NM_000899.4 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:33635144 G>A maps to NM_004795.3 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:33638277 C>A maps to NM_004795.3 S998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr14:104136611 C>T maps to ENST00000445352 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr8:103663554 G>A maps to NM_005655.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr13:74420216 C>T maps to NM_007249.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr3:126071519 G>T maps to NM_014079.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr1:44595666 C>T maps to NM_173484.3 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr2:207988558 G>A maps to NM_003709.2 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr14:50241376 C>G maps to NM_014315.2 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr12:27933701 G>T maps to NM_020782.1 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr1:18807549 C>A maps to NM_152375.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr17:39998266 C>T maps to NM_152467.3 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr17:40011143 T>G maps to NM_018143.1 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:117043744 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:117043379 C>T did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:117043320 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:47364190 C>T maps to NM_025010.4 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr3:47385055 C>T maps to NM_025010.4 Y450Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr15:86312924 A>G maps to NM_022480.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:137034038 C>T maps to NM_017415.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:21674618 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:124664614 G>A maps to NM_001081675.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr23:86869031 G>A did not map to a codon.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr23:86772948 G>A did not map to a codon.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr23:86887364 G>A did not map to a codon.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:86888867 T>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:86773234 G>T did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:86772919 G>C did not map to a codon.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr23:86873047 C>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:21333624 C>A maps to NM_018847.2 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr9:21333628 A>G maps to NM_018847.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr19:51518083 C>T maps to NM_001077500.1 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr19:51519273 G>A maps to NM_001077500.1 H136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:51559890 G>A maps to NM_015596.1 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:51559984 G>A maps to NM_015596.1 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr19:51582706 G>A maps to NM_022046.4 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:51379919 A>C maps to NM_005551.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:51466792 G>T maps to NM_001012964.1 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:187155157 C>T maps to ENST00000511608 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr12:9750671 C>T maps to NM_002258.2 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:9747910 C>A maps to NM_002258.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr12:9985929 A>G maps to NM_016523.1 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:241752098 G>A maps to NM_003679.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr10:135012651 T>C maps to ENST00000368572 D880D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:134999820 G>A maps to ENST00000368572 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:186460081 G>T maps to NM_001102416.2 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr3:186445054 C>T maps to NM_001102416.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:123058870 G>T maps to NM_014708.4 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:123107100 G>A maps to NM_014708.4 A2154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr12:123055445 A>G maps to NM_014708.4 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:117023264 G>A maps to NM_002269.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr1:152733395 G>T maps to NM_001025231.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:25378705 C>A maps to NM_033360.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr12:25380235 A>T maps to NM_033360.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr12:25398258 C>A maps to NM_033360.2 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:25380280 T>C maps to NM_033360.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr12:25362803 T>A maps to NM_004985.3 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr7:149430493 C>T maps to NM_032534.2 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:8273383 G>A maps to NM_213597.2 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:8274822 G>T maps to NM_213597.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr19:10676422 G>A maps to NM_023008.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr7:91851318 C>T maps to NM_194456.1 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr12:75900603 T>C maps to NM_007043.6 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr12:75897752 G>A maps to NM_007043.6 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:38978477 G>A maps to NM_000421.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:39681202 G>A maps to NM_002276.4 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr17:39038873 A>G maps to NM_019010.2 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr17:39084582 A>G maps to NM_015515.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:38855781 G>A maps to NM_019016.2 N425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr17:38926621 G>A maps to NM_181539.4 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:38922814 T>C maps to NM_181539.4 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:38938637 G>A maps to NM_181537.3 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:39553542 C>T maps to ENST00000393998 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr17:39620398 C>T maps to NM_002278.3 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr17:39633379 G>A maps to NM_002280.4 C432C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr17:39580042 C>T maps to NM_003770.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr17:39595538 A>G maps to NM_006771.3 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr12:53207602 A>G maps to NM_002272.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:52909582 G>T maps to NM_000424.3 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:52913942 G>A maps to NM_000424.3 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr12:52883813 G>A maps to NM_005554.3 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:52881632 G>A maps to NM_005554.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr12:52886879 A>C maps to NM_005554.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:52881578 G>A maps to NM_005554.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:52941658 G>A maps to NM_033448.2 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:53005047 G>A maps to NM_175068.2 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:53012017 C>T maps to NM_175068.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:52967108 G>A maps to NM_175053.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:52822461 G>T maps to ENST00000252245 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr12:52827638 G>A maps to ENST00000252245 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr12:53091626 C>T maps to NM_175078.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:53237995 C>A maps to NM_173352.2 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:53292650 G>A maps to NM_002273.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr12:52681406 C>T maps to NM_002281.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:52710780 G>A maps to NM_002282.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr12:52699514 C>T maps to NM_002284.3 N323N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr21:46032346 C>T maps to NM_198695.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr21:31798107 G>T maps to NM_181622.1 C41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:31802973 C>T maps to NM_181600.1 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr21:31812773 G>T maps to NM_181623.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr21:31859610 G>T maps to NM_181608.1 C19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr21:31874204 G>A maps to NM_181611.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:31720882 G>T maps to NM_181624.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:39156084 G>A maps to NM_031959.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr11:71276908 G>A maps to ENST00000422553 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr11:1651168 T>C maps to NM_001001480.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr11:71249124 A>G maps to NM_021046.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr11:71249568 A>G maps to NM_021046.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr11:71249451 C>G maps to NM_021046.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr11:71249586 C>A maps to NM_021046.2 C162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:118405897 C>A maps to ENST00000339824 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:117914279 G>T maps to ENST00000339824 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:117962841 C>T maps to ENST00000339824 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr12:118293320 G>A maps to ENST00000339824 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:119205757 C>T maps to NM_152305.2 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:56083313 A>G maps to NM_001079521.1 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:56118627 T>G maps to NM_001079521.1 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr14:56119763 A>G maps to NM_001079521.1 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr2:143743578 G>A maps to NM_003937.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr23:153134139 G>T did not map to a codon.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr23:153136381 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:153130321 G>A did not map to a codon.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr23:153135085 G>A did not map to a codon.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr14:50734556 C>T maps to NM_024884.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr20:42157977 G>A maps to NM_032107.4 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:130389488 G>T maps to NM_032438.2 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr18:6138290 C>T maps to NM_173464.3 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:108723251 C>A maps to NM_145315.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:63433863 G>T maps to NM_032857.3 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:55019238 C>T maps to NM_002288.3 Y68Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr18:6976064 C>T maps to NM_005559.2 V2120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr18:6959368 C>T maps to NM_005559.2 A2583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:6997743 G>A maps to NM_005559.2 L1601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:7014032 G>A maps to NM_005559.2 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:7017279 G>T maps to NM_005559.2 C935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:7023202 G>A maps to NM_005559.2 D887D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr18:7033009 C>T maps to NM_005559.2 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr18:6958513 C>T maps to NM_005559.2 S2642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr6:129591854 C>T maps to NM_000426.3 D803D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:129794398 G>A maps to NM_000426.3 E2447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:129824403 C>A maps to NM_000426.3 I2842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:129722398 C>T maps to NM_000426.3 R1826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:129813183 T>C maps to NM_000426.3 P2679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr6:129802421 T>C maps to NM_000426.3 V2529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:21481257 G>T maps to ENST00000416669 E2060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:21530074 C>T maps to ENST00000416669 I3200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr6:112461970 G>T maps to NM_001105206.1 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr20:60927303 G>A maps to NM_005560.3 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr20:60898719 C>T maps to NM_005560.3 A1952A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr3:49166569 T>C maps to NM_002292.3 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr7:107704329 G>T maps to NM_007356.2 T979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:107706348 G>T maps to NM_007356.2 Y898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:107743534 G>A maps to NM_007356.2 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr7:107717484 G>A maps to NM_007356.2 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:183086018 C>A maps to NM_002293.3 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:183106902 G>T maps to NM_002293.3 E1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr1:183099545 T>C maps to NM_002293.3 R1116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr1:183079748 G>A maps to NM_002293.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:133946983 C>T maps to ENST00000355048 D1061D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:113974715 C>T maps to NM_005561.3 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:113975968 G>A maps to NM_005561.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:119581784 G>T did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:37431228 G>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:17600149 G>A maps to NM_015907.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr8:98863680 G>A maps to ENST00000378722 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr8:98788260 G>T maps to ENST00000378722 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr22:34022286 G>A maps to NM_133642.3 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr22:34157361 G>A maps to NM_133642.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr5:154181721 T>G maps to ENST00000377643 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:154193631 G>A maps to ENST00000377643 S1089S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:154172312 G>A maps to ENST00000377643 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:128999035 G>T maps to NM_018078.2 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:129121707 G>T maps to NM_018078.2 E733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr4:129012667 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:860950 C>T maps to NM_015155.1 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:863669 C>A maps to NM_015155.1 E564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr10:890956 G>A maps to NM_015155.1 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:71124894 G>A maps to NM_018357.2 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:71125077 G>A maps to NM_018357.2 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:113568041 T>G maps to ENST00000509061 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:45441741 G>A maps to NM_015340.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:64744046 C>T did not map to a codon.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr17:37074955 C>T maps to NM_006148.2 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:73636005 C>T maps to NM_032464.2 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:150001394 G>A maps to NM_004690.2 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr13:21549227 T>C maps to NM_014572.2 E1016E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr20:36982827 G>A maps to NM_004139.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:68118795 C>T maps to ENST00000380035 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:80203458 C>T maps to NM_181714.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:40783685 G>A maps to NM_152505.3 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr21:40778427 C>A maps to NM_152505.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr16:67977992 G>A maps to NM_000229.1 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:152785203 C>T maps to NM_178349.1 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr1:152770575 C>T maps to NM_178352.2 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr1:152759795 G>A maps to NM_178353.1 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:152586483 C>T maps to NM_178433.1 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:30863379 C>A maps to NM_182551.3 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:139635782 G>T maps to NM_001001712.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr9:138557187 G>A maps to ENST00000277526 T135T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AG-4007-01A-01W-1073-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:46708362 C>A maps to NM_002298.4 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:169693866 C>T maps to NM_005565.3 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:136567501 G>A maps to NM_002299.2 F805F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:136594268 G>A maps to NM_002299.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr2:136570466 A>G maps to NM_002299.2 H589H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:136564709 A>G maps to NM_002299.2 S1387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr2:136567003 C>T maps to NM_002299.2 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:103869709 C>A maps to NM_001113407.1 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:16760786 G>A maps to NM_001290.3 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr4:16597493 G>A maps to NM_001290.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:75148026 G>A maps to NM_153486.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr11:36248929 G>A maps to NM_174902.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr23:140271174 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:135286984 T>C maps to NM_002302.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:156710959 G>T maps to NM_001004316.2 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr3:156763175 T>C maps to NM_001004316.2 F572F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr1:153177338 T>C maps to NM_001010857.1 C52C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr6:33740479 G>T maps to NM_181336.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr12:65564797 G>A maps to NM_014319.4 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:127894713 C>T maps to NM_000230.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:66102430 C>A maps to NM_002303.5 I1077I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:66102430 C>A maps to NM_002303.5 I1077I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:43213441 G>A maps to NM_022356.3 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr3:189689719 T>C maps to NM_018192.3 E592E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr8:38250440 C>T maps to ENST00000379957 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:38257890 C>T maps to ENST00000379957 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:63283094 C>T maps to NM_001142535.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr19:39281364 C>T maps to NM_001042507.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr10:95553060 A>G maps to NM_005097.2 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:25014035 C>T maps to NM_018176.3 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr12:71965353 G>A maps to NM_003667.2 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr1:202287419 C>T maps to NM_001017403.1 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr1:202273692 G>T maps to NM_001017403.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr6:63995629 C>T maps to NM_016571.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr13:40175188 A>G maps to NM_005780.2 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:77805754 G>A maps to NM_005779.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:103969334 C>T maps to NM_199000.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr6:35773557 C>T maps to NM_182548.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr1:75602912 C>T maps to NM_001001933.1 C78C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:197890682 C>T maps to NM_020204.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr5:38482731 C>A maps to NM_002310.5 E877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr5:38485936 C>A maps to NM_002310.5 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:38482263 C>T maps to NM_002310.5 E909E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr5:38493780 C>T maps to NM_002310.5 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:48660283 C>T maps to NM_000234.1 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:33310494 C>T maps to NM_013975.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:55146119 C>T maps to ENST00000427581 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3582-01A-01W-0831-10 chr19:54783717 G>A maps to ENST00000391747 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr19:54720982 G>A maps to NM_001081450.1 Y626Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:51883794 G>A maps to NM_030657.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr12:50594643 G>A maps to NM_001113546.1 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr7:73535495 G>A maps to NM_002314.2 W603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:31663017 C>T maps to NM_001031801.1 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr22:31663886 C>T maps to NM_001031801.1 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr4:83905823 G>T maps to NM_194282.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:77907975 G>A maps to NM_032808.5 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr15:77907144 G>A maps to NM_032808.5 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr15:77908089 G>A maps to NM_032808.5 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:27950530 G>A maps to NM_152570.1 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:101110320 C>A maps to NM_001040616.2 G466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:101114186 C>T maps to NM_001040616.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:58855763 C>T maps to NM_000236.2 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr19:42930863 T>C maps to NM_005357.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:90438395 T>G maps to NM_001198829.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr21:15558315 T>G maps to NM_198996.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:15561498 G>A maps to NM_198996.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:90490803 C>T maps to NM_001080518.1 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:99779514 C>T maps to NM_015929.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:145498744 G>A maps to NM_153713.1 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:57006030 G>T maps to NM_005570.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr15:75116784 C>T maps to NM_021819.2 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:176761351 C>T maps to NM_006816.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:70411349 C>T maps to NM_018368.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr6:70410692 T>C maps to NM_018368.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:2431783 G>A maps to NM_032737.2 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:16704218 G>A maps to ENST00000441439 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:123296064 C>T maps to NM_207163.1 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr7:97823748 C>T maps to NM_014916.3 N1324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr19:49001496 C>T maps to NM_001080434.1 A972A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:96314891 G>T maps to NM_005575.2 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:54344806 C>A maps to NM_001126328.1 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr16:48385595 C>T maps to NM_031490.2 N814N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:12594229 G>A maps to NM_152271.3 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:100911972 C>A maps to NM_198461.3 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr23:118147048 T>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:118145801 C>T did not map to a codon.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr23:118108843 A>G did not map to a codon.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr8:23179789 G>A maps to NM_002318.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr6:161020554 C>A maps to NM_005577.2 R1088R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:160952892 G>A maps to NM_005577.2 F1997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:160962146 G>A maps to NM_005577.2 C1862C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:161006105 G>T maps to NM_005577.2 R1421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:161010694 T>C maps to NM_005577.2 G1279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr6:161006214 C>A maps to NM_005577.2 G1384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr6:160977189 G>T maps to NM_005577.2 R1614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr6:160977187 C>T maps to NM_005577.2 R1614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:78010799 G>A did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:78010950 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:48986517 G>T maps to NM_005767.5 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:1463876 G>A maps to NM_024830.3 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:1463837 G>A maps to NM_024830.3 N511N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:211952345 C>T maps to NM_014873.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr1:211956632 A>T maps to NM_014873.2 L222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:82445596 G>A maps to ENST00000370717 K1018K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:62903501 T>C maps to ENST00000506720 S1215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr4:62910253 G>A maps to ENST00000506720 A1267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr4:62775309 T>C maps to ENST00000506720 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr2:11960605 C>T maps to ENST00000396099 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:11960604 G>A maps to ENST00000396099 E868E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:56332200 C>T maps to NM_006151.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr1:99771527 G>A maps to NM_014839.4 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr1:99422192 C>T maps to NM_001037317.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr1:99422173 G>A maps to NM_001037317.1 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr4:155670221 G>A maps to NM_004744.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr4:151336640 T>C maps to NM_006726.3 E2392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr13:47260085 A>G maps to NM_001164211.1 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:197541799 C>A maps to ENST00000425562 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr3:197553750 C>T maps to ENST00000425562 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr19:4538668 G>A maps to NM_052972.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:66512865 C>A maps to NM_015541.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:66430821 G>A maps to NM_015541.2 R1049R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr12:59270242 T>C maps to NM_153377.3 P893P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:85992305 C>A maps to NM_015613.2 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr10:85992225 G>A maps to NM_015613.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr10:85984163 G>A maps to NM_001017924.2 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:25260945 C>A maps to ENST00000354454 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:57548339 C>T maps to NM_002332.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr14:23346660 C>T maps to NM_014045.3 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:105507434 G>T maps to NM_013437.4 S528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:105511578 G>T maps to NM_013437.4 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr2:141115581 G>A maps to NM_018557.2 C3787C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr2:141625385 G>C maps to NM_018557.2 S1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr2:141359135 G>T maps to NM_018557.2 S2291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:141747131 G>A maps to NM_018557.2 S913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr2:141812826 G>T maps to NM_018557.2 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr2:141243075 C>T maps to NM_018557.2 A3087A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:141055479 G>T maps to NM_018557.2 V4288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr2:141460037 G>A maps to NM_018557.2 S2036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr2:141607701 G>A maps to NM_018557.2 N1636N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr2:141751585 G>A maps to NM_018557.2 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr2:141116393 A>T maps to NM_018557.2 C3751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr2:141665449 G>T maps to NM_018557.2 L1172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr2:141267506 T>C maps to NM_018557.2 T2796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr2:170026296 C>T maps to NM_004525.2 Q3804Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr2:170147487 A>G maps to NM_004525.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:170072804 G>A maps to NM_004525.2 I1928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:170025142 G>A maps to NM_004525.2 F3847F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:170003399 G>A maps to NM_004525.2 R4220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr19:33696896 C>T maps to NM_002333.3 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:68191156 G>A maps to NM_002335.2 A1076A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr12:12397415 G>A maps to NM_002336.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr12:12340025 T>C maps to NM_002336.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr2:44132855 C>T maps to NM_133259.3 T1113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:194080362 G>A maps to NM_001135057.2 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:24534943 C>T maps to NM_138360.3 F1170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr14:24533522 C>T maps to NM_138360.3 F1016F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr10:50121828 G>A maps to NM_001006939.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:46574378 C>A maps to NM_024512.3 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:134151130 G>A maps to NM_030626.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:99926273 C>T maps to NM_144598.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:169514579 A>G maps to NM_001172779.1 C287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:67410753 G>A maps to NM_018296.5 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr1:70614266 G>A maps to NM_017768.4 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr12:122670780 G>A maps to NM_001098519.1 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr12:122677339 G>T maps to NM_001098519.1 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr1:3703694 G>A maps to NM_020710.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr19:51022390 C>T maps to NM_001080457.1 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:40136876 C>T maps to NM_020929.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr16:84199421 C>T maps to NM_178452.4 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr11:56954800 C>T maps to NM_001005210.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr7:150034183 T>C maps to NM_023942.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:70225938 C>T maps to NM_020794.2 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr1:70257749 C>T maps to NM_020794.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr9:131671017 C>G maps to NM_001127244.1 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr1:90178693 A>C maps to NM_032270.4 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:90400780 C>T maps to NM_001134479.1 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:238671279 C>T maps to NM_001137552.1 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:37132965 C>A maps to NM_006309.2 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:37125146 C>A maps to NM_006309.2 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr3:37125234 G>A maps to NM_006309.2 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr12:85450451 C>T maps to NM_001079910.1 N627N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:85492677 G>T maps to NM_001079910.1 E1039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:85492677 G>T maps to NM_001079910.1 E1039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:74575236 G>A maps to NM_001105659.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:169555340 G>A maps to NM_001080460.1 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr15:101566294 C>T maps to NM_024652.3 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr15:101605591 G>A maps to NM_024652.3 G1650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:40646786 G>A maps to NM_198578.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:40687399 G>T maps to NM_198578.3 E915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:40716989 A>C maps to NM_198578.3 P1846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr12:40713872 A>G maps to NM_198578.3 K1637K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr12:40668476 A>G maps to NM_198578.3 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr12:40668474 G>T maps to NM_198578.3 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr3:3887422 C>A maps to NM_020873.5 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:110764714 T>G maps to NM_018334.4 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr20:6022339 G>A maps to NM_152611.3 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr20:6022177 G>T maps to NM_152611.3 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:80530140 G>A maps to NM_178839.4 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:138210021 G>A maps to NM_015564.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:68687507 G>A maps to NM_178011.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:76975877 G>A maps to NM_001134745.1 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:38027331 T>C maps to NM_014462.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3584-01A-01W-0831-10 chr19:34687544 C>T maps to NM_001114093.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:14223155 C>T maps to NM_014463.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr11:1874403 C>T maps to NM_002339.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr19:35741410 C>T maps to NM_205834.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr21:47611068 G>A maps to NM_002340.5 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:21172236 G>A maps to ENST00000381541 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr6:31548596 G>A maps to NM_002341.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr14:24780889 C>T maps to ENST00000336557 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:33526596 G>T maps to ENST00000354476 E1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr14:74999243 G>A maps to NM_000428.2 N624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:6499318 G>A maps to NM_002342.1 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr3:46479449 C>T maps to NM_002343.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:144184234 C>T maps to NM_032860.3 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr6:144171287 T>C maps to NM_032860.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:24750802 G>T maps to NM_001009909.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr6:31685454 C>A maps to ENST00000375834 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr8:143784536 G>A maps to ENST00000292430 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:160661610 G>A maps to NM_002349.3 R1705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:160676303 G>T maps to NM_001198759.1 T1362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr4:4285361 G>A maps to NM_017816.2 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:4281194 G>T maps to NM_017816.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr8:143831748 G>A maps to NM_205545.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr19:43965646 G>A maps to NM_014400.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:150071118 T>G maps to NM_177964.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr1:24120367 G>A maps to NM_007260.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:100269603 C>T maps to NM_152449.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr1:235920622 G>A maps to NM_000081.2 L2339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:235973132 G>A maps to NM_000081.2 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr1:235850290 G>A maps to NM_000081.2 C3586C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:29581547 C>T maps to NM_032517.4 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:20110322 G>A maps to NM_021020.2 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:20112506 G>A maps to NM_021020.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr8:20110478 C>T maps to NM_021020.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:36050170 G>T maps to NM_005584.4 C35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr4:151504984 G>A maps to NM_006439.4 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr7:20198969 G>A maps to NM_182762.3 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr1:39824374 C>T maps to ENST00000361689 R1922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:39792958 T>C maps to ENST00000361689 L1521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:39799243 G>A maps to ENST00000289893 K768K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:39852997 G>A maps to ENST00000361689 R2766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:39951333 C>T maps to ENST00000361689 S5387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr1:39853735 G>A maps to ENST00000361689 Q3012Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr1:39905072 T>C maps to ENST00000361689 A4057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr1:39797857 A>G maps to ENST00000289893 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr7:1855714 G>A maps to NM_003550.2 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:47331141 C>A maps to NM_003682.3 I1379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr11:47350616 C>A maps to NM_003682.3 S1620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:166974587 C>T maps to NM_032858.1 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr1:166991079 T>C maps to NM_032858.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr16:79633484 C>A maps to NM_005360.4 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr16:79628416 C>T maps to NM_005360.4 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:35802895 C>T maps to NM_002361.3 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:152482176 T>C did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:152482568 A>G did not map to a codon.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr23:151303309 G>C did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:151303090 C>G did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:151900014 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:151935532 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:151092275 T>C did not map to a codon.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr23:151092777 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:151869682 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:149013406 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:30269012 C>T did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:30268763 T>C did not map to a codon.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr23:35820779 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:35821083 G>T did not map to a codon.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr23:35820648 T>C did not map to a codon.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr23:35820648 T>C did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:35820391 G>A did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr23:26157244 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:30237185 C>A did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:30237239 C>T did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:30236764 G>A did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:30237067 A>G did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:30236764 G>A did not map to a codon.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr23:30237393 T>G did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:30260497 A>G did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:30261249 C>T did not map to a codon.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr23:26212564 C>T did not map to a codon.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr23:140994555 T>C did not map to a codon.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:140995659 A>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:140993372 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:140993857 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:140996067 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:140994173 T>C did not map to a codon.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr23:140996484 T>A did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:140996358 C>T did not map to a codon.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr23:141291465 C>A did not map to a codon.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr23:141291473 C>T did not map to a codon.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr23:141290932 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:141291178 C>A did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:141290855 A>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:140969504 C>A did not map to a codon.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr23:140983313 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:140985435 G>T did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:140984898 C>T did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:140984943 T>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:54841720 G>A did not map to a codon.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr23:54841851 G>A did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:54841193 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:75649459 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:75650295 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:75651049 C>A did not map to a codon.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr23:75649955 A>C did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:75649144 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:75004691 C>T did not map to a codon.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr23:75004572 G>A did not map to a codon.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr23:55479264 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:66023950 C>T maps to NM_001033057.1 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:65376820 G>A maps to NM_001033057.1 N804N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr3:65607704 A>G maps to NM_001033057.1 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:77998480 A>C maps to NM_012301.3 Y365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr23:49022415 C>T did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr12:10758963 T>C maps to NM_018048.3 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:33346628 C>T maps to NM_032509.3 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr18:56390337 C>A maps to NM_006785.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr9:72659527 G>T maps to NM_153267.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr11:95825622 C>A maps to NM_032427.1 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:95712129 G>T maps to NM_032427.1 I1151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr23:149639757 G>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:149638105 C>A did not map to a codon.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr23:149639581 G>A did not map to a codon.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr23:149638894 G>A did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:149638771 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:119510834 G>A maps to NM_005907.2 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr1:117944819 A>G maps to NM_006699.3 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:117963223 C>A maps to NM_006699.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr1:26107552 C>T maps to NM_020379.2 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:12758322 C>T maps to NM_000528.3 E918E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr19:12759994 G>A maps to NM_000528.3 R797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr4:6610848 G>A maps to NM_015274.1 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:103595102 G>T maps to NM_005908.3 S362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr4:103644048 G>A maps to NM_005908.3 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr23:43601276 C>G did not map to a codon.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr23:43662573 C>T did not map to a codon.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:43626759 C>T did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:43628573 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:43814258 C>T maps to ENST00000382031 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr5:71492289 G>A maps to NM_005909.3 P1036P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:71494135 G>T maps to NM_005909.3 E1652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr5:71490970 G>T maps to NM_005909.3 E597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:71490039 C>T maps to NM_005909.3 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:71492952 G>A maps to NM_005909.3 P1257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr5:71490300 G>A maps to NM_005909.3 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:71496021 C>A maps to NM_005909.3 S2280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:210560709 C>A maps to NM_002374.3 T1272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:210561749 C>A maps to NM_002374.3 L1499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr17:21208415 C>T maps to NM_145109.2 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:12032523 C>T maps to ENST00000415385 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr17:12028609 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:67516505 C>A maps to NM_002758.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr19:7975191 C>G maps to ENST00000425613 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr19:40711124 G>A maps to NM_002446.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr12:53875790 T>C maps to NM_001193511.1 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:53878117 G>A maps to NM_001193511.1 R391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr3:185146509 G>A maps to NM_004721.3 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:19379457 G>A did not map to a codon.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr6:161491656 T>C maps to NM_005922.2 D575D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr6:161510472 G>A maps to NM_005922.2 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:161527592 C>T maps to NM_005922.2 R1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr6:161470017 C>G maps to NM_005922.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr6:161455405 C>T maps to NM_005922.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr6:161533757 C>T maps to NM_005922.2 A1526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr6:161530788 A>G maps to NM_005922.2 E1413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:91256989 G>A maps to NM_145331.1 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:91257800 C>A maps to NM_145331.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:71216751 G>A maps to NM_033141.2 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr3:47957777 T>C maps to ENST00000426837 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr2:39570592 C>T maps to NM_003618.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:39552676 G>A maps to NM_003618.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:102503558 G>T maps to NM_145686.2 E1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr23:20033382 C>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:20028971 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:20031203 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:20034396 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:20062573 G>A did not map to a codon.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:135302950 T>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:135308161 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:135326915 T>C did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:135314330 C>T did not map to a codon.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr23:135314028 C>A did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:135313097 T>G did not map to a codon.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr4:156268949 G>A maps to NM_001039580.1 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr22:22160201 A>G maps to NM_138957.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:87023117 G>A maps to NM_138982.2 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:86950394 C>A maps to NM_138982.2 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:36020511 A>G maps to NM_139012.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr16:30128044 C>A maps to NM_002746.2 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:19283131 C>T maps to NM_139034.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr11:45927226 G>A maps to NM_005456.2 Q697Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:179663383 T>G maps to NM_002752.4 *425C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:179669587 G>A maps to NM_002752.4 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr20:31413837 C>T maps to NM_012325.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr2:27248574 T>C maps to NM_012326.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:44039726 C>T maps to NM_001123066.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:44049279 C>A maps to NM_001123066.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:44067362 G>A maps to NM_001123066.3 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr4:164507068 G>A maps to ENST00000514618 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr17:60821764 A>T maps to NM_152598.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr17:60814610 C>T maps to NM_152598.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:217234551 G>A maps to NM_020814.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr2:217234551 G>A maps to NM_020814.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:119750793 C>T maps to NM_006770.3 D449D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:220808815 G>T maps to NM_018650.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:220825397 C>T maps to NM_018650.3 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr1:220809238 T>C maps to NM_018650.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:63667413 C>T maps to NM_001039469.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:57910232 G>T maps to NM_004990.2 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr12:57898051 G>A maps to NM_004990.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr2:198571811 A>G maps to NM_138395.3 P561P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AG-A02N-01A-11W-A096-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:29455364 C>T maps to NM_052967.1 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr6:29455288 A>G maps to NM_052967.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:11086965 G>A maps to NM_006610.2 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:12958768 C>A maps to NM_014975.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr1:46500588 C>T maps to NM_015112.2 A1416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:46290199 G>A maps to NM_015112.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr1:46489482 C>A maps to NM_015112.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:66445358 C>T maps to NM_001164664.1 I1079I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:66461411 G>A maps to NM_001164664.1 P2135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr5:66461969 C>T maps to NM_001164664.1 S2321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:99019809 C>T maps to ENST00000254898 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:99039680 C>T maps to ENST00000254898 I660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:99019770 C>A maps to ENST00000254898 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr20:43932964 G>A maps to ENST00000372754 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:3844906 G>A maps to NM_020746.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr20:3838403 G>A maps to NM_020746.3 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr18:51729416 A>T maps to NM_015832.3 L253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:149248057 C>T maps to ENST00000404807 G1619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:97999257 G>A maps to ENST00000376673 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:131525101 C>A did not map to a codon.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr23:131520694 G>A did not map to a codon.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr17:49272709 C>A maps to ENST00000389496 G416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr17:49272709 C>A maps to ENST00000389496 G416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:84125348 C>T maps to NM_003791.2 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:13884644 G>T maps to NM_000529.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:13885139 C>T maps to NM_000529.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:13885385 G>A maps to NM_000529.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:103349342 G>T did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:103349156 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:112364656 G>A maps to NM_001085377.1 F951F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr23:138701837 T>G did not map to a codon.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr23:138708852 G>T did not map to a codon.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr23:138708818 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:138678794 T>G did not map to a codon.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr13:113739449 G>T maps to NM_001112732.1 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:183056613 G>T maps to NM_015078.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:183097193 G>A maps to NM_015078.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:182897468 A>G maps to NM_015078.2 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:41077325 G>A maps to NM_005297.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:100403891 G>T maps to NM_032503.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:127325638 C>A maps to NM_004526.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:52141211 C>A maps to ENST00000419835 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr6:52138561 T>C maps to ENST00000419835 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:47704008 C>A maps to NM_003906.3 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr21:47684122 C>T maps to NM_003906.3 A1081A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr8:48887409 C>T maps to NM_182746.1 N751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:99695354 G>A maps to NM_005916.3 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr6:119238801 T>C maps to ENST00000316316 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:7591676 C>A maps to NM_020533.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr19:7593141 C>T maps to NM_020533.2 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:94204079 G>A maps to NM_024717.4 C798C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:94046580 G>T maps to NM_024717.4 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:94353133 C>A maps to NM_024717.4 G259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:47324283 A>G maps to NM_001113498.2 N942N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:47426795 G>A maps to NM_001113498.2 R624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr14:47600962 A>G maps to NM_001113498.2 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr14:47530616 G>T maps to NM_001113498.2 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:207611133 C>T maps to NM_001039845.1 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:75689758 C>A maps to NM_005918.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr12:69230471 T>C maps to NM_002392.3 Y287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:90403821 G>A maps to NM_014611.1 V3284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr6:90383051 T>C maps to NM_014611.1 L4459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr11:86152476 G>A maps to NM_001014811.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr11:86158136 G>A maps to NM_001014811.1 C450C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr23:70339906 C>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:70360704 C>T did not map to a codon.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:70342602 G>A did not map to a codon.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr23:70338701 A>G did not map to a codon.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr3:151150579 T>G maps to NM_053002.4 P2142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:151105608 C>A maps to NM_053002.4 V1665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr17:60060306 C>A maps to NM_005121.2 R1019R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:60042386 C>T maps to NM_005121.2 P1608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:116457643 C>T maps to NM_015335.4 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr22:20920884 G>A maps to NM_001003891.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:57472675 C>T maps to ENST00000431606 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:131913539 G>T maps to ENST00000403834 I1159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:131915358 G>A maps to ENST00000403834 R1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr6:131929190 A>G maps to ENST00000403834 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr17:38178691 T>G maps to NM_014815.3 G826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr19:50333402 C>T maps to NM_030973.3 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr19:16687284 C>T maps to NM_004831.3 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:100230588 C>T maps to ENST00000338042 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:3293323 G>A maps to NM_000243.2 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:3297075 G>A maps to NM_000243.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3584-01A-01W-0831-10 chr5:126734451 C>T maps to NM_032446.2 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:126676305 C>T maps to NM_032446.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:66210409 C>T maps to NM_032445.2 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr19:42880527 C>T maps to ENST00000251268 S2713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:42866666 C>T maps to ENST00000251268 S1992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:42847782 C>T maps to ENST00000251268 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:37188834 G>A maps to NM_170675.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:37188834 G>A maps to NM_170675.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:37390244 C>T maps to NM_170675.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:37391658 T>C maps to NM_170675.2 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:47910190 G>A maps to NM_020160.1 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:32157134 C>T did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr11:64571982 A>G maps to NM_130804.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr11:64571898 C>T maps to NM_130804.2 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr6:46793168 C>T maps to NM_005588.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr18:29782964 G>A maps to NM_005925.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr18:29797057 C>T maps to NM_005925.2 R622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr2:112740566 T>C maps to NM_006343.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:81271763 G>T maps to NM_015154.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr15:90321387 C>T maps to NM_001039958.1 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr7:116423414 T>C maps to NM_001127500.1 Y1248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr7:116380996 G>A maps to NM_001127500.1 W540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr17:2323344 A>G maps to NM_024086.3 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr11:28135030 T>C maps to NM_001113528.1 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr10:126453967 G>A maps to NM_212554.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr17:60503801 G>A maps to NM_181725.3 W115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:170669010 G>A maps to NM_014168.2 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:170677647 G>A maps to NM_014168.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:15452881 G>A maps to NM_152396.2 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:82335530 C>T maps to NM_032246.3 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr15:44097660 A>G maps to NM_005926.2 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:170912531 G>T maps to NM_021647.6 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:228197246 A>G maps to NM_020194.4 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:89442928 C>T maps to NM_005928.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr15:89448987 C>A maps to NM_005928.2 G229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr8:8747631 G>C maps to NM_004225.2 T979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:179069713 C>T maps to NM_033540.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:179103428 G>T maps to NM_033540.2 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr3:179096131 T>C maps to NM_033540.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr1:12065897 G>A maps to NM_014874.3 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr11:119213327 G>A maps to NM_031433.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:158527031 G>T maps to NM_022736.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr1:205549973 G>A maps to NM_181644.4 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr2:191301607 G>T maps to NM_017694.3 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr2:191302143 C>T maps to NM_017694.3 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:8701223 G>A maps to NM_152599.3 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr4:678564 C>T maps to ENST00000404286 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr4:128863275 A>G maps to NM_152778.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:103335028 G>A maps to NM_032718.3 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr2:103348856 A>G maps to NM_032718.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr2:103348856 A>G maps to NM_032718.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr15:42041774 G>A maps to ENST00000219905 T2039T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:42021427 C>T maps to ENST00000219905 R1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:42052640 G>T maps to ENST00000219905 E2487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr15:42041564 C>A maps to ENST00000219905 T1969T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr15:42003204 T>G maps to ENST00000219905 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:141705374 G>C maps to ENST00000475668 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr22:39883627 G>A maps to NM_001098270.1 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:39884257 G>A maps to NM_001098270.1 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:179229096 T>G maps to NM_054013.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr12:86373588 T>C maps to ENST00000393205 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:43277226 G>T maps to NM_153361.2 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:131557518 G>T maps to NM_002412.3 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:131334602 C>T maps to NM_002412.3 H60H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:222824035 G>T maps to NM_198551.2 E1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr18:19378062 C>T maps to NM_020774.2 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr11:12281385 T>C maps to NM_014632.2 T1092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr11:12371469 G>A maps to NM_032867.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:10417521 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:10534930 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:10535338 G>A did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:10427779 G>A did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:10417465 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:38664316 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:67450502 G>T maps to NM_001077700.2 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:12089330 C>T maps to NM_021933.2 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:4789437 C>T maps to NM_153827.4 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:7613246 G>T maps to NM_019005.3 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr7:7613281 G>A maps to NM_019005.3 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:24443523 C>A maps to NM_005932.3 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr10:129906139 G>A maps to NM_002417.4 L1322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:129903470 C>T maps to NM_002417.4 T2211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr10:129903299 T>C maps to NM_002417.4 T2268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:129906251 C>T maps to NM_002417.4 A1284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:14340347 G>T maps to NM_014048.3 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:14340859 C>T maps to NM_014048.3 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr16:14339511 T>C maps to NM_014048.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr7:131151087 A>G maps to NM_013255.4 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr7:131155642 A>G maps to NM_013255.4 K657K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:12623703 C>T maps to NM_014160.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:56283519 G>A maps to NM_017777.3 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:56291698 C>A maps to NM_017777.3 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr10:28030375 C>T maps to NM_173576.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:5897568 C>T maps to NM_005511.1 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr12:121132652 C>T maps to NM_014730.2 H147H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:185616498 G>A maps to NM_024629.3 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr12:6859908 A>G maps to NM_005439.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr3:37092042 T>C maps to NM_000249.3 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:37056024 C>T maps to NM_000249.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:37070323 C>T maps to NM_000249.3 R487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr3:37053325 T>C maps to NM_000249.3 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr3:37053588 C>A maps to NM_000249.3 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:75514602 C>A maps to NM_001040108.1 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:75514047 C>A maps to NM_001040108.1 E771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:74708906 G>T maps to NM_152649.2 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr11:118343889 C>T maps to NM_001197104.1 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:118343214 G>A maps to NM_001197104.1 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:118359409 G>T maps to NM_001197104.1 E1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:118373353 C>A maps to NM_001197104.1 V2249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:118373689 G>A maps to NM_001197104.1 S2361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr11:118368706 T>C maps to NM_001197104.1 A1907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr11:118359387 G>A maps to NM_001197104.1 E1464E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr12:49433710 C>T maps to NM_003482.3 S2614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:151945454 G>T maps to ENST00000355193 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr7:151962265 G>A maps to ENST00000355193 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr7:104749519 C>T maps to NM_182931.2 A1200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:104747132 G>T maps to NM_182931.2 E921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:104747949 G>T maps to NM_182931.2 E1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr9:20414186 T>C maps to NM_004529.2 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:168312120 C>A maps to ENST00000400822 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:168351892 C>T maps to ENST00000400822 R1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr6:168352575 G>A maps to ENST00000400822 S1506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr6:33768862 G>A maps to NM_002418.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:122618046 C>T maps to NM_014938.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:146572262 T>G maps to NM_172250.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:154862149 C>T maps to NM_007289.2 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:102647131 C>A maps to NM_002425.2 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:24122864 C>T maps to NM_005940.3 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:102822867 G>A maps to NM_002427.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr14:23311705 A>T maps to NM_004995.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr8:89179994 T>C maps to NM_005941.4 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:89128906 C>T maps to NM_005941.4 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr8:89128915 T>C maps to NM_005941.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr12:132325288 C>T maps to NM_016155.4 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr12:132335617 C>T maps to NM_016155.4 D537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr16:55519307 C>T maps to NM_004530.4 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr16:55519569 T>A maps to NM_004530.4 L238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:5013287 C>A maps to NM_021801.3 Y230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr11:102573487 T>C maps to NM_022122.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr11:102713559 G>A maps to NM_002422.3 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr11:102593392 T>C maps to NM_002424.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:102586131 G>A maps to NM_002424.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr20:44644970 C>T maps to NM_004994.2 Y696Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:88703091 G>A maps to NM_024756.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:28196069 C>T maps to NM_002430.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr1:158813174 G>A maps to NM_002432.1 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:2290265 G>A maps to NM_020310.2 Q560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:1501711 C>T maps to NM_001172223.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr19:2078487 T>C maps to NM_130807.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:33783111 C>T maps to NM_017947.2 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:33846725 T>C maps to NM_017947.2 C808C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr6:29633971 G>A maps to NM_002433.4 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr7:100843713 A>G maps to NM_178176.2 Y64Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr12:62938713 G>T maps to ENST00000393630 G836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:108677967 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:37705951 G>A maps to ENST00000290384 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:2290146 G>A maps to NM_024848.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:14915234 G>T did not map to a codon.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr1:113235544 G>A maps to NM_020963.3 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:113241081 C>T maps to NM_020963.3 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr1:113239067 G>T maps to NM_020963.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr22:50538026 C>T maps to NM_018995.2 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr22:50563960 C>T maps to NM_018995.2 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr22:50572972 G>T maps to NM_018995.2 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:50547127 G>T maps to NM_018995.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:50589165 C>T maps to NM_018995.2 I910I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr22:50546631 C>T maps to NM_018995.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr22:50555768 C>T maps to NM_018995.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:13107074 G>A maps to ENST00000319217 G2034G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:13126571 G>A maps to ENST00000319217 V1525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr11:58980157 G>A maps to NM_001039396.1 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr2:71365675 G>A maps to NM_005791.2 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr16:82203767 G>T maps to NM_005792.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:123645693 C>A maps to NM_022782.2 E972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr12:123649914 C>A maps to NM_022782.2 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr1:43805161 T>C maps to NM_005373.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:56349218 C>T maps to ENST00000340482 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:154009979 G>A did not map to a codon.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr23:154019306 T>C did not map to a codon.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr23:154009974 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:202550671 A>G maps to NM_033066.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr10:28527515 C>T maps to NM_173496.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:28420578 G>A maps to NM_173496.3 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:43831028 G>A maps to NM_001044370.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr11:30516994 T>G maps to NM_001584.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:161276519 G>A maps to ENST00000360451 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr1:161276237 C>T maps to ENST00000360451 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr1:161276171 G>A maps to ENST00000360451 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:167741681 C>T maps to NM_003953.5 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr3:138117397 G>A maps to NM_001085049.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr10:17865238 A>G maps to NM_002438.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3582-01A-01W-0831-10 chr11:94180583 T>C maps to NM_005591.3 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr11:68748292 G>A maps to NM_198923.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:68747869 G>A maps to NM_198923.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr11:68772922 G>A maps to NM_145015.4 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:18956049 G>T maps to NM_147199.3 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:19076974 C>T maps to NM_054030.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr11:18159318 T>C maps to NM_054031.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:78804459 G>T maps to NM_020236.3 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:121444363 C>G did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr6:160218384 G>A maps to NM_014161.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:86434404 C>T maps to NM_016622.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr19:39423123 C>A maps to NM_033363.1 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:56022702 G>A maps to ENST00000426595 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:43642961 C>T maps to ENST00000372118 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:84382148 G>T maps to NM_016067.2 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr7:43908598 G>T maps to NM_032014.2 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr5:44809450 C>T maps to NM_016640.3 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr16:1822398 G>A maps to ENST00000432952 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr11:10647701 G>A maps to NM_001098579.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:60235877 G>A maps to NM_152866.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:60558511 G>A maps to NM_206893.3 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr11:60559757 G>A maps to NM_206893.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:59857287 C>T maps to NM_000139.4 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:59861517 G>T maps to NM_000139.4 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr11:60105329 C>T maps to NM_139249.2 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr8:72755897 G>A maps to NM_005098.3 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr2:47639566 A>G maps to NM_000251.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr2:47637471 C>A maps to NM_000251.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr2:47657019 C>A maps to NM_000251.1 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:48033752 G>T maps to NM_000179.2 E1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:48026931 G>T maps to NM_000179.2 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr3:135913925 G>A maps to NM_018133.3 Y10Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr3:135871146 A>G maps to NM_018133.3 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:11783632 C>T did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr16:830193 G>A maps to NM_001025190.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr23:64951046 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:64951736 G>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:64949551 G>A did not map to a codon.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr8:16026284 G>A maps to ENST00000445506 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr3:49724705 A>G maps to NM_020998.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr3:49723378 T>C maps to NM_020998.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr3:49933984 T>A maps to NM_002447.2 A809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:49933238 C>T maps to NM_002447.2 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:131208174 C>T did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:131202441 G>A did not map to a codon.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr1:155582324 C>T maps to NM_018116.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr5:174151700 C>T maps to NM_002449.4 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:91503014 C>A maps to NM_006980.3 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:242039150 G>A maps to NM_182501.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:107371394 A>G maps to NM_025198.3 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:38281184 C>A maps to NM_005955.2 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:93594850 G>T maps to NM_007358.3 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr14:64920542 C>T maps to NM_005956.3 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:149919216 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:149895774 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:31197153 T>C maps to NM_014967.4 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr17:56569101 G>A maps to NM_004687.4 Y1170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr13:25831345 G>T maps to NM_004685.3 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:63569893 C>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:63488678 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:63563586 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:63568624 C>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:63574763 C>A did not map to a codon.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr23:63490910 C>A did not map to a codon.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr23:63557190 C>T did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:63564990 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:11169361 G>A maps to NM_004958.3 R2505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr1:236998968 C>T maps to NM_000254.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:153311182 T>C maps to NM_019041.5 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:7878149 C>T maps to NM_024010.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:100503083 A>G maps to ENST00000511045 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:17510727 T>C maps to NM_001001924.2 E1117E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AG-3898-01A-01W-1073-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:17611492 C>A maps to NM_001001924.2 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:29600044 G>T maps to NM_001033602.2 G414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:29600575 T>C maps to NM_001033602.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr13:29600214 C>A maps to NM_001033602.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr19:9049722 G>T maps to NM_024690.2 V10636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr19:9075142 G>A maps to NM_024690.2 G4101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr19:9067648 G>A maps to NM_024690.2 T6599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:8987233 G>A maps to NM_024690.2 I13951I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9049837 G>T maps to NM_024690.2 S10598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9057862 G>A maps to NM_024690.2 F9861F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9058849 G>T maps to NM_024690.2 L9532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9059475 C>A maps to NM_024690.2 E9324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9070924 G>T maps to NM_024690.2 A5507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9073639 T>C maps to NM_024690.2 G4602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9085064 G>T maps to NM_024690.2 V2250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9085145 G>A maps to NM_024690.2 S2223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9087068 G>T maps to NM_024690.2 S1582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9089540 T>C maps to NM_024690.2 E758E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr19:9074563 G>A maps to NM_024690.2 S4294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr19:9087431 C>A maps to NM_024690.2 L1461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr19:9047484 A>G maps to NM_024690.2 S11382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr7:100681302 T>C maps to NM_001040105.1 P2202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr7:100679901 A>G maps to NM_001040105.1 E1735E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr11:1092953 G>A maps to ENST00000441003 T1591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr6:30954920 C>G maps to NM_001010909.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr6:30954869 T>C maps to NM_001010909.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:195486079 C>T maps to NM_018406.5 G4967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:195493606 G>A maps to NM_018406.5 F4515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr3:195475798 C>T maps to NM_018406.5 Q5336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:1265444 G>A maps to ENST00000447027 T2448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:1273618 C>T maps to ENST00000447027 Y4973Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr11:1272287 C>A maps to ENST00000447027 S4729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr11:1271177 T>C maps to ENST00000447027 T4359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr11:1270937 T>C maps to ENST00000447027 A4279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:105449657 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:105450220 C>A did not map to a codon.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr23:105451153 A>C did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:105450658 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:113538922 G>T maps to ENST00000189978 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr9:113563217 C>T maps to ENST00000189978 R860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:45797951 G>T maps to NM_001128425.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:45800150 T>C maps to NM_001128425.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr1:45799143 G>A maps to NM_001128425.1 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:70162549 C>T maps to NM_002357.2 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr23:3235843 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:3240134 C>T did not map to a codon.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr23:3238173 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:3229371 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:3238513 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:3239635 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:3248146 C>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:3235153 C>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:3235539 G>A did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:3241420 G>A did not map to a codon.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr23:3235261 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:3229191 T>C did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:3227825 G>T did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:3240723 A>G did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:3241265 A>G did not map to a codon.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr23:3239200 T>C did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr23:3241452 A>G did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr23:3241639 C>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:135518400 C>T maps to NM_001130173.1 D502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:4442901 G>A maps to NM_001105538.1 P1265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr8:67492523 G>A maps to NM_001080416.2 D315D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:67507951 G>A maps to NM_001080416.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:50964827 G>A maps to NM_004533.3 R987R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:203144470 C>T maps to NM_004997.2 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:109837736 C>T maps to NM_001010985.2 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:77718580 G>A maps to NM_015057.4 I2434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr13:77740563 T>C maps to NM_015057.4 G2080G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:48595004 C>A maps to NM_032133.4 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr2:16085897 G>A maps to NM_005378.4 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr15:48458144 G>T maps to NM_016132.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr12:81111114 C>T maps to NM_005593.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr12:81112716 C>T maps to NM_005593.2 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr12:81111303 G>A maps to NM_005593.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr17:10409145 A>G maps to NM_005963.3 Y719Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr17:10409145 A>G maps to NM_005963.3 Y719Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr17:10408264 C>T maps to NM_005963.3 K851K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:8390795 C>T maps to ENST00000360416 A1667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:8409736 C>T maps to ENST00000360416 T1095T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:8411934 C>A maps to ENST00000360416 E1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:8455403 G>T maps to ENST00000360416 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr16:15932004 G>A maps to NM_001040114.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:15869974 G>T maps to NM_001040114.1 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:15878554 G>A maps to NM_001040114.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:15917265 C>T maps to NM_001040114.1 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:10243704 T>C maps to NM_003802.2 G636G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr3:108195348 A>G maps to NM_014981.1 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:108112895 G>T maps to NM_014981.1 A1767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:10443994 C>A maps to NM_017534.5 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:10427101 C>A maps to NM_017534.5 E1759*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AG-A002-01A-01W-A00K-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:10443341 G>T maps to NM_017534.5 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr17:10436603 T>C maps to NM_017534.5 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr17:10541652 C>A maps to NM_002470.2 E1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:10543749 C>A maps to NM_002470.2 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr17:10351934 G>A maps to NM_017533.2 Q1511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:10357936 C>A maps to NM_017533.2 E876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:23851690 G>A maps to NM_002471.3 I1914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr14:23851696 C>T maps to NM_002471.3 A1912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr14:23898993 G>A maps to NM_000257.2 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:23898175 G>A maps to NM_000257.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:23899801 G>T maps to NM_000257.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:23886415 C>A maps to NM_000257.2 E1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:23902385 G>A maps to NM_000257.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr20:33589109 C>T maps to NM_020884.3 G1888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:33577697 C>T maps to NM_020884.3 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr17:10302910 G>T maps to NM_002472.2 R1271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr2:211163164 G>A maps to NM_079420.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:3253331 G>A maps to NM_006471.2 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:3255807 G>A maps to NM_006471.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:111353561 G>A maps to NM_000432.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr12:56549213 C>A maps to NM_002475.4 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:44180601 G>T maps to ENST00000457314 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:123512532 G>A maps to NM_053025.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:46766410 C>A maps to NM_182493.2 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:30387744 C>T maps to NM_013292.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:16670652 C>T maps to NM_012334.2 S1955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:16703248 G>A maps to NM_012334.2 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:18034584 C>T maps to ENST00000205890 F1357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:18054449 G>A maps to ENST00000205890 P2500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:18082114 C>T maps to ENST00000205890 H3508H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr17:18054760 C>T maps to ENST00000205890 F2569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr17:18023658 C>T maps to ENST00000205890 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr22:26176131 C>T maps to ENST00000407587 N728N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr22:26342200 G>A maps to ENST00000407587 T1874T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:192234333 C>T maps to NM_001130158.1 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:192228558 C>T maps to NM_001130158.1 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:192265110 C>T maps to NM_001130158.1 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr15:59455417 G>A maps to NM_004998.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr7:45003710 C>T maps to NM_033054.2 Q894Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr10:26455007 C>T maps to NM_017433.4 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:26414412 C>T maps to NM_017433.4 R664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:26446394 C>T maps to NM_017433.4 R984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr10:26442854 A>G maps to NM_017433.4 A904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr10:26443697 T>C maps to NM_017433.4 R913R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr2:171056661 T>C maps to NM_138995.3 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:171248959 C>T maps to NM_138995.3 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr2:171240248 C>T maps to NM_138995.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr2:171264304 A>G maps to NM_138995.3 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr2:171264304 A>G maps to NM_138995.3 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:47390702 A>G maps to NM_001080467.2 N1217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:47398566 C>T maps to NM_001080467.2 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:47518663 G>T maps to NM_001080467.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:52553237 G>A maps to NM_018728.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr15:52517285 T>C maps to NM_018728.3 E1117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:76540161 G>T maps to ENST00000428345 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:76589595 G>T maps to ENST00000428345 E713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:76596647 C>T maps to ENST00000428345 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr6:76527362 C>G maps to ENST00000428345 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr2:128338351 C>T maps to ENST00000389524 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr15:72311379 C>T maps to ENST00000424560 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:171621526 C>T maps to NM_000261.1 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr17:12608479 G>T maps to NM_001146312.1 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:12666501 A>G maps to NM_001146312.1 E834E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr17:12639604 C>T maps to NM_001146312.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:3079255 C>T maps to NM_003803.3 P1523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr18:3188880 C>T maps to NM_003803.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr8:2091340 C>T maps to NM_003970.2 I1347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr8:2026917 C>T maps to NM_003970.2 R456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:137222998 A>G maps to NM_006790.2 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:69921490 C>T maps to NM_032578.2 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:69934129 G>T maps to NM_032578.2 E761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr10:69926072 C>T maps to NM_032578.2 N541N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr10:69959138 G>A maps to NM_032578.2 P1100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr10:69933945 T>C maps to NM_032578.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr1:59156061 C>T maps to NM_001085487.1 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:59165711 C>A maps to NM_001085487.1 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:76732381 T>G maps to NM_012330.2 L349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr10:76789360 G>A maps to NM_012330.2 Q1593Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr2:1893030 G>A maps to ENST00000399161 D834D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr16:48595971 C>T maps to NM_153029.3 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:33018028 G>A maps to NM_033111.3 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr13:21306019 G>A maps to NM_174928.1 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:153195524 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:41899935 G>T maps to NM_024561.4 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:88557185 G>T maps to NM_024635.3 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:88593189 T>C maps to NM_024635.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:175520972 C>A maps to NM_207015.2 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr19:13246329 G>A maps to NM_052876.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:66857469 C>A maps to ENST00000359087 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr16:66842913 A>G maps to ENST00000359087 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:164069567 C>A maps to NM_138386.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr4:164061372 A>C did not map to a codon.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr22:42466292 C>A maps to NM_000262.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:40693094 G>T maps to NM_000263.3 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr5:70308328 G>A maps to NM_004536.2 Y138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:102029338 C>A maps to NM_052867.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr13:101736092 G>A maps to NM_052867.2 I1184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:105908953 C>T maps to NM_005746.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:72433067 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:92927555 C>A did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:92928038 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:2972544 C>A maps to ENST00000399624 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:47996702 G>T maps to NM_003827.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:50865455 G>T maps to NM_004851.1 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:80441625 C>A maps to ENST00000374611 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr15:60720651 T>C maps to NM_024611.4 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr15:60734741 T>C maps to NM_024611.4 Q766Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr15:60758801 G>C maps to NM_024611.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr15:60734669 T>C maps to NM_024611.4 E790E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr18:55273958 A>G maps to NM_004539.3 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:78285491 A>G maps to NM_024678.4 C14C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr11:78279746 A>G maps to NM_024678.4 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr12:78415550 C>T maps to NM_014903.4 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:78400533 G>T maps to NM_014903.4 G406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:78400517 G>A maps to NM_014903.4 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:78400773 G>T maps to NM_014903.4 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:78573311 C>T maps to NM_014903.4 I1767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:78582426 T>C maps to NM_014903.4 G1953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr12:78510557 T>C maps to NM_014903.4 D881D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr12:78591082 A>G maps to NM_014903.4 G2094G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr12:78582113 T>C maps to NM_014903.4 R1937R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr2:15415751 A>T maps to NM_015909.2 P1860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr13:36006463 C>T maps to ENST00000400445 R2080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr13:36223947 C>T maps to ENST00000400445 R2622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr13:35615219 C>A maps to ENST00000400445 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr3:47042528 C>T maps to NM_015175.1 N1448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr1:19983483 G>T maps to NM_182744.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr8:90990527 T>C maps to NM_002485.4 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr8:90958455 G>T maps to NM_002485.4 S661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:16918426 C>T maps to NM_017940.3 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr1:148004715 C>A maps to ENST00000310701 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr21:22881328 C>T maps to NM_004540.2 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr21:22746199 C>T maps to NM_004540.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr7:158482624 A>T maps to NM_017760.5 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr9:100407909 T>C maps to NM_002486.4 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr9:100431156 C>T maps to NM_002486.4 D682D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr9:100413598 C>T maps to NM_002486.4 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr1:36030903 G>C maps to NM_001014839.1 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr3:136646962 A>G maps to NM_006153.4 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr2:183866719 A>T maps to NM_205842.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr12:54914543 T>C maps to NM_005337.4 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:133538651 G>A maps to NM_207363.2 A1674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr2:133540045 T>C maps to NM_207363.2 E1446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr2:133541425 C>T maps to NM_207363.2 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr12:50190652 C>T maps to NM_001037806.3 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr2:232326410 A>G maps to NM_005381.2 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:232323763 G>T maps to NM_005381.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr20:46255825 A>G maps to NM_181659.2 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr20:46279838 G>A maps to NM_181659.2 Q1255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:46275933 G>T maps to NM_181659.2 G1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:33329435 C>A maps to NM_014071.2 E1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr17:16004936 T>A maps to ENST00000395857 K789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr12:124840067 C>T maps to NM_006312.4 P1104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr16:15790582 C>T maps to NM_001143979.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:23931680 G>A maps to NM_002487.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr14:21489992 G>A maps to NM_201537.1 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:35288784 G>A maps to ENST00000373803 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr16:58545392 G>T maps to NM_001130487.1 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr5:149927841 C>T maps to NM_001543.4 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr2:240960761 G>A maps to ENST00000404554 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:41689206 G>A maps to NM_016013.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr14:92588001 T>G maps to NM_004545.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:206991505 G>T maps to ENST00000455934 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:161179283 G>T maps to NM_004550.4 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr11:47603713 C>G maps to NM_004551.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:44317063 C>T maps to NM_021075.3 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:152393737 C>A maps to NM_001164507.1 E7039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr2:152500442 G>A maps to NM_001164507.1 C2615C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:152349880 C>A maps to NM_001164507.1 E8251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:152423965 G>A maps to NM_001164507.1 Q5958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:152554087 G>A maps to NM_001164507.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr2:152402488 C>T maps to NM_001164507.1 K6830K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:21177027 C>A maps to ENST00000430741 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:21124509 C>A maps to ENST00000430741 G461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:56122105 C>A maps to ENST00000508342 G1317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr15:56207628 G>A maps to ENST00000508342 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:56010289 C>T maps to NM_001144967.1 N510N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr22:29885563 A>G maps to NM_021076.3 E645E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr22:29885566 A>C maps to NM_021076.3 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:29881819 G>T maps to NM_021076.3 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:24810435 C>A maps to ENST00000221169 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr8:24813786 G>A maps to ENST00000221169 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr8:24772211 G>A maps to NM_005382.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr4:178283451 T>C maps to NM_018248.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr4:170523706 T>C maps to ENST00000507142 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr4:170345769 T>C maps to ENST00000507142 K1052K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:27326179 G>A maps to ENST00000396636 R643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:52725363 C>T maps to NM_002498.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:52693532 C>A maps to NM_199289.1 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:52682523 G>A maps to NM_199289.1 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:198248096 T>C maps to NM_133494.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr17:27064864 C>T maps to NM_178170.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:20805359 C>T maps to NM_006157.3 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:44913949 G>A maps to NM_001145107.1 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr1:156640307 C>T maps to NM_006617.1 T1224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr1:156640421 C>T maps to NM_006617.1 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:70417352 G>A maps to NM_153181.2 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr2:242758325 G>A maps to NM_001167599.1 K482K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr2:182543515 G>A maps to NM_002500.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:55420597 G>A maps to NM_021191.2 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr7:31378714 G>A maps to NM_022728.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:113436163 G>A maps to NM_024019.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr17:29528488 C>T maps to NM_001042492.2 R416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr17:29664407 A>G maps to NM_001042492.2 R2150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:29592342 T>G maps to NM_001042492.2 Y1607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr17:29496929 T>C maps to NM_001042492.2 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr17:29562980 C>T maps to NM_001042492.2 R1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr17:29546135 G>A maps to NM_001042492.2 E547E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr17:29684029 A>G maps to NM_001042492.2 S2597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr17:29509616 T>C maps to NM_001042492.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr17:29556850 A>T did not map to a codon.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr17:29664407 A>G maps to NM_001042492.2 R2150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr17:29496966 T>C maps to NM_001042492.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr17:29556398 T>C maps to NM_001042492.2 G922G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr17:29486044 T>C maps to NM_001042492.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr17:29684000 C>T maps to NM_001042492.2 Q2588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr22:30038188 A>G did not map to a codon.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr22:30035155 A>G maps to NM_181832.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr22:30038258 C>A maps to NM_181832.2 Y144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr22:30050665 T>C maps to NM_181832.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr22:30035155 A>G maps to NM_181832.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr22:30054175 A>G did not map to a codon.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr1:204985633 G>A maps to ENST00000367172 T1337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:50048814 G>A maps to NM_012340.3 F837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr16:68156206 T>C maps to NM_173165.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr14:24844903 C>T maps to NM_001136022.1 R701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:178096192 C>A maps to NM_006164.3 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr2:178098831 G>A maps to NM_006164.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:26217628 G>T maps to NM_004289.6 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:94171812 C>A maps to NM_005384.2 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr4:103459064 A>G maps to NM_003998.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr4:103505913 C>A maps to NM_003998.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:35871251 G>A maps to NM_020529.2 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:36387422 C>T maps to ENST00000352614 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr6:44233392 G>A maps to NM_004556.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr8:145661319 G>A maps to NM_013432.4 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr8:145667647 G>A maps to NM_013432.4 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr4:47907325 A>G maps to NM_152995.4 Y148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr2:233834940 T>C maps to NM_019850.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr17:47587819 G>A maps to NM_002507.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr23:102632731 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:25775391 G>A maps to NM_018297.3 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:25761040 G>A maps to NM_018297.3 V625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:103911023 T>G maps to NM_139173.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr4:103867923 C>T maps to NM_139173.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:220012381 G>A maps to NM_024782.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr23:17750347 T>C did not map to a codon.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr23:17743892 A>G did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:17745015 G>A did not map to a codon.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr23:17750557 G>T did not map to a codon.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr23:71358765 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:71360157 C>A did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:71360008 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:71351946 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr23:71359118 G>T did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:71358927 G>T did not map to a codon.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr23:71360136 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:236141259 G>A maps to NM_002508.2 G1217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:236143892 G>A maps to NM_002508.2 D1096D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:236157152 G>A maps to NM_002508.2 C849C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:51224740 G>A maps to NM_020921.3 R1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:51228516 G>A maps to NM_020921.3 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:37019432 A>G maps to NM_133433.3 E1647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:52526284 C>T maps to NM_007184.3 F1434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:52518631 G>A maps to NM_007184.3 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr3:52522564 G>T maps to NM_007184.3 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:161088608 C>T maps to NM_005600.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:100064473 G>T maps to NM_020202.4 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr23:119064063 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:50666239 C>T maps to NM_033119.3 C248C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr23:118724854 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:70384116 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:70389217 C>T did not map to a codon.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr23:70387355 G>A did not map to a codon.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr23:5821192 C>A did not map to a codon.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr23:5821677 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:5811343 T>C did not map to a codon.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr23:5821697 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:5821227 G>A did not map to a codon.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr23:5947387 G>A did not map to a codon.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr23:5811129 C>A did not map to a codon.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr23:5811130 G>A did not map to a codon.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr24:16734311 C>A did not map to a codon.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr24:16734127 A>T did not map to a codon.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr24:16953117 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:26449739 T>C maps to NM_016231.4 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:5461801 G>A maps to NM_033004.3 F738F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:7981568 C>T maps to NM_176821.3 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:56329309 A>C maps to NM_145007.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr19:56320619 G>A maps to NM_145007.3 N452N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:54297341 C>T maps to ENST00000391773 A1050A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:54313910 A>G maps to ENST00000391773 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr19:54301645 G>A maps to ENST00000391773 G927G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr19:54314024 G>A maps to ENST00000391773 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:56436022 C>A maps to NM_176810.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr19:56443515 A>G maps to NM_176810.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:7067968 G>T maps to NM_176822.3 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:7081259 C>A maps to NM_176822.3 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr11:7083735 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:55489156 C>T maps to NM_017852.3 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:55508819 C>A maps to NM_017852.3 T1005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr19:55493980 C>T maps to NM_017852.3 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr1:247611784 C>A maps to NM_004895.4 V1030V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:247586590 G>T maps to NM_004895.4 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr19:56370507 C>T maps to NM_134444.4 N583N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr19:56369445 C>T maps to NM_134444.4 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:56370481 G>T maps to NM_134444.4 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:56369922 G>A maps to NM_134444.4 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr19:56369202 A>G maps to NM_134444.4 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:56515267 A>G maps to NM_153447.4 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:56538690 C>T maps to NM_153447.4 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr19:55450707 G>A maps to ENST00000446217 H521H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr19:55450707 G>A maps to ENST00000446217 H521H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:56467355 G>A maps to NM_176811.2 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:56466500 G>A maps to NM_176811.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:56241246 C>T maps to NM_176820.2 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:56243393 G>T maps to NM_176820.2 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr19:56241219 A>T maps to NM_176820.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr11:119045974 C>T maps to NM_024618.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr6:142396913 C>T maps to NM_002511.2 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:160942825 G>A maps to ENST00000472947 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr1:169279274 C>A maps to NM_013330.3 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:10042654 G>T maps to NM_022787.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr3:139280234 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:151784023 G>T maps to NM_020167.4 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:114167341 G>T maps to NM_006169.2 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr5:43656776 C>A maps to NM_182977.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr5:43704484 T>A maps to NM_182977.2 V1080V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr5:43649357 A>G maps to NM_182977.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:144096941 A>G maps to ENST00000467773 N354N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:96112798 C>A maps to NM_022451.9 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr17:65732800 T>C maps to NM_015462.3 H358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:31432849 G>A maps to NM_003787.4 R625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr9:33463382 G>A maps to NM_022917.4 R1017R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:95060161 G>A maps to NM_017948.5 R1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr10:103912175 C>T maps to ENST00000405356 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr10:103921965 C>T maps to ENST00000405356 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr16:14976467 C>T maps to ENST00000456867 H1015H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr16:16357001 C>T maps to ENST00000263012 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr23:70517754 G>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:2959398 G>A maps to NM_003703.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:2952959 G>A maps to NM_003703.1 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:6672890 C>A maps to ENST00000382421 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:117703129 G>A maps to ENST00000338101 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:117723131 G>A maps to ENST00000338101 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:117726000 G>T maps to ENST00000338101 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:162337007 C>T maps to NM_014697.2 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:162257185 C>A maps to NM_014697.2 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr17:26101432 G>T maps to NM_000625.4 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:169721372 G>T maps to NM_001171631.1 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr9:139390674 C>A maps to NM_017617.3 E2506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr9:139395240 G>A maps to NM_017617.3 N1899N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:120462974 G>A maps to NM_024408.2 R1786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:120459238 G>A maps to NM_024408.2 R2036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:120468217 C>T maps to NM_024408.2 S1407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr1:120491705 A>G maps to NM_024408.2 P841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:145281450 C>T maps to ENST00000454606 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:15289905 C>T maps to NM_000435.2 A1216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr6:32163251 C>A maps to NM_004557.3 E1992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:32166817 G>A maps to NM_004557.3 R1474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:32183112 C>T maps to NM_004557.3 K637K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr8:120428843 T>C maps to NM_002514.3 H24H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:27064619 G>A maps to ENST00000449198 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr14:27066567 C>T maps to ENST00000449198 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:46444011 G>A maps to NM_002516.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:46443210 G>A maps to NM_002516.2 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr23:100117756 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:89135606 C>A maps to NM_016931.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:69341381 C>T maps to NM_024505.3 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr19:47543773 G>A maps to NM_002517.2 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr14:34269534 C>A maps to NM_001164749.1 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr14:33684438 G>T maps to NM_001164749.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:66192121 G>A maps to NM_178864.3 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr11:108044480 T>C maps to NM_002519.2 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:21125097 C>A maps to NM_000271.4 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr20:57289016 C>T maps to NM_024663.3 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:110926030 C>A maps to NM_000272.3 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:5935091 C>T maps to NM_015102.2 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr19:36332648 G>T maps to NM_004646.3 S928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:182783967 G>A maps to NM_030769.1 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr9:35792683 C>T maps to NM_003995.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr7:34698056 T>C maps to NM_207172.1 D11D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr7:98257796 C>T maps to NM_002523.2 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:98254333 C>T maps to NM_002523.2 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr7:24324906 G>T maps to NM_000905.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:156136029 C>T maps to NM_000910.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:69752151 T>C maps to NM_000903.2 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr6:3010338 C>T maps to NM_000904.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr23:30322816 C>T did not map to a codon.
Multiple mappings detected for codon TCGA-DC-6682-01A-11D-1826-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr12:100930769 G>A maps to ENST00000392986 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:161200916 G>T maps to NM_001077482.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr6:108502831 G>A maps to ENST00000368983 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr15:72106356 G>A maps to NM_014249.2 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:142680268 C>A maps to NM_001024094.1 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:142779552 G>A maps to NM_001024094.1 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:142661456 C>T maps to NM_001024094.1 K778K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr4:149181258 G>A maps to ENST00000511528 R590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr1:200012983 G>A maps to NM_205860.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:127302448 G>A maps to NM_033334.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:115393891 G>T maps to ENST00000369358 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr1:115258727 T>C maps to NM_002524.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr2:27664624 C>T maps to ENST00000379863 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr7:107790560 C>A maps to ENST00000379032 G1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr1:52275052 C>A maps to NM_002525.2 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:52285469 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:32505544 C>A maps to NM_013959.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr5:139245140 A>G maps to NM_013982.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr10:84745019 G>T maps to ENST00000404547 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr23:105132355 T>C did not map to a codon.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:105159725 A>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:105167181 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:105190452 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:105137870 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:105167406 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:105189938 A>C did not map to a codon.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr23:105190319 T>A did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:105153286 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:5999313 G>A maps to NM_016588.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr2:206608149 A>G maps to NM_201266.1 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:206608212 C>T maps to NM_201266.1 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr2:51254919 G>T maps to ENST00000404971 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr2:50149357 C>T maps to ENST00000404971 P1456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:50779857 A>G maps to ENST00000404971 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr2:50699460 G>A maps to ENST00000404971 N1113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr2:51254946 G>A maps to ENST00000404971 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:50779938 G>A maps to ENST00000404971 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr5:176721700 G>A maps to NM_022455.4 Q2444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr5:176721628 T>C maps to NM_022455.4 P2420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:152031183 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:152034496 C>T did not map to a codon.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr8:59518549 G>T maps to NM_001144772.1 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr8:59535795 T>C maps to NM_001144772.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:59522171 G>A maps to NM_001144772.1 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:72718371 C>T maps to NM_148956.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr10:18937508 T>C maps to NM_182543.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr10:18937508 T>C maps to NM_182543.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:18765848 G>A maps to ENST00000455492 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:86194983 G>A maps to NM_002526.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr11:132082036 C>A maps to NM_001144058.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:96104369 G>A maps to NM_021229.3 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr9:135073642 C>T maps to NM_032536.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr9:87563462 C>G maps to NM_006180.3 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:11802177 G>T maps to NM_012344.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr2:11798793 G>A maps to NM_012344.3 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:106464624 G>A maps to NM_014840.2 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr12:106480538 G>A maps to NM_014840.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:151064177 C>T maps to ENST00000355851 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr19:49409125 C>T maps to NM_006184.5 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:49404074 G>T maps to NM_006184.5 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:17351715 G>T maps to ENST00000458064 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:205698727 G>T maps to NM_022731.4 Y13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr8:110293375 A>G maps to NM_032869.3 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr8:110293396 A>C maps to NM_032869.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:2289560 C>T maps to NM_198954.1 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:51239149 G>A did not map to a codon.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr11:63995077 C>G maps to NM_032344.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:63995104 C>A maps to NM_032344.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:63994435 G>A maps to NM_032344.2 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:77775651 C>A maps to NM_001105663.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr14:73753995 G>A maps to NM_001005743.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:69103820 G>T maps to NM_020401.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr1:229623210 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:17637603 C>T maps to ENST00000430136 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr5:37307496 C>T maps to NM_153485.1 T935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:47833756 T>G maps to NM_015231.1 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:131767473 C>T maps to NM_015354.1 R1495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr7:135300733 C>T maps to NM_015135.2 T1127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr9:134072981 C>T maps to ENST00000451030 G1368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr22:45571914 T>C maps to NM_007172.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:50411699 G>A maps to NM_012346.4 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:56852628 C>T maps to NM_014669.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr7:23239114 T>C maps to ENST00000413919 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:102334942 C>A did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:102337990 T>C did not map to a codon.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr23:101096736 C>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:101096513 C>T did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr17:722688 G>A maps to NM_022463.3 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:8791029 T>C maps to NM_152745.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr14:24886264 G>A maps to NM_025081.2 E1770E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:24886144 C>A maps to NM_025081.2 I1730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr12:113403674 C>T maps to NM_006187.2 R844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:121458597 G>A maps to NM_003733.2 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr2:192543402 A>G maps to NM_001031716.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:138438724 C>T maps to NM_014582.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr9:138438640 C>T maps to NM_014582.2 Y30Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:228505602 G>A maps to NM_001098623.1 P4620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:228538554 C>T maps to NM_001098623.1 F6110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr1:228526605 C>T maps to NM_001098623.1 Q5713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr1:228468142 C>T maps to NM_001098623.1 R2643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr1:228560699 T>C maps to NM_001098623.1 D7407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:228494621 C>T maps to NM_001098623.1 R3983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr1:228494621 C>T maps to NM_001098623.1 R3983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr1:228525709 G>A maps to NM_001098623.1 T5622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:28117043 C>A maps to NM_000275.2 E702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr15:28196948 A>C maps to NM_000275.2 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr7:5922226 G>A maps to NM_001097622.1 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr23:128691336 A>G did not map to a codon.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr23:128691369 C>A did not map to a codon.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr23:128703309 T>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:128709966 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:128720980 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:103564261 C>T maps to NM_024410.3 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:103564038 C>T maps to NM_024410.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:131233696 G>A maps to NM_153435.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:86820226 C>A maps to ENST00000370567 E556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:86824558 C>A maps to ENST00000370567 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:86847935 C>A maps to ENST00000370567 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:86852673 C>A maps to ENST00000370567 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:199941 A>G did not map to a codon.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr17:8249109 A>C maps to NM_153007.4 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr23:123695613 C>A did not map to a codon.
Sequencing variant TCGA-AG-3582-01A-01W-0831-10 chr23:123780571 A>G did not map to a codon.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr23:123526025 G>A did not map to a codon.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr23:123517986 G>A did not map to a codon.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr23:124029954 T>C did not map to a codon.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr23:123514918 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:123515050 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:123519907 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:123779182 G>T did not map to a codon.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr23:123554301 A>G did not map to a codon.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:123630873 C>A did not map to a codon.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr23:123554279 G>T did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:123631096 T>C did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:124030054 A>G did not map to a codon.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr23:123517633 T>C did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:123514663 G>A did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:124029954 T>C did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr23:123514420 G>A did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr23:123517632 C>T did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr23:123787614 G>A did not map to a codon.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr23:123630961 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:167630769 C>T maps to NM_001122679.1 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr5:167617453 G>A maps to NM_001122679.1 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr5:167420158 C>A maps to NM_001122679.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr4:183696125 C>T maps to NM_001080477.1 Y1708Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:183675615 T>C maps to NM_001080477.1 L1366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:183713935 G>A maps to NM_001080477.1 T2037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:183714058 G>A maps to NM_001080477.1 T2078T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:183664509 C>T maps to NM_001080477.1 G1189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:183713467 C>T maps to NM_001080477.1 F1881F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr4:183696104 C>T maps to NM_001080477.1 D1701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:78380282 G>T maps to NM_001098816.2 V2369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:78381068 G>T maps to NM_001098816.2 L2107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:78381548 G>A maps to NM_001098816.2 F1947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:78433867 G>T maps to NM_001098816.2 I1215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:13764499 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:13764900 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:13762614 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:13769386 G>T did not map to a codon.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr10:50946052 G>A maps to NM_018245.2 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr6:72006227 C>T maps to NM_024576.3 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:9793481 C>T maps to NM_016821.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:70782801 A>G did not map to a codon.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr23:70757808 C>T did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:70757810 T>C did not map to a codon.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr10:74673222 C>T maps to NM_152635.1 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:9971410 G>A maps to NM_058164.2 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr1:102296358 C>A maps to ENST00000338858 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr1:161967993 G>A maps to ENST00000451379 N366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:161954714 A>G maps to ENST00000451379 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:10324612 T>A maps to NM_002543.3 K22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:58999993 C>A maps to NM_145243.3 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr9:95179144 A>G maps to NM_005014.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr9:95179144 A>G maps to NM_005014.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr15:53049844 G>A maps to NM_004498.1 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr11:132307149 C>T maps to NM_002545.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr11:132290087 C>G maps to NM_002545.3 *346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr11:132527045 C>T maps to NM_002545.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr23:67283719 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:67421470 T>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:67652710 C>A did not map to a codon.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr23:67283809 T>C did not map to a codon.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:153420111 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:153421915 G>A did not map to a codon.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr23:153420183 C>T did not map to a codon.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr1:241767753 C>T maps to NM_014322.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr1:29189596 C>T maps to NM_000911.3 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:54142009 G>A maps to NM_000912.3 Y330Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:6891617 C>T maps to NM_001004460.1 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr11:6867548 C>T maps to ENST00000379831 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:7949551 G>A maps to NM_001004461.1 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:22102677 A>C maps to NM_001005466.1 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr11:123886823 G>T maps to NM_001004462.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr19:15918640 G>A maps to NM_013940.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:15917910 C>A maps to NM_013940.2 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr19:15839059 C>T maps to NM_013939.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr11:123847891 G>A maps to NM_001004474.1 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:29394863 G>A maps to NM_013937.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:20666351 T>G maps to NM_001005503.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr14:20711204 C>T maps to NM_001004479.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr9:107298551 G>A maps to NM_001001961.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:107267242 C>T maps to NM_001004485.1 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:130678060 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:130678728 C>T did not map to a codon.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr1:248512496 C>T maps to NM_001001918.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr1:247920898 G>A maps to NM_012353.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:2995870 G>T maps to NM_002548.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:15198472 C>T maps to NM_001004713.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:125273355 C>A maps to ENST00000444856 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr9:125282096 C>A maps to NM_001004452.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:125563048 C>T maps to NM_080859.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:125512902 C>T maps to ENST00000373684 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:57982521 T>C maps to NM_001004458.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:144015543 C>T maps to NM_001005287.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr7:143826870 C>T maps to NM_001001659.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr11:6789690 G>A maps to NM_001004490.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr1:247614761 G>T maps to NM_001004492.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr1:247614572 G>A maps to NM_001004492.1 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr6:29054977 G>T maps to NM_001005226.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr1:247695309 C>T maps to NM_198074.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:6942289 G>T maps to NM_001004684.1 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:6942351 G>A maps to NM_001004684.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr1:247751750 A>G maps to NM_001001915.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:248685810 T>C maps to NM_001013355.1 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:29430434 C>T maps to NM_030883.3 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:248262823 C>T maps to NM_175911.2 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:248224425 G>A maps to NM_001004687.1 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr1:248402331 C>A maps to NM_017504.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr1:248402565 T>C maps to NM_017504.1 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr1:248403030 G>A maps to NM_017504.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:248308949 C>A maps to NM_001004690.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:35957486 C>T maps to NM_019897.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:248570398 C>A maps to NM_030904.1 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:248569429 C>T maps to NM_030904.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:248436681 C>T maps to NM_001004695.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:248737749 C>T maps to NM_001001821.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:29012508 G>T maps to NM_030903.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr17:3182181 G>A maps to NM_002551.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr11:55110865 T>C maps to NM_001005274.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:51412359 G>A maps to NM_001005272.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:55322891 T>G maps to NM_001001920.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:56232577 G>T maps to NM_012374.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:59244932 G>T maps to NM_001004705.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr17:56247303 C>T maps to NM_001004707.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:22134222 G>A maps to NM_001001912.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:102358715 C>A maps to NM_001001674.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr1:69539 G>T maps to NM_001005484.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr14:20404493 C>T maps to NM_001004063.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:20483340 C>T maps to NM_001004712.1 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:20444435 C>A maps to NM_001005486.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:20344473 G>A maps to NM_001005501.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:20248759 C>A maps to NM_001005500.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:22369078 C>T maps to NM_001004719.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr14:20296293 T>C maps to NM_001004723.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:20296065 T>C maps to NM_001004723.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr14:20215735 A>G maps to NM_172194.1 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr14:20215705 G>A maps to NM_172194.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr11:4928865 C>T maps to NM_001004749.1 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr11:5345395 G>C maps to NM_033180.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr11:4843562 C>T maps to NM_001004753.1 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:5020889 T>A maps to NM_001004755.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr11:5020475 G>A maps to NM_001004755.1 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:4903503 C>T maps to NM_001004759.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:5221879 C>T maps to NM_001004760.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:5153355 G>A maps to NM_001005160.2 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:4388942 G>A maps to NM_001005161.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:4389009 C>T maps to NM_001005161.3 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr11:5603050 G>A maps to NM_001005162.2 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:5602882 C>A maps to NM_001005162.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr11:5080594 C>T maps to NM_001005164.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:5906455 G>T maps to NM_001005165.1 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:5906118 C>A maps to NM_001005165.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:4510906 C>A maps to NM_001005171.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:6008034 C>T maps to NM_001005173.2 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr11:6007248 C>T maps to NM_001005173.2 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr11:6048640 C>T maps to NM_001001917.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr11:59210835 C>T maps to NM_001004728.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr11:59211279 G>A maps to NM_001004728.1 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr11:59211351 A>G maps to NM_001004728.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr11:59211349 C>T maps to NM_001004728.1 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:59132602 C>T maps to NM_001004729.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr11:59132242 C>A maps to NM_001004729.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr11:55798205 C>T maps to NM_001001921.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:55798271 C>A maps to NM_001001921.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:58206880 G>T maps to NM_001004733.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:58207352 A>T maps to NM_001004733.2 L91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr11:58190125 A>G maps to NM_001005566.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr11:58275302 G>A maps to NM_001005218.1 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:125551744 C>A maps to NM_001001923.1 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr9:125551915 C>T maps to NM_001001923.1 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr11:55541197 T>A maps to NM_001001967.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr11:55606640 C>A maps to NM_001005496.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr11:55587893 C>G maps to ENST00000395203 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr11:55587290 T>C maps to ENST00000395203 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr3:97888301 C>A maps to NM_001005515.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr3:97983496 T>A maps to NM_001005479.1 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:55703222 G>T maps to NM_006637.1 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:55944803 C>A maps to NM_001005492.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:98110132 C>A maps to NM_001005516.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:98109640 T>C maps to NM_001005516.1 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:55579580 C>T maps to NM_001004738.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr11:56184841 G>T maps to NM_001004744.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:6816051 G>A maps to NM_003696.2 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:143701793 G>A maps to NM_001005281.1 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr12:55714820 T>C maps to NM_001005182.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:55846218 C>A maps to NM_054105.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:55726053 G>A maps to NM_054104.1 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:55945507 C>T maps to NM_001005494.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr12:55886496 T>A maps to NM_001005519.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:247875553 G>A maps to NM_001005286.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr1:158725621 T>G maps to NM_001005184.1 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:123624671 G>A maps to NM_001005188.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr1:158517532 A>T maps to NM_001005189.1 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr19:14952077 C>T maps to NM_001005190.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr19:14910360 G>A maps to NM_198944.1 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:15052890 C>T maps to NM_012377.1 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9362411 G>T maps to NM_001079935.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9213277 G>T maps to NM_001005193.1 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9236888 G>A maps to NM_001001958.1 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr11:56058004 G>A maps to NM_001005199.1 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr11:56057869 G>T maps to NM_001005199.1 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr11:55872964 T>C maps to NM_001005200.1 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr11:55890363 C>T maps to NM_001005201.1 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr11:55861212 C>T maps to NM_001003750.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr11:55861576 C>A maps to NM_001003750.1 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:56086720 A>G maps to NM_001005202.1 *313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr11:56086255 A>G maps to NM_001005202.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr11:55927007 G>T maps to NM_001004058.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr12:48921792 C>T maps to NM_001005203.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:141618902 C>T maps to NM_001001656.1 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:141619010 C>T maps to NM_001001656.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:57947557 C>A maps to NM_001005212.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr11:57958120 T>C maps to NM_001005283.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:69482346 C>T maps to NM_153451.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr7:103801609 C>G maps to NM_002553.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:58111684 C>T maps to NM_006812.3 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:31725524 G>A maps to NM_017784.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:125295034 C>A maps to NM_022776.4 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr18:21897127 A>G maps to NM_080597.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr20:60859122 C>T maps to NM_144498.1 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr11:3143292 G>A maps to NM_020896.3 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:3123490 G>A maps to NM_020896.3 N449N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr2:179247880 T>C maps to ENST00000392505 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:179214084 G>A maps to ENST00000392505 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr12:76780013 G>A maps to NM_020841.4 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:30660018 T>C maps to NM_020530.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr5:38932600 T>C maps to NM_003999.2 P777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr5:38904526 C>T maps to NM_003999.2 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr5:38924609 C>T maps to NM_003999.2 Q653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr2:19553320 C>T maps to NM_145260.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr23:38260658 T>G did not map to a codon.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr23:38211974 T>A did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:38211985 G>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:26684961 G>T maps to NM_194248.2 I1760I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:4199684 G>A maps to NM_177998.1 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:72923855 T>G maps to NM_178160.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:76932774 G>A maps to NM_032109.2 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr4:146072023 T>G maps to ENST00000447906 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:69282895 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:92083454 G>T maps to NM_016023.3 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:57269057 G>A maps to NM_021728.2 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:7716870 G>T maps to NM_198185.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr1:111957637 G>T maps to ENST00000369728 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:41850251 G>A maps to NM_000436.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr3:16312563 C>T maps to NM_138381.3 H35H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:107715280 G>T maps to NM_001198533.1 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr3:38292939 C>T maps to NM_005109.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr11:57135906 A>G maps to NM_002559.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:121659732 C>T maps to NM_002560.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:121666357 G>T maps to NM_002560.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:3592887 C>T maps to ENST00000435558 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr12:121570847 T>C maps to NM_002562.5 N25N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:78216070 C>T did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr23:78216665 T>A did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:78216070 C>A did not map to a codon.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr11:73007691 G>A maps to NM_004154.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:1584786 C>T did not map to a codon.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr10:74804761 C>T maps to NM_001142595.1 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr10:74810942 T>C maps to NM_000917.3 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:74015428 C>A maps to NM_182904.3 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr11:74009334 T>C maps to NM_182904.3 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr17:79813415 C>T maps to NM_000918.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:49039997 C>T maps to NM_177938.2 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr3:49044279 C>A maps to NM_177938.2 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr20:43567343 A>T maps to NM_001124756.1 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr23:90690911 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:90690927 G>T did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr16:88932295 C>T maps to NM_001080487.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:163735865 C>T maps to NM_152410.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:43287078 G>A maps to NM_001184970.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:17567230 C>T maps to NM_013358.2 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:17413183 G>A maps to NM_007365.2 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr1:17708468 G>A maps to NM_207421.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:39877396 T>C maps to NM_019088.2 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr1:26303228 T>C maps to NM_000437.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:26316059 T>C maps to NM_000437.3 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr23:49454024 C>T did not map to a codon.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr23:55117791 A>G did not map to a codon.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr23:55117792 A>G did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr23:55247040 G>A did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr12:103249073 T>C maps to NM_000277.1 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:57318157 C>T maps to NM_001079525.1 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr5:138700308 G>A maps to NM_001033112.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:196509532 G>T maps to NM_002577.4 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr3:196530012 A>G maps to NM_002577.4 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr3:196530021 C>T maps to NM_002577.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr23:110463651 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:110439115 G>A did not map to a codon.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr23:110366489 A>G did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:110463670 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:9561417 C>A maps to NM_177990.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr20:9520156 A>G maps to NM_177990.2 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr20:9525072 A>G maps to NM_177990.2 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:23647325 C>A maps to NM_024675.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:35496274 G>A maps to NM_015430.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:35513592 G>A maps to NM_015430.2 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr13:28851444 A>G maps to NM_175854.7 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr10:91404387 C>T maps to NM_148977.1 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:3888858 G>A maps to NM_153638.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr1:2451297 G>A maps to ENST00000425477 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr22:50617504 G>A maps to NM_052839.3 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr22:50617526 C>T maps to NM_052839.3 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:135197515 G>A maps to NM_152911.2 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:6746443 G>T maps to NM_006999.4 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr14:73729496 C>T maps to ENST00000427855 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr14:73730427 C>T maps to ENST00000427855 D933D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:4901282 G>A maps to NM_020144.4 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:61024274 C>T maps to NM_022894.3 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr9:119028243 T>C maps to NM_002581.3 C947C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr9:118950321 C>T maps to NM_002581.3 H435H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr9:119033667 C>T maps to NM_002581.3 R976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:176526001 G>T maps to NM_020318.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr1:176525832 G>A maps to NM_020318.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr1:176564626 C>T maps to NM_020318.2 H629H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr1:176668548 G>T maps to NM_020318.2 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr3:142681548 G>A maps to NM_198504.2 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:162475137 G>A maps to NM_004562.2 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr4:75937815 T>G maps to NM_015393.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr16:14693793 T>C maps to NM_002582.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr7:139727182 C>T maps to NM_022750.2 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr3:122437032 G>T maps to NM_017554.2 L1372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:122411158 G>T maps to NM_017554.2 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:122446780 C>T maps to NM_017554.2 S1688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:20819269 C>A maps to NM_005484.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:20820418 G>A maps to NM_005484.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:25060322 G>A maps to NM_006437.3 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr22:44489859 C>T maps to NM_001003828.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr23:150842516 A>G did not map to a codon.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr23:150840873 A>G did not map to a codon.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr23:150840855 A>T did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:150842516 A>G did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:150842514 T>C did not map to a codon.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr11:125616234 G>T maps to NM_138294.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:125647895 C>T maps to NM_212555.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr2:223163316 G>A maps to NM_181459.3 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:127254557 C>T maps to NM_006193.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr9:37015163 A>G maps to NM_016734.1 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr9:37015163 A>G maps to NM_016734.1 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:31823108 G>A maps to NM_001604.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:19062433 C>A maps to NM_002584.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:52702600 C>T maps to ENST00000296302 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr3:52643684 T>C maps to ENST00000296302 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr19:19675817 C>T maps to NM_025245.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:66638918 G>A maps to NM_022172.2 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr11:66639504 C>T maps to NM_022172.2 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr3:51994282 G>A maps to NM_033010.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:100809576 G>T maps to NM_000282.3 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr4:134072611 C>T maps to NM_032961.1 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr23:91133862 A>C did not map to a codon.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr23:91137943 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:91132096 C>A did not map to a codon.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr23:91873896 G>A did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr23:91873509 C>G did not map to a codon.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr23:91873532 C>T did not map to a codon.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr23:91090627 A>G did not map to a codon.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr24:5605725 C>A did not map to a codon.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr5:141325080 C>T maps to NM_016580.2 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:141337278 G>A maps to NM_016580.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr10:55996622 C>T maps to NM_001142763.1 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr10:55582385 A>G maps to NM_001142763.1 L1707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:55591100 G>T maps to NM_001142763.1 I1397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:55719535 G>T maps to NM_001142763.1 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:55913041 G>A maps to NM_001142763.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:56077173 G>A maps to NM_001142763.1 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:55626440 G>A maps to NM_001142763.1 D1231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr13:58207477 C>T maps to NM_001040429.2 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr13:58208017 C>T maps to NM_001040429.2 D446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr13:58208284 C>T maps to NM_001040429.2 Y535Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:58299274 G>T maps to NM_001040429.2 R1109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr13:58207642 G>C maps to NM_001040429.2 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr13:58299161 T>C maps to NM_001040429.2 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:138442410 C>T maps to NM_019035.3 T1060T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:138452717 C>T maps to NM_019035.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr4:138442722 C>T maps to NM_019035.3 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr23:99551324 G>A did not map to a codon.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:99551676 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:99663285 C>T did not map to a codon.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr23:99551714 C>T did not map to a codon.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:99662659 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:99551364 C>A did not map to a codon.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr23:99663336 T>A did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:99661860 G>A did not map to a codon.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr23:99662055 C>T did not map to a codon.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr13:61986434 T>C maps to NM_022843.3 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr13:61985846 G>A maps to NM_022843.3 F795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr13:61986436 G>A maps to NM_022843.3 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:53418721 C>T maps to NM_002590.2 P1062P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr13:67801642 C>T maps to NM_203487.2 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr13:67799662 G>A maps to NM_203487.2 D970D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr5:140167965 C>T maps to NM_018900.2 N697N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140167281 G>A maps to NM_018900.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr5:140237090 C>T maps to NM_018901.2 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr5:140250688 G>A maps to NM_018902.3 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr5:140249497 C>T maps to NM_018902.3 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr5:140250874 C>T maps to NM_018902.3 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr5:140250829 G>T maps to NM_018902.3 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr5:140256622 G>A maps to NM_018903.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140255896 G>A maps to NM_018903.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr5:140256832 G>A maps to NM_018903.2 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr5:140263463 G>A maps to NM_018904.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:140262566 C>T maps to NM_018904.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:140176478 C>T maps to NM_018905.2 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr5:140175634 C>T maps to NM_018905.2 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:140183256 A>C maps to NM_031497.1 *825Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr5:140182323 C>T maps to NM_018906.2 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr5:140182269 A>G maps to NM_018906.2 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140188589 G>A maps to NM_018907.2 W606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr5:140203402 G>A maps to NM_018908.2 A681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr5:140202970 C>T maps to NM_018908.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr5:140209751 G>A maps to NM_018909.2 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140208971 G>A maps to NM_018909.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr5:140215401 G>A maps to NM_018910.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr5:140221376 G>A maps to NM_018911.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140221232 C>T maps to NM_018911.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr5:140222315 G>A maps to NM_018911.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr5:140230002 C>T maps to NM_031857.1 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140229708 G>A maps to NM_031857.1 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140230008 G>A maps to NM_031857.1 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr5:140229621 C>T maps to NM_031857.1 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr5:140230197 G>A maps to NM_031857.1 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140307514 G>A maps to NM_018898.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr5:140307376 T>C maps to NM_018898.3 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr5:140432200 C>T maps to NM_013340.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr5:140431258 C>T maps to NM_013340.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr5:140590533 G>T maps to NM_018932.3 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr5:140593772 G>A maps to NM_018933.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140594624 C>T maps to NM_018933.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr5:140626408 C>A maps to NM_018935.2 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140626043 G>T maps to NM_018935.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140564257 C>T maps to NM_020957.1 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr5:140475486 C>T maps to NM_018936.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140480530 G>T maps to NM_018937.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140481091 G>T maps to NM_018937.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140482356 C>T maps to NM_018937.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:140503130 G>T maps to NM_018938.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140517136 C>T maps to NM_015669.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr5:140553438 C>T maps to NM_018940.2 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr5:140559747 G>A maps to NM_019120.2 A711A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr5:140558958 C>T maps to NM_019120.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140710706 C>A maps to NM_018912.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr5:140710661 A>G maps to NM_018912.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:140712128 G>A maps to NM_018912.2 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140793452 C>T maps to NM_018913.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140794469 C>A maps to NM_018913.2 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr5:140794235 C>T maps to NM_018913.2 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140801942 C>A maps to NM_018914.2 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140802449 C>T maps to NM_018914.2 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140811552 C>A maps to NM_003735.2 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140812011 C>A maps to NM_003735.2 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr5:140811648 C>T maps to NM_003735.2 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:140719983 C>T maps to NM_018915.2 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140720177 C>A maps to NM_018915.2 S547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140725321 C>T maps to NM_018916.3 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr5:140724409 C>T maps to NM_018916.3 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140744799 C>A maps to NM_018918.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr5:140744082 C>T maps to NM_018918.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140753847 C>T maps to NM_018919.2 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:140754303 C>T maps to NM_018919.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140764511 C>T maps to NM_018920.2 D682D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140730928 C>T maps to NM_018922.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr5:140740386 C>T maps to NM_018923.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140769028 C>T maps to NM_003736.2 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140778758 C>T maps to NM_018925.2 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:140798469 C>A maps to NM_018927.2 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr2:120397421 C>T maps to NM_001029996.3 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:120362778 T>C maps to NM_001029996.3 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr11:82879948 G>T maps to NM_015885.3 G858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:44571739 T>C maps to NM_022104.3 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:56138151 G>T maps to NM_002591.3 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:82585489 C>T maps to NM_033026.5 K1593K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:82389989 G>A maps to NM_033026.5 R5085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:82581541 G>A maps to NM_033026.5 V2909V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:82582693 T>C maps to NM_033026.5 K2525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:82586070 C>A maps to NM_033026.5 E1400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:82785547 C>A maps to NM_033026.5 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr7:82582363 T>G maps to NM_033026.5 S2635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr7:82578911 A>G maps to NM_033026.5 V3664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:17813058 G>T maps to NM_006197.3 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:17814152 G>T maps to NM_006197.3 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:17843509 G>T maps to NM_006197.3 E1442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr20:5099469 A>T maps to NM_002592.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr20:5099466 T>G maps to NM_002592.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:71511996 C>T maps to NM_014982.2 R1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:71575351 G>A maps to NM_014982.2 S2111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:233161101 G>A maps to NM_014801.3 G1465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:95728863 G>A maps to NM_000439.4 Y701Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr20:17434430 C>T maps to NM_002594.2 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr20:17437009 C>T maps to NM_002594.2 Y373Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr15:101938707 G>A maps to NM_002570.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:101933602 G>A maps to NM_002570.3 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:55509559 G>A maps to NM_174936.3 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr5:148743641 C>T maps to NM_024028.3 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:24593378 A>G did not map to a codon.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr23:24625951 C>T did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:24608201 C>T did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr10:105178279 C>T maps to NM_014976.1 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr10:105202055 T>C maps to NM_014976.1 P1598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr10:105203739 C>T maps to NM_014976.1 Y1731Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:170886649 C>T maps to NM_002598.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr19:34900367 C>T maps to NM_032346.1 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr19:34916979 A>G maps to NM_032346.1 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr10:112653928 T>G maps to NM_014456.4 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr10:112641174 G>A maps to NM_014456.4 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr3:33866732 C>T maps to NM_001162429.1 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr3:33855079 T>C maps to NM_001162429.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:165809815 C>A maps to NM_001130690.1 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:178681636 G>T maps to NM_016953.3 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:178936594 G>A maps to NM_016953.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:14882858 C>T maps to NM_000922.3 R945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:10571762 G>A maps to NM_001111307.1 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:120427076 C>A maps to NM_001083.3 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr4:120528115 C>T maps to NM_001083.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr4:120486474 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:76624825 G>A maps to NM_003719.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr5:76621551 C>A maps to NM_003719.3 C196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:157693889 C>T maps to NM_016205.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr4:157732156 T>A maps to NM_016205.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:55127319 A>G maps to NM_006206.4 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:55143645 G>T maps to ENST00000507166 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr4:55133832 G>A maps to NM_006206.4 W349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:149515192 C>A maps to NM_002609.3 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr5:149495376 C>T maps to NM_002609.3 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:19368188 G>T did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:19373555 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:96761852 C>T maps to NM_005390.4 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:58413898 C>T maps to NM_000925.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:34999701 C>A maps to NM_003477.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr3:122869110 G>A maps to NM_006810.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:20384348 G>T maps to NM_174924.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:173460577 G>T maps to ENST00000392571 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:24546234 C>T did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:24537110 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:97007026 C>T maps to NM_020992.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr8:94934355 T>C maps to NM_001161778.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:33316752 C>T maps to ENST00000400481 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr13:33241959 T>C maps to ENST00000400481 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:107475966 G>T maps to NM_020381.3 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr6:107595388 A>G maps to NM_020381.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:38061643 C>T maps to ENST00000442465 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:32074721 C>T maps to NM_178140.2 G1170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:32088932 C>T maps to NM_178140.2 I1793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr23:153070577 T>C did not map to a codon.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr10:119100489 C>G did not map to a codon.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr10:119042952 G>A maps to NM_173791.3 G1097G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:119049714 G>A maps to NM_173791.3 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:73432827 C>T maps to NM_015009.1 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr3:73432899 C>T maps to NM_015009.1 R939R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:41966704 G>A maps to NM_001164595.1 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr12:41957420 C>T maps to NM_001164595.1 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:41966504 G>T maps to NM_001164595.1 E642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr7:94293391 G>A maps to NM_001172437.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:57327214 G>T maps to NM_006210.2 I865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:57326491 G>T maps to NM_006210.2 I1106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:64322273 C>T maps to NM_020651.3 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:17412848 G>A maps to NM_148172.1 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:33968992 G>A maps to NM_000285.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr2:239162194 C>T maps to NM_022817.2 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:7886607 G>T maps to ENST00000377532 E676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr7:92123678 A>G maps to NM_000466.2 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr7:92147523 G>A maps to NM_000466.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:90226609 A>C maps to NM_003847.1 *248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:45937273 G>A maps to NM_057174.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr6:143792158 C>T maps to NM_003630.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr6:42933492 A>G maps to NM_000287.3 I799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:139661035 C>A maps to NM_002622.4 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:54982636 C>A did not map to a codon.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:54987345 A>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:207228091 C>T maps to NM_006212.2 N10N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr12:48535839 T>C maps to NM_001166686.1 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:3155601 C>T maps to NM_002627.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr11:61017284 C>T maps to ENST00000422676 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:44104786 G>T maps to NM_000290.3 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr12:133294356 C>T maps to NM_001170543.1 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:197781227 C>A maps to NM_024989.3 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr2:197735682 A>G maps to NM_024989.3 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:3838695 C>T maps to NM_014489.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr15:34396123 G>A maps to NM_152595.4 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:230472932 G>A maps to ENST00000321327 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr8:97797187 A>G maps to ENST00000325141 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:75416113 G>A maps to ENST00000405431 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:114557651 C>A maps to NM_005023.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:49753712 G>A maps to NM_138733.4 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr4:37847342 G>A maps to NM_018290.3 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:74047776 C>A maps to NM_173582.3 E597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:83892562 C>T did not map to a codon.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr11:100922293 G>A maps to NM_000926.4 R740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:144074942 C>T maps to NM_001100164.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:144086575 C>T maps to NM_001100164.1 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:58381132 C>T maps to NM_080672.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:58416500 C>T maps to NM_080672.3 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:58420258 G>T maps to NM_080672.3 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr20:58416496 G>A maps to NM_080672.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr23:22117214 G>A did not map to a codon.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr23:22065265 G>A did not map to a codon.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr23:22108570 G>A did not map to a codon.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr17:27241004 T>C maps to NM_001033561.1 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:6679924 C>T maps to NM_153812.2 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:11101435 C>T maps to ENST00000303905 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:133873685 G>A maps to ENST00000448712 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:46917619 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:46913787 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:46918267 G>A did not map to a codon.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr23:46918064 G>A did not map to a codon.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr4:129792843 G>A maps to NM_199320.2 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr9:96436079 C>T maps to NM_005392.3 V854V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:133826883 G>A maps to ENST00000395386 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:133856558 C>T maps to ENST00000395386 V970V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:45957273 T>C maps to ENST00000257821 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:45958051 G>A maps to ENST00000257821 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr11:45967426 A>G maps to ENST00000257821 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:64401723 G>T maps to NM_015153.2 E763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr6:64401917 C>G maps to NM_015153.2 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:54040960 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:79680569 G>A maps to NM_017934.5 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:79707219 G>A maps to NM_017934.5 N704N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:71802366 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:71802289 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:71822974 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:71825179 C>T did not map to a codon.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr23:71830998 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:18911621 G>A did not map to a codon.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr23:18923927 T>C did not map to a codon.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr23:19002034 T>G did not map to a codon.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr23:18954249 C>A did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:18911700 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:47683048 G>A maps to NM_000293.2 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr16:47684504 T>C maps to NM_000293.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr11:118514624 C>T maps to NM_015157.2 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr18:60646087 C>G maps to NM_194449.2 S1526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:60642762 C>T maps to NM_194449.2 R1297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr11:609067 G>A maps to ENST00000264555 A1204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr1:114249244 A>G maps to NM_006608.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:114267406 A>G maps to NM_006608.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr7:77569462 C>G maps to ENST00000427986 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr7:77538203 A>G maps to ENST00000427986 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:13336520 C>T maps to NM_006214.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr8:75761445 T>C maps to NM_015886.3 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr8:75756319 T>A maps to NM_015886.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:25254051 C>T maps to NM_018323.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr4:25258230 A>T maps to NM_018323.3 K231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr22:21119492 G>A maps to NM_058004.2 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:21104264 G>A maps to NM_058004.2 F999F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr1:151274710 A>G maps to NM_002651.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr11:85733486 C>T maps to ENST00000393343 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr2:229890814 G>A maps to NM_017933.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:15339714 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:68060477 G>T maps to NM_004569.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr1:77634962 C>T maps to NM_005482.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr1:77634994 C>A maps to NM_005482.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:160000977 C>A maps to NM_145167.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr18:59825010 G>A maps to NM_176787.4 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr18:59780513 C>T maps to NM_176787.4 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:27120647 C>T maps to NM_017837.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:196454963 G>A maps to NM_001166304.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:98416629 C>T maps to NM_152309.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:17140198 A>G maps to NM_002645.2 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:204394012 G>A maps to NM_002646.3 F1624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr12:18552753 T>A maps to NM_004570.4 L722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:18435101 A>G maps to NM_004570.4 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr18:39576651 T>C maps to ENST00000398870 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr3:178952004 A>G maps to NM_006218.2 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:178947899 C>T maps to NM_006218.2 D925D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr3:178951977 A>G maps to NM_006218.2 P1011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr3:178952139 T>C maps to NM_006218.2 H1065H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr3:178922364 T>C maps to NM_006218.2 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr3:178952067 A>G maps to NM_006218.2 K1041K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr3:178952091 T>C maps to NM_006218.2 G1049G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr3:178952151 A>G maps to NM_006218.2 *1069W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr3:178927981 T>C maps to NM_006218.2 C420C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr3:178928080 A>G maps to NM_006218.2 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr3:178936071 T>C maps to NM_006218.2 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr3:178916663 C>T maps to NM_006218.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr3:178937019 A>G maps to NM_006218.2 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr3:178951998 C>T maps to NM_006218.2 D1018D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr3:178922325 A>G maps to NM_006218.2 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr3:178952034 A>G maps to NM_006218.2 K1030K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr3:178916874 C>T maps to NM_006218.2 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr3:178922364 T>C maps to NM_006218.2 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:138433372 C>T maps to NM_006219.1 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:138403618 A>C maps to NM_006219.1 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr1:9777132 G>A maps to ENST00000361110 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr1:9784119 C>T maps to ENST00000361110 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:106526601 C>T maps to NM_002649.2 F965F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:106508431 G>A maps to NM_002649.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr7:106508179 G>A maps to NM_002649.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:67588950 C>T maps to ENST00000396611 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:67589167 C>T maps to ENST00000396611 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:67589608 G>T maps to ENST00000396611 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:67590465 G>T maps to ENST00000396611 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr5:67589617 C>T maps to ENST00000396611 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr5:67589613 A>G maps to ENST00000396611 K459K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr1:46509455 C>T maps to NM_001114172.1 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr3:130409452 G>C maps to NM_014602.2 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:8731467 G>A maps to NM_001010855.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr2:209207314 C>T maps to NM_015040.3 R1657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:209190768 A>G maps to NM_015040.3 R1078R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:99957092 C>T maps to ENST00000413850 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr7:99955933 G>C maps to ENST00000413850 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr6:37140932 C>T maps to ENST00000373507 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3582-01A-01W-0831-10 chr1:20977045 C>T maps to NM_032409.2 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:10623423 G>A maps to NM_017884.4 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:142832371 G>T maps to NM_002652.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:71509317 G>T maps to NM_003558.2 G179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr23:15509372 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:10728776 G>A maps to NM_001101387.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:28250905 G>A maps to NM_012399.3 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr11:67260479 G>A maps to NM_004910.2 Y1132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr12:123471336 C>T maps to NM_020845.2 T1151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr12:123480132 G>A maps to NM_020845.2 G619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr17:6441379 A>T maps to NM_031220.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:134364639 C>T maps to NM_002653.4 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:25115744 A>G maps to NM_001008496.2 Y834Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:25151833 G>A maps to NM_001008496.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:68381192 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:68382761 G>A did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:108714665 A>G maps to NM_014819.4 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr7:47879157 C>T maps to NM_138295.3 L1885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:47925647 G>T maps to NM_138295.3 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:47947722 G>A maps to NM_138295.3 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr16:81167281 G>A maps to NM_052892.3 R1915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr16:81253924 G>T maps to NM_052892.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:81180944 C>A maps to NM_052892.3 E1716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:102055944 G>A maps to NM_016112.2 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr10:102089791 G>A maps to NM_016112.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:137257337 C>T maps to ENST00000230643 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr22:46654128 G>A maps to NM_006071.1 F1697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:46653324 G>T maps to NM_006071.1 I1965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:46653408 G>T maps to NM_006071.1 V1937V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:46656824 G>A maps to NM_006071.1 R799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr22:46654758 G>T maps to NM_006071.1 Y1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr6:51618062 G>A maps to NM_138694.3 D2962D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr6:51524214 G>T maps to NM_138694.3 S3570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr6:51523857 A>T maps to NM_138694.3 L3689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr6:51889912 A>G maps to NM_138694.3 V1565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:110457590 C>T maps to ENST00000426474 P1831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:110488758 C>A maps to ENST00000426474 S2927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:110530567 C>A maps to ENST00000426474 T3955T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr1:155263068 C>T maps to ENST00000423816 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:155264361 G>A maps to ENST00000423816 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:155265464 G>A maps to ENST00000423816 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:72500984 G>A maps to ENST00000419739 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr15:72499524 C>T maps to ENST00000419739 Q384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:14580254 C>T maps to NM_213560.1 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:131482764 C>T maps to NM_013355.3 G850G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:125281715 G>A maps to NM_022062.2 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr1:201282631 C>A maps to NM_000299.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr12:33031162 G>T maps to NM_004572.3 Y217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:159459595 C>A maps to NM_003628.3 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr2:159481793 G>A maps to NM_003628.3 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr11:63357673 C>T maps to NM_001128203.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr1:20474890 C>A maps to NM_022819.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:186863262 G>T maps to NM_024420.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr1:186901974 C>T maps to NM_024420.2 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:48608676 C>T maps to NM_003706.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:42293406 G>T maps to NM_001080490.1 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:42437839 G>T maps to ENST00000397272 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr1:20416368 G>A maps to NM_000929.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:160806200 G>A maps to NM_007366.4 C1209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:160832604 C>A maps to NM_007366.4 E857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:160901351 C>T maps to NM_007366.4 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:133700588 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:75673382 G>T maps to NM_002658.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr2:28851974 C>T maps to NM_153021.4 F1247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr2:28821612 C>T maps to NM_153021.4 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:8719981 C>A maps to NM_015192.2 I761I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:8722117 C>T maps to NM_015192.2 I807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr20:8769133 G>A maps to NM_015192.2 Q1050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr15:40581104 C>T maps to NM_004573.2 A1123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr11:64033793 A>T maps to NM_000932.2 K1092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr17:43195806 C>T maps to NM_133373.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:39795390 C>T maps to NM_002660.2 F731F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr20:39793964 T>C maps to NM_002660.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:81942035 G>T maps to NM_002661.2 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr16:81922793 T>C maps to NM_002661.2 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr3:155303879 G>A maps to ENST00000340059 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:198948733 G>T maps to NM_006226.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:198950187 C>T maps to NM_006226.3 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr17:4719184 C>T maps to NM_002663.3 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr1:242264039 T>C maps to NM_152666.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:242277235 G>A maps to NM_152666.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:124152832 C>T maps to NM_021622.4 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr2:179350383 G>A maps to NM_019091.3 W19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr2:179355478 G>A maps to NM_019091.3 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr19:49342499 T>C maps to NM_020904.2 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr19:49363680 G>A maps to NM_020904.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:73372619 G>A maps to NM_021200.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr8:96166991 T>C maps to NM_024613.3 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr6:151153150 C>A maps to NM_001029884.1 A968A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr6:151161630 A>T maps to NM_001029884.1 R1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr19:39913400 C>G maps to NM_022835.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:169509 C>A maps to NM_052909.3 R822R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr5:182161 C>T maps to NM_052909.3 H1180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr5:156286 G>A maps to NM_052909.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr1:6529508 C>G maps to NM_198681.2 G722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr12:93150129 C>T maps to NM_001004330.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:68053936 G>A maps to NM_020715.2 G1360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:16060341 C>T maps to ENST00000420314 F1094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr1:908563 A>G did not map to a codon.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr1:150131471 A>G maps to ENST00000443480 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr9:19126235 G>C maps to NM_001122.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr19:4513404 G>A maps to NM_001080400.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr19:4531792 G>A maps to NM_001013706.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr16:23700037 G>A maps to NM_005030.3 W414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr20:21209691 T>C maps to NM_018474.4 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:57750453 G>A maps to NM_006622.2 R672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:128803047 C>A maps to NM_014264.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:128816160 C>A maps to NM_014264.4 I872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:145790388 C>A maps to NM_182943.2 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:103040658 C>A did not map to a codon.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr23:103040642 T>A did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr23:103041612 G>A did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:142389950 G>A maps to NM_001172312.1 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:114864190 G>T did not map to a codon.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr23:114874776 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr3:146239396 T>C maps to NM_021105.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:145917659 T>G maps to NM_020353.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr3:146307457 G>A maps to NM_001085420.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:44540079 G>A maps to NM_006227.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:31829238 C>A maps to NM_130852.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:17476992 C>T maps to NM_031310.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:20432299 C>T maps to NM_032812.7 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr3:126751256 G>T maps to NM_032242.3 V1753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr3:126723976 C>T maps to NM_032242.3 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:208234145 G>A maps to NM_025179.3 R875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr23:153694772 C>T did not map to a codon.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr23:153699911 C>T did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:153695460 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:132192726 G>T maps to NM_020911.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr7:131853172 G>A maps to NM_020911.1 T1392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:132174089 A>C maps to NM_020911.1 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:132193344 C>T maps to NM_020911.1 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr7:131864590 T>C maps to NM_020911.1 A1243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:48453927 G>A maps to NM_001130082.1 F1652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr23:153039022 G>A did not map to a codon.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:153041434 C>T did not map to a codon.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr23:153032488 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:94688287 C>A maps to NM_005761.1 V1302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr12:94543505 C>T maps to NM_005761.1 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr7:6022480 G>A maps to NM_000535.5 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr7:6026615 A>G maps to NM_000535.5 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr7:6038885 C>T maps to NM_000535.5 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr2:219204842 T>C maps to NM_015488.4 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:160232739 C>T maps to NM_173516.1 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr10:118321069 G>A maps to NM_000936.2 W419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr10:118220737 C>T maps to NM_001011709.2 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:118236202 C>T maps to NM_001011709.2 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr10:118196355 A>C maps to NM_001011709.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr10:118220537 C>A maps to NM_001011709.2 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr8:26365182 G>A maps to NM_007257.5 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr8:26365512 C>T maps to NM_007257.5 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr19:46973958 C>A maps to NM_018215.3 E112*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AG-A002-01A-01W-A00K-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:46997933 C>T maps to ENST00000377652 F15F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AG-A002-01A-01W-A00K-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:39650230 A>T maps to NM_002687.3 K440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:44342081 G>A maps to NM_025225.2 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr22:44285723 G>T maps to ENST00000216177 Y149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:7615270 C>T maps to NM_001166111.1 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:89793716 G>A maps to NM_006813.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr5:74984854 G>A maps to NM_001099271.1 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:127379459 G>T maps to NM_015720.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr23:84562262 A>C did not map to a codon.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr1:151384850 C>T maps to NM_015100.3 W567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:151400745 G>A maps to NM_015100.3 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:24766439 G>C did not map to a codon.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr23:24751926 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:24751926 G>T did not map to a codon.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr23:24830826 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr23:24732733 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:42229091 G>T maps to NM_002690.1 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:74329821 G>A maps to NM_006591.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr22:42998969 G>A maps to ENST00000415122 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:133218336 G>A maps to ENST00000455752 F1761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:133236065 G>A maps to ENST00000455752 F1033F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:133256212 G>A maps to ENST00000455752 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr15:89870444 C>G maps to NM_002693.2 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr15:89866640 A>T maps to NM_002693.2 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:74892362 T>C maps to NM_016218.2 N615N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr4:2209941 A>G maps to NM_181808.2 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:121251839 C>A maps to ENST00000393672 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:121207775 C>T maps to ENST00000393672 Q1470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:121240948 C>A maps to ENST00000393672 E522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:7399886 C>T maps to NM_000937.4 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:79741242 G>A maps to NM_007055.3 H1278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:106772091 G>T maps to NM_018082.5 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr16:22334240 C>T maps to NM_018119.2 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3575-01A-01W-0831-10 chr22:41928716 G>A maps to NM_138338.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr7:53103957 C>T maps to NM_182595.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:94992146 G>T maps to NM_000940.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr7:95001482 A>G did not map to a codon.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr13:38153363 A>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr21:14983022 C>T maps to NM_174981.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:42599738 G>T maps to ENST00000342301 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:99283718 C>T maps to NM_005604.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:99283792 C>T maps to NM_005604.2 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr23:82764014 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:82763851 G>A did not map to a codon.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr23:82764139 G>T did not map to a codon.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr23:82764378 G>A did not map to a codon.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr23:82764015 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr23:82763667 C>T did not map to a codon.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr4:147561779 G>A maps to NM_004575.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr5:145719862 C>G maps to NM_002700.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr8:128429031 A>G maps to NM_001159542.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr5:93076992 G>A maps to NM_153216.1 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:93077209 G>A maps to NM_153216.1 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr12:51584191 A>G maps to NM_002702.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:39125629 C>T maps to NM_007252.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:46628101 C>A maps to NM_001001928.2 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr5:149216622 C>T maps to NM_133263.3 R869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr1:42922601 G>A maps to NM_024664.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr23:18767934 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:18779677 T>A did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:70202303 C>A maps to NM_003626.2 A842A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:81732973 G>A maps to NM_003625.2 R845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr12:81799571 A>G maps to NM_003625.2 H252H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr12:81732977 T>C maps to NM_003625.2 K843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr12:82147820 C>T maps to NM_003625.2 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr1:203024712 G>A maps to ENST00000367238 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:27830004 C>T maps to NM_003622.3 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:7631632 G>T maps to NM_003621.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr5:122361520 C>T maps to NM_000943.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr2:170493408 A>G maps to NM_004792.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:170493348 T>C maps to NM_004792.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:102502999 C>T maps to ENST00000451606 R680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:44445124 C>T maps to NM_002706.4 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:57033093 C>A maps to NM_014906.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:202399861 C>T maps to ENST00000367270 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:202409839 G>T maps to ENST00000367270 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr19:55610393 C>T maps to NM_017607.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr19:55603860 G>A maps to NM_017607.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:150569937 G>A maps to NM_030949.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:49377230 C>T maps to NM_014330.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr19:49377361 C>A maps to NM_014330.3 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr7:113518302 C>T maps to NM_002711.3 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr7:113518302 C>T maps to NM_002711.3 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:8998612 A>C maps to NM_024607.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr10:93390321 C>A maps to NM_005398.4 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr10:93390112 G>T maps to NM_005398.4 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:49142835 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:242092954 C>T maps to NM_002712.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:242099782 C>T maps to NM_002712.1 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:242122213 C>T maps to NM_002712.1 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:26227730 G>A maps to NM_001177591.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr4:6331011 T>C maps to NM_181876.2 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr3:135722028 C>T maps to NM_002718.4 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:35565772 T>G maps to NM_017917.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr1:212502525 G>A maps to NM_006243.3 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:212530530 C>T maps to NM_006243.3 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:64697808 C>T maps to NM_006244.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr14:102368207 C>T maps to NM_002719.3 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:102117159 C>A maps to NM_000944.4 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:22389768 G>A maps to ENST00000397775 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:94708198 G>T maps to NM_058237.1 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr14:94712821 C>T maps to NM_058237.1 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:244855278 T>G maps to NM_016076.3 L103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr22:42000088 G>T maps to NM_015704.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:103899314 G>A maps to NM_015062.3 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:42018851 G>T maps to NM_002722.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr17:42018857 T>C maps to NM_002722.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr2:11300651 G>A maps to NM_152391.3 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr1:12837468 G>T maps to NM_001080830.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:12919829 G>A maps to NM_023014.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:11507488 C>A did not map to a codon.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr12:11506649 A>C maps to NM_005039.3 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:11462307 T>G maps to NM_002723.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:91513656 G>A maps to NM_003981.2 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:106555184 G>T maps to NM_001198.3 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:129784891 G>A maps to NM_020228.2 R854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:129787027 G>A maps to NM_020228.2 C777C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr8:70964377 G>T maps to NM_024504.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr8:70971027 G>A maps to NM_024504.2 Y411Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr8:70982041 C>T maps to NM_024504.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:3328497 C>T maps to NM_022114.3 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:121698423 C>A maps to NM_018699.2 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:90126763 G>A maps to NM_001098173.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr4:81123602 G>T maps to NM_001099403.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:23524502 G>A maps to NM_020227.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr5:23527632 C>G maps to NM_020227.2 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:45981392 C>A maps to NM_181697.1 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:12910787 G>A maps to NM_005809.4 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr1:173454528 C>T maps to NM_004905.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr20:47267957 G>A maps to NM_020820.3 R877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:47249037 C>T maps to NM_020820.3 T1469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:47276507 C>T maps to NM_020820.3 Q610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr20:47305234 G>T maps to NM_020820.3 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr20:47248855 C>T maps to NM_020820.3 A1495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr8:69009297 G>A maps to NM_024870.2 K805K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr11:57146258 G>T maps to NM_006093.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:57147239 T>G maps to NM_006093.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:186270757 C>T maps to NM_005807.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:186280684 T>G maps to NM_005807.3 A1250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:64138903 G>A maps to NM_198859.3 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr3:64139007 G>A maps to NM_198859.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:49032335 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:57183363 G>T maps to NM_000947.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:57472419 C>A maps to NM_000947.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr14:94245651 C>T maps to NM_178013.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:57158128 G>A maps to NM_006252.3 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:14203925 A>G maps to NM_002730.3 *352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:71628876 G>A maps to NM_002732.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr7:151478502 G>A maps to NM_016203.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr17:66518948 C>G maps to NM_212472.1 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr3:53212455 C>T maps to NM_212539.1 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:46207444 C>T maps to NM_005400.2 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr19:54395021 G>A maps to NM_002739.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:54401304 A>G maps to NM_002739.3 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr14:61995891 G>T maps to NM_006255.3 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr14:61997204 C>T maps to NM_006255.3 H551H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr3:170009727 T>C maps to NM_002740.5 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:6540491 C>A maps to NM_006257.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr1:2082230 C>T maps to NM_002744.4 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr1:2082317 G>T maps to NM_002744.4 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr14:30105668 C>G maps to NM_002742.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr14:30046613 C>A maps to NM_002742.2 E857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr19:47197330 C>T maps to ENST00000449438 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr19:47214230 C>T maps to ENST00000449438 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr19:47177806 C>A maps to ENST00000449438 G880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr8:48855840 T>C maps to NM_006904.6 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:48840365 C>A maps to NM_006904.6 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:48801168 C>T maps to NM_006904.6 A1440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr8:48752647 G>A maps to NM_006904.6 F2460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr10:53822294 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:53893620 C>T maps to NM_001098512.1 N304N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr4:82065432 T>C maps to NM_006259.1 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:82092946 C>A maps to NM_006259.1 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr4:82065432 T>C maps to NM_006259.1 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr6:22290561 C>G maps to ENST00000397199 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:148559834 C>A maps to NM_138364.2 E796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr1:107599534 C>T maps to NM_018137.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:3662818 C>T maps to NM_019854.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr12:3702264 C>T maps to NM_019854.3 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr20:4680093 C>T maps to NM_001080123.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr17:27030880 A>G maps to ENST00000415329 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:68882440 C>T maps to NM_138964.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:5283114 G>T maps to NM_144773.2 C242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr20:5282913 C>T maps to NM_144773.2 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr4:16002242 C>A did not map to a codon.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr3:93617366 A>G maps to NM_000313.3 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:13642284 G>A maps to NM_003675.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr11:60670224 A>G maps to NM_014502.4 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr11:60666668 G>A maps to NM_014502.4 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr9:116044949 C>T maps to NM_004697.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr2:153514524 C>A maps to ENST00000410080 E924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:4058967 C>T maps to NM_003913.4 R914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:62631084 C>A maps to NM_012469.3 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr17:1579254 C>T maps to NM_006445.3 K882K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr6:42689823 G>A maps to NM_000322.4 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr23:106882651 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:74328350 C>T maps to NM_002766.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr5:120022313 C>T maps to NM_016644.1 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr2:240981463 C>G maps to NM_001080835.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr3:138724642 G>A maps to NM_001134659.1 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr3:138738750 C>T maps to NM_001013650.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr23:37312701 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:37285204 C>A did not map to a codon.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr23:37312394 T>C did not map to a codon.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr23:150869329 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:2868815 G>A maps to NM_006799.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:84234053 G>A maps to NM_153362.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:31153161 G>A maps to NM_173502.3 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:31151646 G>A maps to NM_173502.3 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr1:228005071 C>T maps to NM_183062.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:228033804 G>T maps to NM_183062.2 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr16:58325008 G>A maps to NM_001080492.1 Y39Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr8:10387197 C>T maps to NM_198464.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr8:10396008 C>A maps to NM_198464.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr19:691932 C>T maps to NM_214710.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:79461536 G>A maps to NM_015225.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:79321270 G>T maps to NM_015225.2 A1973A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:79322191 T>C maps to NM_015225.2 E1666E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr9:79270372 G>A maps to NM_015225.2 G2774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr9:79320991 G>A maps to NM_015225.2 A2066A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr9:79461455 G>A maps to NM_015225.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:40900406 G>A maps to NM_181882.2 S1284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr8:143763530 G>A maps to ENST00000301258 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr10:104173749 C>T maps to NM_002779.3 E443E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr5:139192981 C>T maps to NM_032289.2 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr5:139197134 C>T maps to NM_032289.2 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:18393366 C>T maps to ENST00000440756 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr1:227073295 C>T maps to ENST00000391872 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:43372313 G>A maps to NM_006905.2 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:43519304 G>A maps to ENST00000306308 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr19:43233948 T>A maps to NM_021016.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr19:43698573 C>T maps to NM_002780.3 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:43259227 G>T maps to NM_182707.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:43772122 C>T maps to NM_002784.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr9:15469305 C>T maps to NM_001128217.1 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr8:87081680 G>A maps to ENST00000276616 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr8:87076415 G>A maps to ENST00000276616 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr7:103004630 C>T maps to NM_002803.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:40486242 G>T maps to NM_006503.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr19:40480524 C>T maps to NM_006503.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr19:40485748 G>A maps to NM_006503.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:53175093 G>A maps to NM_002806.3 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:53185003 G>T maps to NM_002806.3 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:53185746 G>A maps to NM_002806.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:65353480 C>A maps to NM_002816.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:54159015 A>G maps to NM_014614.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr7:56079455 T>C maps to NM_004577.3 *226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr9:98232132 G>A maps to NM_000264.3 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr9:98231266 C>T maps to NM_000264.3 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr9:98244289 A>G maps to NM_000264.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr9:98221882 T>C maps to NM_000264.3 R962R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr9:98229452 T>C maps to NM_000264.3 E835E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr9:98212179 A>G maps to NM_000264.3 V1164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr9:98231074 A>G maps to NM_000264.3 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr9:98239881 C>A maps to NM_000264.3 G484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr9:98248085 A>G maps to NM_000264.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr9:98248147 G>A maps to NM_000264.3 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr9:98231215 G>T maps to NM_000264.3 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr9:98229649 G>A maps to NM_000264.3 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr23:23411332 C>T did not map to a codon.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr23:23411676 T>C did not map to a codon.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr23:23411776 G>A did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:23397857 C>T did not map to a codon.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr1:11561556 C>T maps to NM_020780.1 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr10:27702771 C>T maps to NM_001034842.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:97316340 C>T maps to NM_014754.1 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr10:89717673 A>G maps to NM_000314.4 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr10:89624270 A>G maps to NM_000314.4 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:89624244 G>T maps to NM_000314.4 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr10:89720775 A>C maps to NM_000314.4 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr10:89725210 A>G maps to NM_000314.4 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr10:89624234 C>T maps to NM_000314.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr10:89624288 C>T maps to NM_000314.4 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr10:89692849 C>T maps to NM_000314.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr10:89711924 G>A maps to NM_000314.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr10:89725042 G>T did not map to a codon.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr10:89692998 A>G maps to NM_000314.4 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr10:89624276 A>G maps to NM_000314.4 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr10:89692998 A>G maps to NM_000314.4 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr10:89692959 A>G maps to NM_000314.4 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr10:89624234 C>T maps to NM_000314.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:89690811 A>G maps to NM_000314.4 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:89692803 A>G maps to NM_000314.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr10:89720721 A>G maps to NM_000314.4 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr10:89692902 A>G maps to NM_000314.4 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr10:89653815 T>C maps to NM_000314.4 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr10:89720727 A>G maps to NM_000314.4 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr10:89725210 A>G maps to NM_000314.4 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr10:89653818 A>G maps to NM_000314.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr1:78958856 T>C maps to NM_000959.3 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr1:78959186 G>A maps to NM_000959.3 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:74340904 T>C maps to NM_152444.2 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:186645251 C>T maps to NM_000963.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:186646897 G>T maps to NM_000963.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:209355365 T>C maps to NM_005048.2 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr12:28116380 G>A maps to ENST00000354417 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:27312076 C>T maps to NM_004103.3 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:43109415 C>T maps to NM_002821.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr6:43126673 T>C maps to NM_002821.3 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:64288416 G>T maps to NM_003463.3 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr10:17636293 C>A maps to NM_014241.3 G232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr10:17636291 T>C maps to NM_014241.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr15:65849210 A>G maps to NM_016395.2 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr9:21029381 C>T maps to NM_001010915.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr3:123303820 G>C maps to NM_198402.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr3:123303823 A>G maps to NM_198402.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr12:112926888 G>A maps to ENST00000392596 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr12:112888196 T>C maps to ENST00000392596 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr12:112926900 A>G maps to ENST00000392596 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr12:112926885 A>G maps to ENST00000392596 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr12:112915743 T>C maps to ENST00000392596 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr12:112926885 A>G maps to ENST00000392596 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:77200460 G>T maps to NM_002835.3 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr7:77230117 T>C maps to NM_002835.3 H230H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:87707063 C>A maps to NM_080685.2 S2112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:87728797 C>T maps to NM_080685.2 F2282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr4:87726443 T>C maps to NM_080685.2 L2228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr1:214549705 C>T maps to NM_005401.4 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr2:131128791 C>T maps to NM_014369.3 D315D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:12859246 G>A maps to NM_002828.2 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:88938682 G>A maps to NM_007039.3 R926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:88971667 T>A maps to NM_007039.3 K166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:114375747 G>A maps to NM_015967.5 R680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr11:18762239 G>A maps to NM_032781.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr20:3007800 G>A maps to NM_002836.3 R581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:70929846 A>C maps to NM_001109754.1 V2013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:70986104 G>T maps to NM_001109754.1 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr1:198711402 C>A maps to ENST00000271610 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:198685891 C>A maps to ENST00000271610 S458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:198711003 G>T maps to ENST00000271610 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr9:8518184 C>T maps to NM_002839.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:129881109 C>T maps to NM_006504.4 F681F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:129868629 C>T maps to NM_006504.4 D403D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr1:44070988 G>A maps to NM_002840.3 Q1088Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:44071003 C>T maps to NM_002840.3 I1093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr3:62189577 C>T maps to NM_002841.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr19:55693157 G>A maps to NM_002842.3 N1104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:48161170 G>A maps to NM_002843.3 A762A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr11:48171646 G>T did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:128326361 G>A maps to ENST00000368210 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr2:220159773 C>T maps to NM_002846.3 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr2:220162095 C>T maps to NM_002846.3 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:157341693 G>A maps to NM_002847.3 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:157926382 G>A maps to NM_002847.3 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:71056291 G>A maps to NM_002849.2 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:71077917 C>A maps to NM_002849.2 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:5212403 C>T maps to NM_002850.3 L1571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr20:40727111 G>A maps to ENST00000373198 F1287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr20:40827934 G>A maps to ENST00000373198 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr20:40730858 G>A maps to ENST00000373198 R1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:29587218 G>A maps to NM_005704.4 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr1:29630427 T>C maps to NM_005704.4 R856R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr7:121624098 C>T maps to NM_002851.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr7:121651199 A>C maps to NM_002851.2 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr7:121653014 C>A maps to NM_002851.2 P1305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr16:1537806 C>T maps to NM_001013658.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr1:31426558 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:20453750 A>G maps to ENST00000361078 T967T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr8:30889623 T>C maps to NM_013357.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr2:61192598 C>T maps to NM_144709.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:61189976 C>A maps to NM_144709.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr2:61180215 T>C maps to NM_144709.2 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:105105784 G>A maps to NM_019042.3 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:105131991 A>C maps to NM_019042.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:44148435 C>A maps to NM_031292.3 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr1:161044046 G>A maps to NM_030916.2 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr2:1653388 C>T maps to NM_012293.1 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:1657474 C>A maps to NM_012293.1 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr2:1667404 G>A maps to NM_012293.1 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr2:1667458 G>A maps to NM_012293.1 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:58368362 C>A maps to NM_017771.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr3:191179196 G>A maps to NM_001083308.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr3:191179139 C>T maps to NM_001083308.1 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:55841113 A>G maps to NM_015617.1 N43N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr12:21590726 G>C maps to NM_024854.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:100144782 G>A maps to NM_032709.2 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:163876326 G>T maps to ENST00000361752 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr6:163987756 G>A maps to ENST00000361752 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr17:74288614 G>T maps to NM_032134.1 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr17:74288734 G>A maps to NM_032134.1 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr12:57648642 A>G maps to ENST00000438036 R1014R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr16:532595 C>T maps to NM_014700.3 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr12:72149034 C>T maps to NM_014999.2 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr4:13371556 C>A maps to NM_004249.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:129318614 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:154490416 C>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:52442636 G>A maps to NM_002867.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr1:220344348 G>A maps to ENST00000358951 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr11:61673946 C>T maps to NM_013401.2 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr23:102755132 C>T did not map to a codon.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr23:102755558 C>T did not map to a codon.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr23:102192955 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:69502680 G>T did not map to a codon.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr1:229433366 A>G maps to NM_004578.2 R143R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AG-3881-01A-01W-0899-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr3:133583484 G>A maps to NM_016577.3 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr3:133583451 G>A maps to NM_016577.3 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:13727174 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:28917054 C>T maps to NM_024816.2 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr9:125751740 A>T maps to NM_012197.3 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:66273977 G>T maps to ENST00000451741 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr3:8983367 C>A maps to NM_020165.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:117868912 G>A maps to NM_006265.2 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr8:117864236 G>A maps to NM_006265.2 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr19:13059031 A>C maps to NM_005053.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:17696941 G>T maps to NM_001099218.2 S914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr14:68301900 A>G maps to NM_133509.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:1042191 T>C maps to NM_134424.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:95412518 C>A maps to NM_012415.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:110969392 G>T maps to NM_152442.3 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr12:110960200 T>C maps to NM_152442.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:55948749 C>T maps to NM_001015885.1 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:150210577 C>T maps to NM_139165.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:150240884 C>T maps to NM_001001788.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:36597746 G>T maps to NM_000448.2 E965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:36595360 G>A maps to NM_000448.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr11:36596671 A>G maps to NM_000448.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr5:34824361 G>A maps to NM_001145521.1 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:34829862 C>T maps to NM_001145521.1 V942V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr23:17819078 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:39745748 C>T maps to NM_005402.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr7:39745750 A>T maps to NM_005402.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr14:36104681 A>G maps to NM_194301.2 N1427N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr9:135983677 T>G maps to NM_006266.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr8:85762214 C>T maps to NM_001100391.1 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr8:85717026 C>T maps to NM_001100391.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr5:170598233 A>G maps to NM_022897.3 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:170610372 C>T maps to NM_022897.3 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:170626765 G>T maps to NM_022897.3 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:170632557 C>T maps to NM_022897.3 R725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:109379748 G>A maps to NM_006267.4 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:109382973 C>T maps to NM_006267.4 S1993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr2:109368374 C>T maps to NM_006267.4 N560N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr9:6013870 T>C maps to NM_012416.2 E579E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr6:13625894 A>G maps to NM_005493.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr22:41647071 T>C maps to NM_002883.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:99264293 G>A maps to NM_001100426.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:134465301 G>A maps to NM_198679.1 F778F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr4:160274959 A>G maps to NM_014247.2 Q1310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr2:173882218 C>T maps to NM_007023.3 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr5:130928156 G>C maps to ENST00000514667 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:130782242 G>A maps to ENST00000514667 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:204354693 C>T maps to ENST00000374493 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:167915735 C>T maps to NM_002887.3 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr5:86629107 C>T maps to NM_002890.1 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr1:178389683 G>A maps to ENST00000263528 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:85605306 G>A maps to NM_152573.2 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:79277357 G>T maps to NM_002891.4 V1151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:79339122 G>A maps to NM_002891.4 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr5:80476045 G>C maps to NM_006909.1 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:64503051 G>A maps to ENST00000320253 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:33774811 G>A maps to NM_170672.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:4766953 G>A maps to NM_014737.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr10:45485158 C>T maps to NM_032023.3 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr1:206757738 G>A maps to NM_182663.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:26208284 T>C maps to NM_001164747.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr12:86198973 G>A maps to NM_005447.3 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:86199585 G>A maps to NM_005447.3 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr13:49027202 T>C maps to NM_000321.2 C590C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:48937069 G>T maps to NM_000321.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr13:48953740 T>G maps to NM_000321.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr13:48947597 A>G maps to NM_000321.2 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr13:48881428 G>T maps to NM_000321.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr13:48923112 T>C maps to NM_000321.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr13:49037877 T>C maps to NM_000321.2 C706C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr13:48947597 A>G maps to NM_000321.2 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr13:48881535 A>G maps to NM_000321.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr13:48941658 A>G maps to NM_000321.2 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr13:48881499 T>C maps to NM_000321.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr13:48881510 G>A maps to NM_000321.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3575-01A-01W-0831-10 chr8:53568949 C>A maps to NM_014781.4 E1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr8:53568974 G>A maps to NM_014781.4 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr8:53570339 T>C maps to NM_014781.4 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr8:53569094 T>C maps to NM_014781.4 E1098E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:53596475 G>A maps to NM_014781.4 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr8:53598017 A>T maps to NM_014781.4 Y4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:16870699 C>T did not map to a codon.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr23:16870189 C>T did not map to a codon.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr23:47044540 C>T did not map to a codon.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr23:47032535 C>T did not map to a codon.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr23:47028789 C>T did not map to a codon.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr23:47028789 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:47045657 G>T did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:47040619 C>T did not map to a codon.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr20:34240766 C>G maps to NM_001198838.1 G826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:34241692 G>A maps to NM_001198838.1 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr20:34242049 C>A maps to NM_001198838.1 G399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:94748487 C>A maps to NM_203390.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr11:66392423 T>G maps to NM_006328.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:51431304 C>A maps to NM_013286.4 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:51430450 C>T maps to NM_013286.4 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:155095157 G>A maps to NM_014892.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr6:155154099 A>G maps to NM_014892.3 R1129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr9:125014164 C>T maps to NM_033117.3 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:114397110 C>T maps to NM_016196.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr13:79911343 G>A maps to ENST00000438737 R877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr13:79896552 C>T maps to ENST00000438737 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr13:79933777 T>C maps to ENST00000438737 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:145613127 G>A maps to NM_018989.1 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:145609403 C>T maps to NM_018989.1 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr7:127953299 G>A maps to NM_018077.2 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr23:48434979 A>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:155537702 G>T maps to NM_053043.2 E796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:235324363 G>A maps to NM_015014.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:55982856 C>T maps to NM_017495.4 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr20:55982631 C>T maps to NM_017495.4 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr20:34312638 T>C maps to NM_184234.1 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:34326902 C>A maps to NM_184234.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:66407508 C>T maps to NM_002896.3 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:66407464 C>T maps to NM_002896.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr2:238726683 T>C maps to NM_001080504.2 C375C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr2:178990776 C>T maps to ENST00000456670 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:155720247 G>T maps to NM_144979.3 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:40440430 C>T maps to NM_001098634.1 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:50151430 G>T maps to NM_005778.2 E556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr3:50098947 T>C maps to NM_005777.2 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr12:56975618 C>T maps to NM_002898.3 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:29476319 C>T maps to NM_001003793.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr3:30029653 T>C maps to NM_001003793.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr23:135956395 G>A did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:129546358 A>G did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:48385872 G>A maps to NM_002900.2 H1073H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr10:48390676 C>T maps to NM_002900.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:30361946 G>T maps to NM_001008712.1 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr9:125622277 A>G maps to NM_001100588.1 Y589Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:32118794 C>T maps to NM_002901.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:77241412 G>A maps to ENST00000320963 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr11:63681554 T>C maps to NM_173587.3 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:167663469 C>T maps to NM_052862.3 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr12:57345980 C>T maps to NM_003708.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:36100334 G>T maps to NM_021111.2 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr2:79384716 C>T maps to NM_138937.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:120342482 G>A maps to NM_032044.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr1:120341216 C>T maps to NM_032044.3 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr11:65425863 G>A maps to NM_021975.3 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr19:45537541 C>T maps to ENST00000221452 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:37650922 G>A maps to NM_001085399.1 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr7:103191533 A>G maps to ENST00000428762 F2094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:103194237 G>A maps to ENST00000428762 I1946I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:103230146 G>A maps to ENST00000428762 C1347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr7:103234212 T>C maps to ENST00000428762 A1276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr7:103113285 T>C maps to ENST00000428762 R3452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:30070142 C>T maps to NM_014012.4 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr20:30064409 T>C maps to NM_014012.4 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:204131290 C>T maps to NM_000537.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:139229910 G>A maps to ENST00000367663 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr1:8421202 T>C maps to NM_012102.3 P788P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:57796625 G>T maps to NM_005612.4 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:43610159 C>A maps to NM_020975.4 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr10:43617395 T>C maps to NM_020975.4 G911G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:100022946 C>A maps to NM_016316.2 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:100027202 C>A maps to NM_016316.2 E767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:111693892 C>A maps to NM_002912.3 E1889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:111695023 G>A maps to NM_002912.3 R1512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:111702605 C>A maps to NM_002912.3 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr6:111632321 T>A maps to NM_002912.3 G2915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr19:1827577 G>A maps to NM_020695.3 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr4:39291551 C>T maps to ENST00000381897 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr3:186508156 G>C maps to NM_181573.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr3:186507805 G>A maps to NM_181573.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:118457549 G>T maps to NM_007370.4 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:29837867 C>T maps to NM_021026.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr22:29837543 G>A maps to NM_021026.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:16358556 G>A maps to NM_015150.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:16475389 G>T maps to NM_015150.1 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:107103123 C>T maps to ENST00000357881 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:107103203 C>T maps to ENST00000357881 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr12:106995105 C>T maps to ENST00000357881 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr15:56385632 T>C maps to NM_022841.5 Q1431Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr23:109696872 G>A did not map to a codon.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr23:109696415 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:109693870 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:109693931 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:109694868 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:109696764 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:109697343 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:109697506 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:109694989 C>G did not map to a codon.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr23:109694988 T>C did not map to a codon.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr23:71350066 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:11508131 G>A maps to NM_001161616.1 R636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:46951190 G>A did not map to a codon.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr5:73166008 C>T maps to NM_001080479.2 V847V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:73128268 T>C maps to NM_001080479.2 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:153332810 C>T maps to NM_012419.4 Q177Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:192780206 C>A maps to NM_002923.3 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:192335139 C>A maps to NM_001039152.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:101076055 C>A maps to NM_015668.3 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:101117606 C>A maps to NM_015668.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr8:101075774 A>G maps to NM_015668.3 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr9:116224395 T>C maps to NM_144488.4 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr15:90021157 G>A maps to NM_016321.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:25628086 C>A maps to ENST00000357542 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:129251527 C>T maps to NM_000539.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr2:20647735 C>G maps to NM_004040.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr10:62634762 C>T maps to NM_014836.4 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:22864339 C>T maps to NM_001160036.1 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:63747756 C>T maps to NM_020663.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr23:119211112 C>T did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:33486947 G>A maps to NM_033103.4 D468D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:53457714 G>A did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr11:8132394 A>G maps to ENST00000309737 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr12:107237686 C>T maps to ENST00000392837 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:12860000 C>A maps to NM_014859.4 S427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:12887968 G>A maps to NM_014859.4 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr17:12888091 C>T maps to NM_014859.4 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:152319838 G>T maps to NM_018151.4 E1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr2:152293374 C>T maps to NM_018151.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr2:152322492 T>C maps to NM_018151.4 P2153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr12:130898849 G>A maps to NM_015347.4 D824D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:130892273 G>A maps to NM_015347.4 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr12:130919421 C>A maps to NM_015347.4 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:8902617 C>T maps to NM_020734.2 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:105261748 A>G maps to NM_001100117.2 G1208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr8:104898095 T>G maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr8:104709325 G>A maps to NM_001100117.2 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:19955748 G>A maps to ENST00000255006 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr14:93118668 G>A maps to NM_024832.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr14:93118467 G>A maps to NM_024832.3 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr7:105183036 T>C maps to NM_021930.4 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr5:96498916 G>A maps to NM_018343.2 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:24807497 G>A maps to NM_006871.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr14:24806434 G>A maps to NM_006871.3 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr6:84563146 G>A maps to NM_001009994.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:155870316 A>C maps to ENST00000368322 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:40704700 G>T maps to NM_012421.3 E1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:73811990 G>A did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr14:21052114 A>G maps to NM_145250.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:12918086 C>T maps to NM_006397.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr19:12918231 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:31486627 C>T maps to NM_013235.4 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:31464405 T>C maps to NM_013235.4 E837E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr2:86847521 G>A maps to NM_005667.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:59348037 G>T maps to ENST00000434298 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:59359276 G>T maps to ENST00000434298 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr15:59373357 T>C maps to ENST00000434298 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr15:59347928 C>A maps to ENST00000434298 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr3:49742128 C>A maps to NM_022064.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:105970342 A>T did not map to a codon.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr3:149613279 A>G maps to NM_007282.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr5:179405270 G>A maps to NM_018434.4 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr4:142053629 C>T maps to NM_020724.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:30325675 C>T maps to NM_015565.2 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr13:25374501 A>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:25367459 G>T maps to ENST00000381927 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:63509431 T>C maps to NM_001113561.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr8:101299868 T>C maps to NM_183419.1 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr8:101299931 A>G maps to NM_183419.1 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:185069001 C>T maps to NM_007212.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr1:6278399 C>T maps to NM_207396.2 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:6270288 C>T maps to NM_207396.2 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:78317011 C>T maps to NM_020914.4 R2073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:78367181 G>T maps to NM_020914.4 E5219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:78320609 C>T maps to NM_020914.4 C2874C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:117150910 G>T maps to NM_207343.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr11:117105071 C>T maps to NM_207343.2 D28D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr22:30776098 C>T maps to NM_001017981.1 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr22:30781915 G>A maps to NM_001017981.1 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:79190224 G>A maps to NM_024546.3 N557N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:79190856 C>A maps to NM_024546.3 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr11:119205978 G>A maps to NM_032015.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:24626831 C>A maps to NM_017999.4 A904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:30043368 C>T maps to NM_025236.3 W66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr12:56604130 G>A maps to NM_194359.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr17:56435546 A>G maps to NM_017763.4 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr13:26788760 T>A maps to NM_005977.3 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:89650879 C>T maps to NM_003800.3 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:78649270 C>A maps to NM_002941.3 E1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:78663873 G>A maps to NM_002941.3 A1453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr3:78663930 C>T maps to NM_002941.3 A1434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:77651533 G>T maps to ENST00000332191 E1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr3:77666709 T>C maps to ENST00000332191 L1114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr11:124740952 T>A maps to NM_022370.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:124765467 G>A maps to NM_019055.5 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:124764190 G>A maps to NM_019055.5 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr18:18547732 C>A maps to NM_005406.2 E1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:11338839 C>A maps to NM_004850.3 E991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr2:11334407 G>A maps to NM_004850.3 S1194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr9:115060127 A>G maps to NM_001163790.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr16:4850569 G>A maps to NM_024589.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr11:62381807 G>C maps to NM_000327.3 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:125694435 G>A maps to NM_001012337.1 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr9:94486945 G>A maps to NM_004560.2 H610H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:77257576 T>C maps to ENST00000396204 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr6:117730796 C>T maps to NM_002944.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr6:117665426 T>C did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr6:117665426 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:55537348 G>T maps to NM_006269.1 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:10470380 C>T maps to NM_178857.5 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:10470413 G>A maps to NM_178857.5 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:10467947 G>A maps to NM_178857.5 D1220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr23:46713274 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:46713159 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:96139421 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:5331501 G>T maps to NM_001033002.3 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:41819229 G>A maps to NM_015540.2 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr1:68905268 G>A maps to NM_000329.2 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:68903977 G>T maps to NM_000329.2 Y340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:68910338 G>A maps to NM_000329.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:111306256 G>A maps to NM_032194.1 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:38158348 G>A did not map to a codon.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr23:38147243 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:21762903 C>T maps to NM_020366.3 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:21816376 G>T maps to NM_020366.3 E1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:53682949 G>A maps to NM_015272.2 R744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:169335 G>A maps to NM_006987.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:88999563 T>C maps to NM_144563.2 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr23:153628260 T>C did not map to a codon.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr1:24022844 C>T maps to NM_000975.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:12877667 G>A maps to ENST00000273223 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:1995892 G>A maps to NM_005061.2 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:35857023 C>T maps to NM_002951.3 N457N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:4995409 G>A maps to NM_006638.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:150432767 T>C maps to NM_015203.3 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:1440146 G>A maps to NM_001018.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr23:71493152 C>T did not map to a codon.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr23:71496025 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:167271689 C>A maps to ENST00000510118 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr6:166836800 G>A maps to ENST00000510118 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:20222186 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:20185792 G>T did not map to a codon.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr23:20185860 T>C did not map to a codon.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr23:20213210 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:91409508 A>G maps to NM_004755.2 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:83361978 G>A did not map to a codon.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr23:83389794 A>T did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr23:83374909 A>G did not map to a codon.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr1:213414658 G>T maps to NM_012424.3 G614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr14:75378074 G>T maps to NM_031464.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:54705147 C>T maps to NM_001013.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:152128410 A>G maps to NM_001122965.1 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:78704376 C>T maps to NM_020761.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr9:19050160 G>A maps to NM_006570.4 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:39318141 G>T maps to NM_022157.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr6:90097190 G>A maps to NM_021244.4 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:90088945 G>T maps to NM_021244.4 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:90097036 G>A maps to NM_021244.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr6:7248753 A>G maps to NM_001003699.3 P1594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr6:7248753 A>G maps to NM_001003699.3 P1594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr4:110757205 A>G maps to NM_006583.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr23:18674814 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:18660160 C>T did not map to a codon.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr2:7030440 T>C maps to NM_080657.4 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr1:114354941 T>G maps to NM_018364.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:77378473 G>A maps to NM_016578.3 R1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:77387909 G>A maps to NM_016578.3 R1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:116949370 G>T maps to NM_001010892.2 G501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:38082189 G>A maps to NM_001038633.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:127469956 C>T maps to ENST00000368317 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr6:127476515 G>A maps to ENST00000368317 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:57255281 C>A maps to NM_133368.1 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:57265110 C>A maps to NM_133368.1 S470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr12:123006783 T>C maps to NM_023012.5 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr10:16796930 A>T maps to NM_012425.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr20:62303952 C>T maps to ENST00000482936 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr20:62298881 G>A maps to ENST00000482936 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:41758425 C>T maps to NM_015138.4 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:63964727 G>A maps to NM_145307.2 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr14:101350471 T>C maps to NM_001134888.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr14:101349853 C>T maps to NM_001134888.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr14:60212552 G>A maps to NM_021136.2 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr19:45998252 G>A maps to NM_005619.3 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:63488413 G>T maps to ENST00000377819 E814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:107019951 A>G maps to NM_032730.4 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr3:186917437 C>T maps to NM_153708.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:67781783 C>A maps to NM_173630.3 E1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr17:41142451 A>G maps to NM_173079.2 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr21:36252866 A>G maps to NM_001754.4 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:93017486 G>A maps to NM_175634.2 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr8:92998513 G>A maps to NM_175634.2 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr8:93004061 G>A maps to NM_175634.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:45515040 G>T maps to ENST00000359524 *590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:155298024 G>A maps to NM_001105203.1 Q833Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:35555270 C>T maps to NM_001135999.1 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:35560482 C>T maps to NM_001135999.1 I1282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:127801414 G>A maps to NM_003707.2 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:159549831 T>A maps to ENST00000440678 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:159568024 G>A maps to ENST00000440678 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr4:159568117 A>G maps to ENST00000440678 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:33937294 C>T maps to NM_016568.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr5:33937618 C>T maps to NM_016568.3 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr3:133921632 T>C maps to ENST00000296084 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:38943557 C>A maps to NM_000540.2 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:38957015 C>T maps to NM_000540.2 I1052I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr19:38956901 G>A maps to NM_000540.2 A1014A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr19:38976775 C>T maps to NM_000540.2 R1827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:38934888 C>T maps to NM_000540.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr19:38976616 G>A maps to NM_000540.2 P1774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:237863700 C>T maps to NM_001035.2 L3101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr1:237947689 G>A maps to NM_001035.2 P4226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:237532884 C>T maps to NM_001035.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr1:237811894 G>A maps to NM_001035.2 A2498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr1:237666610 C>T maps to NM_001035.2 R807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr1:237806694 A>G maps to NM_001035.2 G2430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr1:237580423 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:34047331 G>A maps to NM_001036.3 K2822K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:34072477 G>A maps to NM_001036.3 E3068E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr15:33927941 C>T maps to NM_001036.3 V1101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:33954986 C>T maps to NM_001036.3 P1752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:34047325 C>T maps to NM_001036.3 F2820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr15:33936602 C>T maps to NM_001036.3 C1216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr15:34130561 G>A maps to NM_001036.3 A4127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr15:33893657 G>T maps to NM_001036.3 G609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr15:33855174 C>T maps to NM_001036.3 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr1:153533947 A>G maps to ENST00000368707 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:91616621 C>T maps to NM_005226.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:18257430 C>A maps to NM_006512.3 G15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr11:18105186 T>C maps to NM_138421.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:45785121 C>T maps to NM_014016.3 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr13:23910681 C>A maps to NM_014363.4 E2445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:23907565 T>G maps to NM_014363.4 P3483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:23908735 C>A maps to NM_014363.4 V3093V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:23911195 T>G maps to NM_014363.4 S2273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:23913433 A>G maps to NM_014363.4 N1527N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr13:23932591 C>T maps to NM_014363.4 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr13:23908581 C>A maps to NM_014363.4 E3145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr13:23908972 C>T maps to NM_014363.4 W3014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr19:47656156 G>T maps to NM_005500.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:5613528 C>A maps to NM_014649.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:134993886 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:134992597 G>A did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:134989979 C>T did not map to a codon.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr16:51175490 C>T maps to ENST00000251020 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:51175391 G>A maps to ENST00000251020 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr16:51172862 G>A maps to ENST00000251020 N1090N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr16:51175402 G>A maps to ENST00000251020 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr20:50407572 T>C maps to NM_020436.3 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr20:50406984 G>A maps to NM_020436.3 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr20:50418827 C>T maps to NM_020436.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr20:62607159 C>T maps to NM_080621.4 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr8:119391877 G>A maps to NM_207506.2 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:55203946 C>T maps to NM_015589.4 H306H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:55226886 C>T maps to NM_015589.4 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:55236926 C>T maps to NM_015589.4 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr14:55251327 C>T maps to NM_015589.4 H705H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:92733271 T>C maps to NM_017654.3 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:92732491 G>A maps to NM_017654.3 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr7:92731561 A>G maps to NM_017654.3 N1283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:92761626 C>A maps to NM_152703.2 E1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:92761864 G>A maps to NM_152703.2 N1140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr22:44371982 C>T maps to NM_015380.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr21:15889290 A>C maps to ENST00000285670 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr21:15873050 T>C maps to ENST00000285670 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:128772379 G>A maps to NM_001145928.1 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3575-01A-01W-0831-10 chr11:68343448 C>T maps to NM_001164160.1 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:68326037 G>T maps to NM_001164160.1 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr11:68331812 T>C maps to NM_001164160.1 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr9:136529130 C>T maps to NM_007101.3 S879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr1:109780386 G>A maps to ENST00000369923 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr19:39416934 C>G maps to NM_017827.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr12:108920085 C>T maps to NM_014706.3 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr6:148846473 C>T maps to NM_015278.3 H419H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:148846458 G>A maps to NM_015278.3 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:148848722 C>A maps to NM_015278.3 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:128926970 A>T did not map to a codon.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr23:23803818 G>A did not map to a codon.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr3:18419721 T>C maps to ENST00000332610 E507E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr2:200173512 G>A maps to NM_001172509.1 H570H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr23:84362525 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:9806723 G>A maps to NM_030962.3 R1727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:9853896 G>A maps to NM_030962.3 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr11:9989939 A>G maps to NM_030962.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr19:56041621 G>A maps to NM_001101401.2 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr12:123815037 G>A maps to NM_001167856.1 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr12:123810119 T>C maps to NM_001167856.1 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:39967250 G>A maps to NM_006455.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr9:127764297 G>A maps to NM_173690.4 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr9:127733650 G>T maps to NM_173690.4 R581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr6:28541598 C>T maps to NM_052923.1 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:28542809 C>A maps to NM_052923.1 E558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:28542900 A>C maps to NM_052923.1 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:28543115 C>A maps to NM_052923.1 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr3:47458697 C>A did not map to a codon.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr15:76995211 C>T maps to ENST00000324767 Q793Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr15:77057313 T>C maps to ENST00000324767 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr15:77087665 G>A maps to ENST00000324767 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr8:27824004 G>T maps to NM_173833.5 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr12:125284768 G>T maps to NM_005505.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:83602053 G>A maps to NM_001037582.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:224463934 G>A maps to NM_003469.4 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:35085229 C>T maps to NM_001025591.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr6:25701469 C>T maps to NM_006998.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr6:25665247 G>T maps to NM_006998.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr4:129960212 G>A maps to NM_144643.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:238990837 C>T maps to NM_016510.4 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:41579027 G>A maps to NM_001031694.2 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:17764154 T>A did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:17768145 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:18264795 G>A did not map to a codon.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr23:18348760 T>A did not map to a codon.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr3:38750989 G>A maps to NM_006514.2 N1420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:38768345 C>T maps to NM_006514.2 E946E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:38802854 C>T maps to NM_006514.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr3:38753912 G>A maps to NM_006514.2 G1276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr3:38833623 G>T maps to NM_006514.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:38888583 G>A maps to ENST00000302328 V1659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:38892218 G>A maps to ENST00000302328 F1360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:38927671 C>A maps to ENST00000302328 E965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr3:38968292 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:166904193 A>C maps to NM_001165963.1 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr2:166868747 C>T maps to NM_001165963.1 T1250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:166915078 T>C maps to NM_001165963.1 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr2:166848030 A>G maps to NM_001165963.1 S1918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:166201226 G>T maps to NM_001040142.1 E909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:166211174 C>T maps to NM_001040142.1 S1131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr2:166170617 G>A maps to NM_001040142.1 Q461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr2:166172174 G>A maps to NM_001040142.1 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:118038802 C>A maps to NM_004588.4 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr11:118037754 G>A maps to NM_004588.4 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr2:166012310 T>C maps to NM_006922.3 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:165947004 G>T maps to NM_006922.3 V1886V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:165994618 C>A maps to NM_006922.3 E721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr2:165986779 G>A maps to NM_006922.3 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr2:165994388 C>T maps to NM_006922.3 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr11:123516431 C>A maps to NM_018400.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:62020210 G>A maps to NM_000334.4 F1421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:62026015 G>A maps to NM_000334.4 F1033F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr3:38597230 G>A maps to NM_001099404.1 F1486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:38645238 G>A maps to NM_001099404.1 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:52200540 C>T maps to NM_014191.2 V1757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:167159615 A>G maps to ENST00000303354 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:167141201 C>A maps to ENST00000303354 G580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:167149857 A>G maps to ENST00000303354 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:167108272 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:6457332 G>A maps to NM_001159576.1 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr16:23205521 T>C maps to NM_001039.3 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:10595204 G>A maps to NM_004589.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:174312451 A>G maps to NM_007281.2 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:144886020 C>T maps to NM_182706.3 T1070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr2:120231098 C>T maps to NM_002980.2 W112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:43735137 G>A maps to NM_173050.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:31347354 G>A maps to NM_014654.3 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr14:50280748 A>C maps to NM_004713.3 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:243471468 A>C maps to NM_006642.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr7:4088986 C>T maps to NM_152744.3 T870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:4002367 C>T maps to NM_152744.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:4152938 G>T maps to NM_152744.3 V1151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:71346840 G>A maps to NM_001144952.1 F1949F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:192701019 G>A maps to NM_004657.5 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr2:192711270 C>A maps to NM_004657.5 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:177928079 C>T maps to NM_033127.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:145115871 C>T maps to NM_004892.4 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:39509997 C>A maps to NM_006364.2 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr14:39565309 A>G maps to NM_006364.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr10:121685735 A>G maps to NM_007190.2 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr4:110415906 T>C maps to NM_006323.2 Y461Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr10:75506595 C>T maps to NM_198597.1 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr10:75506595 C>T maps to NM_198597.1 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:83763305 C>T maps to ENST00000505472 A1016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr10:102269147 C>T maps to NM_015490.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:102262141 C>A maps to NM_015490.3 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:49301540 G>A maps to NM_001193489.1 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr14:81964373 C>T maps to NM_005065.4 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr20:13867032 C>A maps to NM_025229.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:13839925 G>A maps to NM_025229.1 H600H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:13846145 G>T maps to NM_025229.1 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr20:13867032 C>T maps to NM_025229.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr1:151337105 C>T maps to ENST00000435071 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:169672531 A>G maps to NM_000655.4 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:169586353 G>A maps to NM_003005.3 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:169565301 G>A maps to NM_003005.3 Y654Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:169582863 G>T maps to NM_003005.3 C183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr12:109017441 A>G maps to ENST00000228463 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:84628805 G>A maps to NM_152754.2 R762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr7:84685071 G>A maps to NM_152754.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:82997279 C>T maps to NM_012431.2 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:83035287 C>A maps to NM_012431.2 G301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr3:52475664 G>A maps to NM_020163.1 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr9:91996162 C>T maps to NM_006378.3 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr2:74900582 G>T did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr2:74900822 C>T maps to NM_004263.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr5:9122871 G>A maps to NM_003966.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:9154664 G>A maps to NM_003966.2 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:9054217 G>A maps to NM_003966.2 C890C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr3:122662371 C>T maps to NM_001031702.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr15:48058182 T>C maps to NM_153618.1 C515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr20:43851052 C>T maps to NM_003008.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr20:43851701 C>T maps to NM_003008.2 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:196626618 C>A maps to NM_152699.4 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:76376477 G>T maps to NM_015571.2 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr6:76373082 A>G maps to NM_015571.2 E281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3578-01A-01W-0831-10 chr3:101066779 C>T maps to NM_020654.3 W591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:101046584 G>A maps to NM_020654.3 C980C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:101049207 C>T maps to NM_020654.3 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:101086820 G>A maps to NM_020654.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr4:25156720 T>A maps to NM_016955.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr4:25160600 G>A maps to NM_016955.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:110303729 C>A maps to ENST00000356688 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr16:4836035 T>A maps to NM_144605.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:55863770 G>A maps to NM_207366.2 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr23:118771000 G>T did not map to a codon.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr7:35942736 G>T maps to NM_001788.4 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:67891861 C>T maps to NM_001018067.1 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:122774930 C>T maps to NM_020755.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:44087293 T>C maps to ENST00000319327 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr14:94756516 G>A maps to NM_001100607.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr14:94964254 G>A maps to NM_173850.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr14:94964310 G>A maps to NM_173850.2 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr14:94964308 C>T maps to NM_173850.2 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr14:95090099 C>T maps to ENST00000393080 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:95033447 C>A maps to NM_006215.2 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr14:94780519 A>G maps to NM_001756.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:105280446 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:105281010 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:61585302 G>A maps to NM_005024.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:61387356 G>T maps to NM_080475.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:61228355 G>A maps to ENST00000382768 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr18:61261695 G>T maps to NM_012397.3 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr18:61645697 C>T maps to NM_198833.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr1:173878852 T>C maps to NM_000488.3 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:100777073 G>T maps to NM_000602.3 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr11:94911900 T>C maps to NM_144665.2 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:42529970 G>A maps to NM_015559.2 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:42530597 C>A maps to NM_015559.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr16:30991489 C>T maps to NM_014712.1 N1461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr3:47084093 G>A maps to NM_014159.6 R2399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr3:47161979 A>G maps to NM_014159.6 A1382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:47164576 C>A maps to NM_014159.6 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr3:47162348 A>G maps to NM_014159.6 G1259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr3:47144859 A>G maps to NM_014159.6 C1631C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:99927566 C>A maps to NM_032233.2 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:9495465 C>A maps to ENST00000407969 S816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr16:58552124 A>G maps to NM_001160305.1 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr12:123892039 C>T maps to NM_020382.3 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:150915097 C>T maps to NM_001145415.1 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr13:50055134 C>T maps to NM_031915.2 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:4355430 C>T maps to NM_006515.3 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:135172395 C>A maps to ENST00000372169 E1943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr9:135150791 A>G maps to ENST00000372169 V2317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:27284489 G>A maps to NM_178860.4 P790P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr17:27286097 C>T maps to NM_178860.4 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:26736452 C>A maps to NM_021115.4 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr11:64544045 T>C maps to NM_201995.2 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:70602202 C>A maps to NM_012426.4 I990I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr22:31927077 C>T maps to NM_001007467.1 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:31927077 C>T maps to NM_001007467.1 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:52947541 C>T maps to NM_016329.3 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:7423836 G>T maps to NM_001018039.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr1:35656296 C>A maps to NM_005066.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr4:154702674 C>T maps to NM_003013.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr4:154702785 C>T maps to NM_003013.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:37955922 G>A maps to ENST00000223214 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:64036932 G>A maps to ENST00000513458 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:19135605 G>A maps to NM_001017392.3 F517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr19:19115058 A>G maps to NM_001017392.3 P949P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:1712546 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:46318816 A>G maps to NM_004719.2 G1200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:42089364 C>T maps to NM_006275.5 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr12:132198666 T>C maps to NM_004592.2 Y90Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr7:94257669 G>A maps to NM_001099401.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:14412243 A>C maps to NM_139167.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr3:153840410 T>A maps to NM_015595.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:153973151 G>T maps to NM_015595.3 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:134492032 G>T maps to NM_001143676.1 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr20:42200774 G>T maps to NM_016276.3 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr8:8197042 G>C maps to NM_001080826.1 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:77472837 G>A maps to NM_024776.2 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr15:77425988 G>T maps to NM_024776.2 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr8:67726109 A>G maps to NM_013257.3 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:108824538 G>T maps to NM_152621.5 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:108831516 C>A maps to NM_152621.5 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:108831603 C>A maps to NM_152621.5 C331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr4:108831579 A>G maps to NM_152621.5 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:201434542 G>T maps to NM_152524.5 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr2:201437639 A>G maps to NM_152524.5 Q857Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:72617371 C>T maps to NM_003901.3 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr2:223423166 C>T maps to NM_152386.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:25264349 C>T maps to NM_001039948.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr17:2266811 T>C maps to NM_014853.2 C242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:2280078 C>T maps to NM_014853.2 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:40801146 C>T maps to NM_015705.4 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr16:28880331 A>G maps to NM_001145795.1 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr12:111886036 G>A maps to NM_005475.2 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:156779562 C>A maps to NM_001161441.1 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr8:19250958 T>C maps to NM_022071.3 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:82363341 G>A maps to NM_207372.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:40847087 G>T maps to NM_007341.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr4:2826420 G>A maps to NM_001145856.1 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr19:4362365 T>C maps to NM_003025.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:19725016 G>T did not map to a codon.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr10:105526903 G>A maps to ENST00000369774 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr2:110015095 C>T maps to NM_001099289.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr2:110259190 C>G maps to NM_001099289.1 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr4:8229577 C>T maps to NM_018986.3 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:148407347 G>A maps to NM_024577.3 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr11:70332476 C>T maps to ENST00000338508 Q1301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr22:51160202 C>T maps to NM_001080420.1 A1330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr1:154942741 T>C maps to NM_001130040.1 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:436638 G>A maps to NM_012435.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr9:91667022 G>A maps to NM_016848.5 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr13:26620911 C>T maps to NM_001007538.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:57626050 C>T maps to NM_005412.5 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:112724662 G>T maps to NM_007373.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:112769478 C>A maps to NM_007373.3 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr3:157823549 T>C maps to NM_003030.4 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:146264907 C>A maps to ENST00000367503 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr3:72842104 G>C maps to NM_018130.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr3:72866502 G>A maps to NM_018130.2 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr3:72881524 A>G maps to NM_018130.2 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr23:9862667 C>A did not map to a codon.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr23:9900581 G>A did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:50350751 T>C did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:50350777 T>G did not map to a codon.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr23:50377222 T>C did not map to a codon.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr3:164785144 T>C maps to NM_001041.3 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:164785144 T>C maps to NM_001041.3 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:124508520 C>A maps to NM_170601.3 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:48396297 C>T maps to NM_001006610.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:46425653 G>A maps to NM_198849.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr3:113329933 C>T maps to ENST00000393830 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr20:3684490 G>A maps to NM_023068.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:52131216 G>A maps to ENST00000222107 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:52033128 G>A maps to NM_001245.5 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:51650039 C>T maps to NM_014385.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:51656390 G>A maps to NM_014385.2 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr19:51961584 T>C maps to NM_014442.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr19:51955689 T>C maps to NM_014442.2 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:111491116 G>T maps to NM_015191.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:116728695 G>T maps to ENST00000445177 S1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr6:100838245 G>A maps to ENST00000262901 N764N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr6:100841612 C>T maps to ENST00000262901 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr21:38092189 C>T maps to NM_005069.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:75706568 G>T maps to NM_001145357.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr15:75702218 G>A maps to NM_001145357.1 C425C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr19:16962242 C>T maps to NM_015260.1 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:39587286 C>T maps to NM_003616.2 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr14:72055680 C>T maps to NM_015556.1 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:72055294 C>T maps to NM_015556.1 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:72055926 C>A maps to NM_015556.1 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:72056031 C>T maps to NM_015556.1 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:72138351 T>G maps to NM_015556.1 V924V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:72055078 A>C maps to NM_015556.1 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:232551264 G>A maps to NM_020808.3 L1579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:232564164 G>A maps to NM_020808.3 R1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr1:232579388 G>A maps to NM_020808.3 P1132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:1460485 C>A maps to NM_001122962.1 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr20:1515072 A>G maps to ENST00000381621 *199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:69647187 C>T maps to NM_012238.4 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:69666546 G>T maps to NM_012238.4 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:61180673 G>T maps to NM_017420.4 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:57196831 C>A maps to NM_182620.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr3:170110051 A>G maps to NM_005414.3 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr3:170110051 A>G maps to NM_005414.3 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr6:31930841 C>T maps to NM_006929.4 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:36168444 G>A maps to NM_005983.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr5:36166731 A>G maps to NM_005983.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:160456958 C>A maps to NM_001184714.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:160460918 G>A maps to NM_001184714.1 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:153716925 C>A did not map to a codon.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr23:153717031 T>C did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:153716357 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:48513122 A>G maps to NM_000338.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr20:44664477 C>T maps to NM_001134771.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr15:34527515 C>T did not map to a codon.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr15:34536251 G>A maps to NM_133647.1 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:34547473 C>A maps to NM_133647.1 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:34530593 G>A maps to NM_133647.1 R881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:1094319 G>A maps to NM_006598.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:122768992 C>A maps to NM_022444.3 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr7:122811856 C>T maps to NM_022444.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr20:45221137 G>A maps to NM_022829.5 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:45216771 G>A maps to NM_022829.5 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:135390915 G>A maps to NM_012450.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr7:135406175 A>G maps to NM_012450.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr7:135406184 C>T maps to NM_012450.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:135412190 G>A maps to NM_012450.2 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr18:43253774 C>T maps to NM_007163.3 I835I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:43205688 C>T maps to NM_007163.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:99378637 G>T maps to NM_005073.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:121631955 G>T maps to NM_021082.3 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:113456731 G>A maps to NM_003051.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr1:113460433 G>A maps to NM_003051.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr17:6941498 G>A maps to NM_201566.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:230910608 G>T maps to NM_152527.4 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:230910901 G>A maps to NM_152527.4 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr23:73751290 A>G did not map to a codon.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:73745669 G>A did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:73751290 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:66268786 G>A maps to NM_004694.4 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr10:61432594 T>C maps to NM_194298.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr11:22399216 G>A maps to NM_020346.2 K560K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr12:100751240 C>T maps to NM_139319.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr20:61597050 C>T maps to NM_022082.3 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:20005551 G>T maps to NM_001135691.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:119003749 A>G maps to NM_003054.4 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr10:119014839 G>A maps to NM_003054.4 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr2:228552898 A>G maps to NM_025243.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr11:35333788 G>A maps to NM_004171.3 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:35302520 G>A maps to NM_004171.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:36680568 C>T maps to NM_004172.4 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr5:36671174 C>T maps to NM_004172.4 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:65243771 C>T maps to NM_003038.4 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr19:15063789 G>A maps to NM_005071.1 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr8:42286359 G>A maps to NM_006749.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:42294775 G>A maps to NM_006749.3 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr3:38307446 T>C maps to NM_004256.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:38317844 C>A maps to NM_004256.3 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr3:38307446 T>C maps to NM_004256.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3582-01A-01W-0831-10 chr6:110746108 C>T maps to NM_033125.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:23816810 G>A maps to NM_020372.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:64990003 G>T maps to ENST00000438990 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:131728296 C>T maps to ENST00000435065 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:62747000 G>A maps to NM_004790.3 C440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr6:43271892 C>T maps to ENST00000372585 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr11:62782409 C>T maps to ENST00000430500 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr5:138714333 C>T maps to NM_152685.3 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:138718270 C>T maps to NM_152685.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:220026720 G>T maps to NM_001144890.1 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr20:19665778 C>T maps to NM_020689.3 N366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:19665961 C>T maps to NM_020689.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:92959950 G>A maps to NM_153646.3 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr15:48431256 C>G maps to NM_205850.2 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr23:129498621 G>A did not map to a codon.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr23:129506896 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:129483268 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:41381511 C>T maps to NM_014252.3 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:70243298 G>A maps to NM_152707.2 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:70276586 G>T maps to NM_152707.2 C48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:6457527 C>T maps to NM_024103.2 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr4:128651780 C>T maps to NM_031291.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr4:128651747 C>T maps to NM_031291.2 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:87476353 G>A maps to NM_018843.3 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr23:118587022 C>A did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:118603755 T>A did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr17:78195517 C>A maps to NM_173626.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:149360113 G>T maps to NM_000112.3 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:149357694 C>A maps to NM_000112.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr7:107314663 C>T maps to NM_000441.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr7:107323967 A>G maps to NM_000441.1 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr7:107342417 T>C maps to NM_000441.1 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:103038398 G>A maps to ENST00000354356 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:103061221 G>T maps to ENST00000354356 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr7:103018943 G>A maps to ENST00000354356 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr19:17608116 C>T maps to NM_198580.1 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:17615279 G>A maps to NM_198580.1 Q600Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:85433734 C>T maps to NM_004213.3 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr9:86903015 A>G maps to NM_022127.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:86917178 G>A maps to NM_022127.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:66136894 G>A maps to NM_001532.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr20:45354682 C>T maps to NM_030777.3 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr6:134350497 G>A maps to NM_145176.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:134328046 G>T maps to NM_145176.2 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr12:7970606 A>G maps to NM_153449.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr3:170723097 A>C maps to NM_000340.1 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:170723154 G>T maps to NM_000340.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr12:8083193 C>T maps to NM_006931.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:7188167 G>A maps to NM_001042.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr1:9100201 C>T maps to NM_003039.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:68396693 C>T maps to NM_022902.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:68412341 G>A maps to NM_022902.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:32445305 C>T maps to NM_001193513.1 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr8:118183324 C>T maps to NM_173851.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:118184847 A>C maps to NM_173851.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:42020144 G>T maps to NM_006345.3 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:42080285 G>T maps to NM_006345.3 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr4:41992691 C>T maps to NM_006345.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr4:25671331 C>T maps to NM_006424.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr4:25671401 G>T maps to NM_006424.2 G257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:48762431 A>G did not map to a codon.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr6:8417715 C>T maps to NM_001142540.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:67519656 C>A maps to NM_015139.2 G14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr6:137245446 G>T maps to NM_001008783.1 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:118596707 C>T maps to NM_001029858.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:234367367 C>T maps to NM_173508.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:58036614 G>T maps to NM_001080455.1 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:114483037 G>A maps to NM_025181.2 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:114492239 G>T maps to NM_025181.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr5:150722454 C>T maps to NM_181776.2 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr11:92895990 C>T maps to NM_152313.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:92881894 C>T maps to NM_152313.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:46602842 C>A maps to NM_030674.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:79226319 C>T maps to NM_001037984.1 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr17:79219805 A>C maps to NM_001037984.1 G970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:165772437 A>G maps to ENST00000409662 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:47162095 G>A maps to NM_018018.4 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:47168837 G>T maps to NM_018018.4 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3575-01A-01W-0831-10 chr16:58701369 G>A maps to NM_018231.1 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:84067036 C>T maps to NM_001080442.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:54960687 G>T maps to NM_173514.2 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:153934788 G>A maps to NM_014437.3 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:196545681 C>T maps to NM_001127257.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr17:70943963 C>T maps to NM_001159770.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:71027781 G>A maps to NM_001159770.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr17:71027796 C>T maps to NM_001159770.1 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr11:47435015 G>A maps to NM_001128225.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:56631496 C>T maps to NM_001135195.1 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:205779239 G>A maps to NM_173854.4 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:1520007 C>A maps to ENST00000382147 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr1:95310925 T>C maps to NM_001114106.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:75685019 C>T maps to NM_152697.4 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:33963849 G>A maps to NM_016180.3 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:29287374 G>A maps to NM_001135919.1 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:19480788 C>T maps to ENST00000395585 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:19609976 G>A maps to NM_152908.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:162820805 C>A maps to NM_001178015.1 V1008V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:3218199 G>A maps to NM_001174090.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr20:3209658 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:220506401 C>T maps to NM_201574.2 F1244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr2:220502424 G>A maps to NM_201574.2 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr2:220494318 C>T maps to NM_201574.2 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:72412158 G>A maps to NM_001098484.2 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:27498145 A>C maps to ENST00000425128 L10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr3:27436594 T>C maps to ENST00000454389 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:51851154 G>T maps to NM_001039960.1 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:24918050 G>A maps to NM_052944.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:26714122 A>G maps to NM_178498.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr16:31499713 G>A maps to ENST00000431354 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr22:32625328 G>A maps to NM_014227.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:17991702 C>T maps to NM_000453.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:17999151 C>T maps to NM_000453.2 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr19:17992828 T>C maps to NM_000453.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr2:27423970 T>C maps to NM_021095.2 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:27423972 G>A maps to NM_021095.2 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:101552061 C>A maps to NM_145913.3 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:48694604 C>T maps to NM_001135181.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr3:10960097 G>A maps to NM_014229.1 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:304438 G>A maps to NM_003044.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:115585562 C>T did not map to a codon.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr23:115588821 C>T did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr23:115584285 G>A did not map to a codon.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr12:85255569 G>A maps to NM_182767.4 H678H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:49796493 G>T maps to NM_014037.2 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:49813000 G>A maps to NM_014037.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:110738256 C>T maps to NM_001010898.2 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:55690764 G>A maps to NM_001043.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:55731915 C>A maps to NM_001043.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr16:55703492 G>A maps to NM_001043.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:20625953 C>A maps to NM_004211.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr23:152958816 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:152959631 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:30107081 G>A maps to NM_003045.4 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr13:30104811 G>A maps to NM_003045.4 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr8:87235282 C>A maps to NM_138817.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:170204103 G>A maps to NM_020949.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr23:70146730 A>G did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr23:70148453 C>G did not map to a codon.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr22:21384275 G>A maps to NM_004173.2 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr16:87870232 G>A maps to NM_003486.5 Y387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:23635554 C>A maps to NM_012244.2 G116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:33353094 G>A maps to NM_014270.4 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:33350769 G>A maps to NM_014270.4 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:111887879 G>T maps to NM_183061.1 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:111918262 C>A maps to NM_183061.1 E810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:111923175 G>T maps to NM_183061.1 I687I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr3:111888082 A>G maps to NM_183061.1 A1004A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr2:103274047 C>T maps to NM_003048.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:67290590 C>T maps to NM_004594.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr16:67300006 C>T maps to NM_004594.2 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:46521555 A>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr20:48456126 G>A maps to ENST00000417961 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:48456126 G>A maps to ENST00000417961 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:21329725 G>T maps to NM_006446.4 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:21370159 C>A maps to NM_006446.4 Y535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr12:21329829 A>G maps to NM_006446.4 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr12:20890175 T>C maps to NM_017435.4 C506C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:20852528 G>T maps to NM_017435.4 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr15:92671649 C>A maps to NM_013272.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:101834230 G>A maps to NM_173488.3 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr5:101748714 A>G maps to NM_173488.3 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:33690346 G>T maps to NM_152270.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:33690784 G>A maps to NM_152270.3 Y14Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:33767976 T>G maps to NM_144682.5 T777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:33768652 C>T maps to NM_144682.5 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:98806508 G>A maps to NM_003061.2 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:20543193 G>T maps to ENST00000273739 E703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:20620553 C>T maps to ENST00000273739 F1517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:168111080 G>A maps to NM_003062.2 N1192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr23:144904518 G>A did not map to a codon.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr23:144906080 G>A did not map to a codon.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr23:144905478 A>G did not map to a codon.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr23:144904612 T>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:144906091 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:144904652 T>G did not map to a codon.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr23:144903996 G>A did not map to a codon.
Sequencing variant TCGA-AG-3582-01A-01W-0831-10 chr3:164907801 G>A maps to NM_014926.2 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr3:164905726 C>T maps to NM_014926.2 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:164906122 C>T maps to NM_014926.2 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr3:164908336 G>T maps to NM_014926.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr3:164906122 C>A maps to NM_014926.2 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3582-01A-01W-0831-10 chr23:142718115 A>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:142717255 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:142718687 G>T did not map to a codon.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr23:142718502 T>C did not map to a codon.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr23:142718464 G>T did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:142718308 C>T did not map to a codon.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr13:88328215 T>C maps to NM_015567.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr13:88329445 C>A maps to NM_015567.1 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr13:86368483 A>G maps to NM_032229.2 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr10:105762747 A>G maps to NM_014720.2 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:105762403 G>T maps to NM_014720.2 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:57898129 C>T maps to ENST00000428312 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr15:59186661 C>T maps to NM_024755.2 E449E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr4:146435884 A>G maps to NM_001003688.1 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr18:48575111 T>C maps to NM_005359.5 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr18:48591808 T>C maps to NM_005359.5 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr18:48591865 A>G maps to NM_005359.5 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr18:48575210 A>G maps to NM_005359.5 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr18:48591808 T>C maps to NM_005359.5 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr18:48586281 T>C maps to NM_005359.5 H317H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr18:48573536 G>T maps to NM_005359.5 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr18:48573542 T>C maps to NM_005359.5 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr18:48591826 A>G maps to NM_005359.5 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr18:48586261 C>T maps to NM_005359.5 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr18:48593496 A>G maps to NM_005359.5 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr18:48575670 C>A maps to NM_005359.5 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr5:135498970 T>C maps to NM_001001419.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:37453772 C>T maps to NM_001127217.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr13:37453598 G>A maps to NM_001127217.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr1:40872451 C>T maps to NM_022733.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:40878690 G>T maps to NM_022733.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr23:128633740 A>C did not map to a codon.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr23:128599876 G>A did not map to a codon.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:128615122 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:128649956 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:128645904 C>T did not map to a codon.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr23:128614768 G>C did not map to a codon.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr23:128649685 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:2032956 C>T maps to NM_003070.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:11152011 C>T maps to NM_001128849.1 I1432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:11114030 G>A maps to NM_001128849.1 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:144447610 A>C maps to NM_003601.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:144468042 G>T maps to NM_003601.2 E879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr4:95206149 T>A maps to NM_001128429.1 I985I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr4:95202678 T>C maps to NM_001128429.1 V890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr3:47719761 A>G maps to NM_003074.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr12:56577681 T>A maps to NM_003075.3 K199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr7:150936209 C>T maps to NM_003078.3 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:150939641 C>T maps to NM_003078.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr22:45789612 A>G maps to NM_148674.3 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr22:45767391 G>A maps to NM_148674.3 R758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr22:45789612 A>G maps to NM_148674.3 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:106864279 G>T maps to NM_001042550.1 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:106885485 G>T maps to NM_001042550.1 E744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:106900419 C>T maps to NM_001042550.1 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:112337594 C>T maps to NM_005445.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:160122244 C>T maps to NM_005496.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:160148845 A>G maps to NM_005496.3 E989E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr9:72967216 G>A maps to NM_015110.3 R1092R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:72893537 C>T maps to NM_015110.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr9:72929698 T>C maps to NM_015110.3 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:17902298 C>A maps to ENST00000381272 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:2666176 G>T maps to NM_015295.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:2784501 C>T maps to NM_015295.2 R1868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr16:18841684 T>C maps to ENST00000389467 L2933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:18859301 C>A maps to ENST00000389467 E1893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:18869531 C>T maps to ENST00000389467 R1398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr16:18882776 T>C maps to ENST00000389467 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr16:18839376 A>G maps to ENST00000389467 I3240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr16:18861442 A>G maps to ENST00000389467 P1763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr16:18882776 T>C maps to ENST00000389467 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr16:18861436 A>G maps to ENST00000389467 D1765D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr1:156230370 T>C maps to NM_015327.2 E718E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr7:128846153 C>T maps to NM_005631.4 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr20:4163143 C>T maps to ENST00000443211 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr11:6413380 C>T maps to NM_000543.4 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr16:68404971 G>A maps to NM_018667.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:98643391 C>T maps to NM_020429.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:88387587 C>T maps to NM_198274.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:246493820 C>A maps to NM_001167740.1 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr22:21213409 C>T maps to NM_004782.3 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr9:15422892 C>T maps to NM_001039697.1 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr9:139277715 G>A maps to NM_003086.2 H635H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr5:121758611 G>A maps to ENST00000379533 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:127544814 C>T maps to NM_014390.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr2:241988532 C>T maps to NM_001080437.1 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:241988475 C>T maps to NM_001080437.1 C514C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:1285731 G>A maps to ENST00000381876 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr2:96944360 G>A maps to NM_014014.3 I1804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr2:96944354 G>A maps to NM_014014.3 D1806D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:96962700 C>T maps to NM_014014.3 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:70122328 G>A maps to NM_006857.1 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:51617191 C>A maps to NM_018967.2 C357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:1251190 C>A maps to NM_018968.3 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:64428563 C>T maps to NM_003099.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr15:64410394 T>C maps to NM_003099.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:46196101 C>T maps to NM_152244.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr6:86223807 G>T maps to NM_153816.3 S846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:130784750 G>A maps to NM_014758.2 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr5:122165297 A>T maps to NM_003100.2 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr4:186267728 T>C maps to NM_031953.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr1:151630868 C>T maps to ENST00000458013 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr15:75942727 C>T maps to NM_153271.1 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr20:17929565 G>A maps to NM_152227.1 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr20:17929563 T>C maps to NM_152227.1 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr12:53509272 G>A maps to NM_003578.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr6:107954899 A>G maps to NM_018013.3 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:55510689 C>T maps to NM_199421.1 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:67992743 C>T maps to NM_004232.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr18:67992659 G>A maps to NM_004232.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr17:36508687 A>G maps to NM_014598.2 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr6:160105982 G>T maps to NM_000636.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr9:138586278 G>A maps to NM_001101677.1 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr13:36744712 G>A maps to ENST00000511166 C481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr16:597983 C>T maps to NM_005632.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr4:186545169 G>A maps to ENST00000355634 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr4:186598555 A>G maps to NM_001145673.1 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:108377916 G>A maps to NM_001013031.1 I970I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:108412301 C>T maps to NM_001013031.1 K771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr10:108357184 C>T maps to NM_001013031.1 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr4:7715968 C>T maps to NM_020777.2 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:7398031 G>A maps to NM_020777.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr10:106937889 C>T maps to NM_014978.1 D656D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:106602566 G>A maps to NM_014978.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:45365691 C>A maps to NM_003104.5 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:5832915 G>C maps to NM_003108.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:204095204 C>T maps to ENST00000367206 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:95364051 C>T maps to NM_007084.2 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr6:21595967 C>T maps to NM_003107.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3578-01A-01W-0831-10 chr12:23998926 G>A maps to NM_006940.4 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr12:23687260 G>A maps to NM_006940.4 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr11:16071409 A>G maps to NM_001145819.1 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:10583418 G>A maps to ENST00000354846 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr16:1033736 C>T maps to NM_014587.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr17:70120102 C>T maps to NM_000346.3 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr17:70120228 C>T maps to NM_000346.3 Q411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr12:53775986 C>T maps to NM_138473.2 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr2:231368940 A>G maps to NM_001080391.1 Q602Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr2:231050788 G>A maps to NM_080424.2 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr2:231112703 G>A maps to NM_007237.4 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:231101920 T>C maps to NM_007237.4 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:231113603 C>A maps to NM_007237.4 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:231174694 C>T maps to NM_007237.4 C705C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr2:231264876 C>T maps to NM_138402.4 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00H-01A-01W-A00E-09 chr2:231254709 A>T maps to NM_138402.4 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr7:21470069 A>G maps to NM_003112.3 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:21469928 A>G maps to NM_003112.3 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr7:21469946 T>C maps to NM_003112.3 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:53722274 C>T maps to NM_001173467.1 W317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:53722439 G>T maps to NM_001173467.1 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:7320330 C>A maps to NM_058201.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr2:215274984 C>T maps to NM_024532.3 D614D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:214162054 G>T maps to NM_024532.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:214204935 C>T maps to NM_024532.3 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:118535238 C>T maps to NM_206996.2 Q1737Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:118584643 G>A maps to NM_206996.2 R946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:118598484 C>A maps to NM_206996.2 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:26912339 C>A maps to NM_006461.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:22676870 C>A maps to ENST00000376603 Y342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:49067096 G>T maps to ENST00000376407 V919V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:49079094 G>A maps to ENST00000376407 R530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:123599596 C>T maps to NM_001174046.1 N368N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:142795458 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:142596916 T>C did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:142596796 T>A did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:142596798 A>T did not map to a codon.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr23:142596796 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:142121905 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:142121984 G>T did not map to a codon.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr5:151045923 G>A maps to NM_003118.2 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr4:88411521 G>A maps to NM_004684.4 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:32379454 C>T maps to NM_014946.3 R581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr3:57108237 C>T maps to NM_181727.1 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:52917875 G>C maps to NM_145263.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:133712401 G>A maps to NM_174927.1 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:48523205 G>A maps to NM_006038.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr14:88904597 T>C maps to NM_018418.4 D544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr5:94994410 C>T maps to NM_031952.3 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr8:145096220 C>T maps to NM_198572.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr2:201281141 A>T maps to ENST00000409151 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:169746017 G>A maps to NM_020675.3 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr7:44042291 G>A maps to NM_175064.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:35807267 G>A maps to NM_024867.3 K1764K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr2:220350101 C>T maps to NM_005876.4 G2548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:16255965 C>T maps to NM_015001.2 G1077G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:16256060 C>A maps to NM_015001.2 S1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:16260807 C>T maps to NM_015001.2 N2691N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr13:46287513 G>A maps to NM_152719.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr13:46287531 C>T maps to NM_152719.1 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:44890502 C>A maps to NM_025137.3 E1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:44941170 C>A maps to NM_025137.3 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr13:36878765 G>A maps to NM_001142294.1 Y579Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:36903629 C>A maps to NM_001142294.1 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:228846459 G>T maps to NM_001142644.1 L1692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:228881999 G>T maps to NM_001142644.1 I1190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:228883583 G>A maps to NM_001142644.1 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:228886493 G>A maps to NM_001142644.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:50926875 G>A maps to NM_003121.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr19:50931487 G>A maps to NM_003121.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr9:33240218 C>T maps to NM_014471.1 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:147503467 C>T maps to NM_001127698.1 R871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:147480972 C>T maps to NM_001127698.1 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:147449938 C>T maps to NM_001127698.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:12449836 C>A maps to NM_001128626.1 E691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr16:89935985 T>C maps to NM_032451.1 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr16:29675990 C>T maps to NM_003123.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr16:28989307 C>T maps to NM_032038.2 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr17:4439610 G>A maps to NM_001124758.1 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr17:4337388 A>C maps to NM_182538.4 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:136448204 C>T maps to NM_004598.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr4:167656167 T>C maps to NM_016950.2 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:167833782 G>T maps to NM_016950.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr4:167656167 T>C maps to NM_016950.2 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:51040896 A>G maps to NM_032802.3 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr19:2344021 G>A maps to NM_152988.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr15:38641630 T>C maps to NM_152594.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr2:65541138 G>A maps to NM_181784.2 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:65541249 G>A maps to NM_181784.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:124323507 C>T maps to NM_199327.1 C254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:80911713 G>A maps to NM_005842.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:155003873 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:155004378 G>T did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:141693947 G>A maps to NM_030964.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr1:158609791 T>C maps to NM_003126.2 Q1581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr1:158626362 G>A maps to NM_003126.2 N963N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:158609680 G>A maps to NM_003126.2 D1618D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:158623164 G>T maps to NM_003126.2 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr1:158589082 G>T maps to NM_003126.2 V2153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr1:158626362 G>A maps to NM_003126.2 N963N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr1:158609791 T>C maps to NM_003126.2 Q1581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:131374462 G>T maps to NM_001130438.2 E1661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr9:131389741 C>T maps to NM_001130438.2 H2218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr9:131353799 G>A maps to NM_001130438.2 P1017P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr14:65241857 G>A maps to ENST00000389723 S1613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr14:65216155 G>A maps to ENST00000389723 T2289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:54873342 G>T maps to NM_003128.2 E1533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr2:54839315 C>T maps to NM_003128.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:66454565 G>A maps to NM_006946.2 S2265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:66466465 G>A maps to NM_006946.2 H1288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:42147123 G>T maps to ENST00000320955 G3158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:18631436 G>A maps to NM_194285.2 R677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr11:18636365 C>T maps to NM_194285.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:142741902 G>A maps to NM_001080415.1 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr16:30731532 T>C maps to NM_006662.2 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr16:30745833 G>C maps to NM_006662.2 L2209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr16:30748692 A>G maps to NM_006662.2 R2444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr16:30735130 C>T maps to NM_006662.2 P1462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr17:17720322 G>A maps to NM_001005291.2 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr22:42293160 C>T maps to NM_004599.2 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:121362758 C>T maps to NM_152546.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr12:64383724 G>A maps to NM_020762.2 W100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:64377748 A>G maps to NM_020762.2 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:64458902 C>T maps to NM_020762.2 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:9055524 T>C maps to NM_014850.2 K605K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr3:9036106 G>A maps to NM_014850.2 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr16:4254627 C>T maps to ENST00000330063 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr16:4254546 G>A maps to ENST00000330063 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:35468784 G>T maps to NM_003136.3 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr14:35492188 G>A maps to NM_003136.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr14:35492182 A>G maps to NM_003136.3 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr11:126135297 G>A maps to NM_003139.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr23:38009099 T>C did not map to a codon.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr23:38019444 T>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:2224605 G>T maps to NM_021947.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr1:24997998 T>C maps to NM_005839.3 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:2813978 G>A maps to NM_016333.3 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:2816535 C>T maps to NM_016333.3 R2003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:2817974 G>A maps to NM_016333.3 T2482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:75894122 G>T maps to ENST00000388802 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr12:119583286 G>C maps to NM_194286.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:100484690 C>T maps to NM_015908.5 Y615Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr7:100482166 C>A maps to NM_015908.5 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:23615837 G>A maps to ENST00000415083 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr20:60747792 G>A maps to NM_198935.1 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:182774684 G>A maps to NM_001130445.1 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr12:109205064 G>A maps to NM_018984.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr12:109185876 C>T maps to NM_001161330.1 *693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:26383753 C>T maps to NM_005086.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr7:149477052 C>T maps to NM_198455.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr7:149482247 T>C maps to NM_198455.2 C975C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:38678866 G>A maps to NM_001049.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:71165604 C>A maps to NM_001050.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr23:48049587 C>G did not map to a codon.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr8:53028936 C>T maps to NM_014682.2 E967E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:53038697 A>C maps to NM_014682.2 L890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr8:53084622 G>A maps to NM_014682.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:134472162 G>A maps to NM_173344.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:44365218 T>C maps to NM_174963.2 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:86071629 G>A maps to NM_003896.3 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:98506952 G>T maps to ENST00000493584 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr11:8739380 T>C maps to NM_005418.3 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr11:8751576 A>G maps to NM_005418.3 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr3:186793464 G>A maps to NM_003032.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr1:76877829 A>G maps to NM_152996.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr1:77510109 C>T maps to NM_030965.1 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr1:77334297 G>A maps to NM_030965.1 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:55024401 C>T maps to NM_015879.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:100231433 G>A maps to NM_005668.4 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr18:44260283 G>A maps to NM_013305.4 N284N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:17362950 C>A maps to NM_001004470.1 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:52540232 G>A maps to NM_015136.2 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr3:52541957 C>T maps to NM_015136.2 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:104049337 C>T maps to NM_017564.9 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:104100655 C>A maps to NM_017564.9 I1361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:104121052 C>T maps to NM_017564.9 F1620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr12:104089564 T>C maps to NM_017564.9 F1175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr12:104086630 C>T maps to NM_017564.9 N1113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr12:104155079 G>T maps to NM_017564.9 T2417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:36587684 C>A maps to NM_003149.1 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:136221552 T>G maps to NM_005862.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:136117665 G>A maps to NM_005862.2 V734V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:136240171 G>A maps to NM_005862.2 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:123164929 C>T did not map to a codon.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:123179200 A>G did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:123200090 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:99797195 G>T maps to NM_012447.2 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr7:99786619 T>C maps to NM_012447.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr10:17730081 A>G maps to NM_003473.2 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:153006732 C>T maps to NM_005843.4 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:90676445 G>T maps to NM_020799.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr13:33703504 G>A maps to NM_178007.2 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr15:81611770 A>G maps to NM_181900.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:67943552 G>A did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:67937559 T>C did not map to a codon.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr12:56750242 C>T maps to NM_005419.3 W38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr2:191905871 G>T maps to NM_003151.2 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr17:40369192 C>G maps to NM_012448.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:74527999 C>T maps to NM_001164380.1 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr8:74464438 T>C maps to NM_001164380.1 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr8:23702525 C>T maps to NM_003155.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:172752876 A>G maps to NM_003714.2 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:89790366 C>A maps to ENST00000433102 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:89854681 G>T maps to NM_152999.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr17:44076663 C>T maps to NM_001007532.2 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr4:27010416 C>T maps to ENST00000382009 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr4:27010416 C>T maps to ENST00000382009 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:63965023 G>T maps to ENST00000358794 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:63964983 C>T maps to ENST00000358794 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr5:171544538 G>A maps to NM_005990.3 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr5:171534791 C>T maps to NM_005990.3 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:171517360 C>T maps to NM_005990.3 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:171488266 C>A maps to NM_005990.3 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr19:1223019 A>G maps to NM_000455.4 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr19:1207079 G>T maps to NM_000455.4 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr19:1207091 C>T maps to NM_000455.4 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:220480909 C>T maps to NM_052902.2 R1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:23809350 C>T maps to NM_031414.3 C563C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr7:23810667 T>C maps to NM_031414.3 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr7:23775221 T>C maps to NM_031414.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr7:23802526 C>G maps to NM_031414.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:146658904 C>A maps to NM_001112724.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr5:146703499 G>A maps to NM_001112724.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr12:27461381 A>G maps to NM_015000.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:26227544 C>A maps to NM_203399.1 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:80553626 C>T maps to NM_007029.3 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:27099208 C>A maps to NM_030795.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:48809173 G>T maps to NM_172311.2 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:48808527 T>C maps to NM_172311.2 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:48818858 T>C maps to NM_172311.2 D666D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr4:184938358 C>T maps to NM_020225.1 S901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr4:184828089 G>A maps to NM_020225.1 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr15:74494575 G>A maps to ENST00000449139 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr9:125909187 T>G maps to NM_018387.4 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:125941322 C>A maps to NM_018387.4 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:47241447 C>A maps to NM_001039877.1 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr23:7175601 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:144508153 G>A maps to NM_003764.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:144508522 C>T maps to NM_003764.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:4426930 G>A maps to NM_016930.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr16:31051087 C>T maps to NM_004604.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:132793476 C>A maps to NM_003569.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr1:109299378 G>A maps to NM_007269.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:53120673 A>G maps to NM_178509.5 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:75659819 C>A maps to NM_016086.2 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:84658637 A>G maps to NM_003849.3 H273H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:84658708 C>A maps to NM_003849.3 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr13:53250435 G>A maps to NM_001130912.1 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr8:70498634 C>T maps to NM_001128206.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3575-01A-01W-0831-10 chr20:46294603 G>A maps to NM_001161841.1 H633H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr22:44225069 C>A maps to NM_014351.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:883125 G>A maps to ENST00000456758 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr7:48046773 C>T maps to NM_152782.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr20:31590399 T>A maps to NM_080675.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr19:39965264 C>T maps to NM_003169.3 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:27002083 G>T maps to NM_003170.3 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr17:27016476 C>T maps to NM_003170.3 A1080A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:114864550 C>A maps to NM_022486.3 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr9:114820788 G>A maps to NM_022486.3 Y676Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr3:33216510 G>A maps to NM_015551.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:75428096 C>T maps to NM_014979.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:113170490 G>T maps to ENST00000374463 L2466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:113170760 G>A maps to ENST00000374463 F2376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:113212478 G>T maps to ENST00000374463 V1321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr9:113341376 C>T maps to ENST00000374463 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:29782171 G>A maps to NM_021738.2 F1330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr10:29782300 C>T maps to NM_021738.2 T1287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr7:138312915 G>A maps to NM_001139456.1 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:115402408 G>T maps to NM_003176.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:115487552 C>T maps to NM_003176.2 R702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr20:58467683 T>C maps to NM_014258.2 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr20:58441386 T>C maps to NM_014258.2 K1427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:15224674 C>T maps to NM_033025.4 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr19:15221023 C>A maps to NM_033025.4 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:85648419 T>C maps to NM_032184.1 K635K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:93650168 C>T maps to NM_003177.5 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:47436857 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:47464410 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:12192756 C>A maps to NM_133625.3 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:86350231 C>A maps to NM_006372.4 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr6:152461138 A>G maps to NM_182961.2 R8468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr6:152737558 G>A maps to NM_182961.2 R2005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr6:152786551 G>A maps to NM_182961.2 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr6:152708290 G>A maps to NM_182961.2 Y2801Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:152551732 C>T maps to NM_182961.2 Q7048Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:152565707 G>A maps to NM_182961.2 V6552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:152708383 G>A maps to NM_182961.2 F2770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr6:152652169 G>T maps to NM_182961.2 C4550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr6:152686148 T>C maps to NM_182961.2 L3326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr6:152477211 C>T maps to NM_182961.2 E7937E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr6:152674795 G>A maps to NM_182961.2 H3670H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr6:152590379 T>A maps to NM_182961.2 T6205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr6:152461138 A>G maps to NM_182961.2 R8468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:64447389 G>T maps to NM_182914.2 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:64519712 G>T maps to NM_182914.2 E3028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:64461911 G>T maps to NM_182914.2 E978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr14:64604533 C>T maps to NM_182914.2 H4892H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr14:64457274 A>G maps to NM_182914.2 K820K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:33411043 C>A maps to NM_006772.2 R905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:34050984 G>A maps to NM_003895.3 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr21:34011220 C>T maps to NM_003895.3 P1343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr21:34004044 G>A maps to NM_003895.3 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr6:158495721 G>A maps to NM_003898.3 K748K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:99672720 G>T maps to ENST00000336292 E1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:150029717 C>T maps to NM_001166209.1 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr5:150028322 T>C maps to NM_001166209.1 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr20:43994314 C>T maps to NM_033542.3 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr11:66812173 G>A maps to NM_001177880.1 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:210273382 G>A maps to NM_001146261.1 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:62536442 G>T maps to NM_031914.2 G216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr14:62541872 C>A maps to NM_031914.2 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr16:19191847 G>A maps to NM_016524.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:51128547 G>A maps to NM_001160329.1 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr19:51135613 C>A maps to NM_001160329.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr1:114682271 C>A maps to ENST00000369545 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr11:61295555 C>T maps to NM_004200.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr11:7441757 C>T maps to NM_175733.3 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:7334913 C>A maps to NM_175733.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:85438945 A>G maps to ENST00000359152 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:85409097 C>A maps to ENST00000359152 E1639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:159166580 G>T maps to ENST00000297239 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr23:37893210 C>T did not map to a codon.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr23:37931342 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:37913672 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:64896041 C>T maps to NM_172230.2 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:30864738 C>A did not map to a codon.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr23:30877656 G>A did not map to a codon.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr23:30872750 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:57407146 C>T maps to NM_013251.3 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr10:123846508 G>T maps to NM_206862.2 L1498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr10:123842776 T>C maps to NM_206862.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3582-01A-01W-0831-10 chr1:166833126 A>G maps to NM_053053.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr4:7056150 G>A maps to NM_152293.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:9828897 C>A maps to NM_006354.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:70617213 G>A did not map to a codon.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:70595133 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:70603904 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:70608138 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:70614067 C>T did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:70595104 G>A did not map to a codon.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr23:70603937 A>G did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr11:6633002 A>G maps to NM_006284.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr1:28931966 G>A maps to NM_005644.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr2:10059940 C>T maps to NM_005680.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:32634962 G>T maps to NM_153809.2 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr9:32635568 G>A maps to NM_153809.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr9:32631659 C>A maps to NM_153809.2 V1306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr9:32633291 A>G maps to NM_153809.2 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr9:32635568 G>A maps to NM_153809.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr9:32635358 C>A maps to NM_153809.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr9:32635358 C>T maps to NM_153809.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:120814212 C>A maps to NM_003184.3 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:8006603 G>A maps to NM_031923.2 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr20:60589623 G>A maps to NM_003185.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr20:60639549 C>A maps to NM_003185.3 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr10:105138094 C>T maps to NM_006951.3 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:105147385 G>T maps to NM_006951.3 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr1:229730578 G>C maps to NM_014409.3 S412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr7:99710478 C>T maps to ENST00000472509 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:100534007 C>A did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:100532685 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:159461768 G>A maps to NM_054114.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:159462391 G>T maps to NM_054114.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:159456923 G>A maps to NM_054114.3 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:159457698 C>T maps to NM_054114.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:32815403 C>A maps to NM_000593.5 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:32818212 G>A maps to NM_000593.5 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr1:234565356 T>C maps to NM_005646.3 Q892Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:33467801 G>T maps to ENST00000455217 E754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:9629253 G>A maps to NM_019599.2 C297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr5:9629598 C>T maps to NM_019599.2 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr12:10978856 T>A maps to NM_023921.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:11061084 G>T maps to NM_023920.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr7:141464108 C>T maps to NM_016943.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr12:11286424 A>T maps to NM_001097643.1 L140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:141478395 C>A maps to NM_016944.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:142919224 C>A maps to NM_176882.1 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:143175840 C>T maps to NM_176883.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:141490820 G>A maps to NM_018980.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:11139423 T>A maps to NM_176890.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr20:13463940 A>G maps to NM_017714.2 C306C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr16:71610249 G>A maps to NM_000353.2 N23N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr3:10302276 C>T maps to NM_014760.3 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr7:27868360 C>T maps to ENST00000409980 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:27809318 G>T maps to ENST00000409980 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:27831746 G>A maps to ENST00000409980 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:27835787 G>T maps to ENST00000409980 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr23:153648063 G>A did not map to a codon.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr10:96260073 T>C maps to NM_015188.1 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:100014146 G>T maps to ENST00000394144 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr15:78322442 A>G maps to NM_144572.1 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:78322511 C>T maps to NM_144572.1 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:75861107 C>T maps to ENST00000431480 T1240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:75898520 G>A maps to ENST00000431480 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr13:75900517 C>T maps to ENST00000431480 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr6:13321190 G>T maps to NM_016495.4 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr2:101654161 G>T maps to NM_001102426.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:106064217 A>G did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:106108791 C>T did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr5:76989141 T>C maps to NM_004607.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr19:36616653 G>A maps to NM_001281.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:80887118 C>T maps to NM_005993.4 R942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr17:80710098 C>T maps to NM_005993.4 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr4:107154747 T>C maps to NM_001163436.1 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:64878185 C>T maps to NM_013254.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3584-01A-01W-0831-10 chr23:9661420 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr24:6942630 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:162274715 T>C maps to NM_006593.2 N284N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr1:119427489 C>A maps to ENST00000369429 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr1:168260607 T>A maps to NM_005149.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:168282179 C>T maps to NM_005149.2 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr17:45822626 C>T maps to NM_013351.1 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr23:79281206 C>A did not map to a codon.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr23:79277902 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:59556058 C>T maps to ENST00000393853 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:114841670 C>T maps to NM_000192.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr23:101395950 G>A did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:102508778 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:13681236 G>T did not map to a codon.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr8:74868289 C>G did not map to a codon.
Sequencing variant TCGA-AG-3894-01A-01W-1073-09 chr18:44561431 G>A maps to NM_016427.2 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:44561563 C>T maps to NM_016427.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr18:44559562 G>A maps to NM_016427.2 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:145838592 G>A maps to NM_006706.3 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:145882991 C>T maps to NM_006706.3 R813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:145883530 G>T maps to NM_006706.3 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr5:145838520 A>T maps to NM_006706.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr5:145887489 C>T maps to NM_006706.3 R989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr22:42606145 T>G maps to NM_005650.1 G1722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:42606742 C>T maps to NM_005650.1 P1523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr2:85532499 C>A maps to NM_031283.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr2:85529701 T>C maps to NM_031283.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr10:114710584 G>T maps to NM_030756.4 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:114912120 G>A maps to NM_030756.4 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr10:114912148 C>T maps to NM_030756.4 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr10:114910882 G>A did not map to a codon.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr1:152085425 G>A maps to NM_007113.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:96178595 G>T maps to NM_021966.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr6:160206463 G>A maps to NM_030752.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:160200076 T>G maps to NM_030752.2 *557C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr21:33956578 T>C maps to NM_144659.5 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr3:196033842 C>G maps to NM_152773.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr12:111057656 C>T maps to NM_001082538.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:115963245 G>T maps to NM_198795.1 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:46656966 C>T maps to NM_001010870.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:46657763 T>C maps to NM_001010870.2 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr14:104508488 G>A maps to NM_153046.2 A1313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:49858607 C>T maps to NM_003598.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr12:3147232 A>T maps to NM_003213.3 K333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:48147492 G>A maps to NM_003215.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:121008364 C>A maps to NM_005422.2 I1059I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr11:121033053 C>T maps to NM_005422.2 T1749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:6704118 G>A maps to NM_053285.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr1:36553585 C>T maps to NM_014466.2 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr2:95542489 C>T maps to NM_144705.2 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:10775926 G>A maps to NM_144674.1 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:53454965 G>A maps to NM_170754.2 E1092E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:20857404 C>T maps to NM_007110.4 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr14:20859204 C>T maps to NM_007110.4 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr5:1264568 G>A maps to NM_198253.2 C931C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr10:70450733 A>T maps to NM_030625.2 T1858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr10:70432670 G>T maps to NM_030625.2 G1565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr10:70333379 T>C maps to NM_030625.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr4:106157489 C>T maps to ENST00000513237 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3890-01A-01W-1073-09 chr4:106156670 G>A maps to ENST00000513237 E545E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:106155524 C>T maps to ENST00000513237 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:106156520 G>A maps to ENST00000513237 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:106157442 G>T maps to ENST00000513237 E803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:74328396 C>T maps to ENST00000409262 P1401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:74328942 G>A maps to ENST00000409262 T1583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr9:103090222 G>C maps to NM_017746.3 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr9:103082639 T>C maps to NM_017746.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:69830385 C>A did not map to a codon.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr23:69749015 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:69749824 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:69960607 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:70026589 C>A did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:69825276 T>C did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:104464717 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:107224540 G>A did not map to a codon.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr17:56676692 C>T maps to ENST00000240361 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:30701274 A>C maps to NM_031271.3 Y1753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:30701384 G>A maps to NM_031271.3 R1717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:30701627 C>A maps to NM_031271.3 E1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:30704933 C>A maps to NM_031271.3 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:30700457 G>A maps to NM_031271.3 Q2026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr8:30699867 A>G maps to NM_031271.3 D2222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr8:30704019 T>C maps to NM_031271.3 K838K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:133476639 G>T maps to NM_001063.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr3:133496020 A>G maps to NM_001063.3 E667E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr3:133485147 A>T maps to NM_001063.3 K453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr3:133473444 C>T maps to NM_001063.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr6:50682842 A>G maps to NM_172238.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:50686804 C>T maps to NM_172238.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr6:50683007 C>G maps to NM_172238.3 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:246729179 G>T maps to NM_022366.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr12:51512473 T>C maps to NM_005653.4 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr3:141692892 C>A maps to NM_001178139.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr23:132351845 C>T did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr6:41658888 C>T maps to ENST00000343317 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr3:100467197 T>C maps to NM_001007565.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr22:26894920 C>T maps to NM_012143.2 E450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr2:188348878 C>T maps to NM_006287.4 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:188368392 C>A maps to NM_006287.4 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:188368483 T>G maps to NM_006287.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr8:133980165 C>A maps to NM_003235.4 G1938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr8:133899527 G>A maps to NM_003235.4 W637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:133899254 G>A maps to NM_003235.4 K546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:134107392 G>T maps to NM_003235.4 E2449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr8:133931747 T>C maps to NM_003235.4 A1502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr8:133913706 T>C maps to NM_003235.4 C1181C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr8:133900727 T>C maps to NM_003235.4 H892H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr8:133925508 C>T maps to NM_003235.4 C1459C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr1:218609480 T>C maps to NM_001135599.2 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:218578554 C>T maps to NM_001135599.2 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr1:218607467 C>T maps to NM_001135599.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr5:135383084 C>T maps to NM_000358.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:101910028 T>G maps to NM_004612.2 L450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:105897176 G>A maps to NM_004257.4 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr24:3447836 G>A did not map to a codon.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr20:36776425 G>A maps to NM_004613.2 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr20:2293560 C>T maps to NM_003245.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr3:44943360 G>A maps to NM_003241.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:44948516 C>T maps to NM_003241.3 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:85553924 C>T maps to ENST00000409015 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr11:2190906 C>T maps to NM_199292.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr16:67876825 G>A maps to NM_020457.2 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:72068115 C>T maps to NM_031435.3 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:39882793 C>T maps to NM_003246.2 D741D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr6:169626378 G>A maps to NM_003247.2 R812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr6:169650826 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:155170941 G>A maps to NM_007112.3 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:151860783 G>A maps to NM_053055.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr6:128134474 C>A maps to NM_001164685.1 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:128176285 C>A maps to NM_001164685.1 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:247928 G>A maps to NM_005131.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:122765682 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:122757089 T>C did not map to a codon.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr23:122772836 A>T did not map to a codon.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:122767821 T>C did not map to a codon.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr23:122820466 T>C did not map to a codon.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr23:122760388 T>C did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr1:36754873 T>C maps to NM_005119.3 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr3:24188295 G>A maps to NM_001128177.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr13:52952781 C>G maps to NM_018676.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:71952906 C>T maps to NM_024817.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:11464375 G>T maps to ENST00000423059 T1110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:137814326 C>T maps to ENST00000272643 C159C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:138413225 C>T maps to ENST00000272643 C1370C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr2:138208521 C>T maps to ENST00000272643 R1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr2:137990529 C>T maps to ENST00000272643 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr11:119291055 C>T maps to NM_006288.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr21:32502558 C>T maps to NM_003253.2 A1339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr21:32525052 C>T maps to NM_003253.2 T1089T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:32617956 G>A maps to NM_003253.2 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr21:32525073 G>A maps to NM_003253.2 D1082D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr21:32589976 A>G maps to NM_003253.2 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:155578057 C>T maps to ENST00000456144 R1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:155450635 G>A maps to ENST00000456144 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:155578071 C>T maps to ENST00000456144 S1670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr1:43783727 C>A maps to NM_005424.2 Y969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr1:43778929 T>C maps to NM_005424.2 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:153691870 G>A maps to NM_145720.2 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr12:56817486 C>T maps to NM_003920.3 Q657Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr16:4393259 G>A maps to NM_016069.8 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr19:7998368 C>T did not map to a codon.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr23:47444706 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:30000918 G>T maps to NM_003257.3 S1565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:30024837 C>A maps to NM_003257.3 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:30058589 C>T maps to NM_003257.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:153549233 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:153537782 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:164394337 G>A maps to NM_032136.4 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:82336718 C>A maps to ENST00000376537 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:2987914 C>A maps to NM_001143986.1 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr4:166976379 C>T maps to ENST00000507499 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:166929161 C>T maps to ENST00000507499 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr10:98156949 C>T maps to NM_012465.3 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:98136532 C>T maps to NM_012465.3 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr9:35703798 A>G maps to NM_006289.3 A2110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:35699389 G>A maps to NM_006289.3 S2279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr15:62949992 C>T maps to NM_015059.2 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr15:63063275 C>T maps to NM_015059.2 L1770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:63040639 C>T maps to NM_015059.2 L1372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:63044598 C>A maps to NM_015059.2 L1435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:63084841 C>T maps to NM_015059.2 I1913I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:38775285 T>C maps to NM_030956.3 E642E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:38775315 G>A maps to NM_030956.3 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:154624905 G>T maps to NM_003264.3 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:187004175 G>T maps to NM_003265.2 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:187005910 C>T maps to NM_003265.2 R867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr1:223285572 G>A maps to NM_003268.5 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:12904320 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:12904026 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:12904836 C>A did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr23:12904055 G>A did not map to a codon.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:12937996 C>A did not map to a codon.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr23:12937315 C>T did not map to a codon.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr23:12938668 C>A did not map to a codon.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr23:12938159 C>T did not map to a codon.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr23:12939148 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:12939077 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:12939261 C>A did not map to a codon.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr23:12937237 G>A did not map to a codon.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr23:12938880 A>G did not map to a codon.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr23:12939055 T>C did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr23:12940020 G>C did not map to a codon.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr10:102893974 G>A maps to NM_005521.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:196051177 C>T maps to NM_138461.2 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:19381885 G>A maps to NM_001001524.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:100211648 G>A maps to NM_004800.1 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr20:30729598 G>A maps to NM_014742.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:30745655 C>T maps to NM_014742.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:2596829 C>A maps to NM_080751.2 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr20:2582874 C>A maps to NM_080751.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr15:81625314 G>A maps to ENST00000454937 D919D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:129390104 G>T maps to NM_001017395.3 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:205210826 C>T maps to NM_014858.3 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr1:205238517 C>T maps to NM_014858.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr12:94975537 G>T maps to NM_020698.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr13:114193724 G>A maps to NM_017905.4 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:79606167 G>T maps to NM_007364.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:77808176 G>A maps to NM_213601.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:72832753 C>T maps to NM_017728.3 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:12269441 A>G maps to NM_018374.3 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:60689288 C>T maps to NM_024092.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:98453721 C>T maps to NM_001134450.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr7:98445720 C>A maps to NM_001134450.1 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:98431765 C>T maps to NM_015348.1 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr2:98392470 T>C maps to NM_015348.1 K1385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr2:98409023 G>A maps to NM_015348.1 P1323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr12:126137054 C>A maps to NM_052907.2 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr12:125834829 C>T maps to NM_052907.2 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr12:126137027 G>A maps to NM_052907.2 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr12:129822277 C>T maps to NM_133448.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:130185031 G>A maps to NM_133448.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr12:129563261 A>G maps to NM_133448.2 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr12:130184521 G>A maps to NM_133448.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:32956183 C>A maps to NM_207313.1 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:86782643 G>T maps to NM_022918.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:61133519 C>A maps to NM_016464.4 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:159165492 G>T maps to NM_018342.4 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:5745964 C>T maps to NM_152784.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:5745964 C>T maps to NM_152784.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:5776305 G>A maps to NM_152784.3 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr6:10730851 C>T maps to NM_016462.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:19232452 G>A maps to NM_017814.1 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr23:109388057 G>C did not map to a codon.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr5:82357694 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:112415337 G>A maps to NM_022484.4 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:112424869 G>T maps to NM_022484.4 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr14:105070790 G>T maps to NM_207379.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr2:103431425 A>G maps to NM_144632.3 *230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:148690510 C>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:148692970 G>A did not map to a codon.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr20:48741642 G>A maps to NM_199129.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:74315726 G>A maps to NM_013390.2 R1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:72699484 G>A maps to NM_001080462.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr15:72691085 G>A maps to NM_001080462.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:75574038 G>A maps to NM_001077416.1 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:102968620 A>C did not map to a codon.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr2:120194856 C>T maps to NM_183240.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:108510452 C>A maps to NM_018112.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:12785414 G>A maps to ENST00000431022 H97H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:25666997 C>A maps to NM_014313.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr21:34828044 A>G maps to NM_006134.5 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr19:18724826 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:77423408 G>T maps to NM_032936.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3575-01A-01W-0831-10 chr6:44120355 C>T maps to NM_018426.1 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr6:44107233 C>T maps to NM_018426.1 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr14:77714713 C>T maps to NM_020431.2 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr8:94809682 C>T maps to NM_153704.5 V695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:74893414 G>A maps to NM_017866.5 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:45423375 C>T maps to NM_001123376.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:112847234 C>T maps to NM_032824.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:426264 C>A maps to NM_021259.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr9:35847066 G>A maps to ENST00000360192 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:154743710 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:154774794 G>T did not map to a codon.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr23:154754253 A>G did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:154743708 T>C did not map to a codon.
Sequencing variant TCGA-AG-A025-01A-01W-A00E-09 chr15:52161472 G>A maps to NM_014547.4 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr15:52181328 A>G maps to NM_014547.4 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:98925612 G>T maps to NM_003276.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:98927457 G>T maps to NM_003276.2 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:98940154 G>T maps to NM_001032283.2 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr3:33135618 G>A maps to NM_001039770.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:69094578 C>A maps to NM_182502.3 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:69095085 C>A maps to NM_182502.3 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:69107479 C>T maps to NM_182502.3 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:68725377 C>T maps to NM_004262.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:68930433 G>A maps to NM_207407.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr4:68934469 G>C maps to NM_207407.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:68956275 C>A maps to NM_207407.2 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:68956345 G>A maps to NM_207407.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:117772977 G>A maps to ENST00000413475 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr21:19666594 G>A maps to NM_002772.2 C826C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:19713768 C>A maps to NM_002772.2 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:19716324 C>T maps to NM_002772.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr21:19725328 A>G maps to NM_002772.2 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr21:43802318 G>A maps to ENST00000380399 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr11:117975478 C>T maps to NM_019894.3 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:111766736 C>T maps to ENST00000443106 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr23:103219129 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:91760122 C>T maps to NM_183049.2 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:29911644 C>T maps to NM_001193451.1 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:83526116 C>T maps to NM_152588.1 R820R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr12:83379734 C>T maps to NM_152588.1 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr13:101316491 G>A maps to NM_032813.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr9:117849481 G>A maps to NM_002160.2 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:117840468 G>T maps to NM_002160.2 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:117793862 C>T maps to NM_002160.2 R1963R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:117846614 G>A maps to NM_002160.2 F668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr9:117798500 C>T maps to NM_002160.2 T1844T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr9:117808872 G>A maps to NM_002160.2 F1647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:26669302 C>T maps to NM_021137.4 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr6:138198219 A>G maps to NM_006290.2 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr6:138199577 A>G maps to NM_006290.2 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr6:138200291 C>T maps to NM_006290.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr6:138200295 C>A maps to NM_006290.2 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:51350200 G>T maps to NM_207381.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:22884761 C>A maps to NM_003842.4 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:23002046 G>T maps to NM_003840.3 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr18:60015456 A>G maps to NM_003839.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:119945383 G>A maps to NM_002546.3 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:12183837 C>T maps to NM_001243.3 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr1:7980912 T>C maps to NM_001561.5 E250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:7993345 C>T maps to NM_001561.5 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr3:172224434 C>T maps to ENST00000382750 W231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:108959223 G>T maps to NM_006573.3 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr9:117666528 C>T maps to NM_001244.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:117666366 C>T maps to NM_001244.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:170828505 G>A maps to NM_015028.2 R761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:170884889 C>A maps to NM_015028.2 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr3:170819362 T>C maps to NM_015028.2 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr4:2744247 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:122079858 C>A maps to ENST00000509841 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr4:122068295 G>A maps to ENST00000509841 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr3:195611886 T>C maps to NM_001010938.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr11:57076323 C>T maps to NM_033396.2 L1287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:57077718 G>A maps to NM_033396.2 D822D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr10:93601072 T>C maps to NM_025235.3 Y569Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr10:93576984 T>C maps to NM_025235.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr1:175116179 G>A maps to NM_022093.1 T1291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:175046850 C>T maps to NM_022093.1 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:175054542 C>T maps to NM_022093.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr1:74957899 C>T maps to NM_001112808.2 F868F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr7:128655104 T>C maps to ENST00000471166 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr7:128612494 T>C maps to ENST00000471166 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr7:128633896 C>T maps to ENST00000471166 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:175299264 G>A maps to NM_003285.2 V1246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:175331865 G>A maps to NM_003285.2 Y929Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:175355351 G>A maps to NM_003285.2 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:175375427 G>A maps to NM_003285.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr1:175355234 G>A maps to NM_003285.2 Y570Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr1:175355222 G>A maps to NM_003285.2 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:40662787 C>T maps to ENST00000454349 R866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr22:40676033 C>T maps to ENST00000454349 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr22:40662787 C>T maps to ENST00000454349 R866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr22:40669465 C>T maps to ENST00000454349 D1015D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:76089173 C>A maps to NM_001142640.1 I1374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr17:76094556 T>C maps to NM_001142640.1 N1516N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr2:218713757 C>T maps to NM_022648.4 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:218675025 C>T maps to NM_022648.4 S1579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:218677938 G>A maps to NM_022648.4 F1547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:218682632 C>T maps to NM_022648.4 P1370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr2:218751338 G>A maps to NM_022648.4 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr2:218678419 G>A maps to NM_022648.4 Q1513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr2:218713688 G>A maps to NM_022648.4 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr2:218713451 C>T maps to NM_022648.4 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:32015688 G>A maps to ENST00000375244 F3382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:48941287 C>A maps to NM_005749.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr1:45808077 C>A maps to NM_025077.3 S172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr14:58874095 G>A maps to NM_207377.2 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:38556216 C>A maps to ENST00000357601 E1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:133362998 G>A maps to NM_007027.3 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr3:133356881 A>G maps to NM_007027.3 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr9:32541756 C>T maps to NM_005802.4 E922E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:132581177 G>A maps to ENST00000437532 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr1:179886701 A>G maps to ENST00000398836 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:179064251 G>T maps to NM_022371.3 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr17:7579590 C>T did not map to a codon.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr17:7577587 G>A maps to NM_001126112.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr17:7577508 C>A maps to NM_001126112.1 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr17:7579590 C>T did not map to a codon.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr17:7577079 T>C maps to NM_001126112.1 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01Y-01A-41W-A096-10 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr17:7577084 C>A maps to NM_001126112.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr17:7578281 G>T maps to NM_001126112.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr17:7579392 A>G maps to NM_001126112.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr17:7579590 C>G did not map to a codon.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr17:7577078 C>A maps to NM_001126112.1 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr17:7578523 G>A maps to NM_001126112.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr17:7578369 C>T did not map to a codon.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr17:7577506 T>C maps to NM_001126112.1 E258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr17:7579535 C>A maps to NM_001126112.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:43739653 C>A maps to NM_001141980.1 E916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:43769883 C>A maps to NM_001141980.1 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:43748581 C>A maps to NM_001141980.1 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr20:44002571 C>T maps to NM_014477.2 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:189455607 G>T maps to NM_003722.4 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:189584532 G>T maps to NM_003722.4 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:83075280 G>A maps to NM_006670.4 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3999-01A-01W-1073-09 chr12:113728004 C>T maps to NM_001143819.1 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr12:113731117 C>T maps to NM_001143819.1 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:113698284 A>C maps to NM_001143819.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:6330997 G>A maps to NM_001001874.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:6330997 G>A maps to NM_001001874.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:72425139 G>T maps to ENST00000389376 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr12:72335392 C>T maps to ENST00000389376 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr15:63335951 G>A maps to ENST00000357980 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:154143174 C>A maps to NM_001043351.1 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:16192748 C>T maps to NM_001145160.1 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:103280244 C>T maps to ENST00000376052 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:103288610 C>A maps to ENST00000376052 S516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:186312585 C>A maps to NM_003292.2 E1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:186324608 C>A maps to NM_003292.2 E702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:186327735 G>T maps to NM_003292.2 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr16:1306346 G>C maps to NM_012217.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:10943003 G>A maps to NM_199261.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr13:20039678 G>A maps to NM_199254.2 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr13:20049727 G>T maps to NM_199254.2 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3601-01A-01W-0833-10 chr20:30370133 G>T maps to ENST00000340513 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr3:185643398 T>C maps to NM_004593.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr9:139815530 G>A maps to ENST00000359662 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr9:139818361 C>T maps to ENST00000359662 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr14:103371895 G>T maps to NM_145725.2 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:103341987 G>T maps to NM_145725.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr2:239237874 C>T maps to NM_015650.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:71520328 G>A maps to NM_014294.5 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr4:118005712 C>T maps to NM_152402.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:36875030 C>A maps to NM_014831.2 E1971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:36876274 C>A maps to NM_014831.2 E1837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:3725372 G>A maps to NM_016292.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr21:45483617 C>T maps to NM_003274.4 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:41127534 G>T maps to NM_018965.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:110100425 G>T maps to NM_003301.4 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr2:12863516 T>C maps to NM_021643.3 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:12880832 G>A maps to NM_021643.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:368759 C>T maps to ENST00000422053 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr20:377084 G>A maps to ENST00000422053 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4008-01A-01W-1073-09 chr6:30128218 C>T maps to NM_006778.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr1:228589823 C>T maps to NM_145214.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr9:100857227 G>A maps to NM_033219.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:64887747 C>A maps to NM_001656.3 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:138262237 C>T maps to NM_015905.2 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr7:138200066 A>G maps to NM_015905.2 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr7:138268671 C>T maps to NM_015905.2 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr6:28876837 A>T maps to NM_006510.4 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:59060555 G>A maps to NM_005762.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr11:5653740 T>C maps to NM_001003819.3 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr17:57126577 A>G maps to NM_015294.3 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:180661306 A>G maps to NM_033549.3 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr3:140401924 C>T maps to NM_152616.4 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr3:140401765 G>A maps to NM_152616.4 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr3:140401870 C>T maps to NM_152616.4 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr11:5701071 G>T maps to NM_033034.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:72732850 G>A maps to NM_178125.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:180687261 G>A maps to NM_032765.2 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:67062667 G>T maps to NM_184085.1 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:67064655 G>T maps to NM_184085.1 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr7:100730764 G>T maps to NM_030961.1 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:100732536 C>T maps to NM_030961.1 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:100731312 G>A maps to NM_030961.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr7:100731828 T>C maps to NM_030961.1 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:248028062 C>A maps to NM_015431.3 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr1:248031151 G>C maps to NM_015431.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr1:231342438 T>C maps to NM_001004342.3 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr11:4622018 A>G maps to NM_018073.5 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:45059655 G>T maps to NM_182985.3 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:45047123 C>T maps to NM_182985.3 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr4:189012814 C>T maps to ENST00000326754 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:189012778 G>T maps to ENST00000326754 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:14291123 G>A maps to NM_007118.2 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr5:14419927 C>T maps to NM_007118.2 F1667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr5:14472721 G>A maps to NM_007118.2 V1978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr22:38109264 C>A maps to NM_001039141.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:6742998 C>T maps to ENST00000313244 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:92461695 C>A maps to NM_004239.3 E1686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr14:92480700 T>C maps to NM_004239.3 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:230672554 C>A maps to ENST00000389044 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr7:100470315 A>T maps to NM_003302.2 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:126332552 C>A maps to NM_001031712.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:3189808 G>T maps to NM_182916.2 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:54956782 T>C did not map to a codon.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr23:54955780 C>T did not map to a codon.
Sequencing variant TCGA-AF-2689-01A-01W-0831-10 chr8:72969250 A>C maps to NM_007332.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr8:72935335 A>G maps to NM_007332.2 T1055T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:72981382 C>A maps to NM_007332.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr3:142455329 C>T maps to ENST00000476941 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr3:142522953 C>T maps to ENST00000476941 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr4:122853893 C>T maps to NM_001130698.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr4:122824120 A>G maps to NM_001130698.1 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:38225389 C>T maps to NM_003306.1 Q697Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:38357362 G>A maps to NM_003306.1 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:38211465 C>A maps to NM_003306.1 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:33609058 C>T maps to NM_015638.2 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:33657148 C>A maps to NM_015638.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr23:111155952 C>T did not map to a codon.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr5:135692751 G>A maps to NM_020389.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:135692631 G>A maps to NM_020389.2 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:135692532 G>A maps to NM_020389.2 H181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr21:45855079 G>A maps to ENST00000397932 T1397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr9:73399088 A>G maps to ENST00000419692 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:73168149 G>A maps to ENST00000419692 I1054I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:73240193 G>A maps to ENST00000419692 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:73240406 G>T maps to ENST00000411705 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr9:73150979 A>G maps to ENST00000419692 N1637N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr9:73151435 T>C maps to ENST00000419692 K1485K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr9:73399067 C>T maps to ENST00000419692 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr19:49703896 C>T maps to NM_017636.3 F936F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr9:77377529 G>A maps to NM_017662.4 R1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr9:77386704 C>T maps to NM_017662.4 E1150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:50891327 C>A maps to NM_017672.4 E1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:234858654 C>T maps to NM_024080.4 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr8:116426340 G>T maps to NM_014112.2 C1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr8:116616107 T>G maps to NM_014112.2 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:116427044 G>A maps to NM_014112.2 Q1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr8:116632237 G>A maps to NM_014112.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr8:116631433 A>G maps to NM_014112.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:116599329 C>T maps to NM_014112.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr8:116616326 C>T maps to NM_014112.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:3475528 G>A maps to ENST00000399756 I717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:3495605 C>T maps to ENST00000399756 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr17:16330136 G>T maps to NM_016113.4 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:3427598 C>A maps to ENST00000381913 E546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:110230180 G>T maps to NM_021625.4 I626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:142605699 C>A maps to NM_019841.4 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr7:142622680 A>G maps to NM_019841.4 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr7:142574334 T>A maps to NM_018646.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr7:98547743 T>C maps to ENST00000359863 R1724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:98548512 C>A maps to ENST00000359863 I1776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:98575944 C>T maps to ENST00000359863 R2826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:98533290 G>A maps to ENST00000359863 A1368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr7:98592256 G>A maps to ENST00000359863 A3351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr7:98555601 A>G did not map to a codon.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr9:135772644 G>A maps to NM_000368.4 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr16:2136354 C>T maps to NM_000548.3 Y1608Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:107018440 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:12574175 C>T maps to NM_025265.3 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr3:12558135 A>G maps to NM_025265.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr3:12558135 A>G maps to NM_025265.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3608-01A-01W-0833-10 chr2:99725860 T>C maps to NM_025244.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:130356606 G>A maps to NM_052933.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:81606199 G>A maps to NM_000369.2 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr14:81610294 C>T maps to NM_000369.2 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr14:81609337 A>G maps to NM_000369.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr20:51871430 C>T maps to NM_173485.5 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:31769276 G>A maps to NM_020856.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:31770404 C>T maps to NM_020856.2 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr19:31768280 C>G maps to NM_020856.2 V806V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr19:31768400 C>T maps to NM_020856.2 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr19:50248604 C>T maps to NM_021733.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:50247576 G>A maps to NM_021733.1 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6702-01A-11D-1826-10 chr19:50251425 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:76507334 C>T maps to NM_015516.3 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr11:76507125 C>T maps to NM_015516.3 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:46649987 C>T maps to NM_005727.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr1:46650756 C>A maps to NM_005727.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:44941421 C>T maps to ENST00000425677 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr1:115596023 G>A maps to NM_005725.4 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:77345213 C>A maps to NM_005724.5 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:99887532 C>A did not map to a codon.
Sequencing variant TCGA-AH-6547-01A-11D-1826-10 chr23:38530640 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:3390928 C>T maps to ENST00000407263 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:53114423 C>A did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:98289372 G>A maps to NM_033512.2 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:3197909 G>A maps to ENST00000398659 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:112770511 G>A maps to NM_032028.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr5:112770458 T>C maps to NM_032028.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:100373977 G>A maps to NM_139246.4 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:43223518 G>A maps to NM_032538.1 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:43044953 A>C maps to ENST00000263802 T1235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr15:43044267 C>T maps to ENST00000263802 W1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:231060653 G>A maps to NM_024525.4 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:231097000 G>T maps to NM_024525.4 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:180321102 G>T maps to NM_133462.3 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr2:3405655 C>T maps to NM_016030.5 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:34863072 G>A maps to NM_144725.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:40094921 C>T maps to ENST00000377543 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:138863337 C>T maps to NM_024926.2 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr21:38523140 G>T maps to NM_003316.3 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:38537936 G>T maps to NM_003316.3 E1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:178482355 G>A maps to NM_152275.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:178415848 A>T maps to NM_152517.2 L548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:109498749 C>T maps to NM_014673.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr2:47233825 G>A maps to ENST00000394850 W417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:91196423 T>C maps to NM_001010854.1 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr9:135251432 G>A maps to NM_007344.2 R863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:135271842 G>A maps to NM_007344.2 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr6:80745120 A>G maps to NM_003318.4 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr2:113286270 G>T maps to NM_153712.4 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr22:43442534 T>G maps to NM_012263.4 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr22:43471559 G>A maps to NM_012263.4 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:90796556 C>T maps to ENST00000438251 C125C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:90801365 C>A maps to ENST00000438251 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr3:9871012 C>T maps to NM_001025930.3 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:219618859 A>G maps to NM_014640.4 K1116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:30522646 C>T maps to NM_001008409.2 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr2:179428319 G>A maps to NM_133378.4 G24945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr2:179669342 C>T maps to NM_133378.4 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr2:179470278 G>A maps to NM_133378.4 R15347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:179425409 G>A maps to NM_133378.4 I25915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr2:179452755 T>A maps to NM_133378.4 V18558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr2:179486704 T>A maps to NM_133378.4 K12414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr2:179586844 G>T maps to NM_133378.4 P6271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179400454 C>T maps to NM_133378.4 W31061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179404445 G>A maps to NM_133378.4 G30214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179404589 T>C maps to NM_133378.4 P30166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179430353 G>T maps to NM_133378.4 V24267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179432767 C>A maps to NM_133378.4 E23463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179449090 C>T maps to NM_133378.4 E19161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179457754 G>A maps to NM_133378.4 V17129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179462763 C>A maps to NM_133378.4 G16477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179482565 G>A maps to NM_133378.4 R13270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179516426 G>A maps to NM_133378.4 V10709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179542572 C>A maps to NM_133378.4 E10112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179547472 G>A maps to NM_133378.4 Y9771Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179575503 G>A maps to NM_133378.4 G8196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179577162 C>T maps to NM_133378.4 T7918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179579139 A>C maps to NM_133378.4 Y7543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179579256 G>A maps to NM_133378.4 V7504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179585316 T>C maps to NM_133378.4 E6480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179596552 A>G maps to NM_133378.4 Y4439Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179605372 G>T maps to NM_133437.3 S4025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179606069 C>A maps to NM_133437.3 E3793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179613320 A>G maps to ENST00000375038 Y4604Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179615266 C>A maps to ENST00000375038 E3956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179621264 C>T maps to NM_133437.3 E3475E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179641739 G>A maps to NM_133378.4 I1617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:179665386 G>A maps to NM_133378.4 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr2:179463493 C>T maps to NM_133378.4 A16413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr2:179424791 T>C maps to NM_133378.4 E26121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr2:179457220 T>C maps to NM_133378.4 P17269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr2:179438324 T>C maps to NM_133378.4 Q21610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr2:179637979 C>A maps to NM_133378.4 E2571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr2:179594276 G>T maps to NM_133378.4 I4958I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr2:179474208 G>A maps to NM_133378.4 Y14708Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr2:179434583 A>G maps to NM_133378.4 S22857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr2:179437808 A>G maps to NM_133378.4 D21782D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr2:179605072 G>C maps to NM_133437.3 S4125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr2:179591844 T>A maps to NM_133378.4 T5505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr2:179447065 G>A maps to NM_133378.4 G19471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr2:179452058 G>A maps to NM_133378.4 D18725D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr2:179459277 C>A maps to NM_133378.4 E16747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr2:179432536 G>A maps to NM_133378.4 Q23540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr2:179629527 C>T maps to NM_133378.4 P3238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr2:179395462 T>C maps to NM_133378.4 K32725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr2:179440586 T>C maps to NM_133378.4 K20856K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr2:179437532 G>A maps to NM_133378.4 A21874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr2:179425004 T>C maps to NM_133378.4 G26050G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:63978614 G>A maps to NM_000370.3 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:54930462 C>T maps to ENST00000391739 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr17:72245193 C>T maps to NM_032646.5 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:72249393 C>A maps to NM_032646.5 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:2689209 G>A maps to NM_025250.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr13:19752430 G>A maps to NM_006001.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr6:30691450 C>T maps to NM_178014.2 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr20:57598985 C>T maps to NM_030773.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:3224999 G>A maps to NM_178012.4 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr4:190904397 G>A maps to ENST00000248151 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr4:190906005 C>T maps to ENST00000248151 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:94558 G>T maps to NM_177987.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr10:93293 G>A maps to NM_177987.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr17:40811901 G>T maps to NM_016437.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:113143947 C>A maps to NM_006322.4 E838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:22868878 C>T maps to NM_052903.4 V917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr22:50662946 T>C maps to NM_020461.3 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr22:50664610 C>T maps to NM_020461.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr22:50656443 C>A maps to NM_020461.3 G1757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr22:50657129 A>G did not map to a codon.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr16:28856081 G>A maps to NM_003321.4 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr6:35473904 G>T maps to NM_003322.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr6:35480008 C>T maps to NM_003322.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:49391470 C>T maps to NM_003323.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr19:49385382 C>T maps to NM_003323.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr12:3040267 C>T maps to NM_001160408.1 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:15508235 G>A maps to NM_006765.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:44189456 A>G maps to NM_002822.3 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr12:44191531 T>C maps to NM_002822.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr7:19156557 G>A maps to NM_000474.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:19744434 A>C maps to NM_001002926.1 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:16857988 C>T did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr16:72120642 A>G maps to NM_001142318.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:672901 C>T maps to NM_001071.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr11:88911234 G>A maps to NM_000372.4 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:12704673 C>A maps to NM_000550.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr19:36235244 G>A maps to ENST00000412391 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:70959097 C>A maps to NM_018003.2 E1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:47062532 C>T did not map to a codon.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr23:47069379 A>G did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:47058302 C>A did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr3:132389865 T>C maps to NM_024818.3 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr9:138836915 G>A maps to NM_016172.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr9:138836918 G>A maps to NM_016172.2 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr9:33988989 G>A maps to NM_018449.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:154241243 G>A maps to NM_014847.3 E994E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:43864743 C>T maps to NM_018961.2 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr11:122671935 C>A maps to NM_032873.4 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr23:118716592 G>A did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr20:44445346 G>C did not map to a codon.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr21:46207990 C>A maps to NM_003343.4 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr7:129479122 G>A maps to NM_003344.2 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:142967458 G>T did not map to a codon.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr23:142967508 C>T did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr17:74392239 G>A maps to NM_022066.3 G926G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr12:109924289 C>T maps to NM_183415.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:109964213 G>T maps to NM_183415.1 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr12:109972418 C>T maps to NM_183415.1 S1013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:10177621 C>T maps to NM_001105562.2 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr1:10231207 C>T maps to NM_001105562.2 R1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr16:4920955 A>G maps to NM_016936.3 Q514Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr23:56591889 C>T did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:56590490 C>T did not map to a codon.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr11:5530317 C>A maps to NM_017481.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr11:5536732 T>C maps to NM_145053.4 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:43309361 C>T maps to NM_174916.2 K986K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr2:170684454 C>T maps to ENST00000442603 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr1:19488940 T>C maps to ENST00000375267 E1643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr1:19499449 A>T maps to ENST00000375267 A1143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:19426953 G>A maps to ENST00000375267 I4379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:19468010 G>T maps to ENST00000375267 S2773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:19488339 C>A maps to ENST00000375267 E1670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr1:19499566 G>A maps to ENST00000375267 I1104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr1:19436958 C>A did not map to a codon.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr1:19487467 G>T maps to ENST00000375267 P1783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3612-01A-01W-0833-10 chr8:103341609 G>A maps to NM_015902.4 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr8:103266661 T>G maps to NM_015902.4 P2756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr14:93681297 C>T maps to NM_175748.3 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:42293102 C>T maps to NM_014233.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr8:59358549 T>C maps to NM_001077619.1 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:196134246 C>A maps to NM_015562.1 G31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:134404927 G>A maps to NM_031432.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr10:13276240 G>A maps to NM_145314.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr4:141483522 G>A maps to NM_021833.4 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:18566205 C>A maps to NM_001040697.1 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:114691814 C>A maps to NM_003358.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:39523017 C>A maps to NM_003359.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr2:128886623 T>C maps to NM_020120.3 N416N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:96506693 G>A maps to NM_020121.3 F1348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:96642325 C>A maps to NM_020121.3 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:96665595 C>A maps to NM_020121.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:234638230 C>T maps to NM_019093.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:70512731 T>G maps to ENST00000514019 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:69434108 C>A maps to NM_001076.2 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr4:70156529 G>A did not map to a codon.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr4:70361242 G>A maps to NM_021139.2 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:36037989 C>A maps to NM_174914.3 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr12:100476886 T>C maps to NM_015054.1 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr12:100476886 T>C maps to NM_015054.1 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr6:150267607 C>G maps to NM_025217.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr12:132405903 T>G maps to NM_003565.2 *1051G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:41977372 C>A maps to NM_017886.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:17750660 G>T maps to ENST00000428389 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:17752350 G>A maps to ENST00000428389 F917F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:35236516 A>G maps to ENST00000396787 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:35295717 C>T maps to ENST00000396787 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr9:35396473 G>A maps to ENST00000396787 E1033E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr15:54542625 C>T maps to ENST00000260323 N1144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr15:54590084 G>A maps to ENST00000260323 K1355K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr15:54306437 G>A maps to ENST00000260323 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr15:54590046 C>T maps to ENST00000260323 R1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr15:54556405 G>A maps to ENST00000260323 K1163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr5:176295868 C>T maps to NM_133369.2 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:73051240 C>T maps to NM_170744.3 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3575-01A-01W-0831-10 chr4:96140171 G>A maps to NM_003728.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:41002621 G>T maps to NM_173561.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr6:41002497 G>A maps to NM_173561.2 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:35584024 G>A maps to ENST00000416672 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr8:35579743 C>T maps to ENST00000416672 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr12:109536403 G>A maps to NM_080911.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:73805933 C>T maps to NM_001080419.1 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr22:24896171 C>T maps to NM_016327.2 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:18974252 C>T maps to ENST00000418384 G880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr10:12039753 T>C maps to NM_015542.2 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr23:118971918 C>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:118971940 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:118972441 C>A did not map to a codon.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr23:118972443 C>T did not map to a codon.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr23:118975080 T>C did not map to a codon.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr19:36164422 C>T maps to NM_007000.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:158978036 G>T maps to NM_001135098.1 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3578-01A-01W-0831-10 chr23:74494246 C>T did not map to a codon.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr16:21968587 T>A maps to NM_003366.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:29698871 G>A maps to NM_006003.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:16134129 G>A maps to NM_001089591.1 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr7:43917672 G>A maps to NM_001077663.1 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:215848532 G>T maps to ENST00000366943 I4240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:215848858 G>A maps to ENST00000366943 L4132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:215953269 G>A maps to ENST00000366943 G3618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:216348704 C>A maps to ENST00000366943 E1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr1:215802378 T>C did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr1:216256827 A>G maps to ENST00000366943 V1756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr1:215963505 A>G maps to ENST00000366943 C3359C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:76721932 G>A maps to NM_003715.2 K564K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:62910999 G>A maps to NM_003368.4 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr16:84806209 C>T maps to NM_005153.2 R688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:84778269 C>T maps to NM_005153.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:47107214 C>A did not map to a codon.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr23:47102926 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:27690730 G>A maps to NM_182488.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:179483557 G>T maps to NM_003940.2 E779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr8:11995189 A>G maps to NM_201402.2 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:119228213 C>A maps to NM_004205.4 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:132620355 G>T maps to NM_001008563.3 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr1:55623037 G>A maps to NM_015306.2 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr1:55613372 A>G maps to NM_015306.2 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr1:55612631 A>G maps to NM_015306.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr21:17250152 A>G maps to ENST00000285681 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:17205775 A>G maps to ENST00000285681 E701E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:17250703 G>A maps to ENST00000285681 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr21:17250150 G>T maps to ENST00000285681 G978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:132159677 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:132160487 T>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:132161837 C>A did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr11:113701631 C>T maps to NM_020886.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3400-01A-01W-0831-10 chr19:57641701 T>C maps to NM_020903.2 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr19:57642199 A>G maps to NM_020903.2 K719K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:23079660 A>C maps to NM_020718.3 G1255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:23085169 C>T maps to NM_020718.3 W736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr17:58365980 A>C maps to NM_032582.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr1:78180332 A>G maps to NM_015017.3 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:61415278 G>A maps to NM_014709.3 V3533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:61441527 G>A maps to NM_014709.3 F2783F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:61546366 G>A maps to NM_014709.3 R1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr2:61436102 T>C maps to NM_014709.3 R2950R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr2:61577701 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:77911745 G>A maps to NM_020798.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:77921073 A>T maps to NM_020798.2 K725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr17:76803073 T>C maps to NM_025090.3 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr2:219418411 G>A maps to NM_020935.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr4:144119067 G>A maps to NM_032557.5 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr4:144135945 C>T maps to NM_032557.5 D939D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr3:49337908 T>C maps to NM_003363.3 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr3:49337908 T>C maps to NM_003363.3 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:99894321 G>A maps to NM_001080481.1 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr4:53468063 G>A maps to NM_022832.3 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:11969589 C>T maps to ENST00000399455 R1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr11:11941794 G>A maps to ENST00000399455 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3878-01A-02W-0899-10 chr1:22021579 C>T maps to NM_032236.5 T954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr1:22033299 C>A maps to NM_032236.5 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr1:22021621 T>C maps to NM_032236.5 K940K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:50835866 C>T maps to ENST00000456636 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:55513911 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:55513973 C>A did not map to a codon.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr23:55514070 C>G did not map to a codon.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr23:55514075 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:75289663 C>A maps to NM_152586.3 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3583-01A-01W-0831-10 chr17:5058850 G>A maps to NM_004505.2 W926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:5041527 G>A maps to NM_004505.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:5073799 G>T maps to NM_004505.2 G1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:9000372 T>C maps to NM_003470.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:9015051 C>A maps to NM_003470.2 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A016-01A-01W-A005-10 chr16:8992420 C>T maps to NM_003470.2 K869K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr16:9014256 G>T maps to NM_003470.2 T190T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G5-6235-01A-11D-1733-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr16:9024252 C>A maps to ENST00000381886 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:50773952 A>G maps to NM_005154.3 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr15:50784957 C>A maps to NM_005154.3 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:40996155 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:41084339 G>T did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr23:41007671 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr24:14887455 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr24:14951945 G>T did not map to a codon.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr6:149285593 C>T maps to NM_005715.2 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr6:149262524 C>T maps to NM_005715.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr23:129060040 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:52604760 C>T maps to NM_021645.5 F607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr13:52604325 T>C maps to NM_021645.5 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr12:101745961 C>T maps to NM_014503.2 L1672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr12:101760431 G>A maps to NM_014503.2 V2074V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:101736729 C>T maps to NM_014503.2 F1436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr12:101764870 C>T maps to NM_014503.2 I2241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:117783831 C>A maps to NM_032334.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:30192429 C>A maps to NM_018428.2 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:30213077 C>T maps to NM_018428.2 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:144768442 C>T maps to NM_007124.2 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:144783843 G>T maps to NM_007124.2 E970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:171678833 G>A maps to NM_003762.4 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr20:56993270 C>T maps to NM_004738.4 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3582-01A-01W-0831-10 chr6:30886628 A>C maps to NM_001167734.1 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr6:30889936 G>A maps to NM_001167734.1 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr1:213125036 C>A maps to NM_024749.3 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:77859261 C>T maps to NM_020927.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr1:108507464 C>T maps to NM_006113.4 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:71159961 G>A maps to NM_012476.2 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr2:71160240 C>T maps to NM_012476.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:154467051 G>C did not map to a codon.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr5:82818042 G>A maps to NM_004385.4 A1306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr5:82834174 G>T maps to NM_004385.4 E1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:82816218 T>G maps to NM_004385.4 T698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:82817253 G>A maps to NM_004385.4 E1043E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:82779402 T>C maps to NM_004385.4 H22H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:82816284 C>T maps to NM_004385.4 V720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:82832869 G>T maps to NM_004385.4 E1350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:82837809 A>G maps to NM_004385.4 P2996P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr5:82785938 G>A maps to NM_004385.4 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr5:82834547 C>A maps to NM_004385.4 S1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:35066723 G>A maps to NM_007126.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:67547157 G>A maps to NM_025054.4 R1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:7811749 G>T did not map to a codon.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr23:8138181 A>G did not map to a codon.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr23:8434340 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr4:177609007 C>A maps to NM_005429.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr3:157099072 G>A maps to NM_001167912.1 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr3:10183611 A>G maps to NM_000551.2 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr3:10188273 T>C maps to NM_000551.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr3:10188207 G>A maps to NM_000551.2 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr3:10188249 C>T maps to NM_000551.2 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr3:10191570 G>A maps to NM_000551.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr3:10191648 A>G maps to NM_000551.2 *214W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:158835800 G>T maps to ENST00000402066 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr9:2651464 G>T maps to NM_003383.3 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr9:2641485 T>C maps to NM_003383.3 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:53770174 G>T maps to NM_173857.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:133004347 G>A maps to NM_004666.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:79908402 G>A maps to ENST00000376646 T1162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:100160232 G>T maps to NM_017890.3 E670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:100168970 G>A maps to NM_017890.3 K736K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:100732574 C>A maps to NM_017890.3 V2245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr8:100454774 T>C maps to NM_017890.3 P1119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr8:100711855 T>C maps to NM_017890.3 S2075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr8:100832313 T>C maps to NM_017890.3 V3011V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr15:62167096 T>C maps to NM_020821.2 R3464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:62169233 G>A maps to NM_020821.2 R3388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:62219468 C>A maps to NM_020821.2 E2113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:62223290 C>T maps to NM_020821.2 S2012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr1:12331174 T>C maps to NM_015378.2 D699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:70916898 C>T maps to NM_004896.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1H8-01A-21D-A152-10 chr11:134114943 C>T maps to NM_052875.3 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:110933822 G>A maps to NM_057180.1 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr11:60901541 G>A maps to NM_017966.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr11:60899363 G>A maps to NM_017966.4 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr15:42479474 T>G maps to ENST00000348544 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr7:38791871 C>T maps to NM_014396.3 Q610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr18:61077590 C>T maps to NM_004869.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:33237314 A>G maps to NM_022553.4 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr6:33232204 G>A maps to NM_022553.4 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:64176172 C>A maps to NM_016516.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr14:97312448 A>C maps to NM_003384.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:58312045 G>T maps to NM_001130480.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:107319438 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:107320326 G>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:118511729 G>A maps to NM_019086.5 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr12:118520061 G>C maps to NM_019086.5 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:124620808 G>T maps to NM_014312.3 Y76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr23:65242692 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:54617552 C>A maps to ENST00000404951 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:25056897 C>A maps to NM_014588.4 *366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr1:117699343 G>A maps to NM_024626.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr17:26695959 G>A maps to NM_000638.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:22163837 G>A maps to NM_173615.3 A1096A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:124006948 C>A maps to NM_014622.4 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:124016639 C>A maps to NM_014622.4 I783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr11:61039218 G>A maps to NM_152718.2 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:6105338 C>T maps to NM_000552.3 Q1964Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:6128533 C>T maps to NM_000552.3 A1350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:6135134 C>T maps to NM_000552.3 E1015E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:6167021 C>T maps to NM_000552.3 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr12:6128299 G>A maps to NM_000552.3 I1428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr1:27744827 A>G maps to NM_006990.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr1:27739085 A>G maps to NM_006990.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr13:27259960 C>T maps to NM_006646.5 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:123336702 C>A maps to NM_003941.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:74687163 C>T maps to ENST00000393972 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr17:73847705 G>A maps to NM_012478.3 N37N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr13:41639400 G>A maps to NM_007187.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:70880998 C>T maps to NM_022479.1 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:73098101 T>C maps to ENST00000423497 Y18Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:224760339 G>A maps to NM_020830.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:85741251 G>T maps to NM_014991.4 S560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:55448378 G>A maps to NM_007086.3 R648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr10:122633432 C>A maps to NM_018117.11 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr10:122649474 T>G maps to NM_018117.11 L766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:122648615 C>T maps to NM_018117.11 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr23:48457273 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:48460468 C>A did not map to a codon.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:48457785 C>T did not map to a codon.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr23:48460236 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:177093608 T>G maps to NM_170710.4 Y1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr4:177069340 C>T maps to NM_170710.4 H608H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:39255633 C>A maps to NM_025132.3 I995I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr14:100848013 C>T maps to NM_001161476.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:100847302 G>A maps to NM_001161476.1 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:100847677 C>A maps to NM_001161476.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:170062509 C>T maps to NM_182552.3 Q305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:128471175 G>A maps to NM_018383.4 R1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3909-01A-01W-1073-09 chr5:110428045 G>T maps to NM_139281.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr5:110440032 C>T maps to NM_139281.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr21:44293683 T>C maps to NM_018669.4 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:76734153 G>A maps to NM_018268.2 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:117527156 C>A did not map to a codon.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr23:117576245 A>G did not map to a codon.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr3:167248969 G>A maps to NM_178824.3 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3896-01A-01W-1073-09 chr3:167293921 A>G maps to NM_178824.3 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr3:167322161 A>G maps to NM_178824.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:113115487 C>T maps to NM_001164496.1 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:196288060 C>A maps to NM_182627.1 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr16:74908247 G>A maps to NM_030581.3 H928H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr3:49052279 T>C maps to NM_018031.3 T1005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr7:158672382 C>T maps to NM_018051.4 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr7:158672482 C>A maps to NM_018051.4 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3575-01A-01W-0831-10 chr1:85583460 G>A maps to NM_145172.3 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr1:241959599 C>T maps to NM_144625.4 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:241946639 G>T maps to NM_144625.4 E878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr1:241912879 G>C maps to NM_144625.4 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr1:241834419 G>A maps to NM_144625.4 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:228750095 G>T maps to NM_178821.1 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:54358451 C>T maps to NM_015285.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:37727009 C>T maps to NM_018034.2 H580H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:53957938 C>A maps to NM_182758.2 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr2:190313192 C>T maps to NM_032168.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:67306289 T>C maps to NM_024763.4 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr7:151093101 G>A maps to ENST00000426624 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr19:33639805 C>T maps to NM_173479.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:33639703 C>T maps to NM_173479.3 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:64066021 A>G maps to NM_080666.2 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr15:90255297 C>A maps to NM_020212.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3580-01A-01W-0831-10 chr1:27622878 C>A maps to ENST00000319394 C312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr1:27609909 G>A maps to ENST00000319394 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr7:141408824 C>T maps to NM_001105558.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:44258514 A>G maps to NM_080753.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr20:44166704 G>A maps to ENST00000396669 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr16:681283 C>T maps to NM_053284.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:175450268 C>T maps to NM_003387.4 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr2:175436914 C>A maps to NM_003387.4 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr7:29923976 T>C maps to NM_001080529.1 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr7:29928973 G>A maps to NM_001080529.1 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:66447015 G>A maps to NM_017983.5 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr17:66429643 C>A maps to NM_017983.5 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr12:1017948 G>A maps to NM_001184985.1 R2640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr12:970297 A>G maps to NM_001184985.1 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr12:994295 T>G maps to NM_001184985.1 V1702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-3913-01A-02W-1073-09 chr23:54263729 G>A did not map to a codon.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr23:54334412 G>A did not map to a codon.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr23:54265375 T>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:54337634 A>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:54263615 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:54278090 C>A did not map to a codon.
Sequencing variant TCGA-AG-A00C-01A-01W-A005-10 chr23:54275518 G>T did not map to a codon.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr23:54328282 G>T did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:54259350 A>C did not map to a codon.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr23:54259357 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:49362093 C>A maps to NM_003394.3 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3594-01A-02W-0831-10 chr11:75898129 C>T maps to NM_004626.2 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:113057613 C>T maps to NM_024494.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr17:44846105 C>T maps to NM_030753.3 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr1:228210496 C>T maps to ENST00000366753 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:228238549 C>T maps to ENST00000366753 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr12:1755210 C>T maps to NM_032642.2 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr1:228112048 G>A maps to NM_003395.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:7606152 C>T maps to NM_018081.2 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:30948014 G>T maps to NM_000553.4 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr12:118490149 G>A maps to ENST00000441406 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr12:108604020 C>T maps to ENST00000261400 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr12:108603966 C>T maps to ENST00000261400 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2692-01A-01W-0831-10 chr11:32421574 G>A maps to NM_024426.4 Y339Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr11:32410609 C>T maps to NM_024426.4 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:160160024 C>T maps to NM_004906.3 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr5:167894877 C>T maps to NM_001161661.1 Q1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:184233555 C>A maps to ENST00000448232 V1173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr4:184190298 C>A maps to ENST00000448232 R795R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr23:10084545 A>G did not map to a codon.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr23:10098061 A>G did not map to a codon.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr23:10094279 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:10085338 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:10047832 G>T did not map to a codon.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr23:10106965 C>A did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:10058884 G>A did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:78420806 C>T maps to NM_016373.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3581-01A-01W-0831-10 chr16:69905709 G>A maps to NM_007014.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:69965464 C>T maps to NM_007014.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr23:52891652 C>T did not map to a codon.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr2:31588406 G>A maps to NM_000379.3 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr23:2729381 A>G did not map to a codon.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr23:2729382 T>C did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr3:39227195 C>T maps to NM_194293.2 P1247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr3:39229115 G>A maps to NM_194293.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:168096387 T>C maps to NM_152381.5 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:168103001 T>C maps to NM_152381.5 G1700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:168115185 C>T maps to ENST00000420519 N743N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr2:168100235 G>A maps to NM_152381.5 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:167760390 C>T maps to NM_152381.5 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:168108197 G>A maps to NM_152381.5 S3432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:168106623 C>T maps to NM_152381.5 Q2908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr2:168100236 T>C maps to NM_152381.5 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr2:168100203 A>C maps to NM_152381.5 R768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:37587405 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:17264658 T>G maps to NM_175878.3 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr8:56436503 C>T maps to NM_052898.1 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:10782207 G>A maps to NM_173683.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr8:10756076 C>T maps to NM_173683.3 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr20:30584380 G>A maps to NM_001011718.1 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:71593400 A>G maps to NM_001011720.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:100169473 G>T did not map to a codon.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr23:100169627 C>T did not map to a codon.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr23:100177922 C>G did not map to a codon.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr23:128888544 A>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:128886228 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:61721178 G>T maps to NM_003400.3 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr13:21357983 A>G maps to NM_022459.4 D1111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:43516062 C>T maps to NM_020750.2 Q665Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:43521126 G>A maps to NM_020750.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:28109918 G>A maps to NM_015171.2 N1106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr16:28112886 G>A maps to NM_015171.2 V1056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr12:64812699 C>T maps to NM_007235.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:180832952 C>T maps to NM_004736.3 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr3:142151540 A>G maps to NM_019001.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:21314217 G>T maps to NM_012255.3 G299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:74618253 G>A maps to NM_182969.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr17:48437546 T>C maps to NM_022167.2 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:33248101 G>A maps to NM_003680.3 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr1:43162404 A>G maps to NM_004559.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr22:21984204 A>G maps to NM_001017964.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:69759618 C>T maps to NM_006530.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr18:746047 C>T maps to NM_005433.3 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr5:143545032 A>T maps to NM_030799.7 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr14:75282965 C>T maps to NM_019589.2 R1855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:75247238 G>A maps to NM_019589.2 Q414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr14:75266068 C>T maps to NM_019589.2 R1357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:61834778 G>A maps to NM_017798.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:61834907 C>T maps to NM_017798.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:1264465 C>T maps to NM_006761.4 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr17:1264492 A>G maps to NM_006761.4 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr22:32352206 C>T maps to NM_003405.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr22:32352208 A>G maps to NM_003405.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:155630671 C>T maps to ENST00000368339 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3602-01A-02W-0833-10 chr23:21874923 C>G did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr23:21875099 G>A did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr23:21874909 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:174055769 C>A maps to NM_016653.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr7:100334191 C>T maps to ENST00000349350 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr7:100361685 C>T maps to ENST00000349350 F1378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:48494992 T>G maps to NM_175619.1 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:2407652 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr22:50277399 T>C maps to NM_014838.2 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr22:50279380 C>T maps to NM_014838.2 Q691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:81411784 G>A maps to NM_001105539.1 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:81412186 G>A maps to NM_001105539.1 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:101370200 C>A maps to NM_014415.3 E991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr6:31868569 A>G maps to NM_181842.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:113934841 G>T maps to NM_001018011.1 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:114112955 G>A maps to NM_001018011.1 Q507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:151694682 G>A maps to NM_020861.1 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr3:114069919 G>A maps to NM_001164342.1 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:109788856 G>A maps to NM_014797.2 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr19:36206337 C>T maps to NM_014383.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr1:197168856 G>A maps to NM_194314.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:197150124 G>A maps to NM_194314.2 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:197169588 T>C maps to NM_194314.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr9:129594889 C>T maps to NM_014007.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:62422077 C>T maps to NM_025224.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr20:62378348 C>T maps to NM_025224.2 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr20:62378363 C>T maps to NM_025224.2 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr1:6648898 C>T maps to NM_005341.2 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:4054675 C>T maps to NM_015898.2 W185*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AG-A014-01A-02W-A00K-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:64719097 C>A did not map to a codon.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr23:64709235 T>G did not map to a codon.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr23:64722696 T>C did not map to a codon.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr13:46541917 C>A maps to ENST00000242848 E1348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr13:46542897 G>A maps to ENST00000242848 R1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr13:46559476 G>A maps to ENST00000242848 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:88690401 A>G maps to ENST00000452588 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr8:144550818 A>G maps to NM_015117.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr2:113074147 A>G maps to NM_198581.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr2:112991732 T>C maps to NM_032494.2 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:138764330 G>A maps to ENST00000464606 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:64138961 C>T did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:117959860 G>A did not map to a codon.
Sequencing variant TCGA-AG-3893-01A-01W-1073-09 chr23:111698286 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:111698216 C>A did not map to a codon.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr23:111698392 C>A did not map to a codon.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr23:77913212 A>C did not map to a codon.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr23:77912907 C>A did not map to a codon.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr9:88937964 G>A maps to NM_024617.3 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr9:88937964 G>T maps to NM_024617.3 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr9:37304240 C>T maps to NM_032226.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:122966081 G>T maps to NM_017612.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr7:100013970 C>T maps to NM_017984.3 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3587-01A-01W-0831-10 chr3:28476707 C>G maps to NM_001040432.1 S147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:28557062 C>T maps to NM_001040432.1 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr2:207172206 C>T maps to NM_020923.1 H985H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:207170017 G>T maps to NM_020923.1 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:207170662 G>T maps to NM_020923.1 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:207172438 G>T maps to NM_020923.1 E1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr2:207162064 G>T maps to NM_020923.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6622-01A-11D-1826-10 chr2:207174441 G>A maps to NM_020923.1 S1730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6681-01A-11D-1826-10 chr5:843814 C>T maps to NM_024786.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr6:158066849 C>G maps to NM_024630.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:74644553 A>C did not map to a codon.
Sequencing variant TCGA-DT-5265-01A-21D-1826-10 chr23:74742740 A>G did not map to a codon.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr23:74698818 A>G did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr3:195936248 C>A maps to NM_001039617.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:113667697 G>T maps to NM_173570.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:6621308 G>A maps to NM_018106.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr22:20134738 C>T maps to NM_001185024.1 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr22:20132829 C>T maps to NM_013373.3 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:128957703 G>T did not map to a codon.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr10:31809186 A>G maps to NM_001174096.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr10:31809579 A>G maps to NM_001174096.1 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr10:31809186 A>G maps to NM_001174096.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr2:145161613 G>A maps to NM_014795.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr2:220072091 C>T maps to NM_138802.1 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:135612792 G>A maps to NM_020863.3 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr8:135521986 G>A maps to NM_020863.3 R1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr12:72028526 C>A maps to NM_144982.4 E773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:72993585 G>A maps to NM_006885.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6655-01A-11D-1826-10 chr8:77766281 C>T maps to NM_024721.4 N2375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr8:77616715 C>T maps to NM_024721.4 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr8:77768156 C>T maps to NM_024721.4 G3000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:77766072 C>T maps to NM_024721.4 R2306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:77767841 C>T maps to NM_024721.4 N2895N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:77768312 G>A maps to NM_024721.4 P3052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr8:77761899 G>A maps to NM_024721.4 T1266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr8:77617810 T>A maps to NM_024721.4 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr8:77765318 T>C maps to NM_024721.4 P2054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr8:77766387 G>T maps to NM_024721.4 E2411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6508-01A-11D-1733-10 chr8:77767925 T>C maps to NM_024721.4 S2923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr19:44831651 T>C maps to ENST00000412927 E903E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr19:44831843 T>A maps to ENST00000412927 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:36832235 G>A maps to NM_020917.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3575-01A-01W-0831-10 chr19:57066699 C>A maps to NM_020828.1 S849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:57065486 G>T maps to NM_020828.1 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:4995231 G>T maps to NM_153018.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:115805940 T>C maps to NM_003408.1 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:115806153 T>C maps to NM_003408.1 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:50769233 G>T maps to NM_018197.2 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr20:50701143 G>A maps to NM_199427.2 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr19:36884212 G>A maps to NM_133466.2 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:58385067 C>A maps to NM_053023.4 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr16:88594494 C>T maps to NM_153813.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3902-01A-01W-1073-09 chr8:106815013 C>T maps to NM_012082.3 R902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:106815060 G>A maps to NM_012082.3 E917E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A014-01A-02W-A00K-09 chr19:3823261 G>T maps to NM_015174.1 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr23:24225593 T>G did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr14:73441631 G>A maps to NM_021260.2 N614N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr3:15126515 T>A maps to NM_022340.2 K143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:52704079 G>T maps to NM_004799.2 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:62340507 G>A maps to NM_032527.4 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:39831593 C>A maps to NM_015035.3 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:57647397 C>A maps to NM_052882.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr19:57647191 G>A maps to NM_052882.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr16:25258336 G>A maps to NM_001012981.4 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr6:28333753 C>T maps to NM_024493.2 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3574-01A-01W-0831-10 chr23:101138644 C>A did not map to a codon.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:101138612 G>T did not map to a codon.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr23:101138643 T>A did not map to a codon.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr5:140084143 G>A maps to NM_144723.1 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr3:178742840 C>T maps to NM_022470.3 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr3:178742983 T>A maps to NM_022470.3 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:40683096 G>A maps to NM_024645.2 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr13:20638636 T>C maps to NM_001190965.1 V1028V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr13:20660012 C>T maps to NM_001190965.1 C1331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:20656205 C>T maps to NM_001190965.1 Y1168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr13:20657132 C>T maps to NM_001190965.1 R1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:70464708 G>T did not map to a codon.
Sequencing variant TCGA-AG-3599-01A-02W-0833-10 chr1:35855605 C>T maps to NM_005095.2 R832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr3:50382647 A>G maps to NM_015896.2 H36H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:42902187 T>G maps to NM_032257.4 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:42902136 G>A maps to NM_032257.4 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr20:45850062 G>A maps to ENST00000471951 Q1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:19788767 G>A maps to NM_033204.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:64167710 T>G maps to NM_016220.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3726-01A-02W-0899-10 chr19:9677158 A>T maps to NM_001008727.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr1:247320092 A>G maps to NM_003431.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr20:18296625 T>A maps to ENST00000401790 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr20:18296628 G>C maps to ENST00000401790 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr19:58131714 A>G maps to NM_003435.3 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:58579255 C>T maps to NM_007134.1 C492C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:12297658 C>T maps to NM_003437.3 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr7:64292096 A>C maps to ENST00000307355 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:19822282 G>A maps to NM_021030.2 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:19822534 G>A maps to NM_021030.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr3:125032391 T>C maps to NM_021964.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EF-5830-01A-01D-1657-10 chr3:125032364 T>C maps to NM_021964.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:58213364 C>A maps to NM_001085384.1 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:47272615 G>T did not map to a codon.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr23:47271999 C>A did not map to a codon.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr19:53572103 T>A maps to NM_001102603.1 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:53572789 G>A maps to NM_001102603.1 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:44609842 G>A maps to NM_018651.2 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:44611915 C>A maps to NM_018651.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:44612831 G>T maps to NM_018651.2 E744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr19:52090210 A>T maps to NM_007147.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:52090273 T>C maps to NM_007147.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:44981206 C>T maps to NM_013256.3 Q497Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:47836136 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:47836689 C>T did not map to a codon.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr23:47836340 G>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:27419905 C>A maps to NM_007149.2 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:104171634 C>T maps to NM_003452.2 R529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:44673978 C>T maps to NM_006991.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:22157349 T>C maps to NM_007153.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:22155720 G>T maps to NM_007153.3 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3609-01A-02W-0833-10 chr20:52198291 C>T maps to NM_006526.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr20:52199014 A>G maps to NM_006526.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr10:45498856 C>G maps to NM_006963.4 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:44470320 G>T maps to NM_013359.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:44470517 G>A maps to NM_013359.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:44536219 C>T maps to NM_001129996.1 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:44536775 G>T maps to NM_001129996.1 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr19:44536078 A>G maps to NM_001129996.1 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:44570385 G>A maps to NM_013361.4 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:44611395 G>A maps to NM_013398.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DF-01A-11D-A152-10 chr19:44611668 A>G maps to NM_013398.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr19:44934172 T>C maps to NM_014518.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:44778459 G>A maps to NM_181756.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:44793148 C>A maps to NM_004234.4 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:44052378 A>C maps to NM_001099284.1 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:44053362 G>A maps to NM_001099284.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:145948333 G>A maps to NM_138367.1 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:145948710 C>A maps to NM_138367.1 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr19:20002520 G>A maps to ENST00000427401 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:20002856 A>C maps to ENST00000427401 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:24289407 G>A maps to NM_203282.2 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:24310307 C>A maps to NM_203282.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr12:133764549 G>A maps to NM_001165881.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr19:58697119 G>A maps to NM_133502.1 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr7:111936290 A>G maps to NM_021994.2 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:53303228 T>G maps to NM_006969.3 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr23:129377604 A>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:129339305 C>T did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:129361683 T>G did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:129380860 C>T did not map to a codon.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr23:129394414 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:129339344 G>T did not map to a codon.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr23:129364599 G>C did not map to a codon.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr23:129364659 A>T did not map to a codon.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr23:129377581 A>T did not map to a codon.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr23:129377604 A>G did not map to a codon.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr15:56959016 G>A maps to NM_017661.2 N571N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:44891986 G>A maps to NM_152354.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:16456562 G>T maps to NM_020653.2 S298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A032-01A-01W-A00E-09 chr6:87970069 C>T maps to NM_015021.1 H2241H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr6:87928402 G>A maps to NM_015021.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr6:87968045 T>C maps to NM_015021.1 L1567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr7:99662464 C>T maps to NM_017715.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9267966 C>T maps to NM_020933.4 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr6:43322830 A>T maps to NM_014345.2 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr1:90473059 C>T maps to NM_182976.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:90484306 G>T maps to NM_182976.2 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:90493068 G>T maps to NM_182976.2 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3885-01A-01W-0899-10 chr19:58639352 G>A maps to NM_024620.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:58640440 C>A maps to NM_024620.3 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:54079952 T>C maps to NM_001079907.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:14826243 G>T maps to NM_032433.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6644-01A-21D-1826-10 chr20:45130462 A>G maps to NM_018102.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2693-01A-02D-1733-10 chr10:38345269 C>T maps to NM_006954.1 Q740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr8:146003459 G>A maps to NM_030580.3 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr20:32379262 T>C maps to ENST00000375200 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:53644384 C>A maps to NM_001172674.1 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:178309989 T>C maps to NM_058230.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:64148202 G>A maps to NM_199451.2 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr5:71756657 G>A maps to NM_152625.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A008-01A-01W-A005-10 chr5:71757092 C>T maps to NM_152625.1 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3882-01A-01W-0899-10 chr19:37100905 G>A maps to NM_032825.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:37118263 G>T maps to NM_032825.3 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr2:180348095 C>T maps to NM_152520.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr3:21465508 C>T maps to NM_024697.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:27368191 G>T maps to NM_001076781.1 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr6:27368952 G>A maps to NM_001076781.1 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr18:32954209 G>T maps to NM_145756.2 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:44378170 T>C maps to ENST00000324394 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:44377348 G>A maps to ENST00000324394 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr18:72775976 C>T maps to NM_017757.2 D2100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr18:72775640 C>T maps to NM_017757.2 A1988A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:72343145 G>A maps to NM_017757.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr18:72592992 C>T maps to NM_017757.2 G1682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:47307475 G>A did not map to a codon.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr23:47308277 C>T did not map to a codon.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr23:47308220 T>C did not map to a codon.
Sequencing variant TCGA-F5-6812-01A-11D-1826-10 chr23:47315382 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:53612634 G>A maps to NM_001164309.1 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6155-01A-11D-1657-10 chr19:53612682 T>C maps to NM_001164309.1 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:58420012 C>A maps to NM_152475.2 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:49671151 G>A maps to NM_015069.2 C637C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3901-01A-01W-1073-09 chr7:148815401 C>T maps to NM_001001661.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr7:148801597 G>A maps to NM_001001661.2 N455N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:12128713 G>A maps to NM_001080411.1 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:12383304 C>A maps to NM_001164276.1 E637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:12541805 C>A maps to NM_005815.4 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:134481163 G>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:134494639 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:134494719 C>T did not map to a codon.
Sequencing variant TCGA-AG-A015-01A-01W-A005-10 chr23:134481165 A>T did not map to a codon.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr23:134493888 A>G did not map to a codon.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr23:134493888 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr5:178391962 C>A maps to NM_182594.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:57802832 C>T maps to NM_006635.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr19:37129788 T>C maps to NM_153257.2 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6683-01A-11D-1826-10 chr19:37130438 C>A maps to NM_153257.2 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr9:109689972 G>A maps to NM_021224.4 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:109690980 C>T maps to NM_021224.4 Y1596Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02G-01A-01W-A00E-09 chr9:109694776 C>T maps to NM_021224.4 R2021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:57088466 G>T maps to NM_001001668.3 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr7:57188620 A>T maps to NM_033273.1 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr9:114304372 G>A maps to NM_133464.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr19:12691347 G>C maps to NM_020714.2 S514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:12691931 C>T maps to NM_020714.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr19:21605923 C>T maps to NM_001076678.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr19:21606036 C>T maps to NM_001076678.2 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr19:21606055 C>T maps to NM_001076678.2 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr19:21606461 C>G maps to NM_001076678.2 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr19:21606545 C>G maps to NM_001076678.2 S362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3600-01A-01W-0833-10 chr3:44763241 G>A maps to NM_033210.4 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:44762969 C>T maps to NM_033210.4 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:19905705 T>C maps to NM_001099269.2 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr19:32851434 A>G maps to NM_014910.4 Q757Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:27844027 C>T maps to NM_032434.2 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr10:97920131 C>A maps to NM_014803.3 I1351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr4:10447325 C>A maps to NM_053042.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr18:22804542 C>A maps to NM_015461.2 T1113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr18:22804989 G>A maps to NM_015461.2 C964C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:52919044 C>T maps to NM_032423.2 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:58117300 C>A maps to NM_020880.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:58118543 G>T maps to NM_020880.3 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3598-01A-01W-0833-10 chr18:56585938 C>T maps to NM_018181.4 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr19:30934549 C>T maps to NM_014717.1 N27N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr19:30934957 C>T maps to NM_014717.1 C163C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4005-01A-01W-1073-09 chr19:31039804 C>T maps to NM_014717.1 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6643-01A-11D-1826-10 chr19:30934885 C>T maps to NM_014717.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr19:30935437 C>T maps to NM_014717.1 H323H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:58772548 G>T maps to NM_014480.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4015-01A-01W-1073-09 chr19:58772535 C>T maps to NM_014480.2 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:58773780 C>A maps to NM_014480.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr19:58773426 G>A maps to NM_014480.2 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3731-01A-11D-1733-10 chr19:57889114 A>G maps to NM_173631.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5337-01A-01D-1657-10 chr19:57889114 A>G maps to NM_173631.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr19:58058833 T>A maps to NM_001039654.1 K219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3593-01A-01W-0831-10 chr19:58319946 G>A maps to NM_024762.3 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:2853044 C>T maps to NM_152791.4 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:2853296 C>T maps to NM_152791.4 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:2878236 C>T maps to NM_024967.1 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr19:2878137 G>A maps to NM_024967.1 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:8931928 C>T maps to NM_144693.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:9577833 C>A maps to NM_152476.2 E597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:36685204 G>A maps to ENST00000355114 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:37427731 C>T maps to NM_198539.2 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6549-01A-11D-1826-10 chr19:37441551 G>A maps to NM_198539.2 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A0XA-01A-11D-A152-10 chr19:37440552 A>G maps to NM_198539.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:37904584 A>C maps to NM_152484.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:37903603 A>G maps to NM_152484.2 H652H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr19:37916781 T>A maps to NM_152484.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:37975754 G>T maps to NM_144694.1 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A026-01A-32W-A096-10 chr19:37975201 C>G maps to NM_144694.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:38230297 T>A maps to NM_001172690.1 K365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr19:53014179 G>A maps to NM_001099694.1 K182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:56895840 T>C maps to NM_144690.1 E315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3578-01A-01W-0831-10 chr19:37643431 T>A maps to ENST00000356958 K457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:37677555 C>A maps to NM_152279.3 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr19:37678048 A>G maps to NM_152279.3 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr19:58290194 A>G maps to NM_017652.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr16:3490873 C>A maps to NM_152457.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:35250484 G>A maps to NM_001007248.2 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr19:35250004 T>C maps to NM_001007248.2 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:38200708 G>A maps to NM_032689.4 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr19:38190767 G>A maps to NM_032689.4 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3586-01A-02W-0831-10 chr5:123984477 G>T maps to NM_020747.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3887-01A-01W-1073-09 chr5:123980113 G>A maps to NM_020747.2 R1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:52869599 G>A maps to NM_001161425.1 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G5-6641-01A-11D-1826-10 chr19:52869755 C>T maps to NM_001161425.1 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:52519386 G>A maps to NM_025040.3 C488C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr9:116811399 C>T maps to ENST00000374126 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6464-01A-11D-1733-10 chr9:116779062 C>A maps to ENST00000374126 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:40574076 C>T maps to NM_001098414.1 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:12256527 G>A maps to ENST00000439556 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:11728452 C>T maps to NM_145295.3 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6620-01A-11D-1826-10 chr19:55994761 G>A maps to NM_033113.2 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3881-01A-01W-0899-10 chr16:30793956 C>T maps to NM_001080417.1 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr23:47918883 T>C did not map to a codon.
Sequencing variant TCGA-AG-3898-01A-01W-1073-09 chr23:47918363 A>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:47918226 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:71650055 G>T maps to NM_014497.3 E1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr2:71654053 A>G maps to NM_014497.3 E1685E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A020-01A-21W-A096-10 chr2:71607378 G>T maps to NM_014497.3 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:91403182 C>A maps to NM_201269.1 E1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:91404287 C>A maps to NM_201269.1 E875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:91404495 A>G maps to NM_201269.1 R805R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2691-01A-01W-0831-10 chr23:22292315 G>T did not map to a codon.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr23:22292067 C>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:22291956 G>A did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:22291956 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr23:22292290 C>T did not map to a codon.
Sequencing variant TCGA-G5-6235-01A-11D-1733-10 chr23:22291523 A>T did not map to a codon.
Sequencing variant TCGA-AF-4110-01A-02D-1733-10 chr16:31091793 G>A maps to NM_014699.3 L1383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr19:52399806 G>A maps to NM_023074.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-2687-01A-02D-1733-10 chr17:47394439 A>G maps to NM_014897.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DG-01A-11D-A152-10 chr9:40773968 C>A maps to NM_033160.5 G436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:44636560 C>T maps to NM_173658.1 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:42956254 T>C maps to NM_001134656.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A011-01A-01W-A00K-09 chr19:53668665 T>C maps to NM_024733.3 S359S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AG-A02N-01A-11W-A096-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr16:31073318 G>A maps to ENST00000417110 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:58231910 C>A maps to ENST00000335820 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:58232189 C>A maps to ENST00000335820 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:58232504 C>A maps to ENST00000335820 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:46332294 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:46359513 T>G did not map to a codon.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr23:46359622 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:46360480 G>A did not map to a codon.
Sequencing variant TCGA-AG-3732-01A-11D-1657-10 chr19:23837044 A>G maps to NM_138330.2 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:23845959 C>A maps to NM_138330.2 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:22363077 C>A maps to NM_001001411.2 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5917-01A-11D-1657-10 chr19:22363447 A>T maps to NM_001001411.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CL-5918-01A-11D-1657-10 chr19:22363648 G>T maps to NM_001001411.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6160-01A-11D-1657-10 chr19:22363609 A>G maps to NM_001001411.2 H303H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:53741151 C>T maps to NM_182609.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:227842251 G>T maps to NM_178549.3 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr1:227842535 A>G maps to NM_178549.3 Q250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr7:63721252 C>T maps to NM_153363.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:23928123 A>C maps to NM_138286.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6624-01C-11D-1826-10 chr16:30616165 G>A maps to NM_138447.1 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:120165627 G>A maps to NM_001080470.1 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A036-01A-12W-A096-10 chr8:146067307 C>T maps to ENST00000446747 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr22:24086664 C>T maps to NM_021916.2 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:53086656 C>T maps to NM_001172655.1 R515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6621-01A-11D-1826-10 chr19:53085917 C>T maps to NM_001172655.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr8:102212325 C>A did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:12575906 C>A maps to ENST00000428311 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:12577564 C>A maps to ENST00000428311 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr15:90611709 C>T maps to NM_198526.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr23:84526277 T>C did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:56006915 T>C maps to NM_182633.1 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr19:21299950 C>T maps to NM_182515.3 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr19:21300527 C>G maps to NM_182515.3 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6158-01A-11D-1657-10 chr19:21300695 C>G maps to NM_182515.3 S409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:80789199 G>A maps to NM_024702.2 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr17:80789310 G>A maps to NM_024702.2 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:134421113 C>A did not map to a codon.
Sequencing variant TCGA-DC-6682-01A-11D-1826-10 chr23:134421515 C>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:30569162 G>A maps to NM_033410.3 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:58018528 G>T maps to NM_198542.1 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr7:150093655 G>A maps to NM_173680.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:40581459 T>A maps to NM_001142577.1 K298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-6157-01A-11D-1657-10 chr19:40553360 C>T maps to NM_001005851.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:38160220 C>A maps to NM_152605.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:38160304 C>A maps to NM_152605.3 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AH-6544-01A-11D-1826-10 chr9:99581836 C>T maps to NM_001001662.1 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:37310281 G>A maps to NM_206894.2 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:37310402 A>C maps to NM_206894.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:38028457 G>T maps to NM_001013659.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr19:58805992 C>T maps to NM_021089.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A00Y-01A-02W-A005-10 chr3:113955261 T>C maps to NM_007136.3 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DY-A1DD-01A-21D-A152-10 chr3:113955428 C>A maps to NM_007136.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6136-01A-11D-1826-10 chr7:127017374 G>A maps to NM_176814.3 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr7:127014459 A>G maps to NM_176814.3 H310H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:127026119 G>A maps to NM_176814.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4001-01A-02W-1073-09 chr2:185800806 C>A maps to NM_194250.1 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6571-01A-12D-1826-10 chr2:185803695 C>A maps to NM_194250.1 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr7:88847566 G>A maps to NM_181646.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr7:88962857 C>T maps to NM_181646.2 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A01W-01A-21W-A096-10 chr7:88964179 T>C maps to NM_181646.2 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr7:88964350 C>T maps to NM_181646.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-5654-01A-01D-1657-10 chr19:53057341 A>G maps to NM_001039886.3 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AF-6672-01A-11D-1826-10 chr23:47775002 T>C did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr23:47775513 G>T did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:47775201 T>G did not map to a codon.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr4:146807010 C>A maps to ENST00000508784 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr13:115090657 T>C maps to NM_032436.2 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:37382999 C>T maps to NM_001171979.1 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:57766268 G>A maps to NM_178457.1 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:57829672 G>T maps to NM_178457.1 E1637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DC-5869-01A-01D-1657-10 chr20:57767042 G>C maps to NM_178457.1 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6811-01A-11D-1826-10 chr20:57766733 C>T maps to NM_178457.1 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02X-01A-01W-A00E-09 chr14:102792653 C>T maps to NM_018335.3 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-4007-01A-01W-1073-09 chr19:9868339 C>T maps to NM_001077624.1 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:12155890 C>A maps to NM_001080404.1 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:23543124 C>A maps to NM_003430.2 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr19:23545419 G>A maps to NM_003430.2 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:22574542 A>C maps to NM_001098626.1 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:22585635 C>A maps to NM_001098626.1 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:22586278 G>A maps to NM_001098626.1 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr19:22941341 C>A maps to ENST00000397104 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3611-01A-01W-0833-10 chr20:47865966 C>T maps to NM_021035.2 S1198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr20:47881339 G>A maps to NM_021035.2 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3727-01A-01W-0899-10 chr11:64883978 C>A maps to NM_014205.2 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr1:86171988 G>A maps to NM_017953.3 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:86171988 G>A maps to NM_017953.3 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:86173447 C>A maps to NM_017953.3 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6465-01A-11D-1733-10 chr19:5455582 G>A maps to NM_181710.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3883-01A-02W-0899-10 chr11:60640727 C>T maps to NM_207341.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr11:60638577 C>A maps to NM_207341.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr16:21210906 G>T maps to NM_003460.1 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3742-01A-11D-1657-10 chr7:76062904 G>A maps to NM_001110354.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6507-01A-11D-1733-10 chr1:238053842 C>T maps to NM_021186.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr7:50097723 A>C maps to NM_007009.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr3:102176649 G>T maps to NM_175056.1 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6510-01A-11D-1733-10 chr3:102187822 T>C maps to NM_175056.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr2:135985517 G>T maps to NM_032143.2 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EI-6506-01A-11D-1733-10 chr23:15821891 G>A did not map to a codon.
Sequencing variant TCGA-DY-A1DC-01A-31D-A152-10 chr19:58564800 C>A maps to NM_182572.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr6:28093466 C>T maps to NM_025231.1 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr15:85164940 C>T maps to NM_181877.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr1:33960167 G>T maps to NM_145238.3 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr19:58850604 T>G maps to NM_181846.2 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3605-01A-01W-0833-10 chr19:56733294 G>C maps to NM_024303.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr2:187693199 G>T maps to NM_182521.2 C471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr11:113609027 G>A maps to NM_004724.2 D614D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CI-6619-01B-11D-1826-10 chr11:113608341 T>C maps to NM_004724.2 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A002-01A-01W-A00K-09 chr23:57935659 T>G did not map to a codon.
Sequencing variant TCGA-AG-A01L-01A-01W-A00K-09 chr23:57935199 T>G did not map to a codon.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr23:57619605 G>A did not map to a codon.
Sequencing variant TCGA-AG-3892-01A-01W-1073-09 chr17:3962534 G>A maps to NM_015113.3 R1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AG-A02N-01A-11W-A096-10 chr17:3917691 G>A maps to NM_015113.3 R2755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F5-6813-01A-11D-1826-10 chr17:3935537 T>C maps to NM_015113.3 G2258G. Only missense variants will be evaluated by CHASM.
